Climate change and biodiversity loss are affecting people and nature and land management will be key to ameliorating the effects of both. Our client a nature conservation charity is seeking a talented conservation scientist with good GIS and analytical skills to join projects examining the spatial conservation and climate change mitigation consequences of land management and restoration in the UK and Europe. Conservation Scientist - Natural Climate Solutions Ref: A Location: Sandy, Bedfordshire or Cambridge Salary: £25,643 to £27,585 per annum. Applicants should expect under normal circumstances to receive an offer at the bottom of the advertised range. Hours: Full Time Contract: 14 month Fixed Term contract You will join a small team working alongside ecological and practical conservationists. You will have a good working knowledge of spatial analytical and statistical techniques using at least two of the following analytical packages (R, SAS, ARC, QGIS). You will be experienced in manipulating and handling large datasets, writing for expert and popular audiences and have a proven scientific publication record. Knowledge and experience of land management, climate change mitigation or restoration science will be an advantage. You will be responsible for establishing and maintaining good relations with internal and external project partners and stakeholders, in the UK and Europe. The post is for 14 months, to assist with the delivery of scenario-based models of landscape-scale land use change and its climate change mitigation potential. Preferably, you will be based in Cambridge or Sandy. Closing date: 11 December 2019 Interview date: 13 January 2020 To Apply and for More Information: Please click the apply button. You will be taken to a simple CHM Recruit form and then redirected to the employer's website. When you make your application please ensure that you include reference number A on any correspondence. This role is covered by the Rehabilitation of Offenders Act. You will be asked to declare unspent convictions and cautions at offer of employment stage. Strictly no agencies, please.
Dec 06, 2019
Contractor
Climate change and biodiversity loss are affecting people and nature and land management will be key to ameliorating the effects of both. Our client a nature conservation charity is seeking a talented conservation scientist with good GIS and analytical skills to join projects examining the spatial conservation and climate change mitigation consequences of land management and restoration in the UK and Europe. Conservation Scientist - Natural Climate Solutions Ref: A Location: Sandy, Bedfordshire or Cambridge Salary: £25,643 to £27,585 per annum. Applicants should expect under normal circumstances to receive an offer at the bottom of the advertised range. Hours: Full Time Contract: 14 month Fixed Term contract You will join a small team working alongside ecological and practical conservationists. You will have a good working knowledge of spatial analytical and statistical techniques using at least two of the following analytical packages (R, SAS, ARC, QGIS). You will be experienced in manipulating and handling large datasets, writing for expert and popular audiences and have a proven scientific publication record. Knowledge and experience of land management, climate change mitigation or restoration science will be an advantage. You will be responsible for establishing and maintaining good relations with internal and external project partners and stakeholders, in the UK and Europe. The post is for 14 months, to assist with the delivery of scenario-based models of landscape-scale land use change and its climate change mitigation potential. Preferably, you will be based in Cambridge or Sandy. Closing date: 11 December 2019 Interview date: 13 January 2020 To Apply and for More Information: Please click the apply button. You will be taken to a simple CHM Recruit form and then redirected to the employer's website. When you make your application please ensure that you include reference number A on any correspondence. This role is covered by the Rehabilitation of Offenders Act. You will be asked to declare unspent convictions and cautions at offer of employment stage. Strictly no agencies, please.
QC Analyst £24,000 - £28,000 depending on experience plus Relocation Package if required Benefits include a company bonus scheme Based in Wiltshire Commutable from Oxford, Reading, Chippenham, Gloucester, Bath An international Pharmaceutical company is looking to appoint 4 experienced QC Analysts to their team based in Wiltshire as part of ongoing expansion plans. Candidates will be expected to work across a number of different products within the QC team and be involved in method transfer as and when required. Any experience of method validation would be highly desirable. Relocation packages are available to the right candidates and please do apply now to be considered. Duties: Transfer new methods into the team and perform routine analysis of in process and finished products Perform development and validation of Analytical techniques Be involved in projects across the department as well as in conjunction with clients Review analytical data to ensure compliance with standard procedures Be involved in any troubleshooting when required Perform all work to cGMP Qualifications and Experience: Minimum qualified to BSc level or equivalent in Chemistry or a related subject At least 12 months experience for entry level positions and ideally at least 2-3 years for higher entry In depth experience in HPLC outside of just following an SOP Motivated, flexible and progression focussed individuals looking for their next career move within a progressive multinational global corporation with opportunities to really develop their career to the next level. For further details and to apply please contact Johnathan Miller at Scantec on 0151._ 666._ 8925 and johnathanm (at) scantec. co. uk Scantec Personnel Limited is acting as an employment business and an employment agency. For contract or interim roles (and unless otherwise stated), all pay rates stated are on a Limited Company basis. Due to the high volume of applications Scantec receives it is not always possible to acknowledge every application. Shortlisted applicants will be contacted within 28 days. If you don't hear from us within 28 days your application has not been shortlisted at this time, to be considered for future vacancies please register with us on our website.
Dec 06, 2019
Full time
QC Analyst £24,000 - £28,000 depending on experience plus Relocation Package if required Benefits include a company bonus scheme Based in Wiltshire Commutable from Oxford, Reading, Chippenham, Gloucester, Bath An international Pharmaceutical company is looking to appoint 4 experienced QC Analysts to their team based in Wiltshire as part of ongoing expansion plans. Candidates will be expected to work across a number of different products within the QC team and be involved in method transfer as and when required. Any experience of method validation would be highly desirable. Relocation packages are available to the right candidates and please do apply now to be considered. Duties: Transfer new methods into the team and perform routine analysis of in process and finished products Perform development and validation of Analytical techniques Be involved in projects across the department as well as in conjunction with clients Review analytical data to ensure compliance with standard procedures Be involved in any troubleshooting when required Perform all work to cGMP Qualifications and Experience: Minimum qualified to BSc level or equivalent in Chemistry or a related subject At least 12 months experience for entry level positions and ideally at least 2-3 years for higher entry In depth experience in HPLC outside of just following an SOP Motivated, flexible and progression focussed individuals looking for their next career move within a progressive multinational global corporation with opportunities to really develop their career to the next level. For further details and to apply please contact Johnathan Miller at Scantec on 0151._ 666._ 8925 and johnathanm (at) scantec. co. uk Scantec Personnel Limited is acting as an employment business and an employment agency. For contract or interim roles (and unless otherwise stated), all pay rates stated are on a Limited Company basis. Due to the high volume of applications Scantec receives it is not always possible to acknowledge every application. Shortlisted applicants will be contacted within 28 days. If you don't hear from us within 28 days your application has not been shortlisted at this time, to be considered for future vacancies please register with us on our website.
We are currently looking for a Associate Director DMPK to join a Global Life Sciences company based in the Cambridgeshire area. As the Associate Director DMPK you will be responsible for providing scientific and strategic leadership to the DMPK / ADME Discovery Group. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Associate Director DMPK will be varied however the key duties and responsibilities are as follows: 1. Collaborate with other departments within the organisation to ensure projects are being successfully progressed through the discovery teams. 2. Offer your expert advice and experience on DMPK, ADME, PK/PD projects and utilise this knowledge for troubleshooting scientific and business related issues. 3. Line management of technical leaders, scientists and managers within the group. You will be instrumental in the development and progression of more junior members of staff. 4. You will facilitate cross-site involvement in projects and be a representative and ambassador for the DMPK / ADME department. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Associate Director DMPK we are looking to identify the following on your profile and past history: 1. Relevant degree in a Bioscience discipline along with significant DMPK / ADME experience. 2. Proven industry experience in managing teams within scientific projects is essential to your application. 3. A working knowledge and practical experience with advancing drug discovery projects within DMPK / ADME / PK/PD through to development candidate selection would be highly advantageous. Key Words: DMPK | ADME | PK/PD | Pharmacokinetics | Drug Metabolism | Drug Discovery | CRO | Life Science | Biotechnology | Pharmaceutical | In Vitro | In Vivo | Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
Dec 06, 2019
Full time
We are currently looking for a Associate Director DMPK to join a Global Life Sciences company based in the Cambridgeshire area. As the Associate Director DMPK you will be responsible for providing scientific and strategic leadership to the DMPK / ADME Discovery Group. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Associate Director DMPK will be varied however the key duties and responsibilities are as follows: 1. Collaborate with other departments within the organisation to ensure projects are being successfully progressed through the discovery teams. 2. Offer your expert advice and experience on DMPK, ADME, PK/PD projects and utilise this knowledge for troubleshooting scientific and business related issues. 3. Line management of technical leaders, scientists and managers within the group. You will be instrumental in the development and progression of more junior members of staff. 4. You will facilitate cross-site involvement in projects and be a representative and ambassador for the DMPK / ADME department. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Associate Director DMPK we are looking to identify the following on your profile and past history: 1. Relevant degree in a Bioscience discipline along with significant DMPK / ADME experience. 2. Proven industry experience in managing teams within scientific projects is essential to your application. 3. A working knowledge and practical experience with advancing drug discovery projects within DMPK / ADME / PK/PD through to development candidate selection would be highly advantageous. Key Words: DMPK | ADME | PK/PD | Pharmacokinetics | Drug Metabolism | Drug Discovery | CRO | Life Science | Biotechnology | Pharmaceutical | In Vitro | In Vivo | Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
Mary Bolt at CK Science is recruiting for a Senior Scientist Translational Research to join a biotechnology company developing cutting edge gene therapies at their site based in Central London on a permanent basis. The Company: Our client are an exciting and expanding biotech developing gene therapy techniques for drug delivery. Location: This role is located in central London so is easily commutable via public transport from the London area or surrounding counties. The Role: Your main duties will be to: - Develop, validate, transfer and troubleshoot immunoassays and cell-based assays internally and at contract research organisations and provide scientific oversight to contracted immunoassays including review of validation protocols and reports. - Develop close and effective partnerships with other nonclinical and clinical pharmacology scientists, safety scientists, research scientists, clinicians and project teams to foster a collaborative work environment. - Complete projects and prepare reports appropriate for internal or external parties within agreed timelines and prepare presentations and represent research internally and externally. Further responsibilities will include to: - Evaluate new assay technologies and other applications for improved performance and efficiency of laboratory activities. - Maintain awareness of current developments in the field through comprehensive reading of the literature and attendance at appropriate scientific meetings. - Represent Translational Research within multidisciplinary project teams and assist and/or train others when appropriate. Your Background: The ideal candidate for this role will have: - Been educated to degree level or above in life science with relevant biotechnology industry experience as well as working knowledge and hands on experience with a wide range of cellular and biochemical immunoassays and state-of-the-art molecular biology techniques. - Experience with bioanalytical method development, validation and troubleshooting of immunochemistry and immunoassay techniques including multiplex approaches e.g. Luminex or MSD platforms. - Demonstrate scientific creativity, critical thinking, and analytical problem-solving skills, with a strong track record of research productivity as evidenced by high-quality publications and excellent collaboration, communication and decision-making skills. - Experience with guidelines and/or working in a GLP/GCP compliant environment. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 46853 in all correspondence.
Dec 06, 2019
Full time
Mary Bolt at CK Science is recruiting for a Senior Scientist Translational Research to join a biotechnology company developing cutting edge gene therapies at their site based in Central London on a permanent basis. The Company: Our client are an exciting and expanding biotech developing gene therapy techniques for drug delivery. Location: This role is located in central London so is easily commutable via public transport from the London area or surrounding counties. The Role: Your main duties will be to: - Develop, validate, transfer and troubleshoot immunoassays and cell-based assays internally and at contract research organisations and provide scientific oversight to contracted immunoassays including review of validation protocols and reports. - Develop close and effective partnerships with other nonclinical and clinical pharmacology scientists, safety scientists, research scientists, clinicians and project teams to foster a collaborative work environment. - Complete projects and prepare reports appropriate for internal or external parties within agreed timelines and prepare presentations and represent research internally and externally. Further responsibilities will include to: - Evaluate new assay technologies and other applications for improved performance and efficiency of laboratory activities. - Maintain awareness of current developments in the field through comprehensive reading of the literature and attendance at appropriate scientific meetings. - Represent Translational Research within multidisciplinary project teams and assist and/or train others when appropriate. Your Background: The ideal candidate for this role will have: - Been educated to degree level or above in life science with relevant biotechnology industry experience as well as working knowledge and hands on experience with a wide range of cellular and biochemical immunoassays and state-of-the-art molecular biology techniques. - Experience with bioanalytical method development, validation and troubleshooting of immunochemistry and immunoassay techniques including multiplex approaches e.g. Luminex or MSD platforms. - Demonstrate scientific creativity, critical thinking, and analytical problem-solving skills, with a strong track record of research productivity as evidenced by high-quality publications and excellent collaboration, communication and decision-making skills. - Experience with guidelines and/or working in a GLP/GCP compliant environment. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 46853 in all correspondence.
PhD Qualified / Postdoctoral Chemist (Formulations) c£32 +Benefits South East AB/J4567 An experienced Postdoctoral chemist with or without experience is required to work very closely with R&D teams. As a PhD chemist qualified in either organic synthesis, formulation or polymer chemistry this a great opportunity to design and synthesise next generation materials for the business. Working closely with business development the successful PhD chemist will complement the R&D team's current skill base and play a critical role in enabling the team to become the High Performance Agile Team that deliver the new components the business needs. Coaching - imparting experience and knowledge to a variety of skill bases and team members. Opportunity to build personal network extensively across range Influence our New Technology Innovation Culture. Greater understanding of market opportunities (short - long term) Exposure to Innovation & road map opportunities. Influence lab set-up & equipment to support the synthesis needs of the business. Key Responsibilities - Proactively contribute to the high safety standard of the group. Innovative and creative approaches to identify opportunities to improve processes and tools to develop our formulation methodologies. Lead projects and contribute to the formulation, development and deployment of next generation fuel additives. Supervise and develop chemists providing colleague mentoring and development coaching. Interface effectively with our internal and external customers Project management Building networks across functions Developing cutting edge technology Qualifications, Knowledge and Experience Required: PhD Chemistry, Polymer chemistry Formulation, Synthetic Chemistry, Organic Chemistry, even pharmaceutical chemistry or a related petroleum subject. All background considered but preferences for synthesis OR formulation, R&D Excellent chemistry background with strong track record of delivering materials to aggressive timescales within a research & development environment. Strong safety focus including networking, communication, a demonstrated ability to deliver high standard risk assessments, make solid safety recommendations when faced with obstacles and influence changes to work differently based on learnings from near miss reporting. Ability to take an objective view of technical problems and address them with creativity and innovation. Strong commitment to HSE and quality values They offer an attractive salary (dependent on experience), commensurate with qualifications and experience as well as associated benefits, including Bonus and Pension Scheme. To Apply: Please contact Alison Basson quoting AB/J4567 on
Dec 06, 2019
Full time
PhD Qualified / Postdoctoral Chemist (Formulations) c£32 +Benefits South East AB/J4567 An experienced Postdoctoral chemist with or without experience is required to work very closely with R&D teams. As a PhD chemist qualified in either organic synthesis, formulation or polymer chemistry this a great opportunity to design and synthesise next generation materials for the business. Working closely with business development the successful PhD chemist will complement the R&D team's current skill base and play a critical role in enabling the team to become the High Performance Agile Team that deliver the new components the business needs. Coaching - imparting experience and knowledge to a variety of skill bases and team members. Opportunity to build personal network extensively across range Influence our New Technology Innovation Culture. Greater understanding of market opportunities (short - long term) Exposure to Innovation & road map opportunities. Influence lab set-up & equipment to support the synthesis needs of the business. Key Responsibilities - Proactively contribute to the high safety standard of the group. Innovative and creative approaches to identify opportunities to improve processes and tools to develop our formulation methodologies. Lead projects and contribute to the formulation, development and deployment of next generation fuel additives. Supervise and develop chemists providing colleague mentoring and development coaching. Interface effectively with our internal and external customers Project management Building networks across functions Developing cutting edge technology Qualifications, Knowledge and Experience Required: PhD Chemistry, Polymer chemistry Formulation, Synthetic Chemistry, Organic Chemistry, even pharmaceutical chemistry or a related petroleum subject. All background considered but preferences for synthesis OR formulation, R&D Excellent chemistry background with strong track record of delivering materials to aggressive timescales within a research & development environment. Strong safety focus including networking, communication, a demonstrated ability to deliver high standard risk assessments, make solid safety recommendations when faced with obstacles and influence changes to work differently based on learnings from near miss reporting. Ability to take an objective view of technical problems and address them with creativity and innovation. Strong commitment to HSE and quality values They offer an attractive salary (dependent on experience), commensurate with qualifications and experience as well as associated benefits, including Bonus and Pension Scheme. To Apply: Please contact Alison Basson quoting AB/J4567 on
Jade Stirk at CK Group is recruiting for a Product Development Specialist to join a leading contract manufacture organisation in Devon on an initial 3 month contract that could lead onto to a permanent position. The Company: Our client is a contract manufacturer of pharmaceutical products serving global markets. Location: This role is located in Devon. The site is easily commutable from Paignton, Dartmouth and Torquay. The Role: Your main duties will be: - Project management of individual product development projects. - Managing a growing base of contract manufacture customers both within the UK and International markets. - Generation of Quality by Design reports and the project plan. - Implementing solutions to problems which may occur during product development projects. - Reviewing of product development projects. - Deputising for the Product Development Manager where required. Your Background: The ideal candidate for this role will have: - A BSc/MSc in Chemistry or a closely related subject. - Experience of working in a GMP environment. - Previous experience working in a pharmaceutical environment. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47031 in all correspondence. INDDIF
Dec 06, 2019
Full time
Jade Stirk at CK Group is recruiting for a Product Development Specialist to join a leading contract manufacture organisation in Devon on an initial 3 month contract that could lead onto to a permanent position. The Company: Our client is a contract manufacturer of pharmaceutical products serving global markets. Location: This role is located in Devon. The site is easily commutable from Paignton, Dartmouth and Torquay. The Role: Your main duties will be: - Project management of individual product development projects. - Managing a growing base of contract manufacture customers both within the UK and International markets. - Generation of Quality by Design reports and the project plan. - Implementing solutions to problems which may occur during product development projects. - Reviewing of product development projects. - Deputising for the Product Development Manager where required. Your Background: The ideal candidate for this role will have: - A BSc/MSc in Chemistry or a closely related subject. - Experience of working in a GMP environment. - Previous experience working in a pharmaceutical environment. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47031 in all correspondence. INDDIF
This is a great opportunity for a chemist or biologist with a background in NMR techniques pertinent to drug discovery to employ these for an R&D-focussed firm near Belfast. The Senior NMR Scientist role is ideal for a recent PhD graduate in the relevant field or an industry-based specialist looking to build a broader skillset for excellent career progression potential. Your day to day duties as a Senior NMR Scientist will be: Researching methods employing NMR towards ligand-binding studies in solution Probing protein instabilities and aggregation phenomena Performing kinetic and competition studies via novel NMR techniques Maintenance of the NMR suite for routine 1D/2D proton NMR service provision Liaising with local internal and external personnel, travelling to academic and industry conferences You will be an ideal candidate with this background: A PhD in a related field employing novel NMR techniques Some data analytical skills and related software expertise The desire to work with both chemists and biologists in the drug discovery process A good team-working approach This client is already shortlisting for the role so I would like you to apply immediately with a CV (Word document format, 2 pages maximum) so as to not miss out on the opportunity. Note my client is unable to sponsor visas for those without eligibility to work in the UK. When choosing your scientific recruitment specialist, why should it be Dr Paul Mears, Head of Chemical recruitment, at Science Solutions? The team I manage here focus solely on matching scientists to positions in the UK speciality chemical industry, and related areas such as drug discovery and agrochemicals, which is where my own experience and network position me best for clients and job seekers alike. Supplemented by a background working in the speciality chemicals and fragrance and flavours sectors, I completed academic studies with a PhD in organic chemistry at the University of Manchester, which came after graduating with a BSc at the University of Leeds' famous Colour & Polymer Chemistry department. Following a short post-doctoral research post I built up four years' experience in recruiting scientists into new jobs. Full references and testimonials of successful assignments such as Technical Directors, Heads of Operations and quick turnarounds for urgent laboratory needs can be found on my LinkedIn profile - search Paul Mears.
Dec 06, 2019
Full time
This is a great opportunity for a chemist or biologist with a background in NMR techniques pertinent to drug discovery to employ these for an R&D-focussed firm near Belfast. The Senior NMR Scientist role is ideal for a recent PhD graduate in the relevant field or an industry-based specialist looking to build a broader skillset for excellent career progression potential. Your day to day duties as a Senior NMR Scientist will be: Researching methods employing NMR towards ligand-binding studies in solution Probing protein instabilities and aggregation phenomena Performing kinetic and competition studies via novel NMR techniques Maintenance of the NMR suite for routine 1D/2D proton NMR service provision Liaising with local internal and external personnel, travelling to academic and industry conferences You will be an ideal candidate with this background: A PhD in a related field employing novel NMR techniques Some data analytical skills and related software expertise The desire to work with both chemists and biologists in the drug discovery process A good team-working approach This client is already shortlisting for the role so I would like you to apply immediately with a CV (Word document format, 2 pages maximum) so as to not miss out on the opportunity. Note my client is unable to sponsor visas for those without eligibility to work in the UK. When choosing your scientific recruitment specialist, why should it be Dr Paul Mears, Head of Chemical recruitment, at Science Solutions? The team I manage here focus solely on matching scientists to positions in the UK speciality chemical industry, and related areas such as drug discovery and agrochemicals, which is where my own experience and network position me best for clients and job seekers alike. Supplemented by a background working in the speciality chemicals and fragrance and flavours sectors, I completed academic studies with a PhD in organic chemistry at the University of Manchester, which came after graduating with a BSc at the University of Leeds' famous Colour & Polymer Chemistry department. Following a short post-doctoral research post I built up four years' experience in recruiting scientists into new jobs. Full references and testimonials of successful assignments such as Technical Directors, Heads of Operations and quick turnarounds for urgent laboratory needs can be found on my LinkedIn profile - search Paul Mears.
Senior drug discovery bioinformatician, innovative biotech in London. Strong data science / ML & NGS/genomics Your new company Hays is exclusively partnered with an exciting pharmaceutical company in central London looking to grow their bioinformatics and data science team. You will be working on multiple drug discovery and development projects to better understand and treat a variety of diseases. This company has a track record of innovation and has recently signed a number of deals with pharmaceutical partners keen to utilise their cutting-edge technology and approaches. Your new role You'll be part of a team bringing innovative data science and bioinformatics approaches to large biological data sets to help draw insights and aid drug discovery research on cutting-edge projects. You will be carrying out a mix of statistical analysis (eg on NGS / SNP data) and programming responsibilities to help drive drug discovery, develop new therapies and aid understanding of disease. Responsibilities will include (but aren't limited to): Identifying and applying appropriate bioinformatics methods to enhance the company's proprietary pipeline for drug target identification, eg tool, pipeline, algorithm or method development/implementation; Hands-on programming in languages such as R, Python, Perl, Java, etc; Act as a technical specialist on bioinformatics and cross-functional projects; Work with genome browsers, public data repositories, etc; Lead technical and strategic projects; Manage and analyse large scale genetic / SNP / NGS datasets using a variety of statistical & computational approaches for drug target identification and/or validation; Maintaining and improving the platform's functionality, eg to enhance R&D capabilities or visualisation functions using R, Shiny, Bash or similar; Horizon scanning to understand what cutting edge approaches, eg tools, methodologies, databases, etc are available and lead the development and implementation of these to increase in-house capabilities; Proactively troubleshoot issues and participate in brainstorming sessions. What you'll need to succeed As well as excellent communication skills, and great problem-solving ability, candidates must have: Strong scripting/programming skills, ideally with Python or R, but other languages such as Perl or Bash are also acceptable, eg for tool, pipeline, algorithm or package development; Experience with statistical software, eg R or Matlab; A very strong background in working with human / clinical NGS data, eg RNA-Seq, WGS, Exome or similar; Data analysis and interpretation skills; At least an MSc (or equivalent experience) in bioinformatics, statistics, biology, computer science, statistical genetics or a similar discipline, with a PhD or similar significantly preferred; Very good communication skills, ideally gained from working with multi-disciplinary teams or researchers in multiple locations; A track record of working on drug discovery projects, with a preference for pharmaceutical / biotech industry experience Experience of Machine Learning or Deep Learning approaches, eg Random Forest, SVM, regression, clustering, knowledge of Keras, scikit-learn or similar would be an advantage for this role. What you'll get in return The opportunity to make a significant contribution to a growing company whilst working on/leading a number of drug discovery projects, a fantastic working environment, and a market-leading salary and benefits structure. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on . If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career, as there are multiple statistical, data science and bioinformatics positions available, for both permanent and contract based opportunities. Keywords: bioinformatics, bioinformatician, data, science, statistics, statistical, biomarker, drug, discovery, genetics, genomics, NGS, PCR, sequence, Bayesian, machine, learning, programmer, programming, scientist, diagnostics, molecular, python, R, C, Bash, platform, project, manager, developer, tool, pipeline, computational, computer
Dec 06, 2019
Full time
Senior drug discovery bioinformatician, innovative biotech in London. Strong data science / ML & NGS/genomics Your new company Hays is exclusively partnered with an exciting pharmaceutical company in central London looking to grow their bioinformatics and data science team. You will be working on multiple drug discovery and development projects to better understand and treat a variety of diseases. This company has a track record of innovation and has recently signed a number of deals with pharmaceutical partners keen to utilise their cutting-edge technology and approaches. Your new role You'll be part of a team bringing innovative data science and bioinformatics approaches to large biological data sets to help draw insights and aid drug discovery research on cutting-edge projects. You will be carrying out a mix of statistical analysis (eg on NGS / SNP data) and programming responsibilities to help drive drug discovery, develop new therapies and aid understanding of disease. Responsibilities will include (but aren't limited to): Identifying and applying appropriate bioinformatics methods to enhance the company's proprietary pipeline for drug target identification, eg tool, pipeline, algorithm or method development/implementation; Hands-on programming in languages such as R, Python, Perl, Java, etc; Act as a technical specialist on bioinformatics and cross-functional projects; Work with genome browsers, public data repositories, etc; Lead technical and strategic projects; Manage and analyse large scale genetic / SNP / NGS datasets using a variety of statistical & computational approaches for drug target identification and/or validation; Maintaining and improving the platform's functionality, eg to enhance R&D capabilities or visualisation functions using R, Shiny, Bash or similar; Horizon scanning to understand what cutting edge approaches, eg tools, methodologies, databases, etc are available and lead the development and implementation of these to increase in-house capabilities; Proactively troubleshoot issues and participate in brainstorming sessions. What you'll need to succeed As well as excellent communication skills, and great problem-solving ability, candidates must have: Strong scripting/programming skills, ideally with Python or R, but other languages such as Perl or Bash are also acceptable, eg for tool, pipeline, algorithm or package development; Experience with statistical software, eg R or Matlab; A very strong background in working with human / clinical NGS data, eg RNA-Seq, WGS, Exome or similar; Data analysis and interpretation skills; At least an MSc (or equivalent experience) in bioinformatics, statistics, biology, computer science, statistical genetics or a similar discipline, with a PhD or similar significantly preferred; Very good communication skills, ideally gained from working with multi-disciplinary teams or researchers in multiple locations; A track record of working on drug discovery projects, with a preference for pharmaceutical / biotech industry experience Experience of Machine Learning or Deep Learning approaches, eg Random Forest, SVM, regression, clustering, knowledge of Keras, scikit-learn or similar would be an advantage for this role. What you'll get in return The opportunity to make a significant contribution to a growing company whilst working on/leading a number of drug discovery projects, a fantastic working environment, and a market-leading salary and benefits structure. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on . If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career, as there are multiple statistical, data science and bioinformatics positions available, for both permanent and contract based opportunities. Keywords: bioinformatics, bioinformatician, data, science, statistics, statistical, biomarker, drug, discovery, genetics, genomics, NGS, PCR, sequence, Bayesian, machine, learning, programmer, programming, scientist, diagnostics, molecular, python, R, C, Bash, platform, project, manager, developer, tool, pipeline, computational, computer
SENIOR CUSTOMER ANALYST CENTRAL LONDON 50,000 - 60,000 Are you looking to get involved with a strong analytics function? Do you have experience in delivering meaningful insights? This is an exciting opportunity for someone looking to develop their career in customer analytics with a well know and growing organisation! THE COMPANY This innovate tech company is looking for a Senior Customer Analyst to come join their collaborative analytics team. Data is at the heart of everything this company does, and you will have the opportunity to get involved with some of the most diverse datasets in this industry and provide actionable insight! THE ROLE As a Senior Data Analyst, you will work alongside a highly talented team of analysts. You will be a key driver in identifying key insights to report back to clients. Your responsibilities will include Building models and delivering insight using SQL and Python and understanding business requirements Being a go-to for analytical problems and being able to propose the best solution Building informative data visualisations to inform key business decisions Be able to translate data and speak to non-technical people about your decisions and recommendations YOUR SKILLS AND EXPERIENCE Strong commercial background in SQL Proven Python or R experience Degree in a STEM subject - 2.1 or higher Solutions driven with a pro-active approach to your work THE BENEFITS On top of a competitive salary, you will be entitled to Great working environment Pension scheme Good holiday package HOW TO APPLY Please register your interest by sending your CV to Gina Falleroni via the apply link on this page.
Dec 06, 2019
Full time
SENIOR CUSTOMER ANALYST CENTRAL LONDON 50,000 - 60,000 Are you looking to get involved with a strong analytics function? Do you have experience in delivering meaningful insights? This is an exciting opportunity for someone looking to develop their career in customer analytics with a well know and growing organisation! THE COMPANY This innovate tech company is looking for a Senior Customer Analyst to come join their collaborative analytics team. Data is at the heart of everything this company does, and you will have the opportunity to get involved with some of the most diverse datasets in this industry and provide actionable insight! THE ROLE As a Senior Data Analyst, you will work alongside a highly talented team of analysts. You will be a key driver in identifying key insights to report back to clients. Your responsibilities will include Building models and delivering insight using SQL and Python and understanding business requirements Being a go-to for analytical problems and being able to propose the best solution Building informative data visualisations to inform key business decisions Be able to translate data and speak to non-technical people about your decisions and recommendations YOUR SKILLS AND EXPERIENCE Strong commercial background in SQL Proven Python or R experience Degree in a STEM subject - 2.1 or higher Solutions driven with a pro-active approach to your work THE BENEFITS On top of a competitive salary, you will be entitled to Great working environment Pension scheme Good holiday package HOW TO APPLY Please register your interest by sending your CV to Gina Falleroni via the apply link on this page.
SENIOR ANALYST CENTRAL LONDON 65,000-75,000 Do you have experience driving and delivering customer insight? Are you confident in working with key stakeholders to influence and deliver recommendations for business growth? THE COMPANY This rapidly growing start-up is looking for a Senior Analyst to come in and hit the ground running. With a unique product, already loved by millions of users, you will help embed and optimise their product roadmap for the future. With a great working culture and complete ownership, this role could be the next step you're looking for. THE ROLE As a Senior Analyst, you will be mentoring a team of analysts and taking lead across all projects you will be involved on. Your main responsibilities will include: Leading projects from extraction to delivery to understand user journey, engagement and trends Identify key insights to enable accurate and actionable recommendations are being delivered across the business using SQL Maintaining the integrity of the data across projects Be comfortable speaking and engaging with key business partners and influencing decision making YOUR SKILLS AND EXPERIENCE Strong proven SQL skills with knowledge GA Experience in mentoring or managing Degree in a STEM background - 2.1 or higher Excellent communication skills THE BENEFITS On top of a competitive salary, you will be entitled to Pension scheme Healthcare Great working culture and nice offices HOW TO APPLY Please register your interest by sending your CV to Gina Falleroni via the apply link on this page.
Dec 06, 2019
Full time
SENIOR ANALYST CENTRAL LONDON 65,000-75,000 Do you have experience driving and delivering customer insight? Are you confident in working with key stakeholders to influence and deliver recommendations for business growth? THE COMPANY This rapidly growing start-up is looking for a Senior Analyst to come in and hit the ground running. With a unique product, already loved by millions of users, you will help embed and optimise their product roadmap for the future. With a great working culture and complete ownership, this role could be the next step you're looking for. THE ROLE As a Senior Analyst, you will be mentoring a team of analysts and taking lead across all projects you will be involved on. Your main responsibilities will include: Leading projects from extraction to delivery to understand user journey, engagement and trends Identify key insights to enable accurate and actionable recommendations are being delivered across the business using SQL Maintaining the integrity of the data across projects Be comfortable speaking and engaging with key business partners and influencing decision making YOUR SKILLS AND EXPERIENCE Strong proven SQL skills with knowledge GA Experience in mentoring or managing Degree in a STEM background - 2.1 or higher Excellent communication skills THE BENEFITS On top of a competitive salary, you will be entitled to Pension scheme Healthcare Great working culture and nice offices HOW TO APPLY Please register your interest by sending your CV to Gina Falleroni via the apply link on this page.
Associate Director - Medicinal Chemistry We are currently working with an award-winning drug discovery company in the East Midlands who are looking to recruit an Associate Director of Medicinal Chemistry . The role: As an Associate Director you will support the strategic leadership of the Chemistry department. Having extensive experience in medicinal chemistry, project management and leadership you will oversee several projects and multidiscipline teams (including DMPK Scientists, Medicinal Chemists, Bioscientists and Computational Chemists) to ensure departmental & company objectives, along with client projects are completed on time and within budget. Responsibilities include: Take a leading role in the Medicinal Chemistry department strategic plans, development and resource management. Act as Project Director having a 'senior' oversight on project design and strategy. Manage and lead groups of Scientists being responsible for their career development. Promote collaborative working between departments. Having expertise in a therapeutic area or scientific process you will act as a subject matter expert for the company. Lead and implement strategies to support overall business growth. Provide financial oversight and input into all project activities (quotes, project reports and presentations). Represent the company externally in at least one key scientific body. Lead the recruitment of new Organic Chemists. To be successful in this role you will have: A PhD in Organic Chemistry or Medicinal Chemistry. Extensive experience leading drug discovery projects. Experience in defining strategies for drug discovery programmes from HTS lead generation to hit-to-lead and/or lead optimization phases. Worked in a strategic leadership role with a proven track record in successful performance management and employee development. Experience working with multiple stakeholders/ divisions you will have excellent engagement and influencing skills at senior management level. If you are interested in joining this highly successful and award-winning company please send your CV to Peter at Rowland Talent Solutions.
Dec 06, 2019
Full time
Associate Director - Medicinal Chemistry We are currently working with an award-winning drug discovery company in the East Midlands who are looking to recruit an Associate Director of Medicinal Chemistry . The role: As an Associate Director you will support the strategic leadership of the Chemistry department. Having extensive experience in medicinal chemistry, project management and leadership you will oversee several projects and multidiscipline teams (including DMPK Scientists, Medicinal Chemists, Bioscientists and Computational Chemists) to ensure departmental & company objectives, along with client projects are completed on time and within budget. Responsibilities include: Take a leading role in the Medicinal Chemistry department strategic plans, development and resource management. Act as Project Director having a 'senior' oversight on project design and strategy. Manage and lead groups of Scientists being responsible for their career development. Promote collaborative working between departments. Having expertise in a therapeutic area or scientific process you will act as a subject matter expert for the company. Lead and implement strategies to support overall business growth. Provide financial oversight and input into all project activities (quotes, project reports and presentations). Represent the company externally in at least one key scientific body. Lead the recruitment of new Organic Chemists. To be successful in this role you will have: A PhD in Organic Chemistry or Medicinal Chemistry. Extensive experience leading drug discovery projects. Experience in defining strategies for drug discovery programmes from HTS lead generation to hit-to-lead and/or lead optimization phases. Worked in a strategic leadership role with a proven track record in successful performance management and employee development. Experience working with multiple stakeholders/ divisions you will have excellent engagement and influencing skills at senior management level. If you are interested in joining this highly successful and award-winning company please send your CV to Peter at Rowland Talent Solutions.
Asbestos Laboratory/Bulk Analyst £18,000 - £22,000 + Benefits Birmingham, West Midlands Our client is a leading asbestos management and environmental testing consultancy that boasts one of the country's largest network of UKAS accredited laboratories in the UK! Due to company growth and new contract wins, they are now seeking additional support to their Birmingham base and require a BOHS P401 qualified Asbestos Bulk Analyst to join their team. The successful applicant can expect to receive a competitive starting salary and benefits package along with excellent training and development opportunities to progress within the company. Key Duties of an Asbestos Analyst : *Preparation of bulk samples for analysis * Logging received samples into in-house systems * Analysing bulk samples for traces of asbestos content using polarised light microscopy * Producing certifications * Generating bulk analysis reports/sampling reports to be issued to clients * Assisting the lab supervisor with any ad-hoc duties In order to be successful, candidates MUST possess the BOHS P401/RSPH qualification, previous experience working within a UKAS accredited laboratory, good level of IT skills, excellent communication skills and knowledge of TEAMS or similar) software. This is a brilliant opportunity to join a market-leading UKAS accredited asbestos consultancy, so if you feel that this opportunity matches your skill-set and experience, don't hesitate to apply! For an informal chat about the position please contact Recruitment on or send your CV across to for immediate consideration. Commutable locations: Dudley, Smethwick, Wolverhampton, Bloxwich, Sutton Coldfield, Stourbridge, Birmingham, Cannock, Lichfield, West Midlands.
Dec 06, 2019
Full time
Asbestos Laboratory/Bulk Analyst £18,000 - £22,000 + Benefits Birmingham, West Midlands Our client is a leading asbestos management and environmental testing consultancy that boasts one of the country's largest network of UKAS accredited laboratories in the UK! Due to company growth and new contract wins, they are now seeking additional support to their Birmingham base and require a BOHS P401 qualified Asbestos Bulk Analyst to join their team. The successful applicant can expect to receive a competitive starting salary and benefits package along with excellent training and development opportunities to progress within the company. Key Duties of an Asbestos Analyst : *Preparation of bulk samples for analysis * Logging received samples into in-house systems * Analysing bulk samples for traces of asbestos content using polarised light microscopy * Producing certifications * Generating bulk analysis reports/sampling reports to be issued to clients * Assisting the lab supervisor with any ad-hoc duties In order to be successful, candidates MUST possess the BOHS P401/RSPH qualification, previous experience working within a UKAS accredited laboratory, good level of IT skills, excellent communication skills and knowledge of TEAMS or similar) software. This is a brilliant opportunity to join a market-leading UKAS accredited asbestos consultancy, so if you feel that this opportunity matches your skill-set and experience, don't hesitate to apply! For an informal chat about the position please contact Recruitment on or send your CV across to for immediate consideration. Commutable locations: Dudley, Smethwick, Wolverhampton, Bloxwich, Sutton Coldfield, Stourbridge, Birmingham, Cannock, Lichfield, West Midlands.
This is a fantastic opportunity for a Lead Colloid Scientist to employ their technical expertise in a laboratory-based role with responsibilities for the project management of new formulations of biocidal products, plus research into new technologies. Based in the East Midlands, the Lead Colloid Scientist role is ideal for an accomplished formulation chemist with a background in new product development from a variety of industries. Your day to day duties as a Lead Colloid Scientist will be: Developing novel formulations of biocidal products Liaison with lab and production staff to ensure reproducibility and regulatory compliance Research into new revenue streams Development of scientists within your team You will be an ideal candidate with this background: A higher degree in a related scientific field Knowledge specifically in colloid chemistry A track record in formulation chemistry in the laboratory The ability to appreciate the commercial factors of a product-driven role This client is already shortlisting for the role so I would like you to apply immediately with a CV (Word document format, 2 pages maximum) so as to not miss out on the opportunity. Note my client is unable to sponsor visas for those without eligibility to work in the UK. Why should your scientific specialist recruiter be Dr Paul Mears, Head of Chemical recruitment, at Science Solutions? The team I manage here focus solely on matching scientists to positions in the UK speciality chemical industry, and related areas such as drug discovery and agrochemicals, which is where my own experience and network position me best for clients and job seekers alike. Supplemented by a background working in the speciality chemicals and fragrance and flavours sectors, I completed academic studies with a PhD in organic chemistry at the University of Manchester, which came after graduating with a BSc at the University of Leeds' famous Colour & Polymer Chemistry department. Following a short post-doctoral research post I built up four years' experience in recruiting scientists into new jobs. Full references and testimonials of successful assignments such as Technical Directors, Heads of Operations and quick turnarounds for urgent laboratory needs can be found on my LinkedIn profile - search Paul Mears.
Dec 06, 2019
Full time
This is a fantastic opportunity for a Lead Colloid Scientist to employ their technical expertise in a laboratory-based role with responsibilities for the project management of new formulations of biocidal products, plus research into new technologies. Based in the East Midlands, the Lead Colloid Scientist role is ideal for an accomplished formulation chemist with a background in new product development from a variety of industries. Your day to day duties as a Lead Colloid Scientist will be: Developing novel formulations of biocidal products Liaison with lab and production staff to ensure reproducibility and regulatory compliance Research into new revenue streams Development of scientists within your team You will be an ideal candidate with this background: A higher degree in a related scientific field Knowledge specifically in colloid chemistry A track record in formulation chemistry in the laboratory The ability to appreciate the commercial factors of a product-driven role This client is already shortlisting for the role so I would like you to apply immediately with a CV (Word document format, 2 pages maximum) so as to not miss out on the opportunity. Note my client is unable to sponsor visas for those without eligibility to work in the UK. Why should your scientific specialist recruiter be Dr Paul Mears, Head of Chemical recruitment, at Science Solutions? The team I manage here focus solely on matching scientists to positions in the UK speciality chemical industry, and related areas such as drug discovery and agrochemicals, which is where my own experience and network position me best for clients and job seekers alike. Supplemented by a background working in the speciality chemicals and fragrance and flavours sectors, I completed academic studies with a PhD in organic chemistry at the University of Manchester, which came after graduating with a BSc at the University of Leeds' famous Colour & Polymer Chemistry department. Following a short post-doctoral research post I built up four years' experience in recruiting scientists into new jobs. Full references and testimonials of successful assignments such as Technical Directors, Heads of Operations and quick turnarounds for urgent laboratory needs can be found on my LinkedIn profile - search Paul Mears.
About Us Diamond Light Source is the UK's national synchrotron; a huge scientific facility designed to produce very intense beams of X-rays, infrared and ultraviolet light. Our scientists use the light to study a vast range of subject matter, from new medicines and treatments for disease to innovative engineering and cutting-edge technology. Diamond is one of the most advanced scientific facilities in the world, and its pioneering capabilities and talented staff are helping to keep the UK at the forefront of scientific research. About the Role We now have an opportunity for a Software Engineer within the Diamond Data Acquisition (DAQ) group to support and develop the Generic Data Acquisition (GDA) software for experiments at Diamond. The DAQ group develops software to interface with and control the hardware which allows experiments to be performed and monitored as well as guiding the end user to tools for data reduction and analysis. The group works closely with scientists, motion and controls engineers to continuously develop and improve software solutions for scientific data acquisition and on-the-fly monitoring and data analysis. Typical experiments will generate tens of terabytes of data per day. Experimental data is acquired with our open source software package for GDA which is responsible for managing and executing experiments, capture and storage of experimental data and real-time visualisation of collected data. GDA is a client-server application written in Java, making use of the Eclipse RCP framework. The GDA server communicates with beamline hardware via EPICS to provide a control and monitor capability and deliver high-level experimental functions. A GDA client provides both a GUI and a Python scripting capability for users to control experiments locally. Some experimental setups at Diamond are highly automated, enabling experiments to be planned and executed remotely. This provides an exciting opportunity to lead in the development of bespoke software to make experiments autonomous. As a Software Engineer you will work alongside other focused science teams for data acquisition in an open and collaborative environment. You will be required to interact with scientists and translate their specifications for scientific capabilities into software requirements. You will liaise with controls and motions engineers to put these requirements into action. You will also potentially participate in international collaborations within this domain, sharing best practice and supporting other facilities and synchrotrons within the collaboration. About You You will be qualified to degree level in a STEM subject, with experience in the full Software Development Lifecycle, using a modern high-level language, and with an understanding of good software design principals and design for usability. Experience of working with large and complex code bases would be an advantage, as would experience of Python, Java, JMS message-oriented middleware, Java RMI, the HDF5 file format and the Eclipse RCP platform. The DAQ group is looking to migrate GDA to a Microservices Architecture, so an understanding of the associated technologies would be beneficial. You should display good communication, interpersonal and analytical skills, with personal interest or experience in a science environment. Benefits Diamond offers an exceptional benefits package to ensure an excellent work/life balance including 25 days' annual leave, 13 days statutory and company holidays, flexible working hours, an onsite nursery, an excellent pension scheme, and social and sporting activities. A relocation allowance may also be available where applicable. To Apply Applicants are required to outline their suitability for this role via the online application process. Please also state where you saw this role advertised. The closing date for applications is 05/01/2020, however, applications will be reviewed and interviewed on an ongoing basis until this vacancy is filled. Full time or part time considered .
Dec 06, 2019
Full time
About Us Diamond Light Source is the UK's national synchrotron; a huge scientific facility designed to produce very intense beams of X-rays, infrared and ultraviolet light. Our scientists use the light to study a vast range of subject matter, from new medicines and treatments for disease to innovative engineering and cutting-edge technology. Diamond is one of the most advanced scientific facilities in the world, and its pioneering capabilities and talented staff are helping to keep the UK at the forefront of scientific research. About the Role We now have an opportunity for a Software Engineer within the Diamond Data Acquisition (DAQ) group to support and develop the Generic Data Acquisition (GDA) software for experiments at Diamond. The DAQ group develops software to interface with and control the hardware which allows experiments to be performed and monitored as well as guiding the end user to tools for data reduction and analysis. The group works closely with scientists, motion and controls engineers to continuously develop and improve software solutions for scientific data acquisition and on-the-fly monitoring and data analysis. Typical experiments will generate tens of terabytes of data per day. Experimental data is acquired with our open source software package for GDA which is responsible for managing and executing experiments, capture and storage of experimental data and real-time visualisation of collected data. GDA is a client-server application written in Java, making use of the Eclipse RCP framework. The GDA server communicates with beamline hardware via EPICS to provide a control and monitor capability and deliver high-level experimental functions. A GDA client provides both a GUI and a Python scripting capability for users to control experiments locally. Some experimental setups at Diamond are highly automated, enabling experiments to be planned and executed remotely. This provides an exciting opportunity to lead in the development of bespoke software to make experiments autonomous. As a Software Engineer you will work alongside other focused science teams for data acquisition in an open and collaborative environment. You will be required to interact with scientists and translate their specifications for scientific capabilities into software requirements. You will liaise with controls and motions engineers to put these requirements into action. You will also potentially participate in international collaborations within this domain, sharing best practice and supporting other facilities and synchrotrons within the collaboration. About You You will be qualified to degree level in a STEM subject, with experience in the full Software Development Lifecycle, using a modern high-level language, and with an understanding of good software design principals and design for usability. Experience of working with large and complex code bases would be an advantage, as would experience of Python, Java, JMS message-oriented middleware, Java RMI, the HDF5 file format and the Eclipse RCP platform. The DAQ group is looking to migrate GDA to a Microservices Architecture, so an understanding of the associated technologies would be beneficial. You should display good communication, interpersonal and analytical skills, with personal interest or experience in a science environment. Benefits Diamond offers an exceptional benefits package to ensure an excellent work/life balance including 25 days' annual leave, 13 days statutory and company holidays, flexible working hours, an onsite nursery, an excellent pension scheme, and social and sporting activities. A relocation allowance may also be available where applicable. To Apply Applicants are required to outline their suitability for this role via the online application process. Please also state where you saw this role advertised. The closing date for applications is 05/01/2020, however, applications will be reviewed and interviewed on an ongoing basis until this vacancy is filled. Full time or part time considered .
Central Employment Agency (North East) Limited
Cramlington, Northumberland
Central Employment are looking for Lab Analyst candidates with a strong science background, for a very reputable, global pharmaceutical company in Northumberland starting in November. The ideal candidate will be either a fresh graduate looking to enter a Scientific field or have a period of employment in a Laboratory environment. There will be a higher salary on offer for candidates with laboratory experience. Role Responsibilities: Test product to pre-determined quality standards to meet customer requirements whilst maintaining the highest level of compliance. As a critical member of the supply chain, you will be planning and schedule testing procedures to ensure excellent documentation recording. Develop and produce new SOP's to maintain and further encourage standard practices and compliance status of the departments. Ensure laboratory investigations/abnormal occurrences are performed within the time frame required and according to the SOP's and to ensure all corrective actions are completed within the agreed time frame. Support the continuous review, improvement and harmonisation of documentation within the departments. Essential Requirements: Excellent understanding of testing and laboratory functions Good time management and prioritisation Scientific related degree (2:1 or higher) Experience working in a laboratory environment Working in a production driven pressurised environment Personal Attributes: Positive and helpful nature Ability to work as part of a team Ability to make good decisions Forward thinking and solution focussed This role is an immediate start so please apply online (attaching your CV) as soon as possible. Please be advised that due to the high volume of applications we receive, we are unable to respond to each application individually, please be assured that we will contact all applicants selected for interview in due course. Central Employment are an equal opportunities Employer.
Dec 06, 2019
Full time
Central Employment are looking for Lab Analyst candidates with a strong science background, for a very reputable, global pharmaceutical company in Northumberland starting in November. The ideal candidate will be either a fresh graduate looking to enter a Scientific field or have a period of employment in a Laboratory environment. There will be a higher salary on offer for candidates with laboratory experience. Role Responsibilities: Test product to pre-determined quality standards to meet customer requirements whilst maintaining the highest level of compliance. As a critical member of the supply chain, you will be planning and schedule testing procedures to ensure excellent documentation recording. Develop and produce new SOP's to maintain and further encourage standard practices and compliance status of the departments. Ensure laboratory investigations/abnormal occurrences are performed within the time frame required and according to the SOP's and to ensure all corrective actions are completed within the agreed time frame. Support the continuous review, improvement and harmonisation of documentation within the departments. Essential Requirements: Excellent understanding of testing and laboratory functions Good time management and prioritisation Scientific related degree (2:1 or higher) Experience working in a laboratory environment Working in a production driven pressurised environment Personal Attributes: Positive and helpful nature Ability to work as part of a team Ability to make good decisions Forward thinking and solution focussed This role is an immediate start so please apply online (attaching your CV) as soon as possible. Please be advised that due to the high volume of applications we receive, we are unable to respond to each application individually, please be assured that we will contact all applicants selected for interview in due course. Central Employment are an equal opportunities Employer.
We are currently looking for a Laboratory Support Supervisor to join a leading Heath Care company based in the Gloucestershire area. As the Laboratory Support Supervisor you will be responsible for overseeing the stability program, performing validation testing, cleaning validation studies, method transfers and analytical method development. As well as equipment procurement, qualification, validation and completing IQ OQ PQ documentation. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Laboratory Support Supervisor will be varied however the key duties and responsibilities are as follows: 1. As the Laboratory Support Supervisor you will Liaise and supervisor laboratory contract service providers. Oversee the Analytical method Development and Validation, schedule and produce annual report for the Validation Master Plan. 2. You will perform analytical work for method transfers and carry out training of Quality Control staff where necessary and associated reporting as well as taking as a supervisory role establishing and maintaining Laboratory Support KPIs. 3. As the Laboratory Support Supervisor you will have an understanding of the process of equipment procurement and lead IQ/OQ/PQ projects for the lab. 4. You will ensure the design and implementation of qualification/validation studies for equipment/systems/processes and subsequent reporting. As well as ensure laboratory equipment is suitably qualified, calibrated and maintained. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Laboratory Support Supervisor we are looking to identify the following on your profile and past history: 1. Relevant degree in a scientific discipline or equivalent industry experience. 2. Proven industry experience in Analytical method development and validation within a Health care or Pharmaceutical company. 3. A working knowledge and practical experience with equipment qualification, validation, calibration and maintenance. Key Words: IQ, OQ, PQ, Cleaning Validation, Equipment Validation, Validation Master Plan, Equipment Qualification, Method Development, Method Validation. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
Dec 06, 2019
Full time
We are currently looking for a Laboratory Support Supervisor to join a leading Heath Care company based in the Gloucestershire area. As the Laboratory Support Supervisor you will be responsible for overseeing the stability program, performing validation testing, cleaning validation studies, method transfers and analytical method development. As well as equipment procurement, qualification, validation and completing IQ OQ PQ documentation. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Laboratory Support Supervisor will be varied however the key duties and responsibilities are as follows: 1. As the Laboratory Support Supervisor you will Liaise and supervisor laboratory contract service providers. Oversee the Analytical method Development and Validation, schedule and produce annual report for the Validation Master Plan. 2. You will perform analytical work for method transfers and carry out training of Quality Control staff where necessary and associated reporting as well as taking as a supervisory role establishing and maintaining Laboratory Support KPIs. 3. As the Laboratory Support Supervisor you will have an understanding of the process of equipment procurement and lead IQ/OQ/PQ projects for the lab. 4. You will ensure the design and implementation of qualification/validation studies for equipment/systems/processes and subsequent reporting. As well as ensure laboratory equipment is suitably qualified, calibrated and maintained. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Laboratory Support Supervisor we are looking to identify the following on your profile and past history: 1. Relevant degree in a scientific discipline or equivalent industry experience. 2. Proven industry experience in Analytical method development and validation within a Health care or Pharmaceutical company. 3. A working knowledge and practical experience with equipment qualification, validation, calibration and maintenance. Key Words: IQ, OQ, PQ, Cleaning Validation, Equipment Validation, Validation Master Plan, Equipment Qualification, Method Development, Method Validation. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
We are currently looking for a Senior Analytical Chemist to join a leading Pharmaceutical company based in the Hertfordshire area. As the Senior Analytical Chemist you will be responsible for providing a range of analytical support to multiple project teams and work on API development. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Senior Analytical Chemist will be varied however the key duties and responsibilities are as follows: 1. As the Senior Analytical Chemist you will take a lead role the development, optimization and validation of analytical methods working on API's, Intermediates, Starting Materials and Raw Materials within a GMP environment. 2. You will provide technical expertise across a range of analytical techniques including HPLC/UPLC, GC, MS and amoung other spectroscopic techniques. 3. As the Senior Analytical Chemist your role will involve troubleshooting and maintenance of equipment and participate in instrument qualification. 4. You will write and review technical documents such as SOPs, protocols and reports, coach and mentor less experienced colleagues as well as review existing processes and provide input into continuous improvements. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Senior Analytical Chemist we are looking to identify the following on your profile and past history: 1. Relevant degree in a Chemistry related discipline. 2. Proven industry experience in analytical techniques such as HPLC and UPLC. 3. A working knowledge and practical experience with ICH guidelines and pharmacopoeias as well as working within a GMP and or GLP environment. Key Words: HPLC, UPLC, Senior Analyst, Senior Scientist, Analytical Development, Validation, Hertfordshire, South East. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
Dec 06, 2019
Full time
We are currently looking for a Senior Analytical Chemist to join a leading Pharmaceutical company based in the Hertfordshire area. As the Senior Analytical Chemist you will be responsible for providing a range of analytical support to multiple project teams and work on API development. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Senior Analytical Chemist will be varied however the key duties and responsibilities are as follows: 1. As the Senior Analytical Chemist you will take a lead role the development, optimization and validation of analytical methods working on API's, Intermediates, Starting Materials and Raw Materials within a GMP environment. 2. You will provide technical expertise across a range of analytical techniques including HPLC/UPLC, GC, MS and amoung other spectroscopic techniques. 3. As the Senior Analytical Chemist your role will involve troubleshooting and maintenance of equipment and participate in instrument qualification. 4. You will write and review technical documents such as SOPs, protocols and reports, coach and mentor less experienced colleagues as well as review existing processes and provide input into continuous improvements. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Senior Analytical Chemist we are looking to identify the following on your profile and past history: 1. Relevant degree in a Chemistry related discipline. 2. Proven industry experience in analytical techniques such as HPLC and UPLC. 3. A working knowledge and practical experience with ICH guidelines and pharmacopoeias as well as working within a GMP and or GLP environment. Key Words: HPLC, UPLC, Senior Analyst, Senior Scientist, Analytical Development, Validation, Hertfordshire, South East. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
A globally-renowned chemical development business based in Oxford is currently recruiting for a Development Chemist to join its R&D team on a permanent basis. As Development Chemist, you will play a vital role in developing new innovative products, assisting with process optimisation and carrying out product application testing (surface analysis). Development Chemist Manage product development projects as directed via Management. Assisting and contribute to process optimisation duties. Carry out routine product application testing (surface analysis). Develop suitable application testing regimes for customer reference. Development of prototype formulations/products and optimising current portfolio of product range. Gain a strong understanding of production capabilities and core technologies to allow new product development to be carried out effectively. Assist with new product development projects. Produce technical datasheets, batch sheets and QC documentation. Carry out new raw material evaluations. Development Chemist requirements You must possess a degree level qualification (BSc/MChem/MSci) in Chemistry. Proven experience working within a commercial R&D laboratory - ideally focusing on development/formulation projects. Ability to work well both independently and as a member of a multi-functional group. Highly motivated coupled with strong problem-solving skills. Strong communication skills with the ability to liaise directly with customers/clients. To bring creativity and innovation to the team. In return, the company can provide an excellent platform to develop a successful career-focused to new product development and highly technical applications. £Comp + excellent company benefits. Development Chemist/Formulation/R&D/Chemistry/Surface Chemistry/Polymers/Emulsions
Dec 06, 2019
Full time
A globally-renowned chemical development business based in Oxford is currently recruiting for a Development Chemist to join its R&D team on a permanent basis. As Development Chemist, you will play a vital role in developing new innovative products, assisting with process optimisation and carrying out product application testing (surface analysis). Development Chemist Manage product development projects as directed via Management. Assisting and contribute to process optimisation duties. Carry out routine product application testing (surface analysis). Develop suitable application testing regimes for customer reference. Development of prototype formulations/products and optimising current portfolio of product range. Gain a strong understanding of production capabilities and core technologies to allow new product development to be carried out effectively. Assist with new product development projects. Produce technical datasheets, batch sheets and QC documentation. Carry out new raw material evaluations. Development Chemist requirements You must possess a degree level qualification (BSc/MChem/MSci) in Chemistry. Proven experience working within a commercial R&D laboratory - ideally focusing on development/formulation projects. Ability to work well both independently and as a member of a multi-functional group. Highly motivated coupled with strong problem-solving skills. Strong communication skills with the ability to liaise directly with customers/clients. To bring creativity and innovation to the team. In return, the company can provide an excellent platform to develop a successful career-focused to new product development and highly technical applications. £Comp + excellent company benefits. Development Chemist/Formulation/R&D/Chemistry/Surface Chemistry/Polymers/Emulsions
12 month contact - Automation Scientist Salary: Basic is negotiable DOE + Bonus + Healthcare (through vitality) + Pension (up to 5% matched) + Secure Car Parking + 28 days Holiday (plus stats) Based: Manchester, UK The Requirements: 5+ years of laboratory experience within an industrial setting, of which 3+ years spent in an automation scientist, Laboratory Scientist, Laboratory Engineer, Laboratory Technician, Researcher, Automation Scientist, Automation Engineer, Automation Specialist role (must have Scripting, Software Integration/ IT experience) related to the Automated/ Robotic machines/ a range of automated liquid handlers, plate readers, automation software and equipment by manufacturers such as Tecan, TTP Labtech, PerkinElmer, Beckman Coulter, Hamilton, Agilent etc. Experience with Tecan liquid handlers, in particular the EVO series, is desirable Software programming skills for robotic operation and graphical user interface, and a good working knowledge of GLP, as well as instrument qualification and validation Able to analyse scientific workflows and recommend changes to improve scientific processes, as well as a good grasp of experimental design and execution The Responsibilities: To design, implement and optimise automation processes to support the design, development verification and validation of molecular diagnostic products for prenatal screening Provide automation expertise on projects, ensuring experimental work is well planned and executed to a high quality in a timely fashion Install, test and validate new automation systems, in particular the Tecan Evo series Ensure that validated systems are maintained in compliance with the Quality System, engage with Scientists and Technicians to automate existing laboratory processes Establish efficient interfaces between automated instruments to enable user friendly workflows Design and optimise automation workflows to ensure they are compatible with test reagents and meet scientific needs and user requirements Enable data transfer and traceability between automation platforms and LIMS (or similar) systems Train and support other team member as well as customers in the use of laboratory automation systems, automated equipment and software The Company and Opportunity: Our client is a molecular diagnostics business that develops and commercialises genetic products and services Their product development, research service and commercial capabilities extend across the lifecycle of DNA test development including regulatory submissions They work in partnership with global leaders in DNA technology to advance diagnostic science Market leaders within the In-vitro Diagnostics Assay development field
Dec 06, 2019
Contractor
12 month contact - Automation Scientist Salary: Basic is negotiable DOE + Bonus + Healthcare (through vitality) + Pension (up to 5% matched) + Secure Car Parking + 28 days Holiday (plus stats) Based: Manchester, UK The Requirements: 5+ years of laboratory experience within an industrial setting, of which 3+ years spent in an automation scientist, Laboratory Scientist, Laboratory Engineer, Laboratory Technician, Researcher, Automation Scientist, Automation Engineer, Automation Specialist role (must have Scripting, Software Integration/ IT experience) related to the Automated/ Robotic machines/ a range of automated liquid handlers, plate readers, automation software and equipment by manufacturers such as Tecan, TTP Labtech, PerkinElmer, Beckman Coulter, Hamilton, Agilent etc. Experience with Tecan liquid handlers, in particular the EVO series, is desirable Software programming skills for robotic operation and graphical user interface, and a good working knowledge of GLP, as well as instrument qualification and validation Able to analyse scientific workflows and recommend changes to improve scientific processes, as well as a good grasp of experimental design and execution The Responsibilities: To design, implement and optimise automation processes to support the design, development verification and validation of molecular diagnostic products for prenatal screening Provide automation expertise on projects, ensuring experimental work is well planned and executed to a high quality in a timely fashion Install, test and validate new automation systems, in particular the Tecan Evo series Ensure that validated systems are maintained in compliance with the Quality System, engage with Scientists and Technicians to automate existing laboratory processes Establish efficient interfaces between automated instruments to enable user friendly workflows Design and optimise automation workflows to ensure they are compatible with test reagents and meet scientific needs and user requirements Enable data transfer and traceability between automation platforms and LIMS (or similar) systems Train and support other team member as well as customers in the use of laboratory automation systems, automated equipment and software The Company and Opportunity: Our client is a molecular diagnostics business that develops and commercialises genetic products and services Their product development, research service and commercial capabilities extend across the lifecycle of DNA test development including regulatory submissions They work in partnership with global leaders in DNA technology to advance diagnostic science Market leaders within the In-vitro Diagnostics Assay development field
We are currently looking for a DMPK Project Leader to join a leading contract research origination based in Cambridgeshire area. This is a great opportunity for an experienced DMPK scientist / project manager that is using DMPK/ADME in integrated drug discovery projects. KEY DUTIES AND RESPONSIBILITIES: Your duties as the DMPK Project Leader will be varied however the key duties and responsibilities are as follows: 1. You will be the technical expert to support the ADME programs, by developing the DMPK strategy. 2. You will impact the drug discovery projects through candidate selection, defining the project direction and the overall strategy. 3. Keep up to date with new technologies and approached in order to define the future of the department. 4. As the DMPK Project Leader, you will collaborate with internal teams to drive the porject further, prepare proposals and present to clients. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Senior Scientist - DMPK we are looking to identify the following on your profile and past history: 1. Relevant degree in a scientific discipline, including but not limited to Biochemisry, Biological Sciences, Molecular Biology etc. 2. Proven industry experience working in DMPK / ADME 3. A working knowledge and practical experience with data processing. Key Words: ADME / PK / DMPK / Project Management / Project Leader / Leadership / Biochemistry / Molecular Biology / Biology / Life Science / ADME / Assay / CRO
Dec 06, 2019
Full time
We are currently looking for a DMPK Project Leader to join a leading contract research origination based in Cambridgeshire area. This is a great opportunity for an experienced DMPK scientist / project manager that is using DMPK/ADME in integrated drug discovery projects. KEY DUTIES AND RESPONSIBILITIES: Your duties as the DMPK Project Leader will be varied however the key duties and responsibilities are as follows: 1. You will be the technical expert to support the ADME programs, by developing the DMPK strategy. 2. You will impact the drug discovery projects through candidate selection, defining the project direction and the overall strategy. 3. Keep up to date with new technologies and approached in order to define the future of the department. 4. As the DMPK Project Leader, you will collaborate with internal teams to drive the porject further, prepare proposals and present to clients. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Senior Scientist - DMPK we are looking to identify the following on your profile and past history: 1. Relevant degree in a scientific discipline, including but not limited to Biochemisry, Biological Sciences, Molecular Biology etc. 2. Proven industry experience working in DMPK / ADME 3. A working knowledge and practical experience with data processing. Key Words: ADME / PK / DMPK / Project Management / Project Leader / Leadership / Biochemistry / Molecular Biology / Biology / Life Science / ADME / Assay / CRO
SPD Development Company Limited
Bedford, Bedfordshire
A rare opportunity has arisen for a Junior Programmer to join our Statistics and Data Management team based at our Bedford site. The primary aim of this role is to provide programming support to the Data Management team as well as providing input into data management strategy within the business, seeking opportunities for improvement and supporting the rollout/upgrade of software. Main Responsibilities Working alongside the Data Management Programmer with key stake holders (team members, project leaders, etc.) to fully understand the requirements of any required applications. Case Record Form (CRF) design using Teleform data capture system according to study protocol. Microsoft Excel workbook and Macro development . Developing new SAS applications which enable efficient processing, storage and summary of data from both internal and external clinical trials and product V&V work. Ensuring all systems are fully documented and validated according to QMS requirements. Contributing to continuous process improvement and seek opportunities for improving efficiency, maximising use and value of technology. Person Specification Educated to degree level with some programming experience or at least 2 years' relevant programming experience. An interest and aptitude in data management technologies . The ability to read and understand a clinical protocol and, with support from Data Management Programmer, to understand what Data Management support. Programming experience and a desire to learn programming in SAS. Some experience of the programming in SAS (SAS/BASE) is required, although further training will be given. Existing knowledge of the technology landscape and practices in clinical data management would be highly advantageous. Experience of designing OCR data forms would be an advantage although full training in Teleform software will be given. Experience of programming in Visual Studio .NET (e.g. VB .NET) would be an advantage. Knowledge of SQL would be an advantage. Experience in developing macros would be an advantage. What we can offer you 25 days paid annual leave (plus bank holidays) Enhanced Maternity and Paternity Pay Private Medical Insurance Medical Cash Plan Scheme Company Pension Scheme Life Assurance Employee Health and Wellbeing Programme Free Parking and Electric Car Charging Points Subsidised Onsite Café Parkland Setting If you require any reasonable adjustments to support you, at any stage during the application process, just let us know how we can help. PLEASE NOTE: We are not able to offer sponsorship at this time. All applicants must have an unrestricted right to work in the UK. About SPD Swiss Precision Diagnostics (SPD) was formed in 2007 as a joint venture between Procter & Gamble (P&G) and Alere, now a wholly owned subsidiary of Abbott, to create, using its parent companies' complementary strengths, one of the world's foremost organisations in consumer diagnostics. We are a leading supplier of home pregnancy and fertility/ovulation tests. These are products designed to give women a better understanding of their own reproductive health and invaluable guidance in their family planning. Our research interests are in the broad application of innovative technologies for use by the consumer at home. We have a strong focus on women's reproductive health and our goals are in the continuing supply of useful diagnostic products which are accurate, simple and affordable. In the achievement of these goals, we believe that SPD consumer diagnostic products will make increasing contributions to personal healthcare and well-being. SPD's Head Office is based in Geneva, Switzerland, and our Innovation Centre is based in Bedford, UK. SPD employs around 180 people.
Dec 06, 2019
Full time
A rare opportunity has arisen for a Junior Programmer to join our Statistics and Data Management team based at our Bedford site. The primary aim of this role is to provide programming support to the Data Management team as well as providing input into data management strategy within the business, seeking opportunities for improvement and supporting the rollout/upgrade of software. Main Responsibilities Working alongside the Data Management Programmer with key stake holders (team members, project leaders, etc.) to fully understand the requirements of any required applications. Case Record Form (CRF) design using Teleform data capture system according to study protocol. Microsoft Excel workbook and Macro development . Developing new SAS applications which enable efficient processing, storage and summary of data from both internal and external clinical trials and product V&V work. Ensuring all systems are fully documented and validated according to QMS requirements. Contributing to continuous process improvement and seek opportunities for improving efficiency, maximising use and value of technology. Person Specification Educated to degree level with some programming experience or at least 2 years' relevant programming experience. An interest and aptitude in data management technologies . The ability to read and understand a clinical protocol and, with support from Data Management Programmer, to understand what Data Management support. Programming experience and a desire to learn programming in SAS. Some experience of the programming in SAS (SAS/BASE) is required, although further training will be given. Existing knowledge of the technology landscape and practices in clinical data management would be highly advantageous. Experience of designing OCR data forms would be an advantage although full training in Teleform software will be given. Experience of programming in Visual Studio .NET (e.g. VB .NET) would be an advantage. Knowledge of SQL would be an advantage. Experience in developing macros would be an advantage. What we can offer you 25 days paid annual leave (plus bank holidays) Enhanced Maternity and Paternity Pay Private Medical Insurance Medical Cash Plan Scheme Company Pension Scheme Life Assurance Employee Health and Wellbeing Programme Free Parking and Electric Car Charging Points Subsidised Onsite Café Parkland Setting If you require any reasonable adjustments to support you, at any stage during the application process, just let us know how we can help. PLEASE NOTE: We are not able to offer sponsorship at this time. All applicants must have an unrestricted right to work in the UK. About SPD Swiss Precision Diagnostics (SPD) was formed in 2007 as a joint venture between Procter & Gamble (P&G) and Alere, now a wholly owned subsidiary of Abbott, to create, using its parent companies' complementary strengths, one of the world's foremost organisations in consumer diagnostics. We are a leading supplier of home pregnancy and fertility/ovulation tests. These are products designed to give women a better understanding of their own reproductive health and invaluable guidance in their family planning. Our research interests are in the broad application of innovative technologies for use by the consumer at home. We have a strong focus on women's reproductive health and our goals are in the continuing supply of useful diagnostic products which are accurate, simple and affordable. In the achievement of these goals, we believe that SPD consumer diagnostic products will make increasing contributions to personal healthcare and well-being. SPD's Head Office is based in Geneva, Switzerland, and our Innovation Centre is based in Bedford, UK. SPD employs around 180 people.
We need an exceptional 2019 Physics Graduate to join a thriving Science & Technology Consultancy based near Cambridge. This is very much a 'hands-on' physics role with a high degree of experimental science, but also requires excellent maths and fundamental understanding of physics from first principles, together with a passion for using science to solve real world problems and develop cutting-edge technologies. This is an exceptional opportunity for a bright physicist who loves science and has a desire to apply their knowledge in a commercial setting. However, make no mistake -it may be called 'consultancy' but this is real, cutting edge R&D science! Projects are varied, all highly innovative in nature and cover a diverse range of technologies for external customers. Typical projects include Scientific Instruments, Medical Devices, Biotechnology, Consumer Electronics and Robotics just to name just a few. Projects are typically 3-6months duration and quick turnaround ensuring that boredom will never be an issue! The company is an excellent employer and the Physicist can expect bespoke training and mentorship programmes, plus excellent future career opportunities and a highly competitive remuneration package. The Graduate Physicist will: Design experimental apparatus and conduct proof-of-principle experiments Develop prototypes involving elements of electronics, optics, sensors, mechanics, etc Analyse systems from first principals, develop scientific solutions to challenging real-world technical problems and take them through the product development process; Identify and research diverse new technologies for possible commercial exploitation Manage tasks as part of a multi-disciplinary product development team; Analyse and report on statistical data from experimental sources, present results and findings to colleagues and external customers. Requirements: A 2.1 or 1st class BSc (Hons) or MPhys Degree in Physics, Applied Physics or similar from a top-tier university, along with AAB grades at A-Level -or direct equivalent. Broad, intuitive and hands-on understanding of how physics effects real processes and products in the real world Strong analytical and mathematical ability Ability to analyse a wide range of data, structure thoughts, draw robust conclusions and communicate results in clear, concise verbal and written English.
Dec 06, 2019
Full time
We need an exceptional 2019 Physics Graduate to join a thriving Science & Technology Consultancy based near Cambridge. This is very much a 'hands-on' physics role with a high degree of experimental science, but also requires excellent maths and fundamental understanding of physics from first principles, together with a passion for using science to solve real world problems and develop cutting-edge technologies. This is an exceptional opportunity for a bright physicist who loves science and has a desire to apply their knowledge in a commercial setting. However, make no mistake -it may be called 'consultancy' but this is real, cutting edge R&D science! Projects are varied, all highly innovative in nature and cover a diverse range of technologies for external customers. Typical projects include Scientific Instruments, Medical Devices, Biotechnology, Consumer Electronics and Robotics just to name just a few. Projects are typically 3-6months duration and quick turnaround ensuring that boredom will never be an issue! The company is an excellent employer and the Physicist can expect bespoke training and mentorship programmes, plus excellent future career opportunities and a highly competitive remuneration package. The Graduate Physicist will: Design experimental apparatus and conduct proof-of-principle experiments Develop prototypes involving elements of electronics, optics, sensors, mechanics, etc Analyse systems from first principals, develop scientific solutions to challenging real-world technical problems and take them through the product development process; Identify and research diverse new technologies for possible commercial exploitation Manage tasks as part of a multi-disciplinary product development team; Analyse and report on statistical data from experimental sources, present results and findings to colleagues and external customers. Requirements: A 2.1 or 1st class BSc (Hons) or MPhys Degree in Physics, Applied Physics or similar from a top-tier university, along with AAB grades at A-Level -or direct equivalent. Broad, intuitive and hands-on understanding of how physics effects real processes and products in the real world Strong analytical and mathematical ability Ability to analyse a wide range of data, structure thoughts, draw robust conclusions and communicate results in clear, concise verbal and written English.
Job Title: Quality Controller Location: East Sussex Job Type: Permanent Salary: £25,000 Clinitemp are looking for a QC Analyst to work in a Cosmetic manufacturer, to be responsible for the creation, development and maintenance of the company's Quality Management System. Responsibilities: To be responsible for the integration, implementation and maintenance of the company's Quality Management System across all areas of the business. To ensure that the company is operating in accordance with the principles and practices contained within the Quality Management System at all times. To ensure that both suppliers and customers are always fully aware of the requirements contained within the company's Quality Management System and operate within these requirements. To ensure that the company's Quality Management System is fully in accordance with the requirements of the company's chosen industry standards and accreditations at all times. To propose, and where required, implement such changes and adjustments as are required to ensure full compliance with the System and linked accreditations. To carry out regular reviews and audits of all internal Quality practices and procedures correctly document findings and act where appropriate and required. Requirements: Auditing experience Previous ISO experience Previous experience within a Production environment
Dec 06, 2019
Full time
Job Title: Quality Controller Location: East Sussex Job Type: Permanent Salary: £25,000 Clinitemp are looking for a QC Analyst to work in a Cosmetic manufacturer, to be responsible for the creation, development and maintenance of the company's Quality Management System. Responsibilities: To be responsible for the integration, implementation and maintenance of the company's Quality Management System across all areas of the business. To ensure that the company is operating in accordance with the principles and practices contained within the Quality Management System at all times. To ensure that both suppliers and customers are always fully aware of the requirements contained within the company's Quality Management System and operate within these requirements. To ensure that the company's Quality Management System is fully in accordance with the requirements of the company's chosen industry standards and accreditations at all times. To propose, and where required, implement such changes and adjustments as are required to ensure full compliance with the System and linked accreditations. To carry out regular reviews and audits of all internal Quality practices and procedures correctly document findings and act where appropriate and required. Requirements: Auditing experience Previous ISO experience Previous experience within a Production environment
This is a fantastic opportunity to join a rapidly growing and evolving global FMCG manufacturer, looking for a quality systems technologist to develop and maintain its systems in support of the quality and food safety function, including driving systems strategy and continuous improvement. This will be on a 12-month fixed-term contract after which there may be the possibility of it becoming a permanent role. Our client is looking for a driven and highly motivated individual to continue the development of the quality systems to satisfy the business needs for all core quality processes and be the go-to expert for all quality systems and processes. The job holder will also be responsible for maintaining all quality related data, providing relevant training and support internally and conducting internal audits. About you You will be qualified by degree (or equivalent) in a related subject and have experience working with quality systems within food manufacturing. You will have a good knowledge of relevant software and computer systems and have an understanding of lean principles associated with the design and development of quality systems and processes. This is an exciting opportunity for an ambitious individual looking to further their career. If you are interested and have a proven track record of success, we would like to hear from you. Please call Camilla Clark at Rockfield Specialist Recruitment or apply now, with your CV, on-line.
Dec 06, 2019
Contractor
This is a fantastic opportunity to join a rapidly growing and evolving global FMCG manufacturer, looking for a quality systems technologist to develop and maintain its systems in support of the quality and food safety function, including driving systems strategy and continuous improvement. This will be on a 12-month fixed-term contract after which there may be the possibility of it becoming a permanent role. Our client is looking for a driven and highly motivated individual to continue the development of the quality systems to satisfy the business needs for all core quality processes and be the go-to expert for all quality systems and processes. The job holder will also be responsible for maintaining all quality related data, providing relevant training and support internally and conducting internal audits. About you You will be qualified by degree (or equivalent) in a related subject and have experience working with quality systems within food manufacturing. You will have a good knowledge of relevant software and computer systems and have an understanding of lean principles associated with the design and development of quality systems and processes. This is an exciting opportunity for an ambitious individual looking to further their career. If you are interested and have a proven track record of success, we would like to hear from you. Please call Camilla Clark at Rockfield Specialist Recruitment or apply now, with your CV, on-line.
Data Scientist - disruptive fintech London £60,000-£75,000 + benefits This an exciting new opportunity for growth and development, quick! You will be joining a rapidly expanding start up, get in early and fast-track your development. As a Data Scientist in this team, you will be focusing on applying machine learning to large data sets, setting up models to analyse customer responsibility. Join an exploratory Data Science team that implements advanced statistical modelling and machine learning techniques. THIS COMPANY: This fast-growing fintech company builds and develops partnerships with its clients to gain any external data sets, they are heavily invested in finding the next top Data Scientist. They are looking for someone to join a team that champions a data-driven approach to all business decisions and pioneers ideas in data science with fintech. You will be working closely with teams across other business areas and communicating technical concepts to non-technical stakeholders. THE ROLE: Working with large world data sets from any external source, building advanced statistical and machine learning models to analyse how customers are using their product and producing insights off the back of this. As a Data Scientist, you will be responsible using alternative data, including transactional and GPS data to build tailored machine learning solutions. You will be encouraged to lead your own research into creating tailored solutions to technical problems and take on as much or as little responsibility as you feel you can manage, with the opportunity to manage in the near future. Applying advanced predictive modelling and machine learning techniques, in Python, to large data sets to set up forecasting Experimenting with machine learning techniques using Python Using SQL for data manipulation Effectively delivering technical concepts to non-technical stakeholders YOUR SKILLS AND EXPERIENCE: Extensive knowledge and use of Python for machine learning and SQL for manipulating data Proven commercial experience building scorecards and machine learning models using Python The successful data scientist will have industrial experience using machine learning techniques, in Python, for forecasting The ideal candidate will have the ability to communicate heavily technical concepts in an effective way and have experience delivering such to non-technical stakeholders THE BENEFITS: £60,000-£75,000 + benefits + bonus Fortnightly meet ups HOW TO APPLY: Please register your interest by sending your CV to Kian Dixon via the Apply link on this page. For more information about similar roles, please get in touch!
Dec 06, 2019
Full time
Data Scientist - disruptive fintech London £60,000-£75,000 + benefits This an exciting new opportunity for growth and development, quick! You will be joining a rapidly expanding start up, get in early and fast-track your development. As a Data Scientist in this team, you will be focusing on applying machine learning to large data sets, setting up models to analyse customer responsibility. Join an exploratory Data Science team that implements advanced statistical modelling and machine learning techniques. THIS COMPANY: This fast-growing fintech company builds and develops partnerships with its clients to gain any external data sets, they are heavily invested in finding the next top Data Scientist. They are looking for someone to join a team that champions a data-driven approach to all business decisions and pioneers ideas in data science with fintech. You will be working closely with teams across other business areas and communicating technical concepts to non-technical stakeholders. THE ROLE: Working with large world data sets from any external source, building advanced statistical and machine learning models to analyse how customers are using their product and producing insights off the back of this. As a Data Scientist, you will be responsible using alternative data, including transactional and GPS data to build tailored machine learning solutions. You will be encouraged to lead your own research into creating tailored solutions to technical problems and take on as much or as little responsibility as you feel you can manage, with the opportunity to manage in the near future. Applying advanced predictive modelling and machine learning techniques, in Python, to large data sets to set up forecasting Experimenting with machine learning techniques using Python Using SQL for data manipulation Effectively delivering technical concepts to non-technical stakeholders YOUR SKILLS AND EXPERIENCE: Extensive knowledge and use of Python for machine learning and SQL for manipulating data Proven commercial experience building scorecards and machine learning models using Python The successful data scientist will have industrial experience using machine learning techniques, in Python, for forecasting The ideal candidate will have the ability to communicate heavily technical concepts in an effective way and have experience delivering such to non-technical stakeholders THE BENEFITS: £60,000-£75,000 + benefits + bonus Fortnightly meet ups HOW TO APPLY: Please register your interest by sending your CV to Kian Dixon via the Apply link on this page. For more information about similar roles, please get in touch!
The Company T he BBI Group offers a portfolio of products and services to the diagnostic, healthcare, research, defence and food industries globally. Our mission is to deliver exceptional products and technologies that people rely on to enjoy a better quality of life. Through innovation, partnership, effective delivery and the collaboration of our people, we constantly strive to help set industry standards, engender trust and build our reputation for excellence. BBI Solutions has served the global diagnostics industry for over 50 years, as a leading developer and manufacturer of raw materials and finished test platforms for the in-vitro diagnostics market. We currently have an opportunity for a Development Scientist to join us at our Global Headquarters in Crumlin. Benefits The salary offered for this role is competitive and makes up part of BBI's attractive benefits package, which includes: 5% contributory pension scheme Life Assurance Private health care scheme Generous annual leave package totalling 32 days (inclusive of bank holidays) Participation in the childcare voucher and cycle to work schemes The Role As a Development Scientist you will be responsible for completing planned laboratory work for projects within the Enzymes team. The Development Scientist is expected to complete and write up experiments accurately utilizing approved formats. The role will also involve analysis and presentation of all results using excel and power point for review and discussion by the project team. Key responsibilities will include but not be limited to; Complete Laboratory work to BBI quality and health and safety requirements. Complete experiemental write ups to QMS requirements and work with appropriate colleagues to review and approve in a timely manner. Review of other scientists/senior scientists experimental write ups to achive consistent quality and meet all QMS requirements. Complete timesheets in an accurate and timely fashion. Requirements As the Development Scientist you will be expected to have significant experience of working within a laboratory environment and be familiar with GLP and working within QMS. Effective communication skills are key, both within the team and also with internal and external customers. It is paramount that you can work independently, accurately and plan experiments with appropriate controls. You will hold a science-based degree and have a good working knowledge in the application of statistical methods (both analytical and descriptive). A knowledge of immunology and analytical techniques such as ELISA would be an advantage. If you are an internal employee applying for this vacancy you and your manager are required to complete an internal transfer form. This needs to be completed in full and attached to your application along with your CV and cover letter.
Dec 06, 2019
Full time
The Company T he BBI Group offers a portfolio of products and services to the diagnostic, healthcare, research, defence and food industries globally. Our mission is to deliver exceptional products and technologies that people rely on to enjoy a better quality of life. Through innovation, partnership, effective delivery and the collaboration of our people, we constantly strive to help set industry standards, engender trust and build our reputation for excellence. BBI Solutions has served the global diagnostics industry for over 50 years, as a leading developer and manufacturer of raw materials and finished test platforms for the in-vitro diagnostics market. We currently have an opportunity for a Development Scientist to join us at our Global Headquarters in Crumlin. Benefits The salary offered for this role is competitive and makes up part of BBI's attractive benefits package, which includes: 5% contributory pension scheme Life Assurance Private health care scheme Generous annual leave package totalling 32 days (inclusive of bank holidays) Participation in the childcare voucher and cycle to work schemes The Role As a Development Scientist you will be responsible for completing planned laboratory work for projects within the Enzymes team. The Development Scientist is expected to complete and write up experiments accurately utilizing approved formats. The role will also involve analysis and presentation of all results using excel and power point for review and discussion by the project team. Key responsibilities will include but not be limited to; Complete Laboratory work to BBI quality and health and safety requirements. Complete experiemental write ups to QMS requirements and work with appropriate colleagues to review and approve in a timely manner. Review of other scientists/senior scientists experimental write ups to achive consistent quality and meet all QMS requirements. Complete timesheets in an accurate and timely fashion. Requirements As the Development Scientist you will be expected to have significant experience of working within a laboratory environment and be familiar with GLP and working within QMS. Effective communication skills are key, both within the team and also with internal and external customers. It is paramount that you can work independently, accurately and plan experiments with appropriate controls. You will hold a science-based degree and have a good working knowledge in the application of statistical methods (both analytical and descriptive). A knowledge of immunology and analytical techniques such as ELISA would be an advantage. If you are an internal employee applying for this vacancy you and your manager are required to complete an internal transfer form. This needs to be completed in full and attached to your application along with your CV and cover letter.
Job Title: Plasma Physicist - Turbulence and Transport Location: Milton Park, Abingdon (OX14) Salary: Competitive, depending on experience Background: The Company has unlocked a new route to scalable fusion power that is cost-effective and does not require huge infrastructure and capital expenditure. The technology could revolutionise the world's energy production - it will be possible to produce more energy, more cheaply and with fewer harmful side effects (e.g. long term nuclear waste or carbon emissions). They aim to accelerate the development of fusion energy by combining two emerging technologies - spherical tokamaks and high-temperature superconductors. The company's innovation has been featured on Channel 4 news, BBC News Click, Reuters internet news channel and they received a Technology Pioneer Award at the World Economic Forum in 2016. This is the chance to join a fast-growing high technology company with an agile, dynamic team and to tackle the challenge of a lifetime. The Role: Do you want to help make fusion power a reality? Are you a plasma physicist looking for a unique and exciting new opportunity? If so, the Company are seeking talented and innovative individuals that are passionate about accelerating the development of fusion power to join the physics team. Their mission is to transform the way the world generates power by creating a clean, safe and sustainable source of energy for current and future generations and their innovative approach to fusion is based on two emerging technologies: spherical tokamaks (STs) and high-field magnets made from high temperature superconductors (HTS). Experimental results from MAST and NSTX have shown that the thermal energy confinement time within spherical tokamaks has a strong favourable dependence on increasing toroidal field (reducing collisionality). When extrapolating to reactor relevant regimes this improved confinement opens the possibility of compact fusion. To investigate the effects of toroidal field on plasma performance the Company has constructed the high field spherical tokamak ST40. To date ST40 has operated with 1.5T toroidal field (already the world's highest field ST) and will soon be commissioned up to its design specification of 3T. They are seeking a talented scientist to interpret experimental results using a transport code (most likely TRANSP). In parallel to the ST40 experimental campaign they are also designing the future tokamaks ST-F1 and ST-E1. The successful candidate will use the transport code to predict the performance of these devices and inform the decision of device parameters (e.g. choosing the toroidal field and plasma current). Finally, they'd like to understand the nature of confinement from a theoretical first-principles perspective and develop reduced transport models. To this end they'd like to develop gyrokinetic turbulence simulations both in-house and through collaborations with world-leading scientific laboratories. Personal Skills and Attributes: Essential Selection Criteria: PhD in plasma physics or closely related equivalent experience Experience working in a research environment Ability to work efficiently on own initiative Willingness to develop new and existing collaborations Highly motivated to deliver against challenging objectives in a compressed timescale Ability to contribute effectively in a multi-disciplinary team of engineers and scientists Willingness to learn and adopt new techniques and technologies Ability to effectively communicate results to both technical and non-technical colleagues Organised approach to tackling complex problems Desirable Selection Criteria: Familiarity with tokamak/plasma modelling codes. In particular any knowledge of transport codes and/or gyrokinetic codes. Experience of programming languages such as Fortran/C++/Matlab/Python/Unix Publication history Benefits: 25 Days Holiday (plus bank holidays) Company Pension scheme: Company contribution of 5% of salary after 3 months' service Eligible for company share option scheme after one years' service Company bonus scheme, discretionary, dependent on performance Private medical insurance after 3 months' service Please note: Only candidates with the relevant skills and experience will be contacted regarding this position. If you do not hear back within 10 days of submitting your application then unfortunately you have been unsuccessful. However, you may be contacted in the future to discuss other opportunities. No terminology in the advert or job description is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the duties of the job. Please click the APPLY button to send your CV and Cover Letter for the role. Candidates with the experience or relevant job titles of; Graduate, Nuclear Physicist, PHD Graduate, Nuclear Scientist, Plasma Scientist may also be considered for this role.
Dec 06, 2019
Full time
Job Title: Plasma Physicist - Turbulence and Transport Location: Milton Park, Abingdon (OX14) Salary: Competitive, depending on experience Background: The Company has unlocked a new route to scalable fusion power that is cost-effective and does not require huge infrastructure and capital expenditure. The technology could revolutionise the world's energy production - it will be possible to produce more energy, more cheaply and with fewer harmful side effects (e.g. long term nuclear waste or carbon emissions). They aim to accelerate the development of fusion energy by combining two emerging technologies - spherical tokamaks and high-temperature superconductors. The company's innovation has been featured on Channel 4 news, BBC News Click, Reuters internet news channel and they received a Technology Pioneer Award at the World Economic Forum in 2016. This is the chance to join a fast-growing high technology company with an agile, dynamic team and to tackle the challenge of a lifetime. The Role: Do you want to help make fusion power a reality? Are you a plasma physicist looking for a unique and exciting new opportunity? If so, the Company are seeking talented and innovative individuals that are passionate about accelerating the development of fusion power to join the physics team. Their mission is to transform the way the world generates power by creating a clean, safe and sustainable source of energy for current and future generations and their innovative approach to fusion is based on two emerging technologies: spherical tokamaks (STs) and high-field magnets made from high temperature superconductors (HTS). Experimental results from MAST and NSTX have shown that the thermal energy confinement time within spherical tokamaks has a strong favourable dependence on increasing toroidal field (reducing collisionality). When extrapolating to reactor relevant regimes this improved confinement opens the possibility of compact fusion. To investigate the effects of toroidal field on plasma performance the Company has constructed the high field spherical tokamak ST40. To date ST40 has operated with 1.5T toroidal field (already the world's highest field ST) and will soon be commissioned up to its design specification of 3T. They are seeking a talented scientist to interpret experimental results using a transport code (most likely TRANSP). In parallel to the ST40 experimental campaign they are also designing the future tokamaks ST-F1 and ST-E1. The successful candidate will use the transport code to predict the performance of these devices and inform the decision of device parameters (e.g. choosing the toroidal field and plasma current). Finally, they'd like to understand the nature of confinement from a theoretical first-principles perspective and develop reduced transport models. To this end they'd like to develop gyrokinetic turbulence simulations both in-house and through collaborations with world-leading scientific laboratories. Personal Skills and Attributes: Essential Selection Criteria: PhD in plasma physics or closely related equivalent experience Experience working in a research environment Ability to work efficiently on own initiative Willingness to develop new and existing collaborations Highly motivated to deliver against challenging objectives in a compressed timescale Ability to contribute effectively in a multi-disciplinary team of engineers and scientists Willingness to learn and adopt new techniques and technologies Ability to effectively communicate results to both technical and non-technical colleagues Organised approach to tackling complex problems Desirable Selection Criteria: Familiarity with tokamak/plasma modelling codes. In particular any knowledge of transport codes and/or gyrokinetic codes. Experience of programming languages such as Fortran/C++/Matlab/Python/Unix Publication history Benefits: 25 Days Holiday (plus bank holidays) Company Pension scheme: Company contribution of 5% of salary after 3 months' service Eligible for company share option scheme after one years' service Company bonus scheme, discretionary, dependent on performance Private medical insurance after 3 months' service Please note: Only candidates with the relevant skills and experience will be contacted regarding this position. If you do not hear back within 10 days of submitting your application then unfortunately you have been unsuccessful. However, you may be contacted in the future to discuss other opportunities. No terminology in the advert or job description is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the duties of the job. Please click the APPLY button to send your CV and Cover Letter for the role. Candidates with the experience or relevant job titles of; Graduate, Nuclear Physicist, PHD Graduate, Nuclear Scientist, Plasma Scientist may also be considered for this role.
I am actively seeking a Inhalation Formulation Scientist in Loughbrough. This is a contract role with possibility of extension/permanent. Please see details below. An opportunity has arisen for an individual to join a global science based technology company who is committed to improving lives and the world. One third of my client's revenue comes from products that didn't exist five years ago and they are looking to better this. In this role, you will be given the freedom to lead the laboratory manufacture of formulations and small-scale product batches. Furthermore, you will be responsible for assisting/leading the characterisation of raw materials and development of formulations. This opportunity will enable you to plan, lead and execute a range of multiple experimental studies working across cross functional teams. This role will allow you to perform research, create, develop and formulate MDI/DPI inhalation products via a QbD framework. You will be tasked on conducting in vitro data analysis and interpretation of data via statistical software. This role will be focusing on product development and formulation of inhalation, with early phase development of new products. Role is predominantly early stage development of new products. You will play a vital role in the lab working with products, getting involved in pre work such as planning, protocol writing and research. Activities will include: * Plan, organise, lead the laboratory manufacture of formulations and small-scale product batches in line with functional/departmental requirements. * Responsible for assisting and leading the characterisation of raw materials, development of formulations and final drug dosage forms for inhalation products. * Novel & new inhalation product development and creation of intellectual property. * Undertake formulation-related testing in line with functional/departmental requirements. * Research/create/ develop/formulate MDI (or DPI) inhalation products via a QbD framework and participate in patent & IP generation. * Use physical characterisation techniques to determine properties of powders and formulations. * Conduct in-vitro data analysis and interpretation of data (preferably inhalation product testing) - via relevant statistical software packages (Excel, Minitab etc). * Research relevant industry developments in the areas of inhalation product development. * Utilise technical/practical knowledge and hands on skills in a laboratory environment using state of the art manufacturing and testing equipment. * Conduct inhalation product testing using existing and new technologies relating to inhalation product characterisation. * Author high level technical protocols / reports and present technical data to all levels within the department. * Plan, lead and execute multiple experimental studies (experimental design) working in cross functional multidisciplinary teams.
Dec 06, 2019
Contractor
I am actively seeking a Inhalation Formulation Scientist in Loughbrough. This is a contract role with possibility of extension/permanent. Please see details below. An opportunity has arisen for an individual to join a global science based technology company who is committed to improving lives and the world. One third of my client's revenue comes from products that didn't exist five years ago and they are looking to better this. In this role, you will be given the freedom to lead the laboratory manufacture of formulations and small-scale product batches. Furthermore, you will be responsible for assisting/leading the characterisation of raw materials and development of formulations. This opportunity will enable you to plan, lead and execute a range of multiple experimental studies working across cross functional teams. This role will allow you to perform research, create, develop and formulate MDI/DPI inhalation products via a QbD framework. You will be tasked on conducting in vitro data analysis and interpretation of data via statistical software. This role will be focusing on product development and formulation of inhalation, with early phase development of new products. Role is predominantly early stage development of new products. You will play a vital role in the lab working with products, getting involved in pre work such as planning, protocol writing and research. Activities will include: * Plan, organise, lead the laboratory manufacture of formulations and small-scale product batches in line with functional/departmental requirements. * Responsible for assisting and leading the characterisation of raw materials, development of formulations and final drug dosage forms for inhalation products. * Novel & new inhalation product development and creation of intellectual property. * Undertake formulation-related testing in line with functional/departmental requirements. * Research/create/ develop/formulate MDI (or DPI) inhalation products via a QbD framework and participate in patent & IP generation. * Use physical characterisation techniques to determine properties of powders and formulations. * Conduct in-vitro data analysis and interpretation of data (preferably inhalation product testing) - via relevant statistical software packages (Excel, Minitab etc). * Research relevant industry developments in the areas of inhalation product development. * Utilise technical/practical knowledge and hands on skills in a laboratory environment using state of the art manufacturing and testing equipment. * Conduct inhalation product testing using existing and new technologies relating to inhalation product characterisation. * Author high level technical protocols / reports and present technical data to all levels within the department. * Plan, lead and execute multiple experimental studies (experimental design) working in cross functional multidisciplinary teams.
PURE KAT CONSULTANCY LIMITED
Cambridge, Cambridgeshire
Position: Senior Data Scientist Location: South Cambridge Salary: £negotiable DOE Contract: Permanent, Full Time Hours: Monday - Friday 37.5 hours Sector: IT & Scientific Do you have a passion for data science with 3 years+ experience in this area or a related field? Are you well versed in Python scripting? Are you looking for a quirky company with a friendly working environment? As Senior Data Scientist you will be responsible for: Solving data analysis questions Supporting R&D activities Leading delivery of technical projects Working alongside new and existing clients regarding company technologies Working with team members to develop solutions for text analytics An ideal candidate for the Senior Data Scientist will have: 3 years+ experience in data science or related field PhD or BSc/MSc in Bioinformatics Knowledege of Python scripting Practical experience in text-analytics & text mining Ideally you will have experience within a similar position. Interviews will take place in South Cambridge, following a registration process by PureKat Consultancy Ltd. If we have not responded to your application within 3-5 days, unfortunately you have not been successful on this occasion, but please feel free to contact us for other opportunities. PureKat Consultancy is acting as an Employment Agency for this permanent vacancy.
Dec 06, 2019
Full time
Position: Senior Data Scientist Location: South Cambridge Salary: £negotiable DOE Contract: Permanent, Full Time Hours: Monday - Friday 37.5 hours Sector: IT & Scientific Do you have a passion for data science with 3 years+ experience in this area or a related field? Are you well versed in Python scripting? Are you looking for a quirky company with a friendly working environment? As Senior Data Scientist you will be responsible for: Solving data analysis questions Supporting R&D activities Leading delivery of technical projects Working alongside new and existing clients regarding company technologies Working with team members to develop solutions for text analytics An ideal candidate for the Senior Data Scientist will have: 3 years+ experience in data science or related field PhD or BSc/MSc in Bioinformatics Knowledege of Python scripting Practical experience in text-analytics & text mining Ideally you will have experience within a similar position. Interviews will take place in South Cambridge, following a registration process by PureKat Consultancy Ltd. If we have not responded to your application within 3-5 days, unfortunately you have not been successful on this occasion, but please feel free to contact us for other opportunities. PureKat Consultancy is acting as an Employment Agency for this permanent vacancy.
Orion Group Sciences are looking for a Technical Writer for our multinational pharmaceutical client based in the Middlesex area on an initial 12-month contract with the potential to extend. Main Responsibilities of the role Translate subject matter expert and stakeholder discussion and/or process model flows into written controlled document procedures Under tight timelines, lead and/or facilitate the writing, review, revision, and formatting/QC of controlled documents; adhering to format, content and style guidelines, giving consideration to usability and ensuring accuracy, consistency and quality according to templates and style guide Serve as a process documentation subject matter expert and point of contact Provide regular status updates to manager/team lead/mentor and/or to business customers to achieve goals and meet deadlines Develops, writes, edits, and formats materials such as Standard Operating Procedures, manuals, and related technical and business process documentation. When creating/revising the documentation Additionally, this position will be required to process documents via the established R&D Document Review process using the electronic document repository (EDM Quality) Need someone with critical thinking skills who is able to work independently with little direction Project manage/lead a cross-functional team of subject matter experts to drive R&D Quality processes including generation and management of MS Project timeline, identifying Quality strategy, oversight of process modeling, and oversight/generation of process documentation Work independently to edit, format and/or write SOPs or User Manuals based on a process map or QC/revise existing documentation according to template/style guide Act as "scribe" writing documents according to template/style guide during meetings with subject matter experts Lead team of subject matter experts to facilitate discussion and review of process and documentation With time, experience, and demonstrated ability, role may serve as a project manager to lead "sub-projects" representing R&D Quality processes from beginning to end including generation of MS Project timeline, strategy for process documentation, oversight of process modeling, and oversight of documentation Role will receive training on R&D structure, initiative/projects, R&D approach to controlled documentation, Quality processes (process mapping/modeling, leading/designing a process-based strategy, and controlled documentation templates and style) Desired Experience and Background of the successful candidate MS Outlook, Word, Excel, and electronic document management repositories. MS Project and Visio experience preferred At least 3 years' prior experience specifically as a technical/business writer for writing controlled process documentation (eg, SOPs, user manuals) in the bio/pharma or medical device industry (other regulated environments may be considered) Excellent verbal and written communication skills/writing skills; active listening skills; attention to detail. strong process/business writing skills Strong analytic/critical-thinking and decision making abilities Must be flexible and able to manage multiple activities and priorities with minimal direction in a rapidly changing and demanding environment Prior experience leading cross-functional team/subject matter experts Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
Dec 06, 2019
Contractor
Orion Group Sciences are looking for a Technical Writer for our multinational pharmaceutical client based in the Middlesex area on an initial 12-month contract with the potential to extend. Main Responsibilities of the role Translate subject matter expert and stakeholder discussion and/or process model flows into written controlled document procedures Under tight timelines, lead and/or facilitate the writing, review, revision, and formatting/QC of controlled documents; adhering to format, content and style guidelines, giving consideration to usability and ensuring accuracy, consistency and quality according to templates and style guide Serve as a process documentation subject matter expert and point of contact Provide regular status updates to manager/team lead/mentor and/or to business customers to achieve goals and meet deadlines Develops, writes, edits, and formats materials such as Standard Operating Procedures, manuals, and related technical and business process documentation. When creating/revising the documentation Additionally, this position will be required to process documents via the established R&D Document Review process using the electronic document repository (EDM Quality) Need someone with critical thinking skills who is able to work independently with little direction Project manage/lead a cross-functional team of subject matter experts to drive R&D Quality processes including generation and management of MS Project timeline, identifying Quality strategy, oversight of process modeling, and oversight/generation of process documentation Work independently to edit, format and/or write SOPs or User Manuals based on a process map or QC/revise existing documentation according to template/style guide Act as "scribe" writing documents according to template/style guide during meetings with subject matter experts Lead team of subject matter experts to facilitate discussion and review of process and documentation With time, experience, and demonstrated ability, role may serve as a project manager to lead "sub-projects" representing R&D Quality processes from beginning to end including generation of MS Project timeline, strategy for process documentation, oversight of process modeling, and oversight of documentation Role will receive training on R&D structure, initiative/projects, R&D approach to controlled documentation, Quality processes (process mapping/modeling, leading/designing a process-based strategy, and controlled documentation templates and style) Desired Experience and Background of the successful candidate MS Outlook, Word, Excel, and electronic document management repositories. MS Project and Visio experience preferred At least 3 years' prior experience specifically as a technical/business writer for writing controlled process documentation (eg, SOPs, user manuals) in the bio/pharma or medical device industry (other regulated environments may be considered) Excellent verbal and written communication skills/writing skills; active listening skills; attention to detail. strong process/business writing skills Strong analytic/critical-thinking and decision making abilities Must be flexible and able to manage multiple activities and priorities with minimal direction in a rapidly changing and demanding environment Prior experience leading cross-functional team/subject matter experts Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
Job Title: Plasma Physicist - MHD and Magnetics Location: Milton Park, Abingdon (OX14) Salary: Competitive, depending on experience Background: The Company has unlocked a new route to scalable fusion power that is cost-effective and does not require huge infrastructure and capital expenditure. The technology could revolutionise the world's energy production - it will be possible to produce more energy, more cheaply and with fewer harmful side effects (e.g. long term nuclear waste or carbon emissions). They aim to accelerate the development of fusion energy by combining two emerging technologies - spherical tokamaks and high-temperature superconductors. The company's innovation has been featured on Channel 4 news, BBC News Click, Reuters internet news channel and they received a Technology Pioneer Award at the World Economic Forum in 2016. This is the chance to join a fast-growing high technology company with an agile, dynamic team and to tackle the challenge of a lifetime. The Role: Do you want to help make fusion power a reality? Are you a plasma physicist looking for a unique and exciting new opportunity? If so, the Company are seeking talented and innovative individuals that are passionate about accelerating the development of fusion power to join the physics team. Their mission is to transform the way the world generates power by creating a clean, safe and sustainable source of energy for current and future generations and their innovative approach to fusion is based on two emerging technologies: spherical tokamaks (STs) and high-field magnets made from high temperature superconductors (HTS). They're looking for a research scientist to join the growing physics team to support ST40 operations and contribute to the design of future high field spherical tokamaks. The role will include analysing ST40 magnetics data to determine equilibrium properties and stability characteristics, as well as assessing and optimising equilibria for future devices. Specific duties will include: producing magnetic reconstructions of ST40 plasmas using EFIT and in-house codes; maintaining magnetics calibrations; developing more advanced reconstructions to include kinetic measurements; performing MHD stability analysis and optimisations; and analysing experimental results. The role will involve working closely with collaborators within the fusion community to expand the spherical tokamak physics basis through research on ST40 and other devices. Personal Skills and Attributes: Essential Selection Criteria: PhD in plasma physics or closely related equivalent experience Familiarity with relevant tokamak/plasma modelling codes (e.g. EFIT, LIUQE, FIESTA, DCON, KNIK, JOREK) Knowledge of magnetic reconstruction and MHD stability Experience working in a research environment or developing novel technologies Ability to work efficiently on own initiative Highly motivated to deliver against challenging objectives in a compressed timescale Ability to contribute effectively in a multi-disciplinary team of engineers and scientists Willingness to learn and adopt new techniques and technologies Ability to effectively communicate results to both technical and non-technical colleagues Organised approach to tackling complex problems Desirable Selection Criteria: Experience of programming languages such as MATLAB/Python/Unix/C++/Fortran Experimental data analysis experience Publication history Willingness to develop new and existing collaborations Benefits: 25 Days Holiday (plus bank holidays) Company Pension scheme: Company contribution of 5% of salary after 3 months' service Eligible for company share option scheme after one years' service Company bonus scheme, discretionary, dependent on performance Private medical insurance after 3 months' service Please note: Only candidates with the relevant skills and experience will be contacted regarding this position. If you do not hear back within 10 days of submitting your application then unfortunately you have been unsuccessful. However, you may be contacted in the future to discuss other opportunities. No terminology in the advert or job description is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the duties of the job. Please click the APPLY button to send your CV and Cover Letter for the role. Candidates with the experience or relevant job titles of; Graduate, Nuclear Physicist, PHD Graduate, Nuclear Scientist, Plasma Scientist may also be considered for this role.
Dec 06, 2019
Full time
Job Title: Plasma Physicist - MHD and Magnetics Location: Milton Park, Abingdon (OX14) Salary: Competitive, depending on experience Background: The Company has unlocked a new route to scalable fusion power that is cost-effective and does not require huge infrastructure and capital expenditure. The technology could revolutionise the world's energy production - it will be possible to produce more energy, more cheaply and with fewer harmful side effects (e.g. long term nuclear waste or carbon emissions). They aim to accelerate the development of fusion energy by combining two emerging technologies - spherical tokamaks and high-temperature superconductors. The company's innovation has been featured on Channel 4 news, BBC News Click, Reuters internet news channel and they received a Technology Pioneer Award at the World Economic Forum in 2016. This is the chance to join a fast-growing high technology company with an agile, dynamic team and to tackle the challenge of a lifetime. The Role: Do you want to help make fusion power a reality? Are you a plasma physicist looking for a unique and exciting new opportunity? If so, the Company are seeking talented and innovative individuals that are passionate about accelerating the development of fusion power to join the physics team. Their mission is to transform the way the world generates power by creating a clean, safe and sustainable source of energy for current and future generations and their innovative approach to fusion is based on two emerging technologies: spherical tokamaks (STs) and high-field magnets made from high temperature superconductors (HTS). They're looking for a research scientist to join the growing physics team to support ST40 operations and contribute to the design of future high field spherical tokamaks. The role will include analysing ST40 magnetics data to determine equilibrium properties and stability characteristics, as well as assessing and optimising equilibria for future devices. Specific duties will include: producing magnetic reconstructions of ST40 plasmas using EFIT and in-house codes; maintaining magnetics calibrations; developing more advanced reconstructions to include kinetic measurements; performing MHD stability analysis and optimisations; and analysing experimental results. The role will involve working closely with collaborators within the fusion community to expand the spherical tokamak physics basis through research on ST40 and other devices. Personal Skills and Attributes: Essential Selection Criteria: PhD in plasma physics or closely related equivalent experience Familiarity with relevant tokamak/plasma modelling codes (e.g. EFIT, LIUQE, FIESTA, DCON, KNIK, JOREK) Knowledge of magnetic reconstruction and MHD stability Experience working in a research environment or developing novel technologies Ability to work efficiently on own initiative Highly motivated to deliver against challenging objectives in a compressed timescale Ability to contribute effectively in a multi-disciplinary team of engineers and scientists Willingness to learn and adopt new techniques and technologies Ability to effectively communicate results to both technical and non-technical colleagues Organised approach to tackling complex problems Desirable Selection Criteria: Experience of programming languages such as MATLAB/Python/Unix/C++/Fortran Experimental data analysis experience Publication history Willingness to develop new and existing collaborations Benefits: 25 Days Holiday (plus bank holidays) Company Pension scheme: Company contribution of 5% of salary after 3 months' service Eligible for company share option scheme after one years' service Company bonus scheme, discretionary, dependent on performance Private medical insurance after 3 months' service Please note: Only candidates with the relevant skills and experience will be contacted regarding this position. If you do not hear back within 10 days of submitting your application then unfortunately you have been unsuccessful. However, you may be contacted in the future to discuss other opportunities. No terminology in the advert or job description is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the duties of the job. Please click the APPLY button to send your CV and Cover Letter for the role. Candidates with the experience or relevant job titles of; Graduate, Nuclear Physicist, PHD Graduate, Nuclear Scientist, Plasma Scientist may also be considered for this role.
Oxford BioMedica is a pioneer of gene and cell therapy and our work is helping to deliver life changing treatments. Gene and cell therapy is the treatment of disease by the delivery of therapeutic DNA into a patient's cells, providing long term and potentially curative treatments for a wide range of diseases. With the potential to transform medicine, the sector holds significant promise with the first commercial products now launched and others rapidly approaching the market. Our recent successes are driving significant growth. As such, we are looking to recruit a Principal Scientist (Team Lead, Analytcial to to lead a team of Scientists and Laboratory Technicians and effectively co-ordinate the daily activities to ensure PR&D timelines are met, whilst maintaining compliance with GLP/GMP & safety regulations, within Process R&D. Specific Work Responsibilities and Deliverables Responsible for the line management of a team of analytical scientists and laboratory technicians; including managing performance, motivating the team and carrying out recruitment activities. Manage and prioritise the team's workload and results, ensuring results are delivered on time and at appropriate levels of quality. Perform assays, report results and QC check assays for release in accordance with local rules. Review and approve training records, and where appropriate organize and conduct training. Contribute to and/or lead trouble shooting and technical investigations. Contribute to and/or lead both departmental and company initiatives/projects. Write, review and approve PR&D Policies, SOPs, forms and technical reports. Responsible for ensuring the GLP (and where necessary GMP) compliance of the laboratory and equipment. Ensure all direct reports or persons involved in projects are fully trained and maintain a high standard of record keeping and documentation of experiments so that information is clearly captured, disseminated and reported. Maintain awareness of upcoming technologies, and keep up to date with current literature and thinking. Promote appropriate, effective communication within team, with members of other departments, and with external collaborators. Contribute to cross departmental activities and provide expert advice and technical input where needed. Maintain a safe working environment by ensuring appropriate H&S training, risk assessments and COSHH assessments are in place. To succeed, you will have: BSc, MSc or PhD (or equivalent) in a relevant Bioscience with an appropriate level of relevant laboratory experience. Previous experience of working within an industrial analytical laboratory environment is beneficial Laboratory technical experience in one or more of the following areas: cell culture, qPCR or ELISA. Good understanding of lentiviral vectors (or other gene therapy vectors), and associated product quality attributes. Line management experience. A sound understanding of basic biopharmaceutical process development activities. In-depth knowledge of the regulatory requirements for analytical work (e.g. product specifications, stability testing guidelines etc) is required. Understanding of laboratory health and safety requirements to ensure reports and junior staff adhere to these. Ability to work within GLP/GMP environment and maintain compliance. Familiarisation with GMP work practices would be a benefit. No agencies please
Dec 06, 2019
Full time
Oxford BioMedica is a pioneer of gene and cell therapy and our work is helping to deliver life changing treatments. Gene and cell therapy is the treatment of disease by the delivery of therapeutic DNA into a patient's cells, providing long term and potentially curative treatments for a wide range of diseases. With the potential to transform medicine, the sector holds significant promise with the first commercial products now launched and others rapidly approaching the market. Our recent successes are driving significant growth. As such, we are looking to recruit a Principal Scientist (Team Lead, Analytcial to to lead a team of Scientists and Laboratory Technicians and effectively co-ordinate the daily activities to ensure PR&D timelines are met, whilst maintaining compliance with GLP/GMP & safety regulations, within Process R&D. Specific Work Responsibilities and Deliverables Responsible for the line management of a team of analytical scientists and laboratory technicians; including managing performance, motivating the team and carrying out recruitment activities. Manage and prioritise the team's workload and results, ensuring results are delivered on time and at appropriate levels of quality. Perform assays, report results and QC check assays for release in accordance with local rules. Review and approve training records, and where appropriate organize and conduct training. Contribute to and/or lead trouble shooting and technical investigations. Contribute to and/or lead both departmental and company initiatives/projects. Write, review and approve PR&D Policies, SOPs, forms and technical reports. Responsible for ensuring the GLP (and where necessary GMP) compliance of the laboratory and equipment. Ensure all direct reports or persons involved in projects are fully trained and maintain a high standard of record keeping and documentation of experiments so that information is clearly captured, disseminated and reported. Maintain awareness of upcoming technologies, and keep up to date with current literature and thinking. Promote appropriate, effective communication within team, with members of other departments, and with external collaborators. Contribute to cross departmental activities and provide expert advice and technical input where needed. Maintain a safe working environment by ensuring appropriate H&S training, risk assessments and COSHH assessments are in place. To succeed, you will have: BSc, MSc or PhD (or equivalent) in a relevant Bioscience with an appropriate level of relevant laboratory experience. Previous experience of working within an industrial analytical laboratory environment is beneficial Laboratory technical experience in one or more of the following areas: cell culture, qPCR or ELISA. Good understanding of lentiviral vectors (or other gene therapy vectors), and associated product quality attributes. Line management experience. A sound understanding of basic biopharmaceutical process development activities. In-depth knowledge of the regulatory requirements for analytical work (e.g. product specifications, stability testing guidelines etc) is required. Understanding of laboratory health and safety requirements to ensure reports and junior staff adhere to these. Ability to work within GLP/GMP environment and maintain compliance. Familiarisation with GMP work practices would be a benefit. No agencies please
Are you a Laboratory Analyst looking to join an international FMCG company with an award winning working culture? DR Newitt is delighted to be partnering with a leading Food and Beverages company to appoint a new Lab Analyst to their dynamic team based in the South East. You will be working for a company that is a key supplier to some of the biggest household names in FMCG and numerous blue chip companies across the globe and is a leader in the most niche, rapidly growing and This business knows that if they look after their staff, then their staff will look after the business, as shown by their outstanding Glassdoor Reviews. They do this by creating a great working culture and offering an impressive package including: Competitive basic salary Flexible working hours Company pension for employee 3.5% contribution and employer 7% contribution + life assurance Private healthcare Free yoga classes and massages Weekly fruit deliveries Free parking 33 days holiday Weekly free fruit Your duties and responsibilities will be as follows: Required to follow up on analytical issues and conduct trouble-shooting investigations Involved in analytical method development/transfer and validation plus report writing Be able to take responsibility for the day-to-day running of the lab Significant input in the authorship of SOPs Have the opportunity to be involved in different internal projects We're looking for: Experience in HPLC analysis and methodology, any UPLC or ICP experience will be beneficial Strong academic background with a-Levels in Science related subjects 2+ years' experience in a lab within either the Food, Drinks, Pharmaceuticals or Nutrition industry Ability to work well in a team If this sounds like you and you'd be interested in working for an amazing business that truly values their staff, then please submit your application below. Keywords: QC / quality control / laboratory analyst / pharmaceuticals / food / beverages / vitamins / minerals / supplements / pharma / medical
Dec 06, 2019
Full time
Are you a Laboratory Analyst looking to join an international FMCG company with an award winning working culture? DR Newitt is delighted to be partnering with a leading Food and Beverages company to appoint a new Lab Analyst to their dynamic team based in the South East. You will be working for a company that is a key supplier to some of the biggest household names in FMCG and numerous blue chip companies across the globe and is a leader in the most niche, rapidly growing and This business knows that if they look after their staff, then their staff will look after the business, as shown by their outstanding Glassdoor Reviews. They do this by creating a great working culture and offering an impressive package including: Competitive basic salary Flexible working hours Company pension for employee 3.5% contribution and employer 7% contribution + life assurance Private healthcare Free yoga classes and massages Weekly fruit deliveries Free parking 33 days holiday Weekly free fruit Your duties and responsibilities will be as follows: Required to follow up on analytical issues and conduct trouble-shooting investigations Involved in analytical method development/transfer and validation plus report writing Be able to take responsibility for the day-to-day running of the lab Significant input in the authorship of SOPs Have the opportunity to be involved in different internal projects We're looking for: Experience in HPLC analysis and methodology, any UPLC or ICP experience will be beneficial Strong academic background with a-Levels in Science related subjects 2+ years' experience in a lab within either the Food, Drinks, Pharmaceuticals or Nutrition industry Ability to work well in a team If this sounds like you and you'd be interested in working for an amazing business that truly values their staff, then please submit your application below. Keywords: QC / quality control / laboratory analyst / pharmaceuticals / food / beverages / vitamins / minerals / supplements / pharma / medical
Introduction of the Company Novogene, headquarters in Beijing with branches in the U.K., U.S. and Singapore, is a leading genomics solution provider with cutting edge bioinformatics expertise and the largest next-gen sequencing capacity in China. Committed to quality service and scientific excellence, Novogene has achieved rapid growth and industry recognition by working in partnership with diverse healthcare, educational and research institutions around the globe to realize the unlimited potential of the rapidly evolving world of genomics. The company has completed numerous major service projects with findings published by top-ranked journals such as Nature and Science. Responsibilities Responsible for the establishment and improvement of NGS sequencing data biological information analysis process To ensure the successful completion of NGS sequencing project Timely summary of the completion of the project, confirm the final delivery data Provide data analysis program, assist sales to resolve the technical problems in the check-in phase of the project Assist the project manager to complete the after-sales problems of our European customers Meet clients and solve problems for clients by communicating with sales and technical team Job requirements Advanced degree in bioinformatics or similar subject More than two years of experience in biologic information analysis or bioinformatics software development in high-throughput sequencing techniques Familiar with the analysis of sequencing data and common bioinformatics analysis software, can establish high-throughput sequencing technology analysis process Master Perl, python, R, C /C++ programming languages, proficient in the use of linux operating system, familiar with basic mathematical statistics knowledge and tools European universities study experience is preferred Must speak Mandarin, Excellent in English All applicants must be eligible to work in the UK Experience Bioinformatics: 2 years (Required) Education Master's (Required)
Dec 06, 2019
Full time
Introduction of the Company Novogene, headquarters in Beijing with branches in the U.K., U.S. and Singapore, is a leading genomics solution provider with cutting edge bioinformatics expertise and the largest next-gen sequencing capacity in China. Committed to quality service and scientific excellence, Novogene has achieved rapid growth and industry recognition by working in partnership with diverse healthcare, educational and research institutions around the globe to realize the unlimited potential of the rapidly evolving world of genomics. The company has completed numerous major service projects with findings published by top-ranked journals such as Nature and Science. Responsibilities Responsible for the establishment and improvement of NGS sequencing data biological information analysis process To ensure the successful completion of NGS sequencing project Timely summary of the completion of the project, confirm the final delivery data Provide data analysis program, assist sales to resolve the technical problems in the check-in phase of the project Assist the project manager to complete the after-sales problems of our European customers Meet clients and solve problems for clients by communicating with sales and technical team Job requirements Advanced degree in bioinformatics or similar subject More than two years of experience in biologic information analysis or bioinformatics software development in high-throughput sequencing techniques Familiar with the analysis of sequencing data and common bioinformatics analysis software, can establish high-throughput sequencing technology analysis process Master Perl, python, R, C /C++ programming languages, proficient in the use of linux operating system, familiar with basic mathematical statistics knowledge and tools European universities study experience is preferred Must speak Mandarin, Excellent in English All applicants must be eligible to work in the UK Experience Bioinformatics: 2 years (Required) Education Master's (Required)
Data Scientist London £50,000 - £55,000 + Benefits The Company This company is a global start-up working across the healthcare sector. As a unicorn start-up they are looking to put accessible and affordable healthcare in the hands of everyone The Role As a Data Scientist, you can expect to be engaging with a range of technology to build the foundations of the data infrastructure and analytics platform. Responsibilities include: Deploying models to scale for commercial use via Python Providing commercially viable applications using deep learning techniques. Developing progressive analytic algorithms through exploiting rich data assets. Creating viable dashboards via Tableau or PowerBi Skills & Requirements: To qualify for this Data Scientist role, you will need: Advanced analytics and programming for models through Python Good SQL/data manipulation skills required including cleaning and managing data. Commercial experience building a variety of dashboards via Tableau or PowerBi HOW TO APPLY: Please register your interest by sending your CV to Sean via the Apply link on this page.
Dec 06, 2019
Full time
Data Scientist London £50,000 - £55,000 + Benefits The Company This company is a global start-up working across the healthcare sector. As a unicorn start-up they are looking to put accessible and affordable healthcare in the hands of everyone The Role As a Data Scientist, you can expect to be engaging with a range of technology to build the foundations of the data infrastructure and analytics platform. Responsibilities include: Deploying models to scale for commercial use via Python Providing commercially viable applications using deep learning techniques. Developing progressive analytic algorithms through exploiting rich data assets. Creating viable dashboards via Tableau or PowerBi Skills & Requirements: To qualify for this Data Scientist role, you will need: Advanced analytics and programming for models through Python Good SQL/data manipulation skills required including cleaning and managing data. Commercial experience building a variety of dashboards via Tableau or PowerBi HOW TO APPLY: Please register your interest by sending your CV to Sean via the Apply link on this page.
At Moove Europe, you will be part of a global manufacturer of quality Industrial and car lubricants and car care chemicals. Chances are you have come into contact with our products more often than you think… In the UK, 1 in 6 cars runs on lubricants produced by us. Our Exxon Mobil brand products are promoted through our motorsport sponsorship. We manufacture private label products for some of the world's biggest vehicle and equipment manufacturers. Our products touch every part of everyday life - from water treatment works to food manufacturing plants. We distribute and sell our products in more than 40 countries worldwide. We're part of a Global company that employs over 40,000 people worldwide We have an opportunity for you at our European Head office based in Gravesend, Kent as a Technical Advisor/Research Analyst for Lubricants. If you have great analytical skills, you thrive working in a fast paced environment and you are looking to develop your career take a look at what we can offer you. Your role will include: Researching new product developments Building relationships with suppliers to understand technology pipeline Researching technology developments that reduce costs whilst upholding product quality Investigating global sourcing opportunities Understanding impact on spend of raw material (base oil and additives) price movements Engaging with suppliers and industry sources to track market movements and support in forecasting spend Providing back up support for escalation of Technical Helpdesk enquires Key Skills required: University degree or equivalent (ideally in science or chemicals) A understanding of oil or lubricants is highly desireable Excellent analytical skills Good relationship building skills What we offer you: Annual company bonus (can be up to 2 months to 4 months of salary) 20 days holiday plus bank holidays (rising to 25 within 2 years) Contributory pension scheme (company match up to 7%) Life Assurance Working hours are Monday to Friday 8.30 to 5.30. Interested in becoming a Moover, being part of a global organisation who truly value their employees, encourage development and progression? If yes please send us your CV and the salary you are looking for to our recruitment team today. We love hearing from you but we also know your personal data is important. You may wish to read our Vacancies Privacy Policy prior to applying for this role. Our Policy covers our compliance with the GDPR (General Data Protection Regulation) in regards to your application. You can find this on our Moove Europe website. Please note we endeavour to reply to everyone but it is not always possible. If you have not heard form us within two weeks of your application please assume in this instance we have not been able to progress.
Dec 06, 2019
Full time
At Moove Europe, you will be part of a global manufacturer of quality Industrial and car lubricants and car care chemicals. Chances are you have come into contact with our products more often than you think… In the UK, 1 in 6 cars runs on lubricants produced by us. Our Exxon Mobil brand products are promoted through our motorsport sponsorship. We manufacture private label products for some of the world's biggest vehicle and equipment manufacturers. Our products touch every part of everyday life - from water treatment works to food manufacturing plants. We distribute and sell our products in more than 40 countries worldwide. We're part of a Global company that employs over 40,000 people worldwide We have an opportunity for you at our European Head office based in Gravesend, Kent as a Technical Advisor/Research Analyst for Lubricants. If you have great analytical skills, you thrive working in a fast paced environment and you are looking to develop your career take a look at what we can offer you. Your role will include: Researching new product developments Building relationships with suppliers to understand technology pipeline Researching technology developments that reduce costs whilst upholding product quality Investigating global sourcing opportunities Understanding impact on spend of raw material (base oil and additives) price movements Engaging with suppliers and industry sources to track market movements and support in forecasting spend Providing back up support for escalation of Technical Helpdesk enquires Key Skills required: University degree or equivalent (ideally in science or chemicals) A understanding of oil or lubricants is highly desireable Excellent analytical skills Good relationship building skills What we offer you: Annual company bonus (can be up to 2 months to 4 months of salary) 20 days holiday plus bank holidays (rising to 25 within 2 years) Contributory pension scheme (company match up to 7%) Life Assurance Working hours are Monday to Friday 8.30 to 5.30. Interested in becoming a Moover, being part of a global organisation who truly value their employees, encourage development and progression? If yes please send us your CV and the salary you are looking for to our recruitment team today. We love hearing from you but we also know your personal data is important. You may wish to read our Vacancies Privacy Policy prior to applying for this role. Our Policy covers our compliance with the GDPR (General Data Protection Regulation) in regards to your application. You can find this on our Moove Europe website. Please note we endeavour to reply to everyone but it is not always possible. If you have not heard form us within two weeks of your application please assume in this instance we have not been able to progress.
We are currently looking for a Software QA Specialist to join a leading Clinical Diagnostics company based in the London area. As the Software QA Specialist, you will be responsible for ensuring the Verification, Validation and Life Cycle Management of Software is compliant and in a timely manner. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Software QA Specialist will be varied. However, the key duties and responsibilities are as follows: 1. You will ensure review, update and approve Software Life Cycle Procedures and Policies, including the Verification and Validation (V&V), whilst acting as the SME in this area and providing training to staff. 2. As the Software QA Specialist, you will review and approve Software Development and Validation documentation, such as User Requirement Specifications (URS), Technical Specifications, Test Protocols and Scripts, and Verification and Validation (V&V) protocols and reports. This will also see you presenting this documentation during client and regulatory audits. 3. You will raise and investigate deviations, implement effective CAPAs and Change Controls, prepare KPIs for the maintenance and improvement of the company's management system and management reviews. 4. As the Software QA Specialist, you will support Information and Cyber Security Compliance, implement Information Security and Privacy objectives, perform internal audits, and qualify and approve software and technology suppliers. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Software QA Specialist, we are looking to identify the following on your profile and history: 1. Experience of Software / Systems Validation ( GAMP / Annex 11 ) in the pharmaceutical or medical device industries, or other software industry. 2. Proven industry experience in writing and reviewing Software Development and Validation documentation. 3. A working knowledge and practical experience with GCP / ISO13485 / ISO27001 regulations and Information System Security and Privacy / GDPR. Key Words: QA | Quality Assurance | CSV | Computer Systems Validation | Software Validation | GAMP | GAMP5 | Annex 11 | Biotechnology | Medical Devices | IT QA | Software Quality Assurance | GCP | ISO13485 | ISO27001 | Internal Audits | Supplier Management | Supplier Qualification | Regulatory Inspections | Compliance | Validation Protocols | Diagnostics Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
Dec 06, 2019
Full time
We are currently looking for a Software QA Specialist to join a leading Clinical Diagnostics company based in the London area. As the Software QA Specialist, you will be responsible for ensuring the Verification, Validation and Life Cycle Management of Software is compliant and in a timely manner. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Software QA Specialist will be varied. However, the key duties and responsibilities are as follows: 1. You will ensure review, update and approve Software Life Cycle Procedures and Policies, including the Verification and Validation (V&V), whilst acting as the SME in this area and providing training to staff. 2. As the Software QA Specialist, you will review and approve Software Development and Validation documentation, such as User Requirement Specifications (URS), Technical Specifications, Test Protocols and Scripts, and Verification and Validation (V&V) protocols and reports. This will also see you presenting this documentation during client and regulatory audits. 3. You will raise and investigate deviations, implement effective CAPAs and Change Controls, prepare KPIs for the maintenance and improvement of the company's management system and management reviews. 4. As the Software QA Specialist, you will support Information and Cyber Security Compliance, implement Information Security and Privacy objectives, perform internal audits, and qualify and approve software and technology suppliers. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Software QA Specialist, we are looking to identify the following on your profile and history: 1. Experience of Software / Systems Validation ( GAMP / Annex 11 ) in the pharmaceutical or medical device industries, or other software industry. 2. Proven industry experience in writing and reviewing Software Development and Validation documentation. 3. A working knowledge and practical experience with GCP / ISO13485 / ISO27001 regulations and Information System Security and Privacy / GDPR. Key Words: QA | Quality Assurance | CSV | Computer Systems Validation | Software Validation | GAMP | GAMP5 | Annex 11 | Biotechnology | Medical Devices | IT QA | Software Quality Assurance | GCP | ISO13485 | ISO27001 | Internal Audits | Supplier Management | Supplier Qualification | Regulatory Inspections | Compliance | Validation Protocols | Diagnostics Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
New opportunity for an experienced Scientist to join an innovative analytical testing laboratory focusing on extractables and leachable studies! Working amongst a dynamic team your primary accountabilities will include the analysis of small molecules and supporting technical staff through problem solving via LC-MS. You will follow established methods to meet stringent sample analysis turnaround times and be responsible for undertaking instrument troubleshooting and maintenance of Waters instrumentation. Applications are invited from candidates who can possess the following: PhD, MSc or BSc in chemistry (or related) Experience of using LC-MS to analyse small molecules and associated data analysis 12 months industry experience Excellent communication skills Apply today to learn more about this unique opportunity! Keywords: HPLC, UPLC, LC-MS, LC-MS/MS, chromatography, mass spectrometry, pharmaceutical, extractables and leachables, QToF, QQQ, high resolution, GLP, GMP, method development, experimental design, data checking, sample preparation, Manchester, VRS6536KF
Dec 06, 2019
Full time
New opportunity for an experienced Scientist to join an innovative analytical testing laboratory focusing on extractables and leachable studies! Working amongst a dynamic team your primary accountabilities will include the analysis of small molecules and supporting technical staff through problem solving via LC-MS. You will follow established methods to meet stringent sample analysis turnaround times and be responsible for undertaking instrument troubleshooting and maintenance of Waters instrumentation. Applications are invited from candidates who can possess the following: PhD, MSc or BSc in chemistry (or related) Experience of using LC-MS to analyse small molecules and associated data analysis 12 months industry experience Excellent communication skills Apply today to learn more about this unique opportunity! Keywords: HPLC, UPLC, LC-MS, LC-MS/MS, chromatography, mass spectrometry, pharmaceutical, extractables and leachables, QToF, QQQ, high resolution, GLP, GMP, method development, experimental design, data checking, sample preparation, Manchester, VRS6536KF
We are recruiting for an LC-MS/MS Analyst to join a client in Manchester on a permanent basis. The company Our client is a contract analytical laboratory specialising in problem solving and analytical development. They have an extensive range of chromatographic and mass spectrometric instrumentation and require an LC-MS/MS Analyst to join the team to cover routine analysis work. What you'll do: You will be analysing samples from various clients including (but not limited to) pharma, agrochemicals and E-Cigarette markets. Core duties for the LC-MS/MS Analyst role are: Be conversant with the Company Health and Safety Policy and work in accordance with Company Operating Procedures. Maintain a clean, tidy and safe working environment. Report any difficulties/problems in following documented procedures to the Scientific or Technical Director prior to making any change/modification. Any change/modification must be authorised by a Director. Be conversant with the content of the Company Quality Manual and carry out work in accordance with such at all times. Maintain an accurate record of all analytical data generated in personal lab book, equipment lab book or study record as appropriate together with any associated quality assurance data. Prepare client samples for analysis including the relevant and appropriate use of standards. Use instrumentation (after having been approved/trained) to acquire and process data for client samples. Report data in client reports. Maintain instrumentation at agreed performance standards and/or report faults/failures to a Company Director. Validate methods as agreed/directed by supervisor/Director. Liase with clients as directed regarding ongoing laboratory work, technical queries etc. When required all work related conducted in support of GLP studies must be performed in compliance with UK GLP regulations You will report to the Laboratory Operations Manager. Your background: As an experienced LC-MS/MS Analyst essential requirements are: A minimum of 1-2 years experience running Waters LC-MS/MS (triple quads) Experience of Waters software Desirable attributes for the LC-MS/MS Analyst : Experience using Waters TQS Working in a GxP or similar environment Experience interpreting MS data Experience/knowledge of organic synthesis in relation to interpreting MS data The package for LC-MS/MS Analyst the is as follows: Salary: £20,000 - £26,000 depending on experience, with generous quarterly AND annual bonus opportunities, a good% contribution pension and 24(+8 bank) holidays a year. On this occasion LiCa Scientific is acting as an employment agency.
Dec 06, 2019
Full time
We are recruiting for an LC-MS/MS Analyst to join a client in Manchester on a permanent basis. The company Our client is a contract analytical laboratory specialising in problem solving and analytical development. They have an extensive range of chromatographic and mass spectrometric instrumentation and require an LC-MS/MS Analyst to join the team to cover routine analysis work. What you'll do: You will be analysing samples from various clients including (but not limited to) pharma, agrochemicals and E-Cigarette markets. Core duties for the LC-MS/MS Analyst role are: Be conversant with the Company Health and Safety Policy and work in accordance with Company Operating Procedures. Maintain a clean, tidy and safe working environment. Report any difficulties/problems in following documented procedures to the Scientific or Technical Director prior to making any change/modification. Any change/modification must be authorised by a Director. Be conversant with the content of the Company Quality Manual and carry out work in accordance with such at all times. Maintain an accurate record of all analytical data generated in personal lab book, equipment lab book or study record as appropriate together with any associated quality assurance data. Prepare client samples for analysis including the relevant and appropriate use of standards. Use instrumentation (after having been approved/trained) to acquire and process data for client samples. Report data in client reports. Maintain instrumentation at agreed performance standards and/or report faults/failures to a Company Director. Validate methods as agreed/directed by supervisor/Director. Liase with clients as directed regarding ongoing laboratory work, technical queries etc. When required all work related conducted in support of GLP studies must be performed in compliance with UK GLP regulations You will report to the Laboratory Operations Manager. Your background: As an experienced LC-MS/MS Analyst essential requirements are: A minimum of 1-2 years experience running Waters LC-MS/MS (triple quads) Experience of Waters software Desirable attributes for the LC-MS/MS Analyst : Experience using Waters TQS Working in a GxP or similar environment Experience interpreting MS data Experience/knowledge of organic synthesis in relation to interpreting MS data The package for LC-MS/MS Analyst the is as follows: Salary: £20,000 - £26,000 depending on experience, with generous quarterly AND annual bonus opportunities, a good% contribution pension and 24(+8 bank) holidays a year. On this occasion LiCa Scientific is acting as an employment agency.
We are currently looking for a Senior Manager within API Development to work at an established Pharmaceutical CMO in Oxfordshire. The role involves project and line management, as well as providing technical expertise within process R&D and organic synthetic chemistry. Key responsibilities and duties: Plan project strategies and ensure they are completed to budget and schedule Direct the project team to achieve objectives and deliverables and ensure tasks are delegated accordingly Manage project meetings and communicate with internal and external bodies on a weekly basis (teleconferences, written reports etc) Supervise, train and provide technical expertise to various members of the API Development team Assist the Director in writing proposals and developing business relationships Review budget, schedule and progress frequently; communicate and update the Director on any issues and ensure appropriate action is taken Ensure H&S, cGMP and correct procedures are followed, and work is to the highest standard of quality Support and lead the development of commercial relationships through the delivery of proposals and project milestones Ideal skills and qualifications: MChem/MSc/PhD in Chemistry or a similar scientific discipline; or equivalent industrial experience Proven commercial experience in project & line leadership, and as part of a management team Experience of working with clients directly Technically competent in organic chemistry, process R&D and API development Flexible approach to organisation structures and resource allocation Ability to work in a fast-paced environment with changing priorities to respond to clients' needs Strong decision-making skills and investigative approach to problem-solving Strong interpersonal and communication skills If you are interested or have any questions about this role, feel free to contact Harriet at CY Partners. The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.
Dec 06, 2019
Full time
We are currently looking for a Senior Manager within API Development to work at an established Pharmaceutical CMO in Oxfordshire. The role involves project and line management, as well as providing technical expertise within process R&D and organic synthetic chemistry. Key responsibilities and duties: Plan project strategies and ensure they are completed to budget and schedule Direct the project team to achieve objectives and deliverables and ensure tasks are delegated accordingly Manage project meetings and communicate with internal and external bodies on a weekly basis (teleconferences, written reports etc) Supervise, train and provide technical expertise to various members of the API Development team Assist the Director in writing proposals and developing business relationships Review budget, schedule and progress frequently; communicate and update the Director on any issues and ensure appropriate action is taken Ensure H&S, cGMP and correct procedures are followed, and work is to the highest standard of quality Support and lead the development of commercial relationships through the delivery of proposals and project milestones Ideal skills and qualifications: MChem/MSc/PhD in Chemistry or a similar scientific discipline; or equivalent industrial experience Proven commercial experience in project & line leadership, and as part of a management team Experience of working with clients directly Technically competent in organic chemistry, process R&D and API development Flexible approach to organisation structures and resource allocation Ability to work in a fast-paced environment with changing priorities to respond to clients' needs Strong decision-making skills and investigative approach to problem-solving Strong interpersonal and communication skills If you are interested or have any questions about this role, feel free to contact Harriet at CY Partners. The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.
We are currently looking for a QC Analyst to join a leading Pharmaceutical company based in the West Sussex area. As the QC Analyst you will be responsible for performing analytical testing and laboratory work to regulated standards, and to undertake Non Conformance and Out of Specification investigations. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows: 1. As a QC analyst you will complete testing of raw materials, intermediates or finished products as required, you will also perform routine laboratory procedures, and to perform project work within the department. 2. To prepare technical documentation within the department and assist in the development and validation of laboratory procedures within the team. 3. As the QC analyst you will understand and follow QC laboratory systems (e.g. equipment, consumable stock management, documentation, compliance programmes), as well as ensuring equipment is calibrated and logged according to procedures. 4. Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the QC Analyst we are looking to identify the following on your profile and past history: 1. Relevant degree in Chemistry or strongly related scientific discipline 2. Proven industry experience in Analytical techniques such as HPLC, UV, FTIR, LCMS, GCMS within a GMP environment. 3. A working knowledge and practical experience with method development and validation using the analytical techniques required. Key Words: HPLC | QC | Quality Control | Raw Materials | Analytical | Method development | Method Validation | GMP | West Sussex| Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
Dec 06, 2019
Full time
We are currently looking for a QC Analyst to join a leading Pharmaceutical company based in the West Sussex area. As the QC Analyst you will be responsible for performing analytical testing and laboratory work to regulated standards, and to undertake Non Conformance and Out of Specification investigations. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows: 1. As a QC analyst you will complete testing of raw materials, intermediates or finished products as required, you will also perform routine laboratory procedures, and to perform project work within the department. 2. To prepare technical documentation within the department and assist in the development and validation of laboratory procedures within the team. 3. As the QC analyst you will understand and follow QC laboratory systems (e.g. equipment, consumable stock management, documentation, compliance programmes), as well as ensuring equipment is calibrated and logged according to procedures. 4. Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the QC Analyst we are looking to identify the following on your profile and past history: 1. Relevant degree in Chemistry or strongly related scientific discipline 2. Proven industry experience in Analytical techniques such as HPLC, UV, FTIR, LCMS, GCMS within a GMP environment. 3. A working knowledge and practical experience with method development and validation using the analytical techniques required. Key Words: HPLC | QC | Quality Control | Raw Materials | Analytical | Method development | Method Validation | GMP | West Sussex| Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
Clinical data & bioinformatics field application specialist for growing company in Cambridge, client facing Your new company Is a rapidly growing pharmaceutical data & bioinformatics company in the Cambridge area, providing bespoke solutions to a range of clients within the pharmaceutical, biotech and genomics fields, using a range of pipelines, software and data analysis tools to make a big difference to their clients, working with multi-omics and clinical trial data sets to fast-track a range of programmes. The company has bright, well-equipped, open plan offices and a collaborative and warm corporate atmosphere. Your new role You will be joining an enthusiastic and talented team, taking on / leading pre-sales support and advice, alongside post-sales training, solutions and troubleshooting for clients on the company's software platform (which is focused on clinical trial, bioinformatics and drug discovery data analysis). For more experienced candidates there is significant scope to input into strategy and company development plans. The major responsibilities include: Managing the pre-sales process with clients; Dealing with RFPs, proposals, and scoping out solutions, including pilot/tester projects; Helping estimate project costs and timelines, including involvement in negotiations; Act as one of the main points of contact with clients, providing regular updates; Providing in-depth training and ongoing support to clients; Providing customer and market feedback to internal development teams to identify market opportunities; Acting as a bridge between customers and the internal development and project teams, ensuring good communication and smooth processes on project work; and Building relationships with clients for future business. This is a fast-paced environment where you will need to deal with people at all levels, from developers through to senior management/C-level executives both internally and externally What you'll need to succeed As well as excellent analytical, organisational and team-working skills, you will need to have an innovative approach to problem solving and be able to work both independently and as part of a larger team. You should have a degree (or equivalent) in bioinformatics, computational biology, computer science, computational chemistry, physics, statistics, mathematics, biology, genetics or a related field, and ideally a post-graduate qualification (MSc or PhD). Experience with clinical trial data, eg from hands-on analysis or as a data manager and/or genomics, drug discovery (eg assay or screening services) or bioinformatics would be a significant advantage. You will also need: A good understanding of pharmaceutical, clinical or similar research, from either academia or industry work experience; Hands-on experience with clinical trial data systems / software (eg RAVE, Medidata or other EDCs), bioinformatics, drug discovery or similar software; An aptitude for creative problem solving, especially within technical problems; The aptitude / ability to lead training and presentation sessions. You must have very strong communication skills due to the interaction with clients. Candidates with related experience but who can evidence / demonstrate a strong ability to learn and adapt to new situations are also encouraged to apply. What you'll get in return An excellent opportunity to join one of the leading pharmaceutical data and bioinformatics companies in the field, a generous salary package, a great working atmosphere, and very good career progression and development opportunities. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on . If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career, as there are a number of bioinformatics, data science and statistics focused positions available. Keywords: clinical, trial, randomised, EDC, Medidata, RAVE, bioinformatics, bioinformatician, genomics, NGS, software, gene, drug, discovery, development, pharmaceutical, assay, programming, statistics, biology, computer, science, data, project, management, field, application, scientist, specialist, client, support, sales, pre-sales, training, product, technical, strategy
Dec 06, 2019
Full time
Clinical data & bioinformatics field application specialist for growing company in Cambridge, client facing Your new company Is a rapidly growing pharmaceutical data & bioinformatics company in the Cambridge area, providing bespoke solutions to a range of clients within the pharmaceutical, biotech and genomics fields, using a range of pipelines, software and data analysis tools to make a big difference to their clients, working with multi-omics and clinical trial data sets to fast-track a range of programmes. The company has bright, well-equipped, open plan offices and a collaborative and warm corporate atmosphere. Your new role You will be joining an enthusiastic and talented team, taking on / leading pre-sales support and advice, alongside post-sales training, solutions and troubleshooting for clients on the company's software platform (which is focused on clinical trial, bioinformatics and drug discovery data analysis). For more experienced candidates there is significant scope to input into strategy and company development plans. The major responsibilities include: Managing the pre-sales process with clients; Dealing with RFPs, proposals, and scoping out solutions, including pilot/tester projects; Helping estimate project costs and timelines, including involvement in negotiations; Act as one of the main points of contact with clients, providing regular updates; Providing in-depth training and ongoing support to clients; Providing customer and market feedback to internal development teams to identify market opportunities; Acting as a bridge between customers and the internal development and project teams, ensuring good communication and smooth processes on project work; and Building relationships with clients for future business. This is a fast-paced environment where you will need to deal with people at all levels, from developers through to senior management/C-level executives both internally and externally What you'll need to succeed As well as excellent analytical, organisational and team-working skills, you will need to have an innovative approach to problem solving and be able to work both independently and as part of a larger team. You should have a degree (or equivalent) in bioinformatics, computational biology, computer science, computational chemistry, physics, statistics, mathematics, biology, genetics or a related field, and ideally a post-graduate qualification (MSc or PhD). Experience with clinical trial data, eg from hands-on analysis or as a data manager and/or genomics, drug discovery (eg assay or screening services) or bioinformatics would be a significant advantage. You will also need: A good understanding of pharmaceutical, clinical or similar research, from either academia or industry work experience; Hands-on experience with clinical trial data systems / software (eg RAVE, Medidata or other EDCs), bioinformatics, drug discovery or similar software; An aptitude for creative problem solving, especially within technical problems; The aptitude / ability to lead training and presentation sessions. You must have very strong communication skills due to the interaction with clients. Candidates with related experience but who can evidence / demonstrate a strong ability to learn and adapt to new situations are also encouraged to apply. What you'll get in return An excellent opportunity to join one of the leading pharmaceutical data and bioinformatics companies in the field, a generous salary package, a great working atmosphere, and very good career progression and development opportunities. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on . If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career, as there are a number of bioinformatics, data science and statistics focused positions available. Keywords: clinical, trial, randomised, EDC, Medidata, RAVE, bioinformatics, bioinformatician, genomics, NGS, software, gene, drug, discovery, development, pharmaceutical, assay, programming, statistics, biology, computer, science, data, project, management, field, application, scientist, specialist, client, support, sales, pre-sales, training, product, technical, strategy
SENIOR RESEARCH ANALYST LONDON 40,000 - 50,000 Do you want to further your career in customer analytics? Do you want to work for a leading eCommerce brand where you will add real value through your insight? This could be the next step you are looking for! THE COMPANY This well-known retail company is looking for a Senior Research Analyst to join their analytics function. With a great working culture, you will be able to add value to the overall successes of the business. THE ROLE As a Senior Research Analyst, you will be responsible for working cross-functionally to support senior leaders in the business. You will be: Using SQL to understand what the data is saying and deliver actionable insight on a weekly basis Be a main driver for quantitative and qualitative research methods for competitor analysis Able to forecast and identify trends to enhance performance Providing deep dive analysis to help shape decision making YOUR SKILLS AND EXPERIENCE Proven experience using SQL Strong knowledge of excel Background in a similar role is desirable Strong communication skills and able to tell a story with the data THE BENEFITS Pension scheme Healthcare Great working environment Internal learning and development HOW TO APPLY Please register your interest by sending your CV to Gina Falleroni via the apply link on this page.
Dec 06, 2019
Full time
SENIOR RESEARCH ANALYST LONDON 40,000 - 50,000 Do you want to further your career in customer analytics? Do you want to work for a leading eCommerce brand where you will add real value through your insight? This could be the next step you are looking for! THE COMPANY This well-known retail company is looking for a Senior Research Analyst to join their analytics function. With a great working culture, you will be able to add value to the overall successes of the business. THE ROLE As a Senior Research Analyst, you will be responsible for working cross-functionally to support senior leaders in the business. You will be: Using SQL to understand what the data is saying and deliver actionable insight on a weekly basis Be a main driver for quantitative and qualitative research methods for competitor analysis Able to forecast and identify trends to enhance performance Providing deep dive analysis to help shape decision making YOUR SKILLS AND EXPERIENCE Proven experience using SQL Strong knowledge of excel Background in a similar role is desirable Strong communication skills and able to tell a story with the data THE BENEFITS Pension scheme Healthcare Great working environment Internal learning and development HOW TO APPLY Please register your interest by sending your CV to Gina Falleroni via the apply link on this page.
Job Title: RF Physicist Location: Milton Park, Abingdon (OX14) Salary: Competitive, depending on experience The Company has unlocked a new route to scalable fusion power that is cost-effective and does not require huge infrastructure and capital expenditure. The technology could revolutionise the world's energy production - it will be possible to produce more energy, more cheaply and with fewer harmful side effects (e.g. long term nuclear waste or carbon emissions). They aim to accelerate the development of fusion energy by combining two emerging technologies - spherical tokamaks and high-temperature superconductors. The company's innovation has been featured on Channel 4 news, BBC News Click, Reuters internet news channel and they received a Technology Pioneer Award at the World Economic Forum in 2016. This is the chance to join a fast-growing high technology company with an agile, dynamic team and to tackle the challenge of a lifetime. The Role: The ECRH system main goal is to provide plasma heating in the range of electron cyclotron frequencies (80 - 170 GHz). This position is responsible for determining and developing effective theoretical and computational approaches for solving a wide range of challenging scientific problems related to tokamak magnetic fusion research. The role will: help determine research directions in key areas including radio frequency (RF) plasma heating and current drive, kinetic and fluid theory and/or integrated simulation perform analytic and computational investigations, including multi-scale simulations of RF absorption, including boundary and plasma interactions prepare integration of the Electron Cyclotron Heating (ECH) & Current Drive (CD) methods into ST40 physics programme implement/develop appropriate plasma-wave interaction modelling tools develop EC/EBW heating based scenarios for plasma start-up, plasma current ramp-up and sustainment support EBW, ECH & CD experiments with predictive modelling and analysis support ECH development, in aspects related to ECH & CD optimisation for future machines Duties will include Participate in the development and integration of RF, boundary, plasma-material interaction, kinetic and fluid theory, and/or core physics codes and their applications to integrated simulation of tokamak experiments Support the overall fusion theory and integrated modelling capability of the Physics Team, including model development and code integration, verification, and validation Participate in the planning and integrated modelling of experiments in the present ST40 tokamak and future devices and perform verification and validation of modelling codes Present and publish research results at professional meetings and refereed journals. Provide documentation and make technical presentations as required and assist in responding to proposals for new or the expansion of existing business opportunities Essential Selection Criteria Requires a master's degree or PhD in scientific or related technical fields and complex scientific experience of four or more years. Equivalent scientific experience may be accepted Must have a complete understanding of scientific concepts, principles, codes, and theory; experience demonstrating a broad application of those concepts; and, an expanding knowledge of principles, concepts, theory, and practices in related technical specialties Must possess the ability to understand new concepts quickly; apply them accurately throughout an evolving environment; organize, schedule, and coordinate work phases; determine the appropriate approach at the task level or, with assistance, at the project level to provide solutions to a range of complex problems Familiarity with boundary and plasma-material interaction physics, RF and kinetic theory, and modern programming languages (particularly C++, Fortran, Python, mpi, CUDA) is desirable Must have strong communication, computer, documentation, presentation, and interpersonal skills; able to perform complex tasks in one scientific area; and, lead a team of less experienced professional employees on semi-routine tasks Original work(s) published in professional scientific journals or formal technical equivalents are highly desirable Benefits 25 Days Holiday (plus bank holidays) Company Pension scheme: Company contribution of 5% of salary after 3 months' service Eligible for company share option scheme after one years' service Company bonus scheme, discretionary, dependent on performance Private medical insurance after 3 months' service Please note: Only candidates with the relevant skills and experience will be contacted regarding this position. If you do not hear back within 10 days of submitting your application then unfortunately you have been unsuccessful. However, you may be contacted in the future to discuss other opportunities No terminology in the advert or job description is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the role Please click the APPLY button to send your CV and Cover Letter for the role Candidates with the experience or relevant job titles of; Graduate, Nuclear Physicist, PHD Graduate, Nuclear Scientist, Radiofrequency Physicist, FR Scientist may also be considered for this role
Dec 06, 2019
Full time
Job Title: RF Physicist Location: Milton Park, Abingdon (OX14) Salary: Competitive, depending on experience The Company has unlocked a new route to scalable fusion power that is cost-effective and does not require huge infrastructure and capital expenditure. The technology could revolutionise the world's energy production - it will be possible to produce more energy, more cheaply and with fewer harmful side effects (e.g. long term nuclear waste or carbon emissions). They aim to accelerate the development of fusion energy by combining two emerging technologies - spherical tokamaks and high-temperature superconductors. The company's innovation has been featured on Channel 4 news, BBC News Click, Reuters internet news channel and they received a Technology Pioneer Award at the World Economic Forum in 2016. This is the chance to join a fast-growing high technology company with an agile, dynamic team and to tackle the challenge of a lifetime. The Role: The ECRH system main goal is to provide plasma heating in the range of electron cyclotron frequencies (80 - 170 GHz). This position is responsible for determining and developing effective theoretical and computational approaches for solving a wide range of challenging scientific problems related to tokamak magnetic fusion research. The role will: help determine research directions in key areas including radio frequency (RF) plasma heating and current drive, kinetic and fluid theory and/or integrated simulation perform analytic and computational investigations, including multi-scale simulations of RF absorption, including boundary and plasma interactions prepare integration of the Electron Cyclotron Heating (ECH) & Current Drive (CD) methods into ST40 physics programme implement/develop appropriate plasma-wave interaction modelling tools develop EC/EBW heating based scenarios for plasma start-up, plasma current ramp-up and sustainment support EBW, ECH & CD experiments with predictive modelling and analysis support ECH development, in aspects related to ECH & CD optimisation for future machines Duties will include Participate in the development and integration of RF, boundary, plasma-material interaction, kinetic and fluid theory, and/or core physics codes and their applications to integrated simulation of tokamak experiments Support the overall fusion theory and integrated modelling capability of the Physics Team, including model development and code integration, verification, and validation Participate in the planning and integrated modelling of experiments in the present ST40 tokamak and future devices and perform verification and validation of modelling codes Present and publish research results at professional meetings and refereed journals. Provide documentation and make technical presentations as required and assist in responding to proposals for new or the expansion of existing business opportunities Essential Selection Criteria Requires a master's degree or PhD in scientific or related technical fields and complex scientific experience of four or more years. Equivalent scientific experience may be accepted Must have a complete understanding of scientific concepts, principles, codes, and theory; experience demonstrating a broad application of those concepts; and, an expanding knowledge of principles, concepts, theory, and practices in related technical specialties Must possess the ability to understand new concepts quickly; apply them accurately throughout an evolving environment; organize, schedule, and coordinate work phases; determine the appropriate approach at the task level or, with assistance, at the project level to provide solutions to a range of complex problems Familiarity with boundary and plasma-material interaction physics, RF and kinetic theory, and modern programming languages (particularly C++, Fortran, Python, mpi, CUDA) is desirable Must have strong communication, computer, documentation, presentation, and interpersonal skills; able to perform complex tasks in one scientific area; and, lead a team of less experienced professional employees on semi-routine tasks Original work(s) published in professional scientific journals or formal technical equivalents are highly desirable Benefits 25 Days Holiday (plus bank holidays) Company Pension scheme: Company contribution of 5% of salary after 3 months' service Eligible for company share option scheme after one years' service Company bonus scheme, discretionary, dependent on performance Private medical insurance after 3 months' service Please note: Only candidates with the relevant skills and experience will be contacted regarding this position. If you do not hear back within 10 days of submitting your application then unfortunately you have been unsuccessful. However, you may be contacted in the future to discuss other opportunities No terminology in the advert or job description is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the role Please click the APPLY button to send your CV and Cover Letter for the role Candidates with the experience or relevant job titles of; Graduate, Nuclear Physicist, PHD Graduate, Nuclear Scientist, Radiofrequency Physicist, FR Scientist may also be considered for this role
Data Scientist, machine learning - AI bioinformatics statistics. Genomics / NGS. Diagnostics company Cambridge Your new company A well-established diagnostics company in the Cambridge area, that are currently undergoing strong growth in their bioinformatics, statistics and biology teams to help drive their new development efforts. The company is heavily focused on genomics & NGS within clinical and in-vitro diagnostics (IVD), and are recruiting several experienced data scientists, bioinformaticians and biostatisticians with strong programming and analysis skills to help drive their company forward and make a real difference in the diagnosis of patients with diseases such as cancer. Your new role You will be focusing on the design, development and implementation of new facets and functionality for their platform, geared towards biomarker discovery and validation; working closely with stakeholders. You will also be involved in the analysis of NGS data from clinical samples to help optimise the company's development efforts for their diagnostic tests. This role is critical to the business, so you will be in a position to make a significant impact on the company. Working as part of a cross-functional team, you will be responsible for managing self-contained Machine Learning projects and collaborating on larger projects with colleagues in departments such as molecular biology, engineering, and software/IT development. Major responsibilities will include: Developing, implementing and testing new Machine Learning / AI models, methods and approaches; Increasing the functionality and effectiveness of the company's technology stack / platform; Biomarker discovery, ID and validation; Project management, including setting timelines and milestones; Hands-on programming, typically in Python, Julia or R; Liaising with major stakeholders; The analysis of large-scale clinical genomic / NGS data sets; Providing training and technical advice to colleagues. What you'll need to succeed As well as strong communication, organisational and time management skills, you should have: An MSc / PhD (or equivalent experience) in data science, machine learning, bioinformatics, computational biology, statistics, computer science, biology or a related subject; A track record of utilising and/or developing Machine Learning, Deep Learning or AI approaches for the analysis of biological data; Ideally exposure to the analysis of genomic (eg sequencing / NGS, RNA-Seq, ChIP-Seq, methylation) or other clinical data; Strong programming skills in a language such as Python, Julia, R or similar, with knowledge of Numpy, Pandas, Tensorflow or similar a distinct advantage; and Good project management skills. Candidates with knowledge / experience of biomarker discovery or validation, clinical diagnostics, commercial product development, or the pharmaceutical / IVD / medical device industry are encouraged to apply. What you'll get in return The chance to work on a range of interesting projects in a great company atmosphere, as well as the ability to directly influence the development of diagnostics products that will make a real difference to patients. You'll also be joining the company as they go into their next growth phase, so there will be chances to further develop your skills and career. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on . If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career, especially as there are a number of other bioinformatics, data science and statistics positions available. Keywords: bioinformatics, bioinformatician, data, science, statistics, statistical, biomarker, discovery, genetics, genomics, NGS, PCR, sequence, Bayesian, biomarker, machine, learning, programmer, programming, scientist, diagnostics, molecular, python, R, C, Bash, medical, device, solution, architect, developer, automation, IVD, platform, project, manager, developer, tool, pipeline, computational, computer, oncology
Dec 06, 2019
Full time
Data Scientist, machine learning - AI bioinformatics statistics. Genomics / NGS. Diagnostics company Cambridge Your new company A well-established diagnostics company in the Cambridge area, that are currently undergoing strong growth in their bioinformatics, statistics and biology teams to help drive their new development efforts. The company is heavily focused on genomics & NGS within clinical and in-vitro diagnostics (IVD), and are recruiting several experienced data scientists, bioinformaticians and biostatisticians with strong programming and analysis skills to help drive their company forward and make a real difference in the diagnosis of patients with diseases such as cancer. Your new role You will be focusing on the design, development and implementation of new facets and functionality for their platform, geared towards biomarker discovery and validation; working closely with stakeholders. You will also be involved in the analysis of NGS data from clinical samples to help optimise the company's development efforts for their diagnostic tests. This role is critical to the business, so you will be in a position to make a significant impact on the company. Working as part of a cross-functional team, you will be responsible for managing self-contained Machine Learning projects and collaborating on larger projects with colleagues in departments such as molecular biology, engineering, and software/IT development. Major responsibilities will include: Developing, implementing and testing new Machine Learning / AI models, methods and approaches; Increasing the functionality and effectiveness of the company's technology stack / platform; Biomarker discovery, ID and validation; Project management, including setting timelines and milestones; Hands-on programming, typically in Python, Julia or R; Liaising with major stakeholders; The analysis of large-scale clinical genomic / NGS data sets; Providing training and technical advice to colleagues. What you'll need to succeed As well as strong communication, organisational and time management skills, you should have: An MSc / PhD (or equivalent experience) in data science, machine learning, bioinformatics, computational biology, statistics, computer science, biology or a related subject; A track record of utilising and/or developing Machine Learning, Deep Learning or AI approaches for the analysis of biological data; Ideally exposure to the analysis of genomic (eg sequencing / NGS, RNA-Seq, ChIP-Seq, methylation) or other clinical data; Strong programming skills in a language such as Python, Julia, R or similar, with knowledge of Numpy, Pandas, Tensorflow or similar a distinct advantage; and Good project management skills. Candidates with knowledge / experience of biomarker discovery or validation, clinical diagnostics, commercial product development, or the pharmaceutical / IVD / medical device industry are encouraged to apply. What you'll get in return The chance to work on a range of interesting projects in a great company atmosphere, as well as the ability to directly influence the development of diagnostics products that will make a real difference to patients. You'll also be joining the company as they go into their next growth phase, so there will be chances to further develop your skills and career. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on . If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career, especially as there are a number of other bioinformatics, data science and statistics positions available. Keywords: bioinformatics, bioinformatician, data, science, statistics, statistical, biomarker, discovery, genetics, genomics, NGS, PCR, sequence, Bayesian, biomarker, machine, learning, programmer, programming, scientist, diagnostics, molecular, python, R, C, Bash, medical, device, solution, architect, developer, automation, IVD, platform, project, manager, developer, tool, pipeline, computational, computer, oncology
