At GAMA Healthcare we help prevent infections and save lives. We offer an extensive range of infection prevention products and services with our flagship range being disinfectant wipes and hand gels. You will find a GAMA product in most UK hospitals, and as infection prevention becomes more important in people's lives, the need for them has never been greater...... click apply for full job details
Jan 25, 2021
Full time
At GAMA Healthcare we help prevent infections and save lives. We offer an extensive range of infection prevention products and services with our flagship range being disinfectant wipes and hand gels. You will find a GAMA product in most UK hospitals, and as infection prevention becomes more important in people's lives, the need for them has never been greater...... click apply for full job details
*Senior Biostatistician (Level I or II) - EMEA - Home based* We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD - thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. Our Biostatistics department are passionate about being data and technically agile, and driving enhanced value for our clients and patients. Determined to improve patient health, we help PPD provide industry-leading statistical, programming and clinical pharmacology contributions through global delivery, consistent quality adherence and scientific insight. We are currently recruiting for an experienced Sr Biostatistician to join our Biostatistics department in EMEA, working fully remotely in the UK or mainland Europe. As a Sr Bios, you will function independently as Lead Statistician on some projects and as support/project statistician on others, your responsibilities will include (but are not limited to) the following: * Develop statistical analysis plans, including analysis database and tables & listing specifications. * Provide randomization schemes and appropriate documentation. * Provide sample size calculations and review protocols for completeness, appropriateness of clinical design and sound statistical analysis. * Coordinate and collaborate with Programmers and Data Management personnel as to database maintenance, updating and documentation. * Work independently as a project lead or as lead statistician to deliver on lead tasks/responsibilities across large and complex projects. * Interact with the sponsor on all aspects of the project and present to sponsor and regulatory agencies as needed. * Lead the project team, conduct team meetings, maintain project timelines, assess resources needed and allocate resources as required. * Provide mentorship to junior team members. *Qualifications:* To be considered for the role you should have the following qualifications and experience: * Master's Degree in Biostatistics, Statistics, Mathematics or related field * 5+ years of experience working in Biostatistics (previous CRO experience is desirable) * Solid SAS programming experience (proficient in BASE, STAT, MACRO and GRAPH) * Strong understanding of statistical principles and excellent statistical skills * Good project management experience, demonstrated through previous experience managing multiple projects * Capable of providing mentorship and promoting teamwork in a multi-disciplinary team setting * Fluency in English is essential At PPD we hire the best, develop ourselves and each other, and recognise the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD you will benefit from an award-winning learning and development programme, ensuring you reach your potential. As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel. - We have a strong will to win - We earn our customer's trust - We are game changers - We do the right thing - We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you. #LI-AD1
Jan 25, 2021
Full time
*Senior Biostatistician (Level I or II) - EMEA - Home based* We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD - thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. Our Biostatistics department are passionate about being data and technically agile, and driving enhanced value for our clients and patients. Determined to improve patient health, we help PPD provide industry-leading statistical, programming and clinical pharmacology contributions through global delivery, consistent quality adherence and scientific insight. We are currently recruiting for an experienced Sr Biostatistician to join our Biostatistics department in EMEA, working fully remotely in the UK or mainland Europe. As a Sr Bios, you will function independently as Lead Statistician on some projects and as support/project statistician on others, your responsibilities will include (but are not limited to) the following: * Develop statistical analysis plans, including analysis database and tables & listing specifications. * Provide randomization schemes and appropriate documentation. * Provide sample size calculations and review protocols for completeness, appropriateness of clinical design and sound statistical analysis. * Coordinate and collaborate with Programmers and Data Management personnel as to database maintenance, updating and documentation. * Work independently as a project lead or as lead statistician to deliver on lead tasks/responsibilities across large and complex projects. * Interact with the sponsor on all aspects of the project and present to sponsor and regulatory agencies as needed. * Lead the project team, conduct team meetings, maintain project timelines, assess resources needed and allocate resources as required. * Provide mentorship to junior team members. *Qualifications:* To be considered for the role you should have the following qualifications and experience: * Master's Degree in Biostatistics, Statistics, Mathematics or related field * 5+ years of experience working in Biostatistics (previous CRO experience is desirable) * Solid SAS programming experience (proficient in BASE, STAT, MACRO and GRAPH) * Strong understanding of statistical principles and excellent statistical skills * Good project management experience, demonstrated through previous experience managing multiple projects * Capable of providing mentorship and promoting teamwork in a multi-disciplinary team setting * Fluency in English is essential At PPD we hire the best, develop ourselves and each other, and recognise the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD you will benefit from an award-winning learning and development programme, ensuring you reach your potential. As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel. - We have a strong will to win - We earn our customer's trust - We are game changers - We do the right thing - We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you. #LI-AD1
My Client, an ever growing and exciting T-Cell therapy Biotech in Oxford is currently looking to expand their CMC team in the form of a Principal Scientist with an expertise in Cell Processing. The role is multifaceted in working closely with the internal research teams on cross-functional projects, such as the development of next gen products, leading cell process and/or analytical development, and the assessment of novel methods and technologies. Further, the role will act as SME on projects with our external partners to establish robust cell processes and analytical methods * Partner with the research team to establish robust GMP compliant cell culture processes and analytics to rapidly advance next gen and new clinical candidates from the pipeline into manufacturing * Transfer knowhow on cell manufacturing and analytical methods to and from external partners under development / GMP tech transfer * Liaise and act as SME with external manufacturing, testing, supply, and development partners * Troubleshoot external manufacturing and supply activities * Clearly communicate problems, risks and potential impact on timelines, as well as recommended solutions to senior management * Develop and execute on project plans to assess novel cell process and analytical technologies and methods internally and with external partners * Author, review, and keep record of protocols, manufacturing and analytical documentation and reports * Provide scientific and technical expertise to and/or lead research and development project teams * Support in development / write documents for regulatory submission packages for IND/ IMPD submissions *Minimum Qualifications and Experience required* * Degree in Life Sciences or related discipline * Substantial and relevant post-graduate experience within academic or industry setting, preferably including an MSc or PhD * Proven experience of working to objectives and timelines * In-depth T-cell biology, process and analytical understanding * Understanding of GMP regulations * Extensive laboratory experience with cell culture and process development, ideally with primary human T cells at various scales * Strong laboratory experience with assay development and analytical methods such as cell counting, phenotypic and functional cell characterisation (flow cytometry, cytokine detection, etc.) * Excellent communicator, both written and verbal * Self-motivated and enthusiastic team player with strong attention to detail * Computer literate and ability to familiarise with different IT systems *Desirable:* * Experience with external contract R&D, cell manufacturing, and suppliers * Hands on experience in global Regulatory filings / submission packages * GMP process / analytical development and validation * Experience with closed and automated process technology * Experience working in project teams * Project and/or people leadership experience If you would like to find out more about this amazing company and opportunity then please reach out ASAP!
Jan 25, 2021
Full time
My Client, an ever growing and exciting T-Cell therapy Biotech in Oxford is currently looking to expand their CMC team in the form of a Principal Scientist with an expertise in Cell Processing. The role is multifaceted in working closely with the internal research teams on cross-functional projects, such as the development of next gen products, leading cell process and/or analytical development, and the assessment of novel methods and technologies. Further, the role will act as SME on projects with our external partners to establish robust cell processes and analytical methods * Partner with the research team to establish robust GMP compliant cell culture processes and analytics to rapidly advance next gen and new clinical candidates from the pipeline into manufacturing * Transfer knowhow on cell manufacturing and analytical methods to and from external partners under development / GMP tech transfer * Liaise and act as SME with external manufacturing, testing, supply, and development partners * Troubleshoot external manufacturing and supply activities * Clearly communicate problems, risks and potential impact on timelines, as well as recommended solutions to senior management * Develop and execute on project plans to assess novel cell process and analytical technologies and methods internally and with external partners * Author, review, and keep record of protocols, manufacturing and analytical documentation and reports * Provide scientific and technical expertise to and/or lead research and development project teams * Support in development / write documents for regulatory submission packages for IND/ IMPD submissions *Minimum Qualifications and Experience required* * Degree in Life Sciences or related discipline * Substantial and relevant post-graduate experience within academic or industry setting, preferably including an MSc or PhD * Proven experience of working to objectives and timelines * In-depth T-cell biology, process and analytical understanding * Understanding of GMP regulations * Extensive laboratory experience with cell culture and process development, ideally with primary human T cells at various scales * Strong laboratory experience with assay development and analytical methods such as cell counting, phenotypic and functional cell characterisation (flow cytometry, cytokine detection, etc.) * Excellent communicator, both written and verbal * Self-motivated and enthusiastic team player with strong attention to detail * Computer literate and ability to familiarise with different IT systems *Desirable:* * Experience with external contract R&D, cell manufacturing, and suppliers * Hands on experience in global Regulatory filings / submission packages * GMP process / analytical development and validation * Experience with closed and automated process technology * Experience working in project teams * Project and/or people leadership experience If you would like to find out more about this amazing company and opportunity then please reach out ASAP!
Microbial, fermentation, process development, upstream, downstream, science jobs, graduate jobs, pharma, bio Your new company My client is one of the leading pharma companies worldwide who maintain a heavy focus on scientific R&D, primarily focussing on immunology, neurology and rare diseases, but also have a very much up-and-coming oncology pipeline...... click apply for full job details
Jan 25, 2021
Full time
Microbial, fermentation, process development, upstream, downstream, science jobs, graduate jobs, pharma, bio Your new company My client is one of the leading pharma companies worldwide who maintain a heavy focus on scientific R&D, primarily focussing on immunology, neurology and rare diseases, but also have a very much up-and-coming oncology pipeline...... click apply for full job details
The Royal Mint group is one of the UK's oldest and most respected organisations. As well as being the home of British coinage for over 1,100 years we offer our global customers a diverse range of products and services which include Consumer and Gifting products; precious metals investment; storage facilities and also a visitor attraction at The Royal Mint Experience...... click apply for full job details
Jan 25, 2021
Contractor
The Royal Mint group is one of the UK's oldest and most respected organisations. As well as being the home of British coinage for over 1,100 years we offer our global customers a diverse range of products and services which include Consumer and Gifting products; precious metals investment; storage facilities and also a visitor attraction at The Royal Mint Experience...... click apply for full job details
Company Description SGS is the world's leading inspection, verification, testing and certification company. We are recognized as the global benchmark for quality and integrity. With more than 95,000 employees, we operate a network of more than 2,400 offices and laboratories around the world. We aim to be the most competitive and the most productive service organization in the world...... click apply for full job details
Jan 25, 2021
Contractor
Company Description SGS is the world's leading inspection, verification, testing and certification company. We are recognized as the global benchmark for quality and integrity. With more than 95,000 employees, we operate a network of more than 2,400 offices and laboratories around the world. We aim to be the most competitive and the most productive service organization in the world...... click apply for full job details
Team Member 2, Forest Operations/Land Management (Higher Education Placement) • Location: Flexible (Mid South, Mid North, South East) • Grade & Salary: Grade 2 - £19,374 • Post number: 202361, 202546, 202700, 202699 • Type of contract: Fixed Term (Monday 6 September 2021 to Friday 26 August 2022) • Work pattern: 37 hours per week (Monday to Friday) Closing date: 31 January 2021 Interviews to take place when/where: Approximately week commencing 15th February 2021 - Due to the current situation with regards COVID19, recruitment is still progressing and interviews will be undertaken by Skype/Microsoft Teams. Benefits: Civil Service pension, 28 days annual leave, rising to 33 days over 5 years, flexible working options, occupational health including counselling and advisory services and eye care and salary sacrifice schemes. Role Purpose: • This is a mid-year placement role for someone who is currently undertaking a higher education qualification, such as an undergraduate qualification in forestry or land management from a higher educational institution. • Under the direction of the line manager, you will support the delivery of programmes within at least one of the following disciplines (dependant on the scale of geographic programmes): • Forest operations; assist with the delivery of operational planning and management including; forest and conservation inventory collection, GIS data collection, monitoring and reporting to ensure statutory compliance. • Land management; monitor the implementation of planned programmes of work, in addition to undertaking landowner liability surveys. Assist with the delivery of the recreational and land management work programmes. • You will work closely with and get direction from the Forest Operations/Land Management Technical Supports, Officers, Senior Officers and Team Leader. Qualifications and Skills: You will have: 1. Currently undertaking an undergraduate degree in either a forestry or land management discipline from a higher education institution. Your undergraduate degree must require a mid-year placement (essential). 2. A good understanding of working in land and forestry management disciplines, including sustainable forest management. 3. Good communication and inter-personal skills with a customer focus. Ability to build effective working relationship with colleagues and partners. 4. Good ICT skills (essential). 5. Full UK driving licence (essential). For more information, please visit our website. TO APPLY PLEASE CLICK THE APPLY NOW BUTTON AND YOU WILL BE REDIRECTED TO BEGIN THE APPLICATION PROCESS
Jan 25, 2021
Full time
Team Member 2, Forest Operations/Land Management (Higher Education Placement) • Location: Flexible (Mid South, Mid North, South East) • Grade & Salary: Grade 2 - £19,374 • Post number: 202361, 202546, 202700, 202699 • Type of contract: Fixed Term (Monday 6 September 2021 to Friday 26 August 2022) • Work pattern: 37 hours per week (Monday to Friday) Closing date: 31 January 2021 Interviews to take place when/where: Approximately week commencing 15th February 2021 - Due to the current situation with regards COVID19, recruitment is still progressing and interviews will be undertaken by Skype/Microsoft Teams. Benefits: Civil Service pension, 28 days annual leave, rising to 33 days over 5 years, flexible working options, occupational health including counselling and advisory services and eye care and salary sacrifice schemes. Role Purpose: • This is a mid-year placement role for someone who is currently undertaking a higher education qualification, such as an undergraduate qualification in forestry or land management from a higher educational institution. • Under the direction of the line manager, you will support the delivery of programmes within at least one of the following disciplines (dependant on the scale of geographic programmes): • Forest operations; assist with the delivery of operational planning and management including; forest and conservation inventory collection, GIS data collection, monitoring and reporting to ensure statutory compliance. • Land management; monitor the implementation of planned programmes of work, in addition to undertaking landowner liability surveys. Assist with the delivery of the recreational and land management work programmes. • You will work closely with and get direction from the Forest Operations/Land Management Technical Supports, Officers, Senior Officers and Team Leader. Qualifications and Skills: You will have: 1. Currently undertaking an undergraduate degree in either a forestry or land management discipline from a higher education institution. Your undergraduate degree must require a mid-year placement (essential). 2. A good understanding of working in land and forestry management disciplines, including sustainable forest management. 3. Good communication and inter-personal skills with a customer focus. Ability to build effective working relationship with colleagues and partners. 4. Good ICT skills (essential). 5. Full UK driving licence (essential). For more information, please visit our website. TO APPLY PLEASE CLICK THE APPLY NOW BUTTON AND YOU WILL BE REDIRECTED TO BEGIN THE APPLICATION PROCESS
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are...... click apply for full job details
Jan 25, 2021
Contractor
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are...... click apply for full job details
We are seeking a highly motivated science graduate to join the NHS Blood and Transplant (NHSBT) Histocompatibility and Immunogenetics (H&I) Service Development Laboratory located at the Colindale Centre, London. You will join a dynamic team and contribute to projects aimed at the development and implementation of new diagnostic tests in HLA, immunogenetics and transplantation, using the latest geno...... click apply for full job details
Jan 24, 2021
Full time
We are seeking a highly motivated science graduate to join the NHS Blood and Transplant (NHSBT) Histocompatibility and Immunogenetics (H&I) Service Development Laboratory located at the Colindale Centre, London. You will join a dynamic team and contribute to projects aimed at the development and implementation of new diagnostic tests in HLA, immunogenetics and transplantation, using the latest geno...... click apply for full job details
MATERIAL SCIENTIST - CERAMICS PERMANENT POSITION. FARNBOROUGH At QinetiQ, we're dedicated to defending sovereign capability, protecting lives, and securing the vital interests of our customers. We are a company of over 6,000 dedicated people providing technological and scientific expertise that helps our customers protect, improve, and advance their vital interests...... click apply for full job details
Jan 24, 2021
Full time
MATERIAL SCIENTIST - CERAMICS PERMANENT POSITION. FARNBOROUGH At QinetiQ, we're dedicated to defending sovereign capability, protecting lives, and securing the vital interests of our customers. We are a company of over 6,000 dedicated people providing technological and scientific expertise that helps our customers protect, improve, and advance their vital interests...... click apply for full job details
Staffline are recruiting for a Research & Development Assistant for our client in Alconbury. Pay for the position will be £8.97 Your Time at Work As a Research & Development Assistant, you will support a range of R&D activities to maximise the shelf life of cut flower products. Reporting to the Research & Development Manager, you will organise and prepare cut flower samples for t...... click apply for full job details
Jan 24, 2021
Seasonal
Staffline are recruiting for a Research & Development Assistant for our client in Alconbury. Pay for the position will be £8.97 Your Time at Work As a Research & Development Assistant, you will support a range of R&D activities to maximise the shelf life of cut flower products. Reporting to the Research & Development Manager, you will organise and prepare cut flower samples for t...... click apply for full job details
Fast growing and extremely innovative scale-up Utilising unique methods for drug discovery Strong career progression opportunities This is an opportunity to join an exciting drug discovery innovator utilising machine learning to vastly improve the drug discovery process and produce more effective therapeutics worldwide...... click apply for full job details
Jan 24, 2021
Full time
Fast growing and extremely innovative scale-up Utilising unique methods for drug discovery Strong career progression opportunities This is an opportunity to join an exciting drug discovery innovator utilising machine learning to vastly improve the drug discovery process and produce more effective therapeutics worldwide...... click apply for full job details
My client is an award-winning AI focused company who are looking to recruit a passionate and knowledgeable Senior Speech Applied Research Scientist who can help lead and improve their innovative speech technology. As a Speech Applied Research Scientist, you will be collaborating with data scientists and engineers to bring research into production...... click apply for full job details
Jan 24, 2021
Full time
My client is an award-winning AI focused company who are looking to recruit a passionate and knowledgeable Senior Speech Applied Research Scientist who can help lead and improve their innovative speech technology. As a Speech Applied Research Scientist, you will be collaborating with data scientists and engineers to bring research into production...... click apply for full job details
Have you recently graduated? Or have you graduated and gained over a year in industry? Who is our client? The company have been working in their field for over 40 years but in the last 10 years staff numbers have grown significantly, with further expansion planned in the next few years. My client is an SME in High Wycombe and specialises in the process of chemical vapour deposition...... click apply for full job details
Jan 24, 2021
Full time
Have you recently graduated? Or have you graduated and gained over a year in industry? Who is our client? The company have been working in their field for over 40 years but in the last 10 years staff numbers have grown significantly, with further expansion planned in the next few years. My client is an SME in High Wycombe and specialises in the process of chemical vapour deposition...... click apply for full job details
Package: Salary up to £27,500 (FTE) plus benefits This role is for a part-time (0.6 FTE) position at Heyford Park (HP) Innovation Centre, Upper Heyford with immediate effect but is expected to become a full-time position during April 2021, to include the Wood Centre for Innovation (WCFI) at Headington, Oxford (0...... click apply for full job details
Jan 24, 2021
Full time
Package: Salary up to £27,500 (FTE) plus benefits This role is for a part-time (0.6 FTE) position at Heyford Park (HP) Innovation Centre, Upper Heyford with immediate effect but is expected to become a full-time position during April 2021, to include the Wood Centre for Innovation (WCFI) at Headington, Oxford (0...... click apply for full job details
JOB TITLE: Senior R&D Quality Engineer LOCATION: Pilot, Chandler's Ford, Hampshire Responsible for leading QA Activities in Concept Research Control or Design Control activities, Risk Management in the R&D and Manufacturing, ensuring that clinical trial samples, new products and new processes meet all requirements established by CooperVision procedures and appropriate regulatory requirements...... click apply for full job details
Jan 24, 2021
Full time
JOB TITLE: Senior R&D Quality Engineer LOCATION: Pilot, Chandler's Ford, Hampshire Responsible for leading QA Activities in Concept Research Control or Design Control activities, Risk Management in the R&D and Manufacturing, ensuring that clinical trial samples, new products and new processes meet all requirements established by CooperVision procedures and appropriate regulatory requirements...... click apply for full job details
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are...... click apply for full job details
Jan 24, 2021
Full time
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are...... click apply for full job details
Flakt Woods specialises in the design, test, certification and manufacture of axial fans for a wide range of industrial, life applications. Flakt Woods has one of the largest certified axial ranges in the world. Our approach is based on offering high levels of customisation across our range of products and services to create maximum value for our customers and end users...... click apply for full job details
Jan 24, 2021
Full time
Flakt Woods specialises in the design, test, certification and manufacture of axial fans for a wide range of industrial, life applications. Flakt Woods has one of the largest certified axial ranges in the world. Our approach is based on offering high levels of customisation across our range of products and services to create maximum value for our customers and end users...... click apply for full job details
*SENIOR SCIENTIST, DOWNSTREAM PROCESS VIRAL VECTOR* *JOB PURPOSE* You will join Process Development team as the downstream process development (DSP) Senior Scientist where you will be involved in all aspects of DSP process development for viral vector products. This is a brilliant opportunity for a talented scientist to take a leading role in the development novel viral vector products. You will work closely with the CMC DSP team for transferring and supporting developed processes internally to CMC-Manufacturing and externally to cGMP contract manufacturing organisations. Our client is looking for someone with the ability to succeed within a small biotech environment, with the ability to train, mentor, motivate, innovate and deliver a high standard of results! *KEY RESPONSIBILITIES* * Lead decision making of technical and scientific issues that affect, or have the potential to affect, the development and execution of DSP for the manufacture of biologics. * Develop, optimise, and establish robust, scalable and industry leading DSP processes to produce high quality novel viral vector products, meeting the requirements for quality and titre. * Provide scientific and technical leadership, in downstream process development and transfer into CMC Manufacturing or cGMP - for example process risk assessments, technology transfer and scale-up. * Deliver product specific and platform DSP documentation, process flow diagrams and reports ensuring appropriate quality of documentation to support inclusion of data and information in regulatory filings. * Work collaboratively with Research, Cell Line Development, Upstream Process Development, Analytical Development, CMC-Manufacturing and Quality to develop and establish new techniques and recommend alternative approaches and potential solutions to downstream processing issues. * Ensure a healthy and safe working environment and compliance to GMO/ACDP requirements. *PROFILE SUMMARY* *Education and Qualifications:* * PhD or BSc/MSc in Cell Biology, Biochemistry, Biotechnology, Food Science, Biological Sciences, Biochemical Engineering or a related field. A highly motivated ambitious scientist with: * Ability to work independently. * Good conceptual, analytical thinking, problem solving, and organisational skills. * Ability to work in a high paced team environment, meet deadlines, and prioritise work from multiple projects. * Strong interpersonal and communication skills with demonstrated ability to work within a team environment. * Ability to balance multiple priorities and projects at the same time and be able to change priorities as needed by the business. * Experience in downstream process development/purification of viral vector products, from cell culture harvesting through to drug substance/purified product. This would have preferably been gained working with viral vectors such as LVV, AAV or AV. * Experience with chromatography systems such as Akta Purifier/Pure/Avant and a good understanding of chromatography techniques e.g., IEX/SEC/HIC/Affinity. Experience and understanding of tangential flow filtration are also desirable. Experience of scale-up of downstream processes to pilot scale would be a bonus. * Experience of routine analytical techniques such as SDS-PAGE, Western Blotting and biochemical assays is desirable. * Experience in the application DoE. * Knowledge of regulatory requirements for the development and manufacture of biologics using from mammalian cell culture is desirable. *DURATION* Permanent / full-time *SALARY* Attractive package *LOCATION* South East UK - commutable from Berkshire, Buckinghamshire and Oxfordshire *ABOUT PLANET PHARMA* Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
Jan 24, 2021
Full time
*SENIOR SCIENTIST, DOWNSTREAM PROCESS VIRAL VECTOR* *JOB PURPOSE* You will join Process Development team as the downstream process development (DSP) Senior Scientist where you will be involved in all aspects of DSP process development for viral vector products. This is a brilliant opportunity for a talented scientist to take a leading role in the development novel viral vector products. You will work closely with the CMC DSP team for transferring and supporting developed processes internally to CMC-Manufacturing and externally to cGMP contract manufacturing organisations. Our client is looking for someone with the ability to succeed within a small biotech environment, with the ability to train, mentor, motivate, innovate and deliver a high standard of results! *KEY RESPONSIBILITIES* * Lead decision making of technical and scientific issues that affect, or have the potential to affect, the development and execution of DSP for the manufacture of biologics. * Develop, optimise, and establish robust, scalable and industry leading DSP processes to produce high quality novel viral vector products, meeting the requirements for quality and titre. * Provide scientific and technical leadership, in downstream process development and transfer into CMC Manufacturing or cGMP - for example process risk assessments, technology transfer and scale-up. * Deliver product specific and platform DSP documentation, process flow diagrams and reports ensuring appropriate quality of documentation to support inclusion of data and information in regulatory filings. * Work collaboratively with Research, Cell Line Development, Upstream Process Development, Analytical Development, CMC-Manufacturing and Quality to develop and establish new techniques and recommend alternative approaches and potential solutions to downstream processing issues. * Ensure a healthy and safe working environment and compliance to GMO/ACDP requirements. *PROFILE SUMMARY* *Education and Qualifications:* * PhD or BSc/MSc in Cell Biology, Biochemistry, Biotechnology, Food Science, Biological Sciences, Biochemical Engineering or a related field. A highly motivated ambitious scientist with: * Ability to work independently. * Good conceptual, analytical thinking, problem solving, and organisational skills. * Ability to work in a high paced team environment, meet deadlines, and prioritise work from multiple projects. * Strong interpersonal and communication skills with demonstrated ability to work within a team environment. * Ability to balance multiple priorities and projects at the same time and be able to change priorities as needed by the business. * Experience in downstream process development/purification of viral vector products, from cell culture harvesting through to drug substance/purified product. This would have preferably been gained working with viral vectors such as LVV, AAV or AV. * Experience with chromatography systems such as Akta Purifier/Pure/Avant and a good understanding of chromatography techniques e.g., IEX/SEC/HIC/Affinity. Experience and understanding of tangential flow filtration are also desirable. Experience of scale-up of downstream processes to pilot scale would be a bonus. * Experience of routine analytical techniques such as SDS-PAGE, Western Blotting and biochemical assays is desirable. * Experience in the application DoE. * Knowledge of regulatory requirements for the development and manufacture of biologics using from mammalian cell culture is desirable. *DURATION* Permanent / full-time *SALARY* Attractive package *LOCATION* South East UK - commutable from Berkshire, Buckinghamshire and Oxfordshire *ABOUT PLANET PHARMA* Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
*SENIOR SCIENTIST, UPSTREAM PROCESS VIRAL VECTOR* *JOB PURPOSE* You will join Process Development team as the Upstream Process (USP) Senior Scientist where you will be involved in all aspects of USP process development for viral vector products. This is a brilliant opportunity for a talented scientist to take a leading role in the development novel viral vector products. You will work closely with the CMC USP team for transferring and supporting developed processes internally to CMC-Manufacturing and externally to cGMP contract manufacturing organisations. Our client is looking for someone with the ability to succeed within a small biotech environment, with the ability to train, mentor, motivate, innovate and deliver a high standard of results! *KEY RESPONSIBILITIES* * Design, and execute experiments to develop and optimise mammalian cell culture batch and fed batch processes for novel viral vector products. * Apply statistical approaches for process optimisation (DoE, QbD) at small scale and translation of small-scale results to process scale-up. * Scale up of upstream processes (10-200L) to confirm process performance. * Generate harvest material for purification by the downstream development group. * Support technology transfer activities for clinical manufacturing. * Ensure that all experimental and analytical data is documented following data integrity principles. * Work collaboratively with Research, Cell Line Development, Downstream Process Development, Research Manufacturing and Quality to develop and establish new techniques and recommend alternative approaches and potential solutions to upstream process development issues. * Ensure a healthy and safe working environment and compliance to GMO/ACDP requirements. *PROFILE SUMMARY* *Education and Qualifications:* * PhD or BSc/MSc in Cell Biology, Virology or Biochemistry, Biotechnology, Molecular Biology, Biological Sciences, Biochemical Engineering with a viral vector focus, e.g., AAV, LVV, AV. A highly motivated ambitious scientist with: * Industry experience in mammalian suspension cell culture: batch and fed-batch process development, transient transfection, optimisation and scale up gained through the development of viral products. * Some experience of basal medium and feed development, control, and optimisation. * Some experience of developing upstream process control strategies. * Understanding and experience of development and establishment of in-process analytical methods as applied to mammalian cell culture processes producing viral vector products. *DURATION* Permanent / full-time *SALARY* Attractive package *LOCATION* South East UK - commutable from Berkshire, Buckinghamshire and Oxfordshire *ABOUT PLANET PHARMA* Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
Jan 24, 2021
Full time
*SENIOR SCIENTIST, UPSTREAM PROCESS VIRAL VECTOR* *JOB PURPOSE* You will join Process Development team as the Upstream Process (USP) Senior Scientist where you will be involved in all aspects of USP process development for viral vector products. This is a brilliant opportunity for a talented scientist to take a leading role in the development novel viral vector products. You will work closely with the CMC USP team for transferring and supporting developed processes internally to CMC-Manufacturing and externally to cGMP contract manufacturing organisations. Our client is looking for someone with the ability to succeed within a small biotech environment, with the ability to train, mentor, motivate, innovate and deliver a high standard of results! *KEY RESPONSIBILITIES* * Design, and execute experiments to develop and optimise mammalian cell culture batch and fed batch processes for novel viral vector products. * Apply statistical approaches for process optimisation (DoE, QbD) at small scale and translation of small-scale results to process scale-up. * Scale up of upstream processes (10-200L) to confirm process performance. * Generate harvest material for purification by the downstream development group. * Support technology transfer activities for clinical manufacturing. * Ensure that all experimental and analytical data is documented following data integrity principles. * Work collaboratively with Research, Cell Line Development, Downstream Process Development, Research Manufacturing and Quality to develop and establish new techniques and recommend alternative approaches and potential solutions to upstream process development issues. * Ensure a healthy and safe working environment and compliance to GMO/ACDP requirements. *PROFILE SUMMARY* *Education and Qualifications:* * PhD or BSc/MSc in Cell Biology, Virology or Biochemistry, Biotechnology, Molecular Biology, Biological Sciences, Biochemical Engineering with a viral vector focus, e.g., AAV, LVV, AV. A highly motivated ambitious scientist with: * Industry experience in mammalian suspension cell culture: batch and fed-batch process development, transient transfection, optimisation and scale up gained through the development of viral products. * Some experience of basal medium and feed development, control, and optimisation. * Some experience of developing upstream process control strategies. * Understanding and experience of development and establishment of in-process analytical methods as applied to mammalian cell culture processes producing viral vector products. *DURATION* Permanent / full-time *SALARY* Attractive package *LOCATION* South East UK - commutable from Berkshire, Buckinghamshire and Oxfordshire *ABOUT PLANET PHARMA* Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
Metallurgist An exciting opportunity has arisen for a Metallurgist to further their career as part of our employee focused company. Luxfer MEL Technologies is a global leader in the development, manufacture and supply of Magnesium and Zirconium based products and services to technology industries worldwide...... click apply for full job details
Jan 24, 2021
Full time
Metallurgist An exciting opportunity has arisen for a Metallurgist to further their career as part of our employee focused company. Luxfer MEL Technologies is a global leader in the development, manufacture and supply of Magnesium and Zirconium based products and services to technology industries worldwide...... click apply for full job details
Johnson Matthey ('JM') is a global leader in science that enables a cleaner and healthier world. With over 200 years of sustained commitment to innovation and technological breakthroughs, we improve the function, performance and safety of our customers' products. Our science has a global impact in areas such as low emission transport, pharmaceuticals, chemical processing and making the most efficie...... click apply for full job details
Jan 24, 2021
Full time
Johnson Matthey ('JM') is a global leader in science that enables a cleaner and healthier world. With over 200 years of sustained commitment to innovation and technological breakthroughs, we improve the function, performance and safety of our customers' products. Our science has a global impact in areas such as low emission transport, pharmaceuticals, chemical processing and making the most efficie...... click apply for full job details
Johnson Matthey ('JM') is a global leader in science that enables a cleaner and healthier world. With over 200 years of sustained commitment to innovation and technological breakthroughs, we improve the function, performance and safety of our customers' products. Our science has a global impact in areas such as low emission transport, pharmaceuticals, chemical processing and making the most efficie...... click apply for full job details
Jan 24, 2021
Full time
Johnson Matthey ('JM') is a global leader in science that enables a cleaner and healthier world. With over 200 years of sustained commitment to innovation and technological breakthroughs, we improve the function, performance and safety of our customers' products. Our science has a global impact in areas such as low emission transport, pharmaceuticals, chemical processing and making the most efficie...... click apply for full job details
Laboratory Technician Superb career opportunity for an individual with a strong work ethic and experience with AI biology, or a biology aptitude with a background of working within a commercial laboratory environment, to join the quality focused team within the Laboratory at Cogent located in Aldford near Chester...... click apply for full job details
Jan 24, 2021
Full time
Laboratory Technician Superb career opportunity for an individual with a strong work ethic and experience with AI biology, or a biology aptitude with a background of working within a commercial laboratory environment, to join the quality focused team within the Laboratory at Cogent located in Aldford near Chester...... click apply for full job details
We have a new Senior Scientist role within our growing Analytical Development team at our Swindon manufacturing site. The Senior Scientist is responsible for project management and execution of analytical activities. All work within the Analytical Development group is to be performed in accordance to cGXP requirements, including analytical investigations, adhering to project timelines and maintain...... click apply for full job details
Jan 24, 2021
Full time
We have a new Senior Scientist role within our growing Analytical Development team at our Swindon manufacturing site. The Senior Scientist is responsible for project management and execution of analytical activities. All work within the Analytical Development group is to be performed in accordance to cGXP requirements, including analytical investigations, adhering to project timelines and maintain...... click apply for full job details
Specialist Would you like to be part of an organisation which is committed to improving patient lives worldwide through education, collaboration and innovation? Do you want to make a difference? If the answer is 'yes' then you're just the kind of person we're looking for! We have new exciting opportunities for Specialists to work in our Production Support Department...... click apply for full job details
Jan 24, 2021
Full time
Specialist Would you like to be part of an organisation which is committed to improving patient lives worldwide through education, collaboration and innovation? Do you want to make a difference? If the answer is 'yes' then you're just the kind of person we're looking for! We have new exciting opportunities for Specialists to work in our Production Support Department...... click apply for full job details
To be successful in your application to this exciting opportunity as the Formulation Chemist we are looking to identify the following on your profile and past history: 1. Relevant degree in pharmaceutical science or another related discipline 2. Proven industry experience in pharmaceutical or cosmetics industry 3...... click apply for full job details
Jan 24, 2021
Full time
To be successful in your application to this exciting opportunity as the Formulation Chemist we are looking to identify the following on your profile and past history: 1. Relevant degree in pharmaceutical science or another related discipline 2. Proven industry experience in pharmaceutical or cosmetics industry 3...... click apply for full job details
Job Title: Lab Technician Location: Ipswich Salary: £10-£14/hour Are you a keen scientist looking for a position to work in a medical laboratory? We are currently looking to fill multiple Lab Technician positions, with a potential start date of February. Your duties will include: Performing a range of routine healthcare science activities under the supervision of a Specialist Biomedical Scient...... click apply for full job details
Jan 24, 2021
Contractor
Job Title: Lab Technician Location: Ipswich Salary: £10-£14/hour Are you a keen scientist looking for a position to work in a medical laboratory? We are currently looking to fill multiple Lab Technician positions, with a potential start date of February. Your duties will include: Performing a range of routine healthcare science activities under the supervision of a Specialist Biomedical Scient...... click apply for full job details
Senior Regulatory Scientist This is a great opportunity to join a company of over 200 dedicated Regulatory Affairs experts offering consulting services to global clients across the life sciences sector including pharmaceuticals, biotechnology and medical devices. The position is a permanent role, offering a great career growth plan and exposure to multiple RA projects in various products including ...... click apply for full job details
Jan 24, 2021
Full time
Senior Regulatory Scientist This is a great opportunity to join a company of over 200 dedicated Regulatory Affairs experts offering consulting services to global clients across the life sciences sector including pharmaceuticals, biotechnology and medical devices. The position is a permanent role, offering a great career growth plan and exposure to multiple RA projects in various products including ...... click apply for full job details
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
Jan 24, 2021
Full time
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
Jan 24, 2021
Full time
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
SRG is searching for laboratory technicians to work in and around Royal Leamington Spa in a state of the art, high output diagnostics laboratory environment. The lab is seeking Junior Lab Technicians to work variable shifts on a fixed-term contract as part of the UK's NHS Test and Trace programme. The Junior Laboratory Technician role comes with a competitive salary and benefits package, including ...... click apply for full job details
Jan 24, 2021
Contractor
SRG is searching for laboratory technicians to work in and around Royal Leamington Spa in a state of the art, high output diagnostics laboratory environment. The lab is seeking Junior Lab Technicians to work variable shifts on a fixed-term contract as part of the UK's NHS Test and Trace programme. The Junior Laboratory Technician role comes with a competitive salary and benefits package, including ...... click apply for full job details
Role: Synthetic Organic Chemist Location: Stevenage Duration: 12 Months (possible temp to perm opportunity) Rate: Up to £20/hour We are looking for a Synthetic Chemist to work with our expert Chemistry team with employees across the world. Do you have a passion for employing synthetic chemistry skills to produce functional materials? Then we would love to hear from you. What you'll do Use a range of synthetic chemistry's to produce functionalised membrane materials Functionalise membranes with biological or chemical ligands for use in the next generation of affinity chromatgraphy applications, towards expansion of Fibro range of products Work closely with Materials Scientists, Engineers and Biologists to support activities including chemical analysis, reactor design, device fabrication, reactor and applications testing Take detailed lab notes and use these to write up accurate protocols and technical reports Carry out and document COSHH and Risk Assessments Who you are Minimum MSc or equivalent in chemistry from an accredited institution, with modules including organic chemistry Experience carrying out a range of practical organic chemistry techniques in a laboratory environment is essential >6 months experience of synthetic organic chemistry working in industry (Chemical or Biotechnology) is highly desirable Experience or good working knowledge of chemical analysis techniques such as GC-FID, SEC-HPLC, Raman Spectroscopy is desirable Proven aptitude for problem solving, flexibility to adapt to changing project priorities, good attention to detail and a strong team player Who we are Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you'll feel right at home here. If you're flexible, curious and relentless, you'll belong. If you are excited about a global culture, this can be the place to further your career. To apply please send your CV's in the first instance
Jan 24, 2021
Contractor
Role: Synthetic Organic Chemist Location: Stevenage Duration: 12 Months (possible temp to perm opportunity) Rate: Up to £20/hour We are looking for a Synthetic Chemist to work with our expert Chemistry team with employees across the world. Do you have a passion for employing synthetic chemistry skills to produce functional materials? Then we would love to hear from you. What you'll do Use a range of synthetic chemistry's to produce functionalised membrane materials Functionalise membranes with biological or chemical ligands for use in the next generation of affinity chromatgraphy applications, towards expansion of Fibro range of products Work closely with Materials Scientists, Engineers and Biologists to support activities including chemical analysis, reactor design, device fabrication, reactor and applications testing Take detailed lab notes and use these to write up accurate protocols and technical reports Carry out and document COSHH and Risk Assessments Who you are Minimum MSc or equivalent in chemistry from an accredited institution, with modules including organic chemistry Experience carrying out a range of practical organic chemistry techniques in a laboratory environment is essential >6 months experience of synthetic organic chemistry working in industry (Chemical or Biotechnology) is highly desirable Experience or good working knowledge of chemical analysis techniques such as GC-FID, SEC-HPLC, Raman Spectroscopy is desirable Proven aptitude for problem solving, flexibility to adapt to changing project priorities, good attention to detail and a strong team player Who we are Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you'll feel right at home here. If you're flexible, curious and relentless, you'll belong. If you are excited about a global culture, this can be the place to further your career. To apply please send your CV's in the first instance
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
Jan 24, 2021
Full time
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
Jan 24, 2021
Full time
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
Jan 24, 2021
Full time
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
Jan 24, 2021
Full time
RPS islooking for an experienced and commercially minded Ornithologist to join ourhighly respected Ecology Team at Principal level. Our work covers UK on shoreand off shore projects and we are particularly interested to hear fromornithologists based in Scotland or those with particular experience inrenewable energy project work. Byjoining RPS, you will become part of a leading global multi-discipl...... click apply for full job details
Watford, BSBI Consulting Solution Sponsorship is available for international students BSBI Consulting is recruiting for a Graduate Data Scientist/Insight Analyst (Internship) to support the move to advanced modelling and machine learning development using Python or R to derive meaningful insight from customer and operational data to improve services and performance...... click apply for full job details
Jan 24, 2021
Seasonal
Watford, BSBI Consulting Solution Sponsorship is available for international students BSBI Consulting is recruiting for a Graduate Data Scientist/Insight Analyst (Internship) to support the move to advanced modelling and machine learning development using Python or R to derive meaningful insight from customer and operational data to improve services and performance...... click apply for full job details
Organic Chemist Temporary contact - 6 Months Immediate / ASAP start Lancaster Our client is a large organisation in several Global Top-10's for their business categories (Chemicals, Healthcare and Instrumentation). At their site near Lancaster, they produce Organics, Organometallics, Inorganics, and other speciality / bulk chemicals alongside Catalysts...... click apply for full job details
Jan 24, 2021
Seasonal
Organic Chemist Temporary contact - 6 Months Immediate / ASAP start Lancaster Our client is a large organisation in several Global Top-10's for their business categories (Chemicals, Healthcare and Instrumentation). At their site near Lancaster, they produce Organics, Organometallics, Inorganics, and other speciality / bulk chemicals alongside Catalysts...... click apply for full job details
Analytical Chemist Temporary contact - 6 Months Immediate / ASAP start Lancaster Our client is a large organisation in several Global Top-10's for their business categories (Chemicals, Healthcare and Instrumentation). At their site near Lancaster, they produce Organics, Organometallics, Inorganics, and other speciality / bulk chemicals alongside Catalysts...... click apply for full job details
Jan 24, 2021
Seasonal
Analytical Chemist Temporary contact - 6 Months Immediate / ASAP start Lancaster Our client is a large organisation in several Global Top-10's for their business categories (Chemicals, Healthcare and Instrumentation). At their site near Lancaster, they produce Organics, Organometallics, Inorganics, and other speciality / bulk chemicals alongside Catalysts...... click apply for full job details
Excellent Package & Benefits Felling, Gateshead Having gained extensive experience in manufacturing operations and process technology, ideally in a polymer & powder coatings production, you are seeking your next senior level role. This Powder & Polymer Process Technology Manager role with AkzoNobel is exactly what you are looking for...... click apply for full job details
Jan 24, 2021
Full time
Excellent Package & Benefits Felling, Gateshead Having gained extensive experience in manufacturing operations and process technology, ideally in a polymer & powder coatings production, you are seeking your next senior level role. This Powder & Polymer Process Technology Manager role with AkzoNobel is exactly what you are looking for...... click apply for full job details
* About the Role: * We are looking to recruit a Programme Manager with a scientific background. This role will report into the Head of the Programme Management Office within PPI. Using their knowledge and experience they will manage an assigned large scale programme(s). The job is based at our Cambridge (UK) site but the job holder will work closely with other stakeholders in other global locations to deliver the programme to strict timelines. * Roles & responsibilities: * * To plan and design complex multi-disciplinary programmes, identifying success criteria, setting controls and ensuring programme assurance, quality assurance and appropriate change management processes are in place with routine updates/checks. Proactively monitoring and reporting on progress through the governance framework. * To maintain and ensure delivery of the portfolio/programme delivery map, having an overall view of finance tracking using an established system and resources, ensuring the projects within the programme have adequate resources to deliver and develop strategies to address resource gaps. * To communicate changes in timelines in a timely manner to stakeholders and works to resolve issues to get project back on track, skillfully managing and influencing all levels within Abcam, managing risks (threats and opportunities) and issues across the programme, ensuring regular reporting and escalation to senior stakeholders as appropriate. * To establish and supports programme governance and decision making by acting as a link between the programme and business governance. Prepares milestone reports as required particularly for higher level stakeholders including board level. Holding self and programme team accountable for delivery. * To ensure relevant stakeholders interests are identified and addressed. Working collaboratively to build effective relationships and achieve buy-in to the overall programme objectives. * To build and manage strategic relationships with multiple diverse stakeholders across the projects and Abcam and drives to build a consensus that maintains focus and ensures programme objectives are met. * To develops and maintain the programme plan and regularly provides status reports on programme progress to sponsors and executive stakeholders at senior management meetings. * To identify and establish a working program team that enables the program to move forwards. Chair regular team meetings and provide minutes to key stakeholders. Influence project members to ensure timely delivery of the project deliverables. * About you * Our ideal candidate will have a strong project management background, with experience of working within the life sciences industry, and a MSc or PhD in biological science or equivalent experience. A formal project management qualification is highly preferred (such as Prince 2). You will have extensive experience of managing and delivering large scale projects with multiple stakeholders and will have extensive years project management experience. You will be highly organised, be comfortable working to deadlines and prioritising different aspects of the project. You will be able to work independently and have outstanding attention to detail. If this sounds like you and you'd like to be a part of a fast-paced, growing business with the vision to become the most influential company and best-loved brand in life sciences, please apply now! * Pay and Benefits * In addition to competitive salaries, we offer an attractive and flexible benefits package (including our award-winning share scheme, 18 weeks full paid maternity leave and 6 weeks full paid paternity leave), a culture focused on well-being and opportunities for growth and development, and a highly flexible working environment. What's more, as a WORK180 Endorsed Employer, we are recognized globally as an organization that's diverse, inclusive and supports women in the workplace. * About Us * An idea conceived in a University of Cambridge laboratory in 1998, * Abcam plc () * began life as an innovative and entrepreneurial start-up, spearheaded by like-minded individuals who shared a common purpose of providing the scientific community with quality antibody reagents, as well as trustworthy and up-to-date information about their uses and limitations. Abcam has now grown to become a leading supplier of protein research tools to life scientists, whilst always maintaining the core collaborative values assumed at its inception. Abcam now supports life science researchers in their quest to understand the cause of disease and ultimately offer improvements to diagnoses and treatments. To achieve this outcome, the company both develops and manufactures its own products in specialist facilities across the globe, and sources from over 400 partners, offering scientists the newest, most innovative and highest quality research tools available globally, regardless of source. With a customer base of research scientists who require high performance products with detailed technical specifications, 64% of global researchers use Abcam products. * Inclusion & Diversity * Abcam is an Equal Opportunity Employer and makes all employment decisions without regard to age, national origin, race, ethnicity, religion, creed, gender, sexual orientation, disability, veteran status, or any other characteristic protected by law.
Jan 24, 2021
Full time
* About the Role: * We are looking to recruit a Programme Manager with a scientific background. This role will report into the Head of the Programme Management Office within PPI. Using their knowledge and experience they will manage an assigned large scale programme(s). The job is based at our Cambridge (UK) site but the job holder will work closely with other stakeholders in other global locations to deliver the programme to strict timelines. * Roles & responsibilities: * * To plan and design complex multi-disciplinary programmes, identifying success criteria, setting controls and ensuring programme assurance, quality assurance and appropriate change management processes are in place with routine updates/checks. Proactively monitoring and reporting on progress through the governance framework. * To maintain and ensure delivery of the portfolio/programme delivery map, having an overall view of finance tracking using an established system and resources, ensuring the projects within the programme have adequate resources to deliver and develop strategies to address resource gaps. * To communicate changes in timelines in a timely manner to stakeholders and works to resolve issues to get project back on track, skillfully managing and influencing all levels within Abcam, managing risks (threats and opportunities) and issues across the programme, ensuring regular reporting and escalation to senior stakeholders as appropriate. * To establish and supports programme governance and decision making by acting as a link between the programme and business governance. Prepares milestone reports as required particularly for higher level stakeholders including board level. Holding self and programme team accountable for delivery. * To ensure relevant stakeholders interests are identified and addressed. Working collaboratively to build effective relationships and achieve buy-in to the overall programme objectives. * To build and manage strategic relationships with multiple diverse stakeholders across the projects and Abcam and drives to build a consensus that maintains focus and ensures programme objectives are met. * To develops and maintain the programme plan and regularly provides status reports on programme progress to sponsors and executive stakeholders at senior management meetings. * To identify and establish a working program team that enables the program to move forwards. Chair regular team meetings and provide minutes to key stakeholders. Influence project members to ensure timely delivery of the project deliverables. * About you * Our ideal candidate will have a strong project management background, with experience of working within the life sciences industry, and a MSc or PhD in biological science or equivalent experience. A formal project management qualification is highly preferred (such as Prince 2). You will have extensive experience of managing and delivering large scale projects with multiple stakeholders and will have extensive years project management experience. You will be highly organised, be comfortable working to deadlines and prioritising different aspects of the project. You will be able to work independently and have outstanding attention to detail. If this sounds like you and you'd like to be a part of a fast-paced, growing business with the vision to become the most influential company and best-loved brand in life sciences, please apply now! * Pay and Benefits * In addition to competitive salaries, we offer an attractive and flexible benefits package (including our award-winning share scheme, 18 weeks full paid maternity leave and 6 weeks full paid paternity leave), a culture focused on well-being and opportunities for growth and development, and a highly flexible working environment. What's more, as a WORK180 Endorsed Employer, we are recognized globally as an organization that's diverse, inclusive and supports women in the workplace. * About Us * An idea conceived in a University of Cambridge laboratory in 1998, * Abcam plc () * began life as an innovative and entrepreneurial start-up, spearheaded by like-minded individuals who shared a common purpose of providing the scientific community with quality antibody reagents, as well as trustworthy and up-to-date information about their uses and limitations. Abcam has now grown to become a leading supplier of protein research tools to life scientists, whilst always maintaining the core collaborative values assumed at its inception. Abcam now supports life science researchers in their quest to understand the cause of disease and ultimately offer improvements to diagnoses and treatments. To achieve this outcome, the company both develops and manufactures its own products in specialist facilities across the globe, and sources from over 400 partners, offering scientists the newest, most innovative and highest quality research tools available globally, regardless of source. With a customer base of research scientists who require high performance products with detailed technical specifications, 64% of global researchers use Abcam products. * Inclusion & Diversity * Abcam is an Equal Opportunity Employer and makes all employment decisions without regard to age, national origin, race, ethnicity, religion, creed, gender, sexual orientation, disability, veteran status, or any other characteristic protected by law.
*Brief Description*: The Nurse Clinician - RN [Field Based] - New York City, NY is responsible for understanding all client program education and training aspects and contract deliverables. The RN may work with multiple program stakeholders that can include Patients in various settings, including home, HCP office, etc. The RN may also be responsible for HCP interactions in addition to other parties such as program specific Sales Representatives or Reimbursement Specialists. The RN is expected to Identify and track trends for analytics reporting to ensure clinical criteria program integrity. Maintain a professional and ethical behavior at all times as outlined by the Nurse Practice Act along with applicable company and client expectations and policies. Presents a professional work appearance. Meets Client specifications to ensure patients and other stakeholders are serviced accurately and timely. Completes all charting or data entry into program databases accurately and timely. *Specific job duties may include:* * Performs territory management and route planning * Reports AE/PC/OSF as required by program guidelines * Ensures patient privacy by keeping related PHI, documents and demo supplies in a secure location * Provides product education and training for both patients and/or HCPs per program guidelines * Maintains program database and responds to member and physician inquiries regarding clinical programs. Makes recommendations regarding escalation of issues, and follows through with escalation process. * Completes program specific training as requested and within required timelines * Submits weekly program related expense reports and mileage * Special projects/assignments as needed. *Supervisory Responsibility: * N/A *Desired Skills and Qualifications:* * Nursing degree * 2 - 5 years' experience in a clinical or commercial setting * Registered Nursing Licensure in good standing * Registered Nurse License in good standing in the state in which you work and/or cross-licensed in other states * Telephonic nursing roles must have (or be willing to obtain) a compact nursing license; additionally, the employee must be willing to obtain additional state licenses upon request. * General PC knowledge including Microsoft Office, Internet and email * Previous clinical criteria review experience preferred * Active professional affiliations and/or national certification in related clinical specialty preferred * Able to adapt to flexible work schedule * Able to travel within defined territory * Self-driven with proven ability to work independently *ABOUT UBC* United BioSource Corporation (UBC) is a leading provider of pharmaceutical support services, partnering with life science companies to make medicine and medical products safer and more accessible. Our services support the full lifecycle of medicine and medical products, including development, commercialization, and long-term value and safety. While UBC offers employment within Patient Support, Nursing, Pharmacy and Corporate, two main focus areas for the company are Clinical Development & Research and Safety & Risk Management. Members of the Clinical Development and Research teams help evaluate study protocol, target study population, recruit physicians and patients, and collect, clean, validate and report data. As a result, sponsors are able to submit findings to regulatory authorities or make a no-go decision in a timely and clear-cut manner. Additionally, our Safety and Risk Management teams develop, deliver, and report evidence to reinforce safe and appropriate product use. Through our Patient Access services, we help patients begin therapy quickly and remain on therapy, building strong relationships with patients to ensure optimal care. You can find out more by visiting []()
Jan 24, 2021
Full time
*Brief Description*: The Nurse Clinician - RN [Field Based] - New York City, NY is responsible for understanding all client program education and training aspects and contract deliverables. The RN may work with multiple program stakeholders that can include Patients in various settings, including home, HCP office, etc. The RN may also be responsible for HCP interactions in addition to other parties such as program specific Sales Representatives or Reimbursement Specialists. The RN is expected to Identify and track trends for analytics reporting to ensure clinical criteria program integrity. Maintain a professional and ethical behavior at all times as outlined by the Nurse Practice Act along with applicable company and client expectations and policies. Presents a professional work appearance. Meets Client specifications to ensure patients and other stakeholders are serviced accurately and timely. Completes all charting or data entry into program databases accurately and timely. *Specific job duties may include:* * Performs territory management and route planning * Reports AE/PC/OSF as required by program guidelines * Ensures patient privacy by keeping related PHI, documents and demo supplies in a secure location * Provides product education and training for both patients and/or HCPs per program guidelines * Maintains program database and responds to member and physician inquiries regarding clinical programs. Makes recommendations regarding escalation of issues, and follows through with escalation process. * Completes program specific training as requested and within required timelines * Submits weekly program related expense reports and mileage * Special projects/assignments as needed. *Supervisory Responsibility: * N/A *Desired Skills and Qualifications:* * Nursing degree * 2 - 5 years' experience in a clinical or commercial setting * Registered Nursing Licensure in good standing * Registered Nurse License in good standing in the state in which you work and/or cross-licensed in other states * Telephonic nursing roles must have (or be willing to obtain) a compact nursing license; additionally, the employee must be willing to obtain additional state licenses upon request. * General PC knowledge including Microsoft Office, Internet and email * Previous clinical criteria review experience preferred * Active professional affiliations and/or national certification in related clinical specialty preferred * Able to adapt to flexible work schedule * Able to travel within defined territory * Self-driven with proven ability to work independently *ABOUT UBC* United BioSource Corporation (UBC) is a leading provider of pharmaceutical support services, partnering with life science companies to make medicine and medical products safer and more accessible. Our services support the full lifecycle of medicine and medical products, including development, commercialization, and long-term value and safety. While UBC offers employment within Patient Support, Nursing, Pharmacy and Corporate, two main focus areas for the company are Clinical Development & Research and Safety & Risk Management. Members of the Clinical Development and Research teams help evaluate study protocol, target study population, recruit physicians and patients, and collect, clean, validate and report data. As a result, sponsors are able to submit findings to regulatory authorities or make a no-go decision in a timely and clear-cut manner. Additionally, our Safety and Risk Management teams develop, deliver, and report evidence to reinforce safe and appropriate product use. Through our Patient Access services, we help patients begin therapy quickly and remain on therapy, building strong relationships with patients to ensure optimal care. You can find out more by visiting []()
Provide statistical leadership and statistical expertise into clinical development plans, concept sheets and protocols for clinical development projects, represent Cytel and the statistical team on the Product Development Teams of sponsors. Lead statistical teams on clinical development projects, ensuring alignment of objectives and delivery of statistical output on time and meeting project requirements, coordinating all statistical aspects across clinical trials of each assigned project. Provide statistical input into study protocols, Case Report Forms, and data management plans, write statistical analysis plans, review or create analysis dataset specifications, and perform statistical analyses. Review and contribute to study reports and clinical and statistical sections of regulatory submission dossiers, lead electronic submissions of clinical data to regulatory authorities, and participate to meetings with regulatory authorities. When in the Lead Biostatistician role for a project: manage biostatisticians and statistical programmers with respect to statistical strategy, deliverables and processes. Generate the use of innovative statistical methodology approaches by identifying, adapting, developing or using optimal statistical research methodologies and techniques appropriate to each project, and contribute internally and externally to the development and visibility of the company and of the Clinical Services department through her/his expertise and customer orientation. Contribute to the development of sourcing strategy for projects.
Jan 24, 2021
Full time
Provide statistical leadership and statistical expertise into clinical development plans, concept sheets and protocols for clinical development projects, represent Cytel and the statistical team on the Product Development Teams of sponsors. Lead statistical teams on clinical development projects, ensuring alignment of objectives and delivery of statistical output on time and meeting project requirements, coordinating all statistical aspects across clinical trials of each assigned project. Provide statistical input into study protocols, Case Report Forms, and data management plans, write statistical analysis plans, review or create analysis dataset specifications, and perform statistical analyses. Review and contribute to study reports and clinical and statistical sections of regulatory submission dossiers, lead electronic submissions of clinical data to regulatory authorities, and participate to meetings with regulatory authorities. When in the Lead Biostatistician role for a project: manage biostatisticians and statistical programmers with respect to statistical strategy, deliverables and processes. Generate the use of innovative statistical methodology approaches by identifying, adapting, developing or using optimal statistical research methodologies and techniques appropriate to each project, and contribute internally and externally to the development and visibility of the company and of the Clinical Services department through her/his expertise and customer orientation. Contribute to the development of sourcing strategy for projects.
Provide statistical leadership and statistical expertise into clinical development plans, concept sheets and protocols for clinical development projects, represent Cytel and the statistical team on the Product Development Teams of sponsors. Lead statistical teams on clinical development projects, ensuring alignment of objectives and delivery of statistical output on time and meeting project requirements, coordinating all statistical aspects across clinical trials of each assigned project. Provide statistical input into study protocols, Case Report Forms, and data management plans, write statistical analysis plans, review or create analysis dataset specifications, and perform statistical analyses. Review and contribute to study reports and clinical and statistical sections of regulatory submission dossiers, lead electronic submissions of clinical data to regulatory authorities, and participate to meetings with regulatory authorities. When in the Lead Biostatistician role for a project: manage biostatisticians and statistical programmers with respect to statistical strategy, deliverables and processes. Generate the use of innovative statistical methodology approaches by identifying, adapting, developing or using optimal statistical research methodologies and techniques appropriate to each project, and contribute internally and externally to the development and visibility of the company and of the Clinical Services department through her/his expertise and customer orientation. Contribute to the development of sourcing strategy for projects. * * *Qualifications and Experience: * *Minimum Education: *Ph.D. or MS in Statistics, Biostatistics or related discipline. *Minimum Work Requirements: * At least 6 years of experience as biostatistician in the Pharmaceutical/Biotechnology industry in clinical development. t least 3 years of experience as a Lead Biostatistician for clinical development projects. *Job Description * Knowledge of relevant international regulatory guidelines applicable to clinical development, and some experience of regulatory interactions and data e-submission to FDA. Fluent in English (French or German is a plus). Working SAS & CDISC knowledge. * * *Skills: * Works effectively in international teams, effectively operates within a matrix organization and with multi-disciplinary groups. Understands and anticipates customer needs and responds to their inquiries. Verbal and written communication is effective with multi-disciplinary groups. Work is well-organized, of high-quality, meeting timelines. Able to balance concurrent tasks and responsibilities. Excellent time management. Brings creative ideas and makes suggestions for optimization. Exhibits leadership for the biostatistics team working on the same clinical development teams. Exhibits the ability to mentor and develop statistical colleagues.
Jan 24, 2021
Full time
Provide statistical leadership and statistical expertise into clinical development plans, concept sheets and protocols for clinical development projects, represent Cytel and the statistical team on the Product Development Teams of sponsors. Lead statistical teams on clinical development projects, ensuring alignment of objectives and delivery of statistical output on time and meeting project requirements, coordinating all statistical aspects across clinical trials of each assigned project. Provide statistical input into study protocols, Case Report Forms, and data management plans, write statistical analysis plans, review or create analysis dataset specifications, and perform statistical analyses. Review and contribute to study reports and clinical and statistical sections of regulatory submission dossiers, lead electronic submissions of clinical data to regulatory authorities, and participate to meetings with regulatory authorities. When in the Lead Biostatistician role for a project: manage biostatisticians and statistical programmers with respect to statistical strategy, deliverables and processes. Generate the use of innovative statistical methodology approaches by identifying, adapting, developing or using optimal statistical research methodologies and techniques appropriate to each project, and contribute internally and externally to the development and visibility of the company and of the Clinical Services department through her/his expertise and customer orientation. Contribute to the development of sourcing strategy for projects. * * *Qualifications and Experience: * *Minimum Education: *Ph.D. or MS in Statistics, Biostatistics or related discipline. *Minimum Work Requirements: * At least 6 years of experience as biostatistician in the Pharmaceutical/Biotechnology industry in clinical development. t least 3 years of experience as a Lead Biostatistician for clinical development projects. *Job Description * Knowledge of relevant international regulatory guidelines applicable to clinical development, and some experience of regulatory interactions and data e-submission to FDA. Fluent in English (French or German is a plus). Working SAS & CDISC knowledge. * * *Skills: * Works effectively in international teams, effectively operates within a matrix organization and with multi-disciplinary groups. Understands and anticipates customer needs and responds to their inquiries. Verbal and written communication is effective with multi-disciplinary groups. Work is well-organized, of high-quality, meeting timelines. Able to balance concurrent tasks and responsibilities. Excellent time management. Brings creative ideas and makes suggestions for optimization. Exhibits leadership for the biostatistics team working on the same clinical development teams. Exhibits the ability to mentor and develop statistical colleagues.
