1472 Science jobs

Data Scientist Deep Learning/Machine Learning London £70,000 - £80,000 OVERVIEW Harnham are currently working with a global tech company in central London who are looking to hire three Data Scientists with a specialism in deep learning and computer vision to tackle problems related to recommender systems. There are a number of roles being recruited for and my client is looking for a range of data scientists with experience in the following areas for a number of research-related projects: deep learning, computational linguistics, NLP, computer vision and machine learning. This is the perfect role for someone keen to stay at the forefront of their discipline and use the latest techniques in the data science space to help solve real-world problems which will go on to impact millions of people. THE ROLE On a daily basis you will be: Researching and developing deep learning algorithms to help solve computer vision problems Work within a core group of Research Scientists and Engineers Championing the use of data/data science within the business SKILLS AND EXPERTISE Experience programming with Python Extensive experience in deep learning An MSc or Ph.D. in Computer Science, Machine Learning, Artificial Intelligence, Deep Learning etc. Experience with SQL HOW TO APPLY To be considered for this exciting opportunity, please submit your details using the Apply button on this page. Or for more information regarding other roles please contact Nick Mandella at Harnham. SALARY This pays up to £80,000 + benefits. KEYWORDS Python, R, SQL, Hadoop, NoSQL, computer science, machine learning, artifical intelligence, deep learning, computer vision, natural language processing, NLP, Data Scientist, Data Science, Xpath, Regex.

Excellent opportunity for a team leader position within an international food/Cannabinoid testing laboratory! This is a permanent role based in Acton/London paying a competitive salary Search Scientific consultancy is a recruitment partner to an international Food testing company who are looking for a Technical Team Lead to help establish and grow and new analytical service based in Acton. This is a great opportunity to gain experience with a desirable employer, where the successful individual will be performing Specialist Cannabinoid Analysis using LC-MS and UPLC. Key responsibilities: To support the set up, validation and accreditation of the 16 component Cannabinoid analysis via UHPLC/LC-MS to ISO17025:2017 To develop additional methods to enhance the CBD proposition as required, ex client specific methods for encapsulated products or LC-MS To manage the subcontracting of associated analysis Responsible for validating CBD methods for the basic CBD testing Responsible for managing the work flow in the laboratory and all aspects of CBD Testing Supporting development of methods as the industry and legislation evolves. Validate and accredit lab and tests methods for the analysis of Cannabinoids to UKAS 17025 standards Lead the Analysis of CBD via UPLC and LC-MS Develop additional methods to improve offering available to clients Support staff and train new team members Requirements: Degree in Science or related field Experience within laboratory environment working as a Senior Analyst or team leader Essential to have experience in working in a food or water testing laboratory Excellent experience in people management within a UKAS ISO17025 laboratory. Experience of chromatography method development, ideally UHPLC and/or LC-MS previous experience of Analysing Cannabinoids would be a distinct advantage If you are interested in this role, please apply or get in touch via / Search is an equal opportunities recruiter and we welcome applications from all suitably skilled or qualified applicants, regardless of their race, sex, disability, religion/beliefs, sexual orientation or age.

We are currently looking for an experienced and ambitious Senior Scientist - Neuroscience to join a leading life sciences company based in the Edinburgh area. Our client are known for offering specialist preclinical contract research services to Pharmaceutical & Biotechnology companies focussed on Immuno-Oncology, Immunology, Neuroscience and specialised multiplex Histology. As the Senior Scientist - Neuroscience you will be responsible primarily for research into assay development and client project delivery within the field of neuroscience and neurodegeneration (focussing on Stroke, Parkinson's and Alzheimer's disease). KEY DUTIES AND RESPONSIBILITIES: Your duties as the Senior Scientist - Neuroscience will be varied however the key duties and responsibilities are as follows: 1. Producing and maintaining primary cell cultures and cell lines. Additionally, utilising molecular and cellular biology, protein biochemistry and functional neuroscience background to develop, validate and run assays. Accurate record-keeping and data analysis. 2. Active reviewing and analysis of scientific literature to understand relevant therapeutic targets with relation to individual projects. 3. Working as part of the company team and with academic contacts and clients to ensure delivery of high quality client projects, including implementing quality control steps and developing and updating SOPs. 4. Taking an active role in nurturing new and expanding client relationships, including presenting at conferences to capture new commercial opportunities. 5. As the Senior Scientist - Neuroscience, you will line manage Scientists and delegate project tasks across the team to ensure accurate and timely delivery of client data and reports. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Senior Scientist - Neuroscience we are looking to identify the following on your profile and past history: 1. A degree (ideally PhD) in a relevant life sciences discipline, ideally within Neuroscience plus significant relevant industry experience working in a CRO/Pharma/Biotech setting. 2. Evidence of a strong conceptual understanding of the field, with demonstrable laboratory experience within cellular and molecular biology. 3. Conference presentation and client discussion experience would be advantageous. Key Words: Neuroscience | Assays| CRO | Immuno-oncology | Senior Scientist | Pharmaceutical | Biotech | Immunology | Cell Biology | Molecular Biology

QC Chemistry Analyst 6 months Contract The Company Consult Search and Selection are currently recruiting for two analytical chemists to join a successful pharmaceutical services business that support drug development. They have two 6 month contracts available in their small and effective analytical team where they perform a variety of raw materials, stability and batch release testing to GMP standards. The Opportunity Reporting into the operations manager as an analytical chemist you will work alongside a small team of analysts and technicians performing day to day analysis of pharmaceutical products and/or raw materials. Tests will be for batch release or stability testing using a variety of analytical techniques. You will document results and interpret the data, working to GMP standards. Some of the role responsibilities include: Generating, recording and reporting analytical data Investigating atypical results Working to GMP Use of techniques such as HPLC, GC, IR, UV and wet chemistry to analyse products About You Due to the nature of these two positions being initial contracts of 6 months and joining a small team, my client is looking for experienced analytical chemists that have worked to GMP standards testing pharmaceutical products. This experience can be either from a manufacturing environment or contract testing company and will be on top of a relevant degree such as Chemistry, Pharmaceutical sciences or similar. To apply or find out more about this and our other similar roles, please contact Sophia at Consult Search and Selection.

Share you integrity by helping us to ensure compliance across our processes. We are looking for a motivated & creative GMP specialist interested in using their knowledge to author and co-ordinate our manufacturing documentation. You may off already have some SOP writing experience or similar or perhaps looking to move into this type of career, either way we would be like to hear from you. Duties & Responsibilities: Authoring of clear and concise GMP documentation to support manufacturing of clinical and commercial grade lentiviral vectors Co-ordinates the document update and review with other departments in order to ensure project time lines are achieved with minimal disruption to other activities within the facility Ensuring of adherence to manufacturing schedules to allow for timely availability of the batch manufacturing records. Work with the Senior Technical Writer to improve GMP documentation to minimise errors Work effectively alongside manufacturing teams and process compliance to ensure documentation is delivered in a timely manner. Education, Skills & Experience: Graduate in a science based subject, and/or experience of working to GMP standard within an aseptic manufacturing environment Proven experience working to GMP standards Past experience working within a GMP manufacturing facility is beneficial Competent with authoring clear and concise GMP documentation such as SOP's or Batch Manufacturing Records (BMR's) Competent user of MS Office applications Clear communicator in both written & spoken English. We look forward to receiving your application. No Agencies please

Senior Technologist with Continuous Flow c£up to 45k +Benefits South East AB/J4386a An experienced chemist or chemical engineer with flow chemistry experience preferably PhD qualified is required to work very closely with R&D teams. This a great opportunity to design and synthesise next generation materials for the business. There are also opportunities to influence multiple interfaces (like performance differentiation, Innovation, Manufacturing Technology, external outsourcing and Safety). The successful candidate will complement the R&D team's current skill base and play a critical role in enabling the team to become the High Performance Agile Team that deliver the new components the business needs (incremental, step-out & disruptive). This is a great role for a chemist or chemical engineer who wants to be involved in Coaching - imparting experience and knowledge to a variety of skill bases and team members. Opportunity to build personal network extensively across range Influence our New Technology Innovation Culture. Greater understanding of market opportunities (short - long term) Exposure to Innovation & road map opportunities. Development of external outsourcing relationships. Influence lab set-up & equipment to support the synthesis needs of the business. Key Responsibilities Lead safety initiatives to continue to build on the strong safety culture, deliver risk assessments and consistently demonstrate the highest standards of safety and quality. Deliver robust routing scouting to deliver materials in a time efficient manner. Supervise, develop & coach laboratory based chemists. Prepare a variety of materials in an agile and efficient manner. External focal lead for assigned chemical outsourcing. Provide design solutions to a variety of programs to enable science teams to prove or disprove the working hypothesis. Communicate progress, challenges and delivery through a variety of communication media. Qualifications, Knowledge and Experience Required: PhD Chemistry, Chemical Engineering, Synthetic Chemistry, Organic Chemistry, or a related engineering or petroleum subject. Technical background - significant experience in related fuels, diesels, pharma or oils markets, Strong track record of delivering materials to aggressive timescales within a research & development environment. Strong safety focus including networking, communication, a demonstrated ability to deliver high standard risk assessments, make solid safety recommendations when faced with obstacles and influence changes to work differently based on learnings from near miss reporting. Ability to take an objective view of technical problems and address them with creativity and innovation. Strong commitment to HSE and quality values They offer an attractive salary (dependent on experience), commensurate with qualifications and experience as well as associated benefits, including Bonus and Pension Scheme. To Apply: Please contact Alison Basson quoting AB/J4386a on

An exciting opportunity has arisen for an experienced Analytical Study Director to join a successful and rapidly expanding scientific company. Do you have experience conducting Bioanalysis and/or small molecules analysis studies in a GLP environment? Are you confident preparing study plans, updates and reports? Are you seeking a senior position with significant responsibility? Then this could be the role for you! You will act as Study Manager/ Director for a range of studies in the Bioanalysis/Small Molecules area and ensure work is conducted within set timeframes and to the highest scientific and regulatory standards. Your responsibilities will also include preparation of study plans, updates and reports as well as data review and QC checking. Successful applicants will have: - Significant experience conducting Bioanalysis/Small molecules analysis studies in a GLP environment - Experience of study management or project management - Excellent communication skills - High attention to detail - Experience working as a Study Director is desirable but not essential Apply to VRS today to be considered for this rewarding opportunity! Keywords: Study Director, Chemist, Analyst, Analysis, Chemistry, environmental, soil, water, food, pharmaceutical, biological, sample analysis, GLP, GMP. GCP, good laboratory practice, Northamptonshire, Northampton, Huntingdon, Kettering, Midlands, VRS6073FP Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.

An exciting opportunity has arisen for an experienced E-Fate Study Director to join a successful and rapidly expanding scientific company. Do you have experience conducting Environmental fate and/or metabolism studies in a GLP environment? Are you confident preparing study plans, updates and reports? Are you seeking a senior position with significant responsibility? Then this could be the role for you! You will act as Study Manager/ Director for a range of studies in the Environmental area and ensure work is conducted within set timeframes and to the highest scientific and regulatory standards. Your responsibilities will also include preparation of study plans, updates and reports as well as data review and QC checking. Successful applicants will have: Significant experience conducting E-fate/Metabolism studies in a regulated (GLP, OECD) environment Experience of study management or project management Excellent communication skills High attention to detail Experience working as a Study Director is desirable but not essential NB: For the right candidate, our client is willing to provide visa sponsorship. ? Apply to VRS today to be considered for this rewarding opportunity! Keywords: Study Director, efate, e-fate, environmental fate, environmental, Chemist, Analyst, Analysis, Chemistry, environmental, soil, water, food, pharmaceutical, biological, sample analysis, GLP, GMP, GCP, OECD, good laboratory practice, Northamptonshire, Northampton, Huntingdon, Kettering, Midlands, VRS6073FP Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.

Exciting new opportunity for an experienced Characterisation Chemist to join a world-leading laboratory at an exciting time of expansion! Playing a key role in supporting projects focused on oligonucleotide analysis within GxP environments; you will be routinely performing and developing methods (MS, NMR) and approaches to elucidate the structure of biopharmaceutical products. You will be responsible for scheduling, undertaking and reporting your own workload to ensure that studies are completed efficiently and effectively, to the highest level of quality. Applicants possessing a Chemistry (or related) degree and experience with structural elucidation using mass spectrometry, alongside strong attention to detail and teamworking skills are encouraged to apply. Apply to VRS now to learn more! Key words: MS, NMR, LCMS, liquid chromatography, mass spectrometry, oligo, oligonucleotide, pharma, biopharma, pharmaceutical, biopharmaceutical, GMP, GLP, GCP, analysis, Analyst, Scientist, development, validation, science, laboratory, Manchester, Greater Manchester, North West, VRS6025HQ Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.

Exciting Medical Devices Development company seeks a highly self-motivated and enthusiastic Senior QA/RA Officer. Reporting to the QMS Manager the Senior QA/RA Officer is responsible for helping to maintain and improve the Quality Management System by identifying potential improvements and developing, revising and implementing Quality procedures and policies. The company are certified to ISO 13485:2016, work in compliance with BS EN ISO 14971 and develop software according to IEC 62304. About the role: Compile and maintain Medical Device Files, Technical Files and Device Master Records in preparation for Regulatory submissions in various markets globally with guidance from the Regulatory Manager. Take an active role in the product risk management process. Take an active role in software development compliance review and approval. Support design review and control of change processes during product development. Maintain an up-to-date awareness of relevant regulations which may impact the QMS and communicate this effectively. Help to implement systems that facilitate productivity, improve processes and guarantee efficacy. Be involved in and lead training sessions to ensure the understanding and compliance of all employees. Administer, prepare, conduct and report internal quality system audits and external vendor assurance audits as necessary. Work within the QA/RA team to maintain the company's electronic Quality Management System, Q-Pulse, including monitoring and progression of CAPA and audit actions. Promote the benefits of the quality system to all employees. Plan, conduct and report validation of QMS-related software packages. Duties may include: Performing a combination, but not necessarily all, of the following duties: Work within the Quality team to maintain focused, effective progression in line with Company Quality objectives. Support other members of the Quality team by providing training and mentoring on areas of expertise. Effectively interact with Technical, Development and Planning teams to ensure research and development is performed in accordance with company procedures. Work with the software development team to ensure compliance with ISO 62304 is evident and maintained in accordance with company procedures. Support the Regulatory Affairs Manager to ensure compliance with relevant national and international standards and legislation. Ensure policies and procedures are properly understood, carried out and evaluated and that modifications are investigated if necessary. Help to train staff in Quality and Regulatory requirements. Facilitate the continued work toward established goals, objectives, policies, procedures and systems pertaining to the QMS. Investigate relevant standards and establish clearly defined Quality methods for staff to apply. Define Quality procedures in conjunction with operating staff. Maintain process controls and documentation procedures and identify areas for improvement and efficiency. Support product design review and change control systems. Participate in the Company audit schedules for both internal and external Quality audits. Monitor Quality indicators and helping to gather and track relevant data. Identify relevant Quality-related training needs and delivering training. QA/QC review of contractor documentation relating to validation and verification activities as well as device manufacture records when required. Perform other duties that may be required from time to time. Skills and experience: Degree level education in a relevant scientific or engineering-based subject. Experience of ISO 13485 and ISO 14971. Experience in working in quality assurance in the IVD sector. Ability to communicate effectively with all departments within the company and to represent the company in external audits. Experience in preparing and delivering training packages relating to Quality and Regulatory Affairs topics. Be eligible to work full time in the UK without restriction. Outstanding teamwork, a great sense of humour and ability to work in a fast-paced, cross-functional group environment, with a willingness to be hands-on across a wide range of responsibilities. Experience of working in compliance with IEC 62304. Awareness of radio equipment directive and knowledge of global radio regulations. Experience with ISO 60601 and its sub-standards. Experience in commercialisation of IVD products including knowledge of regulatory approval pathways in EU, US, and Asia. Experience of WHO prequalification for diagnostics.

PE Global is currently recruiting for an Epidemiologist (research) for a leading multi-national Biotech client based in Uxbridge. The role: The epidemiology position will be responsible for writing Statistical Analysis Plans (SAPs), guiding data analysts to explore client's real-world data (RWD) assets and interpreting the output. Prior experience with large databases such as CPRD or THIN is strongly desired. Experience in SAS or other statistical software is also highly desired. Responsibilities: • Responsible for writing of SAPs • Contributes to projects using real-world healthcare data assets • Guiding the analysts to explore RWD • Contributes to research strategy within the product team and epidemiology TA • Provides input into epidemiology department meetings • Stays abreast of the latest developments in the field of epidemiology and drug development, healthcare RWD and contributes to the field • Promotes epidemiologic awareness • Promotes understanding and use of RWD and epidemiologic methods • Communicate significant scientific information to a variety of audiences Requirements: • Master's degree in Epidemiology or other subject with high epidemiologic content • Experience in epidemiologic research • Experience in the design, execution, and analysis of epidemiology studies within Pharmaceutical or Public Health setting • Experience in research to support drug development Interested candidates should submit an updated CV. Please click the link below to apply, call Amparo on + or alternatively send an up to date CV Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert.

Data scientist London, United Kingdom £70,000+ Benefits Are you an enthusiastic Computer Vision expert, who is willing to work on Machine Learning projects and looking for something more? Join this adventurous company that is exploring complex data to impact and provide solutions to new computer vision and advanced technologies. The aim of this company being to covert text to images, as a Data Scientist you will take ownership of projects, getting data to write predictive models, this is a unique opportunity to work in a niche field of analytics. THE COMPANY Join a company full of world class developers that focus on the expansion of Artificial Intelligence and Computer Vision to produce breakthroughs through data transformation. Work with other Data Scientists in a collaborative environment, who are all keen to develop new ideas that impact the real world. THE ROLE This role will be an exciting opportunity to develop new solutions and work with Computer Vision and Artificial Intelligence. This role will allow you to solve complex roles on a daily basis and work with a variety of data, more details of the role are as follows: Using Computer Vision and Machine Learning to develop solutions -Working on an existing platform to develop the technology Problem solving on a daily basis Provide expertise when it comes to computer vision Work on data and projects to excite and please the audience Challenge and build on existing solutions YOUR SKILLS AND EXPERIENCE Enthusiastic problem solver Ability to lead and explore ideas with team Educated in a numeric discipline PhD also required Ability to work as a team and also independently Machine learning and Computer Vision experience Customer segmentation and Deep Learning experience Commercial experience and also experience using TensorFlow and PyTorch T HE BENEFITS Earning potential up to £70,000 + Benefits HOW TO APPLY Please register your interest by sending your CV to Charlotte York via the apply link on this page

Natalie Wood is currently recruiting for a Laboratory Analyst to join a fast growing dynamic and successful team within a FTSE 100 company based in Farnborough. This well known company provides quality and quantity measurement, inspection, and laboratory testing services to the global oil, gas, petrochemical, petroleum refining and distribution, natural gas, biofuels, marine, and chemical industries. This role is offered on a full time permanent basis and comes with a salary of £18,000 - £27,000 dependant on experience. This company has one of the largest networks of analytical testing laboratories in the world. Using advanced analytical technologies, our experienced chemists, material scientists, technicians and lab managers provide clients with key purity and component testing, able to measure elements and compounds into the parts-per-trillion level. Your main responsibilities in this role will be to analyse greases and lubricants within the test laboratories. Further responsibilities include: • Undertaking and coordinating testing using established test methods; • Interpretation of test data and provision of meaningful conclusions based on test results; • Providing advice to customers on results of testing and other issues relating to product analysis; • Maintenance of existing test equipment and developing/commissioning of new test methods and equipment as required; • Ensuring compliance with relevant quality and accreditation procedures. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: •Good IT literacy skills (including Microsoft Word and Excel) •Previous experience of working in a laboratory environment ideally within the fuels and lubricants sector •Demonstrable laboratory experience with experimental test methods •Full driving license Skills and experience required: •Good IT literacy skills (including Microsoft Word and Excel) •Previous experience of working in a laboratory environment ideally within the fuels and lubricants sector •Demonstrable laboratory experience with experimental test methods Personal qualities •Ability to demonstrate exceptional customer service •Motivated, self-starter •Highly organised with strong attention to detail •Confident communicator (written, email, text & oral) and able to build rapport, quickly and effectively •Demonstrates flexibility and resilience in order to meet the demands of the role The company would also consider taking on candidates with a chemistry degree without industrial xperience as long as they are enthusiastic and willing to learn. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 46658 in all correspondence.

CK Group is recruiting for a Senior Statistician to join a company in the Pharmaceutical industry on a fully remote, contract basis for 12 months and has an hourly rate of £65. The Company: Our client is a global pharmaceutical company with a major presence in the UK. Their purpose is to deliver life-changing medicines and to do this they are completely science-led and like to share this with the scientific, healthcare and business communities within the UK. The Role: In this role you will provide statistical expertise for complex design and interpretation of clinical studies, regulatory submissions and commercialisation. You will also act as a coach/guide for less experienced statisticians in the production of analysis, supporting graphics and analysis tables for CSRs, GMA studies or publications. You will also: - Analyse internal and external information to inform design decisions and the development of decision criteria. - Develop a Statistical Analysis plan for complex studies and/or project deliveries. - Provide support to the complex study analysis, regulatory submissions including specification of overview documents and response to regulatory questions. - Contribute to the regulatory submissions including specification of overview documents and response to regulatory questions. - Identify opportunities for the application of modelling and simulation to improve study design. - Identify and apply statistical methodology to improve the process and delivery activities. - Perform ad hoc and exploratory data analyses. - Contribute to the development of best practice to improve quality, efficiency and effectiveness. Your Background: You should have the following key skills, knowledge and experience for the role: - Phase 3/4 Oncology Submission experience. - Experience in design work, study execution and delivery. - Experience as a lead statistician. - Excellent communication skills - able to work with a large team, globally. - MSc or PhD in Statistics, Biostatistics, or Mathematics (containing a substantial statistical component). - Knowledge of the technical and regulatory requirements related to the role and able to guide others on these. - Experience in drug development, study design, and data analysis and interpretation. - Excellent communication skills and ability to build strong relationships. - Excellent collaboration skills required - the energy to work across global & functional boundaries, both internally and externally. - Project management skills. - Ability to apply statistical expertise to complex problems, problem solving and quality focus. Desirable qualifications include: - Experience in Oncology product development. - Coaching skills. - Experience in commercial or early development support work. - Expert statistical programming skills (SAS and R). - Level (Statistical Science Director vs Principal) to be commensurate with experience and abilities. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47116 in all correspondence.

R&D Analyst - Derbyshire - One of UK's leading Building Materials & Construction Company - Competitive Salary My client is one of the UK's leading building materials and construction companies looking for a Research and Development Analyst who will be responsible for project delivery and the ongoing support and development of Lime products. You will be reporting directly into the Lime Senior Technical Manager, with main responsibilities including the development of current and new products with continued support from Operations, Commercial and Quality teams over 2 sites. Key Responsibilities: Development of new test methodologies to support project requirements. Continued collaboration over 2 site's Operational Teams to ensure all product development complies to quality and manufacturing standards. Cross team working to ensure coordination and optimisation of the companies approach to Lime R&D. Maintaining a continued pipeline of projects that complies to customer and market needs. Delivering new products to market by coordination of research and trial methods. Requirements: Degree in Chemistry or related field. Previous experience in Laboratory Testing and Calibrations. Proven experience Researching and Developing new products. Knowledge of Quality Assurance and ISO 9001. Ability to analyse and interpret data. Benefits: Competitive salary £30,000 - £35,000 depending on experience Excellent Training and Development opportunities Collaborated on some of the UK's biggest construction projects Expansive Benefits package If you think you match the skills listed above and are looking for a new challenge, then please apply with your CV or call Thomas Nash on for a completely confidential chat about your situation.

Quality Control Microbiology Analyst Liverpool Shift pattern: 4 on, 4 off, 11 hour shifts. 6 month temporary contract My client, a pharmaceutical company in Liverpool, are looking to appoint a Quality Control Microbiology Analyst to join them to perform routine microbiological analytical testing. * The Quality Control Microbiology Analyst will be responsible for various duties and tasks within the Microbiology laboratory. * These include preparation and quality control of media, sample preparation, sub-culturing, plating out, streaking and reading plates; all via aseptic techniques and GMP. * This role is also required to calibrate and clean microbial equipment whilst assisting with environmental monitoring and bioburden testing. The ideal candidate: * Will have a BSc or equivalent in Microbiology * previous experience of microbiological testing in a pharmaceutical environment is desirable * Must have knowledge of GMP If you are an experienced Microbiologist with previous experience from the pharmaceutical industry looking for a new challenge please apply now! Search is an equal opportunities recruiter and we welcome applications from all suitably skilled or qualified applicants, regardless of their race, sex, disability, religion/beliefs, sexual orientation or age

An exciting opportunity for an individual with method development experience to join an industry leading analytical services company. In this diverse and challenging role, you will be providing method development and validation services for a broad range of sponsor studies, covering an array of sample matrices. Working within a GLP and GMP environment, you will develop and validate methods on IC, HPLC, GC, LC-MS and GC-MS. The ideal candidate will be confident developing methods and analysing samples by one or more of the above chromatography techniques and using a range of detection methods. Preferably you will be experienced the full spectrum of analytical projects within a GxP environment, including planning, performing studies and report writing. Applicants must possess strong communication skills, be highly enthusiastic and confident in training others. Apply to VRS now to be considered for this excellent opportunity! Key words: GC-MS, mass spectrometry, gas chromatography, pharmaceutical, pharma, HPLC, Liquid chromatography, LC-MS, LC-MS/MS, GC-MS/MS, analyst, analytical chemist, Method development, validation, GxP, GLP, Leeds, Bradford, Huddersfield, West Yorkshire, VRS6538RS Follow VRS Recruitment on LinkedIn to view all our latest vacancies! Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.

Business Analyst £350 - £400 PD 1 Day a Week Your new company A leading pharmaceuticals organisation in Cambridge is seeking a Business Analyst to assist the team in Cambridge working closely with the IT Solutions team. Your new role You will need to be able to efficiently run a large transformation programme to a high standard of quality in keeping with this companies' reputation. The right candidate will be able to work in an agile environment whilst communicating with colleagues from multiple sectors both internal and external to the organisation. Your focus on late sciences whilst maintaining this leading organisations values. What you'll need to succeed To succeed in this role, you will need to be able to: Document current systems within SEUIT whilst identifying and designing improvements through to implementation. Be able to work and communicate with DevOps automation engineers and automate systems where suitable Be a highly motivated and reliable individual with experience in problem solving Experience with BPM software and mapping of IT processes What you'll get in return Experience working for the 4th largest pharmaceuticals company in the world. £400 PD one day a week. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Hays EA is a trading division of Hays Specialist Recruitment Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk

On behalf of our client, we are looking to recruit a Bioinformatician with good experience in programming and knowledge integration, to join the Early Stage Research Team within Product Safety, providing technical leadership in bioinformatics, helping to develop and deploy tools which help to predict the impact of new chemicals on the environment and human health. Basic Requirements: Expertise in at least one of the following Programming languages (e.g. Python, Java, R) Workflow systems (e.g. KNIME and PipelinePilot) Relational database querying (SQL, SPARQL) Web APIs Knowledge of databases such as UniProtKB, Ensembl, CheEMBL, IPA, KEGG etc. Demonstrable ability to lead projects or tasks within projects and deliver technical leadership Strong communication and interpersonal skills including the ability to quickly develop key relationships and to communicate within and across multidisciplinary teams The ability to quickly learn and apply new skills. Qualified to degree level in bioinformatics, biochemistry, biology, genetics, microbiology or computer science, with post-graduate experience or qualifications in the application of Bioinformatics The ability to work in the UK without the need for visa sponsorship Duties and Responsibilities: Integrate biological, chemical and environmental knowledge/data from internal databases and external sources (e.g. ChEMBL, OpenTargets, Ensembl) for chemical-target safety reviews Develop approaches to determine molecular mechanisms underlying toxicological endpoints (Adverse Outcome Pathway) Deliver solutions which utilise technologies, for example microbiomics to aid the prediction of environmental fate of chemicals and soil health Seek out latest tools, databases and workflows and assess their potential use to support early stage research Liaise with toxicology, ecotoxicology, environmental fate and modelling scientists to understand requirements and define bioinformatics solutions Work with contract organisations and/or academic collaborators to define and develop solutions/tools/workflows to support scientists Support the company's scientific credibility within the wider scientific and regulatory communities Network within the company and the external bioinformatics community to ensure best use of resources and opportunities Agenda and its clients only recruit people who are passionate about animal care and welfare, people with integrity who are honest and trustworthy and who have a great work ethic. To enable us to hire the very best people we will conduct a full and comprehensive background and pre-employment screening as an essential part of the recruitment process.

We are currently looking for a Medicinal Chemist for a growing Drug Discovery company in the East Midlands. The role: Joining this award-winning company, you will support Medicinal Chemistry projects in early stage drug discovery by developing novel small molecule drugs at the hit-to-lead and lead optimization stage. Duties include: Solve complex medicinal and synthetic chemistry problems. Design and carry out experiments using standard laboratory techniques. Develop synthetic routes and perform synthesis of agreed target molecules. Compile and review customer reports and documentation. Ideal candidates will: Have a PhD in Organic Chemistry or Medicinal Chemistry, with experience in multi-step organic synthesis or a degree/ masters with some industrial experience working as an Organic Chemist. The company pride themselves on staff development and offering continuous learning opportunities. Key words: Medicinal Chemist, Synthetic, Synthesis, Organic Chemist, Drug discovery, Drug Development, Pharmaceutical, PhD, Post Doc, Chemistry, Researcher

This is an excellent opportunity to join a successful and fast growing business as a Senior Geologist, which offers excellent long-term career prospects and remuneration package. Job Title: Senior Geologist Location: Conwy Salary: Competitive Salary + Benefits (as below) The Company We are a joint venture company between PetroStrat Ltd and Hafren Scientific Ltd (including Chemostrat and Origin Analytical) to undertake high quality multidisciplinary workflows, integrated wellsite solutions, integrated reservoir quality studies and regional studies and to provide a one-stop shop for stratigraphic and related reservoir solutions. The primary aim of the joint venture is to bring complementary stratigraphic disciplines together to develop tailored and targeted stratigraphic solutions to the oil and gas industry We combine the resources, analytical facilities and technical backgrounds of world leading stratigraphy companies to unlock world class stratigraphic solutions. Primary Responsibilities Gather and analyse geological data, provide geological inputs, manage projects, build and maintain models and develop integration workflows in the geological understanding of the reservoirs. Complete your own technical interpretation, integration and reports and manage technical delivery from subcontractors' teams . Strong knowledge of stratigraphy, biostratigraphy, sedimentology and chemostratigraphy and multidisciplinary integration ideally in data visualisation software, GIS, Spotfire, etc. In conjunction with the General Manager, you will perform all tasks necessary to achieve the annual sales budgets and forecasts. To supervise the work of geologists in the team and subcontractors. Manage, delivery, technical quality of geological reports undertaken by geologists. Input into Business Development and direction of Proprietary and MC technical services. Input to the R&D of stratigraphic and sedimentological development and of technical services. Requirements Master of Sciences (Geology), or equivalent. At least ten (10) years working experience in the oil industry with at least seven (7) years of experience working as a Geoscientist / Geologist. Good interpersonal and communication skills that will allow you to communicate and exchange technical opinions with other staff both internally and externally. A through and methodical approach to geological problem solving. Ability to work in a team, a highly motivated self-starter, evidence of self-sufficiency and self-assurance, ability to take responsibility for important decisions Benefits Annual salary is based upon company remuneration scales, with a weighting for local living costs. Bonus scheme. Company pension scheme. Fun working atmosphere. Long-term career prospects. Next Steps To apply to our vacancy for a Senior Geologist, please click on Apply to upload your CV for consideration. We look forward to hearing from you.

Asad at CK Science has an amazing opportunity for a QC Analyst/Analytical Chemist to work within the Pharmaceutical Analytical division of a global contract development and manufacturing organisation. This role will be based in Leicestershire on a permanent basis. Job Summary: You will be responsible for conducting chemical testing following set procedures, maintain accurate records of work and conduct all analysis following GMP and/or internal procedures. Responsibilities include: - Undertaking the chemical analysis of raw materials, intermediates and products according to set procedures and methods. - Preparing reagents, mobile phase and solutions according to set procedures and pharmacopoeial methods. - Carrying out the analysis of stability samples. On offer is a competitive salary plus excellent benefits (pension, healthcare, flexible working, childcare vouchers, free parking, health promotions, death in service benefits and more). Qualifications, Skills and Experiences: ESSENTIAL: - BSc. (or equivalent) in Chemistry or a Life Science subject with a significant chemistry portion. DESIRABLE: - Experience working within a laboratory environment. - Experience in analytical techniques (UV, IR, KF, HPLC, GC and dissolution analysis). - Previous experience with analytical method transfer and validation. - Experience in GMP raw material testing for API, Excipients & packaging. - Experience in the use of LC-MS systems. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47129 in all correspondence.

Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability. This role can be based at either our UK Head Office situated in Uxbridge or be fully home-based anywhere in the UK. We are near to both Uxbridge train station as well as the town centre and the building has plenty of free onsite parking. The office is open planned, and you will be working in an innovative and collaborative environment. This is an excellent opportunity for an advanced level graduate from a medical, life sciences, pharmacy discipline that is looking to begin and develop a career in medical writing within the commercial medcoms industry. As the Senior Medical Writer you will research, create, and edit all documents associated with clinical research. Responsibilities will also include: acting as primary client contact for medical writing projects,working with other Parexel departments and clients to set and meet internal/external deliverable timelines, project leadership, and training and support of junior medical writing staff. Key Accountabilities: Author Clinical Documents - Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and integrated summaries of safety and efficacy. Quality Control - Ensure that all work is complete and of high quality prior to team distribution or shipment to client. - Provide medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copyediting and content review. Document Project Management - Act in the capacity of project manager/lead for medical writing projects, which may entail serving as the primary client contact, negotiating deliverable timelines, and resolving project-related issues. Project management of contractual and financial aspects may only be performed with the guidance of medical writing management. - Serve as the Medical Writing representative on assigned project teams and demonstrate document leadership: communicate content requirements, coordinate and conduct interdepartmental team review of draft and final documents. Training/ Compliance - Attend and complete mandatory, corporate, project-specific, and departmental training as required. - Keep abreast of professional information and technology through workshops and conferences (when approved), and assure appropriate transfer of that information to the department. General - Attend departmental and company meetings as necessary. - Comply with departmental procedures and requirements, such as completion of project assignment and workload trackers on the applicable software platform. Education: - Bachelor's degree in Life Sciences/Health Related Sciences or equivalent Skills: - Excellent interpersonal, negotiation, verbal, and written communication skills. - A flexible attitude with respect to work assignments and new learning. - Motivation to work consistently in a fast-paced, rapidly changing environment. - Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail, e.g., organizational skills. - Competent working in a matrix environment and values the importance of teamwork. Possesses team leadership skills and cross-cultural sensitivity. - Exhibits sound judgement: escalates issues to project teams or departmental management as appropriate. Presents solutions and follows through to ensure problems have been satisfactorily resolved. - Ability to negotiate on behalf of medical writing to ensure resources, timelines and expectations are aligned. - Understands and satisfies client needs. - Establishes a connection with the client beyond one's project, to gain repeat business and/or to widen existing scope and services. Ability to gain trust and confidence within the company. Knowledge and Experience: - Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, e.g., ICH-GCP. - Extensive clinical/scientific writing skills. - Scientific background essential; writing experience includes multiple clinical documents: study reports, study protocols, or CTD documents or similar. - Advanced word processing skills, including MS Office (expertise in Word); software and systems knowledge or ability to learn and adapt to various IT systems: document management systems, collaborative authoring (e.g., SharePoint), and file conversion and databases (Excel). - Fluent in written and spoken English with appropriate attention to phraseology, grammar, and punctuation. In return we will be able to offer you a structured career pathway and development within the role including awareness and understanding of the industry. Your hard work will be rewarded with a competitive salary, as well as a benefits package including 25 days holiday per year

Senior Research Assistant - London - 31k Senior Research Assistant - London - 31k NGS, biotechnology, research, scientist, associate, biology, biochemistry, biomedical, PCR, IVD A new position has opened in a revolutionary Biotech company based in London, working on a cutting edge technology diagnostics platform. They are expanding their New Application Research team and looking for Senior Research Assistant to support the development of DNA sequencing technology. The Role: Responsible for novel oncology library preparation Supporting technology development for Oncology Running experiments daily Routine testing, debugging and maintenance of laboratory equipment. Generation of data, data analysis Effective management of required documentation. The candidate: BSc, MSc in Molecular Biology, Biochemistry or other Biomedical discipline. Molecular biology techniques such as qPCR, including primer design. Product development or assay development experience based on PCR. Workflow development experience of IVD or NGS systems. Experience working with Biosafety Category 2 certified micro-organisms. The Benefits: Rapidly expanding Biotech working on cutting edge technology diagnostic platform. Complex and Exciting Projects. Great Progression Opportunity. Highly Competitive Salary £25-31K plus an excellent Benefits Package. Company is based in London. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk

This is a fantastic opportunity for a Lead Formulation Scientist to employ their technical expertise in a laboratory-based role with responsibilities for the project management of new formulations of biocidal products, plus research into new technologies. Based in the South East, the Lead Formulation Scientist role is ideal for an accomplished formulation chemist with a background in new product development from a variety of industries. Your day to day duties as a Lead Formulation Scientist will be: Developing novel formulations of biocidal products Liaison with lab and production staff to ensure reproducibility and regulatory compliance Research into new revenue streams Development of scientists within your team You will be an ideal candidate with this background: A higher degree in a related scientific field A track record in formulation chemistry in the laboratory The ability to appreciate the commercial factors of a product-driven role This client is already shortlisting for the role so I would like you to apply immediately with a CV (Word document format, 2 pages maximum) so as to not miss out on the opportunity. Note my client is unable to sponsor visas for those without eligibility to work in the UK. Why should you work with Dr Paul Mears as your scientific specialist recruiter at Science Solutions? I focus solely on matching scientists to positions in the UK speciality chemical industry, which is where my own experience and network position me best given a background working in the speciality chemicals and fragrance and flavours sectors. I completed academic studies with a PhD in organic chemistry at the University of Manchester, which followed a BSc in the University of Leeds' famous Colour & Polymer Chemistry department. Following a short post-doctoral research post I built up three years' experience in recruiting scientists into new jobs. Full references and testimonials of successful assignments such as Technical Directors, Heads of Operations and quick turnarounds for urgent laboratory needs can be found on my LinkedIn profile - search Paul Mears.

Posting date: 2 December 2019 Closing date: 30 December 2019 Hours: Monday to Friday, 9am to 5pm About RethinkX RethinkX is an independent not-for-profit think tank, founded in 2016. We analyse the speed and scale of technology and business innovation disruptions, and their broader economic, social and environmental implications across society. We produce impartial, data-driven analyses that identify pivotal choices facing investors, businesses, policymakers, and civic leaders. We are a small, collaborative organisation present in both the USA and UK. See for more information and to download our reports. About the Role RethinkX (UK) Limited is seeking a Sector Research Analyst for its London office. The successful applicant will assist other sector analysts on various research projects related to the different sectors of the economy including but not limited to transportation, food and agriculture, and energy. Additionally, involvement in other collaborative projects between RethinkX (UK) Limited, RethinkX in the US and partner organisations is likely. This vacancy is ideal for candidates with significant relevant experience of researcher, analyst or other post-degree experience. Duties and responsibilities The role will involve secondary research, analysis, synthesis, and modelling on: the current inputs, outputs and economics of conventional food production and consumption in the US, and globally; the path of potential for a range of new 'alternative proteins' (eg plant- based meats, fish, and milk, cell-cultured meats), including cost analyses and projections for the speed and extent of adoption by consumers; work on other aspects of food disruptions, including vertical/indoor farming, recirculating aquaculture systems, and advances in automation within field crop agriculture; the establishment of autonomous electric vehicles, transportation-as-a-service and related industries/technologies country by country and globally; the establishment of solar electric power and related industries/technologies electric vehicles, transportation-as-a-service and related industries/technologies country by country and globally; and framing your research in readable and non-technical language for use in a report. The position requires contributing to the production of deliverables such as: long-form, in depth research reports (see our reports Rethinking Transportation (2017) and Rethinking Food and Agriculture (2019)); editing existing reports and drafts; rolling updates to previously published works; overseeing day to day project administration of projects including team-wide updates, progress reports and report distribution; and communications materials such as blogs, social media content, podcast episodes etc. Person Specifications Qualifications minimum of a bachelor's degree or educational equivalent in a relevant field of study; relevant postgraduate degree desirable; and Significant relevant professional experience in research and analysis. Essential skills and experience Excellent evidence-based research and analytical skills (with a background in Science, Economics, Market and/or Investment Analysis); broad understanding of recent advancements in technology (and ideally specific research experience) in the food and agriculture sector, transportation sector, and energy sector; demonstrated modelling capability, preferably with regards to systems dynamics and non-linear relationships; experience of accurately proofreading documents for publication; ability to speak and write in English professionally, with the skills to adapt communications for different audiences ranging from highly technical to non-technical; strong attention to detail; strong team working and collaborative skills with the ability to work remotely with team members in different time zones; flexible and proactive approach to working; ability to organise and manage own work programme independently; familiarity with aspects of business theory such as technology disruption and other fundamental concepts of RethinkX's previous work; solid grasp of advanced economic concepts and the finance sector; ability to challenge traditional mainstream approaches to "linear" analyses, assumptions and business models; excellent administration skills; ability to work under pressure, manage competing deadlines and priorities; and strong IT skills including proficient working knowledge of Microsoft Office applications and databases. Desirable skills/experience experience in project management; experience with graphic design and visual communication of complex concepts; willingness to present research findings to a large audience; experience of managing multiple projects at once; and experience of website editing and using social media as a business tool. To apply, please forward your CV and cover letter no later than the closing date to Anna Strebel with a description of why you would be a great asset to our team and help further our cause.

GCMS Analyst £23,000 - £30,000 North Manchester Are you an experienced GCMS Analyst with experience in the fragrance industry? I am currently seeking a passionate and enthusiastic GCMS Analyst to join a family run organisation based in North Manchester. The ideal candidate will have previous experience working in a GCMS Analyst role within the flavours or fragrances industry. In addition to these, I am potentially looking for a candidate who has experience within leadership and would have the confidence to lead an analytical team to assist in their growth and development. Key Duties: Preparation, analysis and quantification of products from various products such as perfumes, soaps, candles and fragrance oils using GC with MS and FID detectors. Preparation of samples may require solvent extraction techniques such as SPME arrow. Use GCMS to identify different substances in a test sample. Analyse samples and be able to perform maintenance and trouble shooting Preparation of samples for analysis on GCMS-FID Preparation and analysis of samples using GCMS-FID using relevant software and instrumentation. To keep up date on new fragrance ingredients/components within the market and to add these to library accordingly. To continuously undertake method development to help improve runtime and quality of analysis from the instrumentation. Key Skills: Chemistry or related science degree Experience working as a GCMS Analyst Experience within flavours and fragrance. Desirable to have experience using Mass Hunter software.

SENIOR DATA SCIENTIST £65,000-£80,000 + COMPETITIVE BENEFITS CENTRAL LONDON Are you looking for an opportunity to join one of the UK's most renowned retailers as a Senior Data Scientist where you will be working to build algorithms for huge data sets? You will be working in a collaborative and friendly environment as part of a committed team of Data Scientists to provide measurable benefits to the company through the use of cutting edge methods and technologies. THE COMPANY: Our client is a very well-known brand which has a huge presence in both the UK and internationally and over 25,000 employees. With over a thousand stores and a massive online presence you will have access to huge data sets and the ability to spend your time on a variety of interesting projects. THE ROLE: You will be joining a team of highly skilled and like-minded Data Scientists and analysts where you will be helping to lead complex and diverse Machine Learning projects which will provide real commercial benefit to the company. In specific, you can expect to be involved in the following: Help to lead the delivery of complex and diverse projects with a commercial focus through the use of your expert knowledge in machine learning and statistical techniques. Working on projects across a range of areas such as Marketing, Logistics or Merchandising and then be able to report your findings back to non-technical stakeholders. Deliver end to end data science solutions through the use of Python and SQL that will help the business stay competitive. Help to coach more junior Data Scientists and advise the rest of team on best practice and focus areas for upskilling. YOUR SKILLS AND EXPERIENCE: The successful Senior Data Scientist will have the following skills and experience: Proven extensive experience developing and implementing Machine Learning algorithms using Python or R. Be an expert in mining large & very complex data sets. Have considerable experience using SQL and NoSQL databases and Apache Spark. Proficient programming in Python, Java, R, Spark, SQL etc. Hold a PhD or Masters degree in a numerate discipline. Preferably have experience in a similar senior position where you have held responsibility for managing or mentoring junior team members. THE BENEFITS: Competitive benefits available. HOW TO APPLY: Please register your interest by sending your CV to Lillie via the Apply link on this page.

Product Development Team Leader (NPD) - Medical Devices/FMCG Are you looking for a challenging, and worthwhile career opportunity where your contributions will help to accelerate healthcare technology and make a difference in people's lives? A new opportunity for a Product Development Team Leader has become available to join a dynamic and innovative company that operates in the medical device industry. You will be responsible for leading projects for the development of new products and changes to existing products within budget and on time. The Role: * Provide scientific leadership and oversight to a team of cross-functional product development scientists to deliver pipeline launch projects for the Science and Innovation Team * You will have the responsibility of managing multiple projects; this will involve developing formulations of varying complexities in response to company objectives * Provide technical support to ensure key documentation and deliverables are in place to allow progression of NPD projects through the stage gate development process. * Liaise and collaborate with internal management team where appropriate to ensure continual pipeline drive through Stage-Gate process The Candidate: * We are interested in speaking to individuals who have experience in formulation science within relevant sectors such as Medical devices, Biocides, Pharmaceutical or Cosmetics. * You will have a strong background and experience in developing and delivering products to market within a commercially focused environment. * You will have experience of team leadership and also developing staff There are opportunities to develop and to take on more responsibility. This is a fantastic opportunity for someone seeking the next step in their career within the formulation sector, in a high profile environment. Search is an equal opportunities recruiter and we welcome applications from all suitably skilled or qualified applicants, regardless of their race, sex, disability, religion/beliefs, sexual orientation or age.

Qualification or good experience in chemistry. Understand the processes required for developing, testing and reporting new technology. This candidate will be required to develop new and innovative methods of dispensing fragrance suitable for commercial areas. The individual will be working for the engineering manager and will be working closely with product design engineers. This position will be suitable for somebody with 2 years + experience. Matchtech acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers and is part of Gattaca Plc. Gattaca Plc provides support services to Matchtech and may assist with processing your application.

Project Management Team Leader Are you looking for a challenging, and worthwhile career opportunity where your contributions will help to accelerate healthcare technology and make a difference in people's lives? A new opportunity for a Project Management Team Leader has become available to join a dynamic, innovative company that operates in the medical device industry. You will be responsible for leading projects for the development of new products and changes to existing products within budget and on time. The Role: * Lead multiple, key, cross-functional, strategic projects, liaising with R&D, Quality Assurance and Regulatory Affairs Teams. Introducing effective project controls to highlight risks which could impact the projects * You will make day-to-day decisions that will determine the success of projects, resolve issues within scope of the project. * Develop, manage and maintain strong collaborative relationships with key internal stakeholders (i.e. Marketing, Regulatory, Quality, Sales, Graphic Design & Packaging) to achieve project critical goals * Manage internal and external stakeholder expectations and prioritise own workload * Assist with the project direction for junior team members, typically but not limited to overseeing their daily project interactions The Candidate: * You will have a degree or equivalent qualification in a science based subject * Strong demonstrable cross functional project management experience within relevant sector such as Medical devices, Biocides, Pharmaceutical or Cosmetics * The ability to lead complex multifunctional projects, flag critical issues and align key stakeholders to decisions/recommendations * Experience with project management systems to produce GANTT charts * Fluency across chemistry, microbiology, and highly regulated categories such as medical devices and cosmetics There are opportunities to develop and to take on more responsibility. This is a fantastic opportunity for someone seeking the next step in their career within the formulation sector, in a high profile environment. Search is an equal opportunities recruiter and we welcome applications from all suitably skilled or qualified applicants, regardless of their race, sex, disability, religion/beliefs, sexual orientation or age.

Our client is a truly pioneering, venture capital backed Health Technology company, now entering a new and tremendously exciting phase of its development, looking to accelerate its growth to turn over more than £1bn. It's an amazing time to join a company with incredible potential to improve the lives of many millions of people globally, playing a key role in its development as Chief Commercial Officer/CCO, a key member of the Executive Team reporting directly to the CEO. Part of a highly experienced, lean and visionary team, the role is primarily concerned with ensuring the commercial success of the organisation through a combination of strong business development and technical selling solution skills. As Chief Commercial Officer/CCO your responsibilities will include: • Driving the development and execution of the business' commercialisation strategy. As products are developed, there will be a need to convince clinicians and a wider ecosystem that they work. • When appropriate funding is in place, building the commercialisation infrastructure, and organisation, to drive market adoption of the company's products, being responsible for revenue growth within the organisation • Taking a global perspective on market opportunities and leading in the assessment and prioritisation of the same - geographic as well as between different market segments • Generating awareness of and excitement for the company's vision with a range of interested parties including Government, investors, healthcare providers, insurers and, eventually, consumers • Inspiring confidence and generating excitement, enthusiasm and commitment as the company executes its business plans - internally as well as externally • Making sure that all functions of the organisation are aligned to meet its strategic commercial objectives within the overall business plan • Developing and driving the pricing strategy of the organisation As Chief Commercial Officer/CCO you'll be/need: • A proven leader with an outstanding track record gained delivering transformative diagnostic technologies, perhaps most likely in a similar Chief Commercial Officer/CCO, Senior Commercial Manager, Director of Business Development, Chief Revenue Officer/CRO, Sales Director, Senior Business Development Manager (BDM) or Senior Sales Manager type role, accessing pharma and diagnostic companies • Demonstrable experience in developing and executing successful commercialisation strategies in early-stage companies - comfortable and/or experienced working in a small (say, medical device/(IVDs)) company for several years, even in a very senior role • The ability to build the team of your dreams to take on the world as the company grows • Marketing skills will be welcome, but there will be other marketing capability in house and externally • Knowledge/experience of venture capital, grant funding, UK healthcare or health insurance industries, NHS and/or organisations like the National Physics Laboratory (NPL) , Laboratory of the Government Chemist (LGC) advantageous • Experience in the development of the regulatory framework for diagnostic products and of government initiatives such as Accelerated Access Review (AAR) and Innovation and Technology Payment (ITP) also desirable Additional Chief Commercial Officer/CCO personal attributes: • An incredibly hands-on approach - keen to be involved with, and perhaps experienced in, the start of commercialisation efforts • Highly persuasive, able to generate awareness of and excitement for the company's vision - capable of, and perhaps experienced in, activity such as convincing an industry giant that our client's protein measurement system, suitably automated, should form a big part of their next generation hospital analysers. Similarly, a proven ability to open doors, talk passionately and build working relations with some/all of government, healthcare providers, insurers and consumers will be regarded favourably. • Strong strategic, creative thinking, communication, negotiation and analytical skills to develop solutions to complex business challenges, products and routes to market • A great deal of flexibility and an exceptionally innovative approach • Good organisational, IT and administrative skills • The capacity and willingness to undertake extensive business travel in the UK and internationally, potentially at weekends and outside of normal business hours - a full, clean UK driving licence is attractive Salary range: up to £100,000 per annum + share option package + bonus Please note: High levels of interest mean we will only contact you if your application is shortlisted and this will happen within five working days. You must also be eligible to work in the UK.

CADD role for global pharmaceutical company in M4 Corridor. Computational chemist, modelling & drug discovery Your new company Is a leading pharmaceutical company, with a track record of innovation, looking to grow their computational chemistry / CADD team working on a number of large scale drug discovery and Hit ID projects for small molecules across multiple therapy / disease areas. Your new role You will be working closely with the wider CADD and computational chemistry team to develop new tools, models and software to support them on a variety of molecular modelling and computer-aided drug design projects to boost the company's portfolio and advance their drug discovery efforts across multiple therapy areas. The role will also involve interaction with a number of other teams and departments, eg medicinal chemistry. As well as hands-on software development work - mainly in Python / C++ - for the computational chemistry teams (for aspects such as molecular dynamics, virtual screening, SAR and modelling work), duties will include project management, prototyping of tools and working closely with research teams & stakeholders to understand their needs and translate these requirements into software. What you'll need to succeed As well as strong communication, organisational and project management skills, you should have: A PhD (or significant equivalent work experience) in computational chemistry / cheminformatics, bioinformatics, computer science, or related discipline; Strong programming skills in languages such as C++ and/or Python, or other languages such as Java; Exposure to drug discovery, molecular modelling, or hit ID projects; Knowledge of molecular dynamics, or molecular simulations (eg modelling binding affinities, force fields, protein-ligand or protein-protein interactions); Knowledge of packages such as Desmond, AMBER, GROMACS, SIRE, NAMD, etc; Exposure to KNIME, CDK, OpenEye, MOE or other similar packages/toolkits; Experience of working with structure based modelling and/or small molecule design teams in the pharmaceutical or biotech industry is an advantage but not essential for this position. What you'll get in return The opportunity to make a significant contribution to drug discovery and development projects, a fantastic working environment, excellent career development, and a very generous hourly pay rate. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Keywords: Python, C++, computational, chemistry, computer, data, science, cheminformatics, molecular, modelling, model, dynamics, molecule, design, small, drug, discovery, pharmaceutical, science, structure, tool, KNIME, CDK, OpenEye, MOE, Keras, Scikit, deep, machine, learning, Desmond, AMBER, GROMACS, CHARMM, SVM, regression, neural, net, R, Matlab, programming, programmer, neuroscience, oncology, therapy, disease, CADD, Hit

Johnson Matthey, a FTSE 100 company, is a global leader in sustainable technologies specialising in catalysis, precious metal products, chemicals and process technology. With operations in over 30 countries, we employ more than 13,000 people. Johnson Matthey uses science to make the world cleaner and healthier. Over the past two centuries we have built our reputation and place as a global leader through quality, integrity, and innovation. Today, more than 93% of the group's sales come from products and services which provide sustainability benefits through the positive impact they have on the environment, resource efficiency and human health, but that's not enough. We have ambitious plans for growth and need talented individuals to help shape and lead us into our next century. We are currently recruiting for an Analytical Senior Scientist based in our Health Analytical Development team in Edinburgh. The postholder will be responsible for leading the development, validation and evaluation, and implementation of analytical test methods in support of research, GMP production, and stability testing. In addition the Analytical Senior Scientist will be responsible for mentoring and providing advice, guidance, and direction to junior analysts on technical and project management issues, as well as guiding their professional development. Key responsibilities Develop efficient, selective, robust and scientifically sound analytical procedures Assists with the transfer of the methods developed. Mentor, coach and develop junior analysts. Reviews supplied data packages, researches the literature and outlines the project work proposal and estimates the required timelines. Participates in project management activities including: creating and meeting objectives for timelines, budgets, and project goals and presenting project results internally and with customers Provides leadership for employee relations through effective communication, coaching, training, and development, and ensures staff acts in accordance with Johnson Matthey policies and practices with respect to GLP, environmental, EHS and other related regulatory requirements. Troubleshoots, analyses and leads investigations when required. Prepares high quality written documentations (SOPs, analytical methods, summary reports) and assists with regulatory documentation. Reports experiments accurately and promptly, keeping laboratory notebooks up to date in accordance with the company's quality procedures. Contributes to problem-solving, brain-storming sessions, seminars and other scientific discussions. Are you the ideal candidate? Analytical Chemistry or equivalent qualification with significant experience with chromatography method development for small molecule APIs Considerable experience with HPLC/UHPLC, GC, hyphenated MS and wet chemistry Experience with Process Development of APIs Demonstrates flexibility and adaptability, with a "can do" attitude and the tenacity to see tasks through to the end. Able to effectively plan the work of self and the team to meet customer timelines. Excellent analytical, written and verbal communication skills with customers and colleagues. Proven ability to lead projects and provide direction to analytical scientists. Ability to work independently and in a team environment. Ability to write clear and concise technical reports, business correspondence and procedure manuals.

A fantastic opportunity is available for a DNA analyst to join the Genomics team at a thriving Biotechnology company. My clients is seeking a candidate with experience of DNA extraction, NGS Sequencing and CRISPR. The ideal candidate for this role will be a life sciences graduate with strong work ethic and a desire to learn. You will be joining a growing team and be offered a competitive salary if successful. Please apply now! Search is an equal opportunities recruiter and we welcome applications from all suitably skilled or qualified applicants, regardless of their race, sex, disability, religion/beliefs, sexual orientation or age.

Post Doctoral Future and Novel Materials Researcher Fixed Term for 2 years employed directly with the client. Our client is currently seeking a Post-Doctoral Researcher to join their Visionary Enterprises team. Your role will involve investigating potential new research topics and projects based on advanced materials. In addition, you will help identify sub-themes and opportunities where unique materials needs can be found. This position is an exciting opportunity to direct our clients future research activities. Working as a member of a dynamic interdisciplinary team of physicists, chemists, biochemists and engineers, you will identify from a broad spectrum of areas unique material needs which will grow our clients research expertise. These identified needs will feed directly into potential research areas teams In addition, you will have the opportunity to attend events in both industry and academia in order to expand your knowledge in emerging new technologies as well as extend our clients contacts network. Excellent academic credentials are essential for this role, including a PhD in Physics or Electro-optical Engineering. Multidisciplinary research experience with a keen awareness of recent trends as well as cutting edge materials technologies is highly desirable. You will be eager to learn about new technologies, and will have a demonstrated ability to research, understand, and summarise complex scientific concepts and will be able to make recommendations without access to full details or information. Furthermore, you will be successful at identifying hidden gaps or unmet needs in material development. A high level of competency in effectively communicating and presenting to a wide audience, and the ability to network and connect with people in industry and academia across multiple scientific disciplines are of vital importance. This is an exciting opportunity for a creative and talented researcher to make an important contribution towards shaping the future R&D program.

The post holder will: Develop or verify methods for the testing of incoming materials as well as developing methods for intermediates and products manufactured using these materials. Carry out analysis to GMP standards and monitor the levels of compliance within the Laboratory. Maintain records of all analytical work carried out on incoming materials, intermediates and products. Monitor the systems in place within the Laboratory to ensure that procedures are being followed. Report and investigate incidents of out of specifications results within the Laboratory. Advise and assist staff in troubleshooting methods. Review new methods with respect to their application within the Laboratory. Delegate and monitor the progress of work on a daily basis with regard to the overall schedule of work within the department. Liaise with senior department staff and other departments to update them on the progress of work. Compile SOP's specifications and protocols for various development projects. To perform any other duties deemed appropriate by their Manager Matchtech acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers and is part of Gattaca Plc. Gattaca Plc provides support services to Matchtech and may assist with processing your application.

Our Client is a very successful pharmaceutical company based in Hertfordshire where a wide variety of medicines and healthcare products are developed and tested. They are now seeking a QC Analyst to join their existing team of analysts who form the QC team. This position is a full-time permanent role. Key Areas of Responsibility The role as a QC Analyst will involve assisting with the Quality Control of raw materials, bulk and finished products in accordance with prescribed protocols using analytical techniques such as HPLC and GC Involvement in the swabbing and analysis of samples for cleaning verification of the pilot production facility Take equal part in the overall running of the laboratory, including equipment maintenance, calibration of apparatus and other general duties such as solvent disposal Perform manual and automated tests and assays in a methodical and scientific fashion to a high level of accuracy and precision and to operate associated analytical equipment Use computer software packages, such as Chromatography Data Handling, LIMS and Excel, for the collection, processing and reporting data Qualifications / Experience A degree (or equivalent) in a chemistry-based discipline Some relevant experience in an analytical testing role, preferably in a pharmaceutical environment Some experience in the techniques of HPLC and GC analysis In return our client is offering a basic salary of £25,000 per annum plus comprehensive benefits for the successful Candidate Please send your C.V to Lorraine Roger, Director at Atom Recruitment Ltd.

Analytical Chemist We currently have a great opportunity for an Analytical Chemist to join a leading Pharmaceutical development company in Kent. The role: As an Analyst you will support a range of analytical projects using an array of analytical instruments including HPLC, GC and LC-MS. This is an Analytical Development role and as such you will carry out method development and validation. Responsibilities include: Ensure all work is carried out to the required standards (GMP and ICH guidelines). Carry out analytical testing using a HPLC, LCMS and GC. Carry out analytical method development and validation. Write and review analytical documentation and SOPs. Ensure all analytical instrumentation is maintained and validated ready for use. Ideal candidates : Will be degree qualified in Analytical Chemistry or a similar subject and have experience in a range of analytical techniques including HPLC, LCMS and GC. Experience in NMR is desirable. You will have experience in method development, validation and troubleshooting within the Pharmaceutical industry. This is a fantastic opportunity to join a dynamic and growing company as an Analytical Chemist. For further information or to apply please contact Peter at Rowland Talent Solutions Key words: Analytical Chemistry, HPLC, UPLC, LC-MS, chromatography, GMP, Pharmaceutical, , analytical Chemist, Method development, Method validation.

An opportunity had arisen for a laboratory analyst to join an award-winning analytical testing laboratory at its UKAS accredited facility just outside of Cambridgeshire. As a laboratory analyst you will work as part of the analytical team carrying out various tests using GC, GC-MS, ICP-MS & OES and HPLC instruments. You will also be responsible for interpreting the test data and compiling reports for clients; finally ensuring all laboratory activities are carried out in accordance with ISO17025. To be successful you should ideally hold a degree in a relevant scientific discipline, possess experience within a commercial laboratory and have strong communication skills. Laboratory Analyst Responsibilities: Carry out various sample tests using GC, GC-MS, ICP-MS & OES and HPLC instruments. Interpret the test data and compile reports for clients. Support with the maintenance for the laboratories analytical instrumentation. Ensure stocks, equipment and storage areas are well kept and meet company standards. Ensure all aspects of your work comply with H&S and ISO regulations. Laboratory Technician Requirements: Hold a degree in a relevant scientific discipline, (i.e. chemistry, analytical, forensic science) Possess hands-on experience within a commercial laboratory. A sound understanding of UKAS/ISO17025 regulations. Excellent communication skills, written and verbal. Ability to work well independently as-well-as in a team. Proficient in the use of Microsoft applications, Word, Excel, Outlook etc. Salary: £17,000-£21,000 + Benefits - 25 days holiday + Banks - Company Pension Contribution - Life Assurance Hours: 37.5 hrs per week - 9.00am to 5.00pm Monday to Friday - 30min Lunch If you are a have commercial laboratory experience and are looking to be part of a like-minded, growing organisation then get in touch with Lewis at Cranleigh Scientific with your CV.

Laboratory Technician Rowland Talent Solutions are currently looking for a Laboratory Technician or Analytical Chemist to join a leading contract testing company in Cambridgeshire. This role is open to recent graduates in Chemistry, Analytical Chemistry or Forensic Sciences (or similar subject) with some experience in GC or HPLC analysis. Duties include: Setting up and running experiments to test environmental samples. Support and/ or carry out, after full training, GC, GC-MS and GC-FID or HPLC analysis. Follow SOPs and ensure work is carried out to UKAS and ISO 17025 guidelines. Sample preparation and conduct wet chemistry tests. Ideal candidates will be degree qualified in a Chemistry subject or have some laboratory experience in an analytical testing laboratory. Experience of HPLC, GC OR GC-MS is desirable however full training is provided. For further details please contact Peter at Rowland Talent Solutions. Key words: Lab Tech, Laboratory, Analyst, Analytical Chemist, Graduate, Science, GC, HPLC, Chemistry, GC-MS.

Senior Statistical Programmer - Global Pharma Company - Buckinghamshire - £salary is competitive depending on experience The Company This excellent role sits with the world's largest and most broadly-based healthcare company, who are committed to using their reach and size for good. They are a Global Pharma Company who are continuously expanding their client base, opening huge opportunities for you to work across multiple projects and boost your career. Multiple opportunities to progress and develop career Focus on the patients and changing lives, as well as their people Excellent benefit package and salary The Role The Sr. Statistical Programmer Analyst is an individual contributor in the Statistical Programming and Analysis Department, that will be accountable for development, verification, and documentation of SAS code on the assigned clinical project. This role is that of a SAS programmer who is capable of supporting programming requests of medium to high complexity in support of clinical trial reporting and submissions, with minimal guidance. Critically reviews requirements and data, identifies gaps, suggests solutions and applies expertise on clinical R&D statistical programming activities. Completes programming tasks of medium to high complexity and maintains documentation as appropriate. Perform quality control in support of clinical R&D analysis and reporting. Design and development of statistical programs for the assigned project. You A Bachelor's degree or higher in Computer Science, Mathematics or other scientific fields is required. In-depth knowledge of SAS statistical software with a minimum of 5 years. SAS programming experience with increasing responsibility is required. Experience working with programmers in a team environment is preferred. Knowledge and experience in SDTM and ADaM are required. What should you do next? This role will not be open for long so apply ASAP to avoid disappointment. Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

We are currently looking for a Bioinformatician to join a leading scientific company based in the Berkshire area. As the Bioinformatician you will be responsible for providing technical leadership by developing tools that will contribute towards the prediction of how new chemicals effect human and environmental health. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Bioinformatician will be varied however the key duties and responsibilities are as follows: 1. As a Bioinformatician you will be responsible for developing solutions and technologies that can help predict toxicological properties of chemicals. 2. Integration of biological and chemical data from various databases including ChEMBL, Ensembl, OpenTargets for safety reviews of chemical targets. 3. As a the technical expert you will be working in a collaborative environment by liaising with scientists from other disciplines by understanding their requirements and implementing bioinformatics solutions. 4. You will keep up to date with the latest technologies, tools and databases that will support early stage research. This may involve networking within the wider scientific community and working with academic collaborators and contract organisations. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Bioinformatician we are looking to identify the following on your profile and past history: 1. PhD or MSc in a relevant subject such as Bioinformatics, Microbiology, Computer Science or another related discipline. 2. Proven industry experience in building workflows systems (e.g KNIME, PipelinePilot) that allow you to query data for bioinformatic application. 3. A working knowledge of databases (UniProKB, Ensembl, CheEMBL, IPA, KEGG) and strong programming ability (e.g. Python, R, Java). Key Words: Bioinformatics, Data, Workflows, Database, Programming, Python, R, Java, Chemical, KNIME, SQL, SPARQL, Toxicology

Hyper Recruitment Solutions are currently searching for a Technology Transfer Manager to join a world class research company based in the London area. As the Technology Transfer Manager you will be responsible for Intellectual Property management of research projects. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Technology Transfer Manager will be varied however the key duties and responsibilities are as follows: 1. Deliver a consistent approach for all Intellectual Property (IP) management. 2. Manage a portfolio of commercialisation projects and engage with all relevant external bodies. 3. Provide IP training to the project management team and scientific staff 4. As the Technology Transfer Manager, you will lead ongoing health research projects by providing strategy to all scientific members of the team. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Technology Transfer Manager we are looking to identify the following on your profile and past history: 1. Degree, Masters or PhD in Life Sciences 2. Expert knowledge of scientific intellectual property 3. Industry experience in academia, scientific research or healthcare Key Words: Technology transfer manager, intellectual property, IP, research, scientific, healthcare.