We found 198 job(s) for you:

  • Engineer

    Salary: £0 Location: Stevenage

    The client: My client is a science driven company in the pharmaceutical sector specialising in cell and gene therapies. Their vision is to drive the growth of the industry by helping cell and gene therapy organisations across the world translate early stage research into commercially viable and investable therapies. Wanting to be the global leader in development, delivery and commercialisation of cell and gene therapy, they have state-of-the-art viral vector laboratories and a £55million GMP manufacturing centre. They are currently hiring for an Engineer to undertake the day to day mechanical, electrical engineering & facilities management activities within the manufacturing centre. The role will involve providing expert support in the event of plant failure and reporting & repair of faults in a timely manner. You will take a leading role in setting up the facility, maintain facility asset databases and technical SOP’s. Most candidates will have: - Experience working in a GMP environment. Preferably pharmaceutical - Specific experience working in clean room environments and HVAC - Knowledge in one of EU/MHRA/HTA/HFEA as well as FDA requirements - Good verbal communication skills - Experience working with PPM systems and some building services - Educated to degree level or other relevant technical qualifications A very competitive salary with company benefits including call out allowance and overtime paid extra. If you are interested in the role and want to find out more or see if you’re suitable, please feel free to contact me on 0161 236 8200 or send your cv over to and I’ll be happy to get back to you.

  • Research Technician in Molecular Microbiology

    Salary: £0 Location: Aberdeen

    Research Technician in Molecular Microbiology- Aberdeen Initially this is a 9-month maternity cover vacancy, however due to growth there is the potential for this to be made perm. Based in Aberdeen, my client is a leading biotechnology company, involved in ground-breaking R&D, mostly focusing on the treatment of autoimmunity, inflammation, oncology and CNS disease. This role will be a working closely with the molecular microbiology team, involved in applying functional genomic approaches in the study of LBPs. Previous relevant experience in the area of molecular microbiology is essential to this position as is the ability to record data with a high level of accuracy. Experience / Qualifications Required BSc or higher genetics, molecular biology or microbiology with at least 1 year’s relevant experience in the research area. Experience in a range of molecular microbiology techniques including: nucleic acid extractions, primer design, cloning, and bacterial mutagenesis approaches. Competitive salary State of the art facilitates

  • Environmental lMonitoring Compliance Officer

    Salary: £0 Location: Salisbury

    Based in Wiltshire my client is a specialist biopharmaceuticals manufacturer and CMO. Due to continued growth they are currently looking for an experienced Environmental Monitoring Compliance officer to join their Biological services, QC team. You will be responsible for: • Managing the GMP databases for water quality, clean steam quality and microbiological environmental monitoring. • Co-ordinate and review water quality, clean steam quality and microbiological environmental monitoring activities as required. • Preparing and analysing technical and numerical information from the databases and preparing trend analysis data as graphs, charts and / or diagrams. • Investigating OOS water and environmental monitoring test results and reviewing resulting Non-Conformances. • Preparing environmental summary reports of production batches and process simulations for inclusion in the batch manufacturing records. • Reviewing particle monitoring data from the manufacturing areas. • Reviewing and managing the environmental monitoring SOPs. • Liaising with production, quality and engineering services to promote GMP compliance. Reviewing facility, utility and equipment documentation and monitoring data to prepare facility release reports. • Carrying out facility release and other internal and external audits You will have: BSc, equivalent or higher in microbiology, chemistry or pharmacy Experience of working with in a GMP environment Strong knowledge of QA within with in a Biopharm, pharma or biologics company is desirable Competitive salary Great training developments

  • Lab Manager

    Salary: £0 Location: Cambridge

    The client: My client is a biotech company based in Cambridge. They are developing biotherapeutics to meet the growing demand for the next generation of drugs to compete with monoclonal antibodies. Its benefits are its smaller size, higher expression yields and stability. They are expanding rapidly given the escalation in their demand. We have an opportunity for a Laboratory Manager to join our expanding team. In this diverse role you will manage a small Laboratory Support team and work closely with our scientists to play a vital role in the daily operations of our laboratories. You will be responsible for maintaining a high quality, safe laboratory environment and supporting the scientists in their everyday work, by taking responsibility for all aspects of lab management, including instruments, equipment and supplies needed to ensure the labs run smoothly. Most candidates will have: - Graduate qualification or equivalent in a biological science or other relevant discipline - Previous experience in managing a biological lab - Knowledge of regulatory requirements - Able to work to a high degree of autonomy - Ability to negotiate with third parties will be highly desirable but not essential - Previous experience of SAGE will be a distinct advantage, but not essential to apply We are located very conveniently, in state-of-the- art laboratories, offering an exciting and innovative environment where you will have the opportunity to develop your career. We offer an attractive benefits package that includes competitive salaries and company pensions. For more information about the role or for a chance to apply, please contact Philip Adebiyi on 0161 250 5049 or and I’ll be happy to help

  • Senior Scientist, Molecular Biology

    Salary: £45000 Location: Oxford

    Senior Scientist, Molecular Biology– Oxford (permeant) My client is an Oxford-based biotechnology company, developing the next generation cancer immunotherapy. The company is looking for a motivated, Senior Scientist, in Molecular Biology, working to deliver transformative therapeutics for people with common cancers. Working as part of the research team, you will be engaged in molecular engineering and preclinical testing of therapeutics, with a focus on developing technology for clinical trial. You will have: MSc or higher, in a life sciences subject (please note, people with solely academic experience would not be suitable for this role) Prior industry experience working with molecular cloning; molecular biology, virology and in vitro or in vivo techniques. Good organisation and the ability to work on multiple project streams in parallel. Experience with molecular biology, virology and/or in vitro assays; cell viability, proliferation, migration, flow cytometry Salary: £32,000.00 to £45,000.00 (based on experience) Excellent career development

  • Modelling and Simulation Research Fellow

    Salary: £0 Location: Nottingham

    My client is passionate about innovating and transforming drug development to help their customers develop new medicines for patients in need. As a respected member of the drug development world, my client specialises in delivering high quality innovative solutions that integrate formulation development, real time GMP manufacturing and clinical testing. Due to recent expansion and growth, there is now an exciting opportunity for a scientist specializing in physiologically based pharmacokinetic (PBPK) modelling and simulation (M&S) to join their consulting group. The Modelling and Simulation Research Fellow will provide hands-on M&S scientific support and input throughout a project lifecycle (design, planning, delivery and reporting) to ensure client’s study objectives are achieved. What you will do • Develop a thorough understanding of the biopharmaceutic, pharmacokinetic and metabolism profile of assigned compounds. • Independently build and rigorously test PBPK models to support evaluation of absorption and systemic exposure potential for NCE’s. • Use in vitro data and in silico tools to predict or describe the impact that formulation strategy/technology can have on in vivo performance. • Provide in silico simulations to aid interim decision making during clinical studies regarding dose escalation and formulation selection. • Investigate the existence of correlations between in vitro dissolution data and human plasma concentration-time data (IVIVCs) using either mechanistic models or traditional numerical deconvolution approaches. • Review data packages and generate proposals for potential new projects. • Train, mentor and support existing and new members of staff What you will need • Must be degree qualified, ideally with a PhD, in a discipline with a significant component of Modelling and Simulation • Relevant pharma, CRO/CDMO experience • Hands on experience in the use of M&S in a pre-clinical/translational setting (late stage discovery/early clinical R&D), is essential • Experienced in one or more of WinNonlin Phoenix, GastroPlus or SimCYP. • Should have a broad cross-functional knowledge of early drug development, be an effective member of multi-disciplinary teams and be able to deliver multiple projects to stringent timelines. What you will get • Excellent training and development • State of the art facilities • Highly competitive salary • Generous benefits package This is an exciting opportunity for an enthusiastic scientist to be part of a dynamic team that helps the development of new medicines to market. Get in touch today to ensure that you don’t miss out!

  • Senior Medical Writer

    Salary: £0 Location: Chelsea

    The Client: My client is dedicated to bringing new solutions to patients for the detection, prevention and treatment of blood clots. My clients research is driven by the needs of patients so that innovations and new treatments flow seamlessly from theory to practice. They have become a world leader in the developing field of real-world outcomes research, developing and executing pioneering global programmes. They are currently on the lookout for a Senior Medical Writer who will be responsible for creating high-quality written materials across a range of media, including slides, manuscripts, posters, meeting reports and websites in collaboration with our clinical advisors and PR team. The successful applicant will be able to present complex information in a clear and concise manner and work with a team of statisticians to ensure accuracy of clinical data presented. The role includes some mentoring of junior writers as well as assisting with strategic publication planning and meetings’ support. Requirements: - PhD or MSc in life sciences - Sound scientific understanding and strong writing ability - Previous experience in publication planning - Project management experience - Minimum 3 years experience in medical writing - Some mentoring experience will be highly desirable - Familiarity with ICMJE, GPP2, STROBE or some publication standards - Ability to work independently and effectively in a team across multiple projects - Excellent communication and interpersonal skills - Ability to find and correct errors in spelling, punctuation, grammar and check text for consistency, clarity and accuracy For more information about the role or for a chance to apply, please contact Philip Adebiyi on 0161 250 5049 or and I’ll be happy to help

  • French Speaking CTA

    Salary: £0 Location: Chelsea

    The Client: Based in Central London, my client is a leading Clinical organisation looking to take on an experienced French Speaking, CTA, working as a key member of the project team. This role will provide in-house operational support to study teams, ensuring standardisation and consistency of tracking across studies in accordance with SOPs. Key Responsibilities: • Day to day operational support to Lead Ops, CPMs, CRAs for defined tasks during study • Collects, co-ordinates and maintains essential documents and the Trial Master File (TMF) • Logistics of investigator and monitor meetings organised including the development of presentation materials under direction of PM • Active membership of projects meetings: meetings booked, minutes taken and communicated • Documents learnings and recommendations from study debriefs and best practice identified and implemented in collaboration with manager and colleagues • Study area managed according to standards including set up, access rights and maintenance of study related documents • Development and maintenance of study specific documents and tracking tools under direction of PM • General filing and adhoc administrative task • Documentation provided to support the preparation of clinical study reports and publications • Health Authority/ IRB submissions and approvals tracked • Awareness of and compliance to all policies and procedures including: Finance, Procurement, IT and Legal Most Candiates will have: Experience work as a CTA or another role with similar capabilities, in a clinical setting. Experince in full project life cycle monitoring Be fluent in French (Reading, Verbal, and Written) Strong organisational skills and the ability to work over multiple projects Salary: Daily rate (discussed at point of application) Contract term: 1 year For more information on this role or for a chance to apply, please contact Philip on or call on 0161 250 5049 and Ill be happy to help

  • (Senior) Research Scientist

    Salary: £0 Location: Saffron walden

    My client is an industry leading biotech company dedicated to providing the industry with the fastest and most efficient engine for therapeutic antibody discovery. Working with their industrial pharmaceutical partners, they are driven by their goal to help patients though more affordable medicines and faster access to potentially life changing treatments. Based in Saffron Walden (close to Cambridge), my client is now looking for an enthusiastic and innovative scientist to join their dynamic team. Working in a state-of-the-art facility, your role will be to design and carry out selections and screening campaigns on their antibody fragment libraries using phage display, in order to identify therapeutic candidates. What you will need • An MSc or a PhD in a biological discipline • More than 2 years’ experience in a relevant field • Knowledge and practical experience in phage display • Knowledge of molecular and biology techniques like DNA purification, PCR setup, SDS-PAGE, ELISA and western blot What you will get • State-of-the-art laboratories • Competitive Salary • Great Benefits Package This a great opportunity for talented individuals who are seeking a dynamic career at the cutting edge of biopharmaceutical research. Get in touch today to ensure that you don’t miss out!

  • Executive Manager – Quality Assurance

    Salary: £0 Location: Petersfield

    Quality Assurance Executive Manager- Permanent Based in Hampshire, my client is one of the market leaders in the cosmetic and personal care sectors and is looking for a Quality Assurance Executive Manager. Reporting to the VP of Quality assurance the ideal candidate will have extensive experience managing the quality function for a company preferably with experience in personal care, Cosmetics and OTC manufacturing, Pharma or FMCG (At the request of my client, company and salary details will only be provided to candidates, suitable for the role and wishing to be considered for the position) You will be responsible for a team of 3 direct reports and accountable for- + The QMS &, leading annual management reviews. + Managing spending within the budget. + Be at the forefront of the QA team, leading by example and striving to drive improvement within the department. + Encouraging teamwork and promoting professional development within the quality team + Track and manage compliance of the plant with corporate quality policies and procedures + Ensure OTC complaints and quality enquiries are dealt with + Delegating product release specifications, effectively with in the QA team. + Use a risk-based approach to take decisions on disposition of materials You will have- A BSc in Chemistry, Cosmetics, Pharma Applied sciences or another relevant sector. Extensive experience as a QA manager with in the Pharmaceutical, Cosmetic, Personal care, FMCG or another relevant sector. Competitive Salary (dependant on experience) Excellent benefits Fantastic opportunity to work with a high end, international company.


« previous 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 next »