Do you have aMasters or BSc degree in Biology, Biomedical Science, Immunology or similar, together with some experience gained in an analytical lab in a GMP environment? Do you have a strong grounding in Flow Cytometry and PCR? If so, this brand-new opportunity near London Bridge could be a fantastic career move!
This is a permanent QC Associate role with a salary up to £35,000, plus excellent benefits including annual bonus, pension, healthcare and 25 days’ holiday. You will join an exciting, pioneering company who have secured significant investment and are expanding the business in line with moving into Phase 1 clinical trials in early 2022.
We are looking for an adaptable, energetic, collaborative, honest and versatile person to join this pioneering company who are developing new approaches to autoimmune and inflammatory diseases, as well as tackling organ transplantation rejection.
Your role will include:
Supporting clinical trial manufacturing through QC testing across multiple disciplines including microbiology, mammalian cell culture, flow cytometry, qPCR and potency testing
Participating in supporting QC activities e.g. OOS / Deviations / Change controls
Assisting with the qualification and validation of test methods and processes to ensure their suitability for use in support of Clinical Trial manufacturing
Participating in equipment qualification activities
Assisting with technology transfer of QC test methods from the analytical development group
Supporting QC stability programmes
Authoring reports and regulatory documentation
Working with external 3rd party QC service providers
This is a permanent role with a salary up to £35,000 depending on experience. In addition, the company will invest significantly in your training and development and offers annual bonus, 25 days’ holiday, great pension, private medical cover, life assurance and a very supportive team around you!
Skills and Experience Required:
Experience with Flow Cytometry and qPCR gained within ideally in a Biologics, Cell Therapy / ATMP, sterile manufacturing or Biopharmaceutical organisation
Daily usage experience of running these analytical techniques is essential. Experience of developing or validating methods would be an advantage but is not essential
Strong grounding in GMP
Life science qualification – ideally a degree minimum (preferably a Masters) in a biological discipline
Excellent communication skills and ability to work with people at all levels
Proactive, driven, pragmatic, open-minded, emotionally intelligent, positive and respectful approach to your work
Full details will be provided on application. This is a permanent role near London Bridge. You will be required to visit another site in the local area on occasion as well.