I have an excellent opportunity as a Senior QA Specialist for an innovative and rapidly growing cell and gene organisation based in London, giving you the chance to work in a fast-paced environment and the ability to make a huge impact.

This opportunity will give you a chance to take on a critical role within the QA department ensuring all activities and products are compliant with the high-quality GMP and GDocP standards.

This role will offer you

• Exposure to numerous clinical projects which have the potential to save lives
• Exposure to high visibility from the senior leadership team
• Opportunity to join one of the most rapidly expanding biopharmaceutical company
• Work at the forefront of science

You will be responsible for

• Lead from a QA SME perspective
• QA duties from a Batch review perspective
• Ensuring GMP and GDocP compliance by implementing continuous improvement strategies on the Pharmaceutical Quality System
• Reviewing and qualifying the critical quality documentation and records e.g. deviations, Change Controls, Risk Assessments, CAPAs, etc
• Supporting the site QMS ensuring activities are carried out compliantly

You will bring the following

• Previous experience in a QA role within a GMP and GDocP-compliant environment
• Experience within Steriles or Cleanrooms. Cell and gene experience is a bonus
• Experience with BMR and Batch release documentation and document control
• BSc or MSc in a relevant Life Sciences subject

If you want to be part of an innovative, growing company where you can grow and expand your current knowledge, GET IN TOUCH - Please email me at sarah.ghaziri@biotalent.com if you think you could be a good match.