I have an excellent opportunity as a QA Officer for an innovating and rapidly growing cell and gene organisation, giving you the opportunity to work in a fast-paced environment and the ability to make a huge impact.

This opportunity will give you the chance to take on a critical role within the QA department ensuring all activities and products are compliant with the high quality GMP 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 companies
• Work at the forefront of science

You will be responsible for

• Ensuring GMP compliance by implementing continuous improvement strategies on the Pharmaceutical Quality System
• Reviewing and qualifying the critical raw material suppliers including frequent audits and inspections
• Deviation management including coordinating risk assessments and change controls
• Supporting the site QMS ensuring activities are carried out compliantly

You will bring the following

• Extensive QA experience within a GMP compliant environment
• Experience with ATMPs or Cell and Gene therapy
• Experience with holding or hosting audits and inspections

• BSc or MSc in a relevant Life Sciences subject

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