If so, this will be an excellent career opportunity for you. I am currently working with a leading cell and gene therapy CDMO based in the golden triangle. This company has been founded in 2016, and since then, they have been providing their clients with a number of services such manufacturing in their GMP suites, QC testing, process development, warehouse and office spaces.
This company supports clients with complex, breakthrough therapies for a globally diverse market. They are looking for a Senior Quality Assurance Officer to lead QMS, regulatory and compliance activities for the successful manufacture of ATMP’s.
To qualify, you should possess a BSc degree in life sciences and have prior experience working in a QA position within GMP and ATMP’s. This is a permanent, full time position that requires your presence on-site in Cambridge.
Key responsibilities for the QA role:
• Lead QMS, regulatory and compliance activities
• Train members of the team
• Ensure all suppliers meet regulatory and compliance requirements
• Develop strategies and undertake risk assessments Knowledge/Skills Requirements:
• BSc within life sciences
• Strong QA experience within GMP and ATMP’s
• Strong QMS, regulatory and compliance experience