We are supporting a successful CDMO in their search for a new QA Compliance Manager. This role is to support business growth and to work closely with the QA Director to lead their expanding Quality department.
The QA Compliance Manager will support the Production team in ensuring compliance of process development in Gene therapies. It is imperative that you have a thorough understanding of GMP and an appreciation of ATMPs. Overseeing a team of 3 QA Officers, you will also deputise for the QA Director in their absence.
Cored duties include, but not limited to:
- Ensure QMS is compliant with relevant standards
- Identify, investigate and correct CAPAS
- Lead Site Management review meetings
- Produce quarterly and annual quality reports
- Monitor change control process
Applicants will be expected to have achieved a degree (or equivalent) in a relevant life sciences discipline. Significant experience and knowledge gained in the manufacutre of cell and/or gene therapy products is essential. Apply today for immediate consideraiton. Full job description available on request.