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| Job Location | Cambridge |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent , full-time |
CK Group are recruiting for a Quality Assurance Pharmaceutical Quality System (PQS) Manager on behalf of a growing Cell Therapy CDMO to be based at their site in Cambridge on a permanent basis.About the Company:Our client is based in state of the art facilities for multi-product GMP manufacturing. Their facilities include GMP research lab space and process development suites, GMP manufacturing suites, QC lab space and cryogenic storage.Job Summary:The main purpose of this role is to to lead the development and continuous improvement of the Pharmaceutical Quality System supporting the development and manufacture of Advanced Therapy Medicinal Products (ATMPs) in a continuously growing and expanding ContractDevelopment Manufacturing Organisation (CDMO). About the role:The QA PQS Manager will be responsible for monitoring, controlling and overseeing process performance and maintaining a state of control, as well as ensuring that appropriate systems for training all staff are maintained, delivered and continuously improved.About you: