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 Contract Development 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: MSc or equivalent experience in a life sciences subject Significant experience working as a quality manager within a GMP Quality department in the manufacture of cell and/or gene therapy products.Experience of working with regulatory bodies and preparing sites for regulatory inspection.Experience of managing, developing and supporting a team Strong organisational skills and ability to prioritise, work under pressure.Ability to engage and influence at senior management level. To Apply:It is essential that applicants hold entitlement to work in the UK. Please quote job reference 56402 in all correspondence.