If you answered yes, then I might have a great opportunity for you!
Our client is a cell therapy CDMO who are currently managing the development of a state-of-the-art facility for multiproduct GMP production, which will allow the scale up of current commercial production and initiate the provision of contract manufacturing services to meet the growing demand for such services in the UK.
They are currently seeking a Quality Assurance Compliance Manager to join their site in Cambridge on a full time basis. You will be in charge of leading the establishment of the quality framework for the successful manufacture of ATMPs, as well as leading a Quality team.
Responsibilities:
- Overseeing the risk, change and non-conformance management.
- Monitoring trends.
- Working closely with Regulatory bodies and preparing the company for the inspections
- Line management of small Quality Team
- Developing continuous quality improvement and quality awareness in the company.