QA/ Site Compliance Manager – Pharmaceutical
Liverpool
6- 12 month maternity cover
£24 PH
Cpl Life Sciences are currently recruiting for a Site Compliance Manager to join a leading Pharmaceutical company that is one of the worlds largest vaccine companies. This role will support with the site compliance across Quality Systems, documents and GMP related tasks.
Key Responsibilities;
- Provide support on Quality systems to ensure compliance with the companies standards and GMP regulatory guidelines
- Develop, maintain and improve GMP related QC systems including SOPs
- Support with quality systems – Validation, LIMS, Calibration, Document Management, Deviations, CAPA, Change control
- Write and manage validation plans
- Support with internal audits and 3rd party quality audits
Qualifications/ experience;
- Degree in a science related subject
- 5 years experience in quality systems in a Pharmaceutical Manufacturing environment
- GMP experience
- QA experience, deviations, CAPA, change control
For more information please contract mark.bathe@cpl.com