Description
QA GMP Supervisor
An important vacancy has recently become available for an experienced QA GMP Supervisor to join a well-respected European pharmaceutical organisation. The successful candidate will provide QA support to the Biology QC department, acting as back up of the Supervisor/Manager for QA operations.
Description of the role:
- Prepare weekly deviation meetings with QA technician if relevant
- Approve life cycle validation reports and intra-site transfer report in accordance with procedures and timelines
- Review and challenge the QC change controls (R1 - R2) in accordance with procedures (Matrix) and timelines
- Review and challenge the QC deviations and CAPA of its QC department
- Review at least on monthly basis the quality system status of its QC department (D0, E3, E6, CP, RPC/R2)
The successful candidate will have:
- 2-5 years experience in pharmaceutical environment
- Experience in FDA/EU/WHO inspection
- Good knowledge of FDA/EU/ICH/CDN/AUS guidelines
- Experience in biologicals manufacturing/testing processes
- Good knowledge of current Good Manufacturing Practices
- Good manufacturing and laboratories process knowledge
Do not miss the chance to further your career by working for this renowned pharmaceutical company as the position will not be open for long. If you believe you are suitable for the role, or would like to hear more please send your CV
Furthermore we offer a generous referral bonus of euro;400 for any referral that results in employment, so if you know of anyone please get them in touch.