GMP Facility Quality Manager
Vor 4 Tagen
Join us at DINAMIQS, a dynamic Contract Development and Manufacturing Organization (CDMO) in Switzerland, focused on viral vector production for gene therapies.
We offer a comprehensive range of services, including vector design optimization, process development, and analytics, to support gene therapy projects.
We are seeking a skilled GMP Facility Quality Manager to join our team and contribute to the success of our operations.
In this role, you will be responsible for implementing quality systems, managing documentation control systems, preparing facilities for regulatory inspections, and reviewing quality documents.
You will also support supplier qualification, act as the primary QA contact on the shop floor, and conduct root cause analysis.
To succeed in this position, you should have a B.Sc or M.Sc in Biotechnology, Virology, or Molecular Biology and at least 5 years of experience in a GMP-regulated biopharmaceutical environment, with at least 2 years in QA.
Key benefits include:
- A challenging and rewarding career opportunity
- Competitive salary and benefits
- Flexible working hours and holidays
- Professional growth and development
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