Quality Manager - Sterile Manufacturing
- Employment type
- Full-time
- Location
- Basel
- First posted
- 22 juillet 2026
- 100%
- Durée indéterminée
- anglais (Courant)
- 4001 Basel
- Se connecter pour voir l-estimation de salaire de jobup.ch
French-Speaking Switzerland | GMP | Quality & Compliance ##
Looking for more visibility, responsibility and impact in Quality?
Join a specialized sterile pharmaceutical manufacturing site where you will work closely with Production, QA, QC and the Qualified Person, driving GMP compliance and operational quality activities in a highly regulated environment.
Your Responsibilities
- Support batch review and release activities
- Review GMP documentation and manufacturing records
- Manage deviations, CAPAs and Change Controls
- Provide quality support to production, laboratories and warehouse operations
- Maintain strong shopfloor presence and drive continuous improvement
- Act as compliance contact for customers and external partners
- Support inspections and client audits
Your Profile
- Degree in Pharmacy, Chemistry, Life Sciences or Engineering
- Experience in GMP-regulated pharmaceutical manufacturing
- Strong exposure to sterile / aseptic production
- Experience with deviations, investigations and Change Controls
- Operational mindset and willingness to work close to production
- Fluent French and good English
What-s on Offer?
- High visibility role within a specialized pharmaceutical manufacturing site
- Broad quality responsibilities with direct impact on operations
- Close collaboration with Production, QA, QC and Release teams
- International environment with short decision paths
- Excellent opportunity to further develop towards broader Quality and QP responsibilities
Posted 4 days ago