Posted 3 months ago
Quality Manager – Sterile Manufacturing
Basel, SwitzerlandOn-site
AI Summary
A Quality Manager in sterile pharmaceutical manufacturing supports batch release, GMP compliance, and operational quality activities, collaborating closely with Production, QA, QC, and the Qualified Person.
About this role
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
Skills
Aseptic ProcessingBatch ReleaseCAPAChange ControlDeviation ManagementEnglishFrenchGMPPharmaceutical ManufacturingQuality ComplianceSterile Manufacturing
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