Quality Manager – Sterile Manufacturing

gloor & lang ag

4001 BaselFestanstellungVeröffentlicht 22.7.2026

Über den Job

Specialized sterile pharmaceutical manufacturing site in French-Speaking Switzerland. You will work closely with Production, QA, QC and the Qualified Person, driving GMP compliance and operational quality activities in a highly regulated environment.

Aufgaben

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

Profil

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

Rahmenbedingungen

Ort: French-Speaking Switzerland

Benefits

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

GMP-ComplianceSterile / aseptische ProduktionBatch Review und FreigabeAbweichungsmanagement (Deviations)CAPA und Change ControlBehörden- und KundenauditsStudium Pharmazie/Chemie/Life SciencesFliessend Französisch und gutes Englisch

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