Quality Manager – CDMO Services Parenterals

gloor & lang Pharma and Biotech Recruiting; Bezirk Solothurn; Vor Ort; CHF 90.000 - 150.000; Vollzeit

Benefits dieser Stelle

High visibility role

Broad quality responsibilities

Close collaboration with teams

International environment

Path to QP responsibilities

Zusammenfassung

gloor & lang Pharma and Biotech Recruiting is hiring for a French-speaking Switzerland GMP Quality & Compliance role. You will support batch review, deviations, CAPAs and change controls, working closely with Production, QA, QC and the Qualified Person to ensure GMP compliance in a sterile manufacturing site.

Fluent French and good English are required, with a degree in Pharmacy, Chemistry, Life Sciences or Engineering and hands-on GMP experience.

Qualifikationen

• 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.

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.

Kenntnisse

GMP experience

Sterile production

Deviation investigations

Ausbildung

Degree in Pharmacy, Chemistry, Life Sciences or Engineering

Jobbeschreibung

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