CQV Engineer / Quality Manager
We are currently looking for a Quality Manager with a background in CQV Engineering for a leading pharmaceutical company in Switzerland.
This is a 6 month contract with high likelihood of extension.
About the Role
In this position, you will be responsible for the qualification and validation of process equipment and facilities. You will play a key role in optimizing processes, systems, and internal workflows, ensuring compliance and supporting continuous improvement throughout the system life cycle.
Key Responsibilities
Prepare commissioning and qualification documentation for new installations and support modification, expansion, and greenfield projects.
Lead PQs for critical systems in new construction projects and manage system life cycle (SLC) activities post-handover.
Manage deviations, changes (GEP and GMP), and CAPAs.
Coordinate internal teams, external service providers, and suppliers.
Present qualification documentation during audits and inspections.
Provide project support as a qualification specialist.
Your Profile
Degree from a technical college (HF/FH/University) in engineering or a related field.
Several years of experience in a regulated environment (commissioning, qualification, validation of process systems, clean utilities, cleanrooms, or process equipment).
Independent, structured, and flexible working style with strong communication skills.
Proficient in Microsoft Office; experience with COMOS, DMS, TrackWise, and SAP is an advantage.
Fluent in German (written and spoken); good command of English.
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