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.