Overview
We are seeking an experienced Quality Manager to oversee site quality matters for a pharmaceutical construction project in Switzerland. This role requires a seasoned professional to establish/maintain the highest quality standards throughout the construction and commissioning phases of a pharmaceutical manufacturing facility.
Responsibilities
The successful candidate will be responsible for implementing comprehensive quality management systems, ensuring GMP compliance, and managing all quality-related activities from construction through to facility handover and validation.
1. Establish and maintain project quality management systems aligned with pharmaceutical industry standards
2. Ensure all construction activities comply with GMP requirements and regulatory standards
3. Direct daily quality activities across all construction disciplines and contractors
4. Oversee quality documentation, IQ/OQ protocols, and validation master plans
5. Coordinate internal and external quality audits, regulatory inspections, and client assessments
6. Lead investigation and resolution of quality issues and deviations
7. Monitor subcontractor quality performance and compliance with project specifications
8. Deliver quality training programs for project teams and contractors
Qualifications
9. Degree in Engineering, Science, Quality Management, or related discipline
10. Minimum 8+ years in quality management roles on major construction/engineering projects
11. Proven experience in pharma facility construction quality management
12. Deep understanding of GMP and Belgian/EU pharmaceutical regulations
13. Extensive experience with ISO 9001, quality management systems, and validation processes
14. Fluent English essential; German/French advantageous
Candidates must have :
15. Right to work in Europe
16. English Language Skills - German highly desireable