Overview
PM Group are seeking an experienced Quality Lead to oversee all site quality matters for a major pharmaceutical construction project in Geel, Belgium. This critical role requires a seasoned professional to establish and maintain the highest quality standards throughout the construction and commissioning phases of a state-of-the-art 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 Good Manufacturing Practice 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; Dutch/French advantageous
15. Qualified internal auditor with experience managing regulatory inspections
16. Professional quality qualification advantageous
17. Experience with cleanroom construction and controlled environment validation advantageous
18. Understanding of pharmaceutical engineering standards
D&I
Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.
PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.
For more company information visit our company website > Meet Our Team - careers | PM Group
#LI-GS1
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.
19. Establish and maintain project quality management systems aligned with pharmaceutical industry standards
20. Ensure all construction activities comply with Good Manufacturing Practice requirements and regulatory standards
21. Direct daily quality activities across all construction disciplines and contractors
22. Oversee quality documentation, IQ/OQ protocols, and validation master plans
23. Coordinate internal and external quality audits, regulatory inspections, and client assessments
24. Lead investigation and resolution of quality issues and deviations
25. Monitor subcontractor quality performance and compliance with project specifications
26. Deliver quality training programs for project teams and contractors
27. Degree in Engineering, Science, Quality Management, or related discipline
28. Minimum 8+ years in quality management roles on major construction / engineering projects
29. Proven experience in pharma facility construction quality management
30. Deep understanding of GMP, and Belgian/EU pharmaceutical regulations
31. Extensive experience with ISO 9001, quality management systems, and validation processes
32. Fluent English essential; Dutch/French advantageous
33. Qualified internal auditor with experience managing regulatory inspections
34. Professional quality qualification advantageous
35. Experience with cleanroom construction and controlled environment validation advantageous
36. Understanding of pharmaceutical engineering standards
D&I
Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.
PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.
For more company information visit our company website > Meet Our Team - careers | PM Group
#LI-GS1