CQV-Manager

FAT,SAT-Projects - GMP - Oral Solid Dosage

You don’t just execute projects — you drive them.
You understand GMP, OSD manufacturing, and complex validation environments.
And you’re ready to take ownership of a critical tableting area revamp.
This is your opportunity to step into a Manager / Engineering role where your expertise in commissioning & qualification (C&Q) directly shapes manufacturing excellence.
You will lead the qualification activities for the revamping of a pharmaceutical Oral Solid Dosage (OSD) tableting manufacturing area

• Own Design Qualification, FAT, SAT, Qualification, Handover & Close-Out
• Drive commissioning and qualification of OSD process equipment & computerized systems
• Lead C&Q activities on capital projects — on time and within budget
• Author and approve validation strategies, protocols & reports
• Interface cross-functionally with engineering, QA, MS&T, suppliers & contractors
• Support audits and health authority inspections as SME

You’ll operate within a structured stage-gate project environment and influence across organizational boundaries

• Degree in Engineering or Science (Mechanical, Chemical, Life Sciences, etc.
• 5+ years in pharmaceutical validation, ideally within OSD in GMP environments
• Experience managing complex capital projects
• Strong problem-solving and communication skills
• Experience with inspections and regulatory interactions
• Project & change management expertise
• English and French fluent

• Starting Date 01. April
• 6 Months (high probability for prolongation)
• 100 % on-Site

• Lead instead of follow
• Influence instead of execute only
• Deliver measurable impact within a high-standard GMP environment
• Strengthen your profile in capital project C&Q leadership