Interim CQV Manager

Walker Cole International has recently partnered with an established pharmaceutical client based in France, who are looking to onboard an experienced CQV manager to oversee all commissioning and qualification activities of a new build sterile manufacturing facility.

You will be responsible for:

• Lead and manage all CQV activities for pharmaceutical manufacturing projects, from planning through execution and closeout.
• Manage the vendors, contractors, and consultants to ensure deliverables meet quality/schedule expectations.
• Collaborate with engineering, operations, quality, and vendors during design, construction, and start-up phases.
• Manage CQV documentation control in line with company and regulatory standards.
• Ensure compliance with FDA, EMA, and other relevant regulatory requirements.
• Provide technical guidance, training, and mentorship to CQV engineers and project team members

The successful candidate will have:

• 10+ years of experience in CQV management in the life science/pharmaceutical industry (ideally in a sterile environment).
• Proven experience managing complex CQV projects from concept to handover.
• Familiarity with global regulatory guidelines (FDA, MHRA, GAMP 5)
• Excellent leadership, project management, and stakeholder communication skills.
• Capable of working independently and cross-functionally when required.
• Proficiency in risk-based validation approaches

Contract details:

• Length - 12 months
• Full-time onsite, 5 days per week
• Start date - Immediate
• Location - France
• Pay - 95-105 Euros per hour

C&Q | CQV | Validation | Pharmaceutical | Commissioning| Qualification | Manager | Management | Leadership | Pharma |Biopharma| Life Sciences | Manufacturing | Steriles | GMP | Good Manufacturing Practice