CQV & CSV Engineering Roles – France

About the role

KPC International is seeking experienced CQV (Commissioning, Qualification & Validation) and CSV (Computer System Validation) professionals for upcoming pharmaceutical and biopharma projects in France. Start dates are expected between Q3 and Q4 2025, with options for both contract and permanent employment.

Key responsibilities

• Support global pharma and biopharma clients through all phases of plant facility start‑up, from strategic planning to operational readiness.
• Deliver high‑impact validation activities for equipment, processes, and computer systems.
• Work on‑site for the duration of each project, ensuring compliance with regulatory standards.

Required profile

• Proven experience in CQV or CSV roles within pharmaceutical or biopharma environments.
• Full working rights in France and willingness to be based on‑site.
• French language skills strongly preferred; fluent English also considered.
• Local candidates or those with prior experience working in France.
• Experience with DeltaV control systems.

Required skills

• CQV (Commissioning, Qualification & Validation)
• CSV (Computer System Validation)
• DeltaV systems

What we offer

• Excellent rates and working conditions.
• Opportunities on both contract and permanent bases.
• Projects with recognised global clients across France, Ireland, the UK, and wider Europe.