Validation Engineer

Are you an experienced CSV Specialist looking for an exciting new opportunity? We are seeking a skilled professional to join a dynamic team working on computer system validation within the pharmaceutical industry.

Role: CSV specialist

Start: As soon as possible

Duration: 12 months

Location: South-Holland, Hybrid working possible

Contract: Freelance Contract via Amoria Bond

Responsibilities:

• Execute and manage CSV activities across the full validation lifecycle (URS, IQ, OQ, PQ)
• Ensure systems comply with GxP, GMP, and regulatory requirements
• Develop and review validation documentation, protocols, and reports
• Perform risk assessments and support audits and inspections
• Collaborate with cross-functional teams including QA, IT, and Engineering

What We’re Looking For:

• Proven experience in ...