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 Computer System Validation within the pharmaceutical
• Strong knowledge of GxP, GMP, and regulatory guidelines (e.g., GAMP5)
• Hands-on experience with validation documentation and testing methodologies
• Excellent analytical, documentation, and problem-solving skills
• Strong communication skills and ability to work in multidisciplinary teams
• Fluent in Dutch and English

Amoria Bond operates as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age or experience, and we confirm that we are happy to accept applications from persons of any age or experience for this role.