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Validation Engineer


Freelance Validation Specialist About the Opportunity To support ongoing expansion, we are seeking experienced freelance validation professionals to collaborate on projects within the pharmaceutical and life sciences sector. Role Overview As an independent validation specialist, you will reinforce project teams at client sites. Your focus will be on planning, executing, and documenting qualification and validation activities in compliance with current GMP and GxP requirements. Assignments may vary in duration (short- or long-term) depending on project scope, your expertise, and availability. Engagements are primarily located across Belgium and the Netherlands. Key Responsibilities Depending on your background and strengths, responsibilities may include: Qualification of laboratory equipment Commissioning and qualification of facilities and utility systems Process validation and/or cleaning validation Computerized System Validation (CSV) Preparation and review of validation documentation Ensuring compliance with applicable regulatory standards Profile 3–5+ years of hands-on experience in validation within a regulated environment Solid understanding of GMP, GxP, and life sciences regulatory frameworks Able to work autonomously with a structured and methodical approach Strong communication skills and comfortable interacting with clients and stakeholders Fluent in Dutch and English

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