Job Title: Freelance QA Support – Process & Cleaning ValidationLocation: Province of Antwerp, Flemish RegionRole Overview:We are seeking an experienced QA professional to provide freelance support in process and cleaning validation within the pharmaceutical/biotech sector. This role focuses on ensuring compliance with GMP standards, supporting validation projects, and maintaining high-quality documentation.Key Responsibilities:Process Validation:Support New Product Introduction (NPI) and technology transfer activities.Assist with CPV / lifecycle validation projects.Provide audit support and ensure readiness for regulatory inspections.Cleaning Validation:Develop and implement cleaning validation strategies.Prepare and review master plans, protocols, reports, and monitoring activities.Perform Cleaning Quality Reviews and MACO calculations.Documentation & Compliance:Review and approve quality documents with accuracy.Maintain compliance with GMP and Annex 15 requirements.Ensure consistent application of QA processes across projects.Requirements:3–5+ years of experience in GMP QA.Strong knowledge of Annex 15 and quality systems.Solid understanding of organic chemistry.Proven experience in process and cleaning validation.Excellent documentation, review, and approval skills.Contract Type: Freelance – 4 days on site one day remoteApplication:If you are a proactive QA professional with a strong track record in process and cleaning validation, this freelance role offers the opportunity to work on impactful projects with flexible arrangements.