CQV Engineer
Location: Antwerp Region, Belgium
Work Pattern: 3-4 days onsite / 1–2 days remote
Contract Type: Freelance / Long-term Contract
Start Date: ASAP
Language: Dutch preferred, English considered for exceptional candidates
Key Responsibilities
- Plan, execute, and document qualification activities (IQ/OQ/PQ) for process and utility equipment including:
- Reactors (glass-lined and stainless steel)
- Centrifuges, dryers, and vessels
- Process piping, skids, and associated systems
- Review and approve FAT/SAT documentation and vendor files.
- Prepare and maintain qualification documentation, URS, FDS, and traceability matrices in line with GMP and Annex 15 requirements.
- Collaborate with Engineering, QA, and Production teams to align qualification activities with project and operational timelines.
- Manage deviations, non-conformances, and CAPAs related to qualification scope.
- Support audits and inspections by providing qualification documentation and technical explanations.
- Participate in risk assessments (FMEA, change control) for new or modified equipment.
- Provide technical support during commissioning and troubleshooting.
Key Skills & Experience
- 5–15 years’ experience in Equipment Qualification / Validation Engineering within pharma or chemical API manufacturing.
- Proven experience executing IQ/OQ/PQ for process equipment (reactors, centrifuges, dryers, vessels, piping).
- Strong understanding of GMP
- Excellent documentation and communication skills.
- Fluent in Dutch (preferred) or English (fluent required).
If you’re an experienced Equipment Qualification Engineer with a background in pharma or chemical API environments, and you’re ready for a hands-on role in Belgium, please get in touch with your updated CV or contact our team for a confidential discussion.
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