CQV Engineer
CQV Engineer.
CQV Engineer
Beuningen
|Contract
|CQV
Freelance CQV Engineer - Greenfield Pharmaceutical Project
2 Year Project
We are looking for an experienced Freelance CQV Engineer to support a Greenfield pharmaceutical project. This is an ideal position for an expert looking to contribute to a cutting-edge facility startup.
The ideal professional must be based in the Netherlands.
Responsibilities:
- Develop and execute commissioning, qualification, and validation plans for project phases.
- Conduct risk assessments to ensure compliance with cGMP, FDA, and EU regulations.
- Lead the preparation and execution of IQ/OQ/PQ protocols for systems, utilities, and equipment.
- Review design documentation and collaborate with project stakeholders on system integration.
- Troubleshoot and resolve commissioning/validation issues in a timely manner.
- Generate and maintain detailed technical reports and documentation for regulatory approvals.
Requirements:
- Bachelor's degree in Engineering, Life Sciences, or a related discipline.
- Minimum 3 years of CQV experience in the pharmaceutical or biotech industry.
- Proven track record working on Greenfield projects or facility startups.
- Expertise in IQ/OQ/PQ protocol development and execution.
- Familiarity with regulatory guidelines (cGMP, FDA, EU) and validation procedures.
- Experience with CQV-related software/tools is a plus.
- English Speaking
Must be based in the Netherlands. If you feel like you could be suited for this then please send your CV to James.Gregory@darwinrecruitment.com
Darwin Recruitment is acting as an Employment Business in relation to this vacancy.
James Gregory
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