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