About the job
What you'll do
The CQV Engineer will execute commissioning, qualification, and validation activities for process, utility, and facility systems in a GMP environment. They will also collaborate with multidisciplinary teams to ensure project delivery, system startup, and regulatory compliance.
What they're looking for
Candidates must have previous CQV experience within pharmaceutical, biotech, or life sciences manufacturing environments. A strong understanding of commissioning methodologies and GMP documentation is required, along with the legal right to work in the EU.
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