Senior CQV Engineer — GMP Validation & Commissioning
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Engineering
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Quality Assurance - QA/QC
Job Description & How to Apply Below
Adryan is seeking a hands-on commissioning, qualification and validation (CQV) engineer for life sciences projects in the United States. You will manage CQV activities for GMP facilities, equipment, and utilities, ensuring compliance with FDA/EU guidelines and quality standards.
You will design, execute, and document IQ/OQ/PQ processes and generate final reports.
Required:
Bachelor’s in engineering or related field, 5+ years GMP, 3+ years CQV, and strong teamwork, communication, and
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Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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