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About the role

Adryan is seeking a seasoned CQV engineer to join the US life sciences team. You will own commissioning, qualification, and validation activities for GMP facilities and critical systems, ensuring regulatory and internal quality compliance. Responsibilities include designing CQV documentation, IQ/OQ/PQ execution, data analysis, and final reporting. A strong GMP background and 10+ years of experience are preferred in a fast-paced project environment.

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JOB OVERVIEW

Experience level

Senior

Location

Brooklyn, NY

Occupation

Validation Engineers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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