Elanco is seeking an experienced Senior CQV Engineer for our Central Engineering team. You will lead validation lifecycle activities across bioprocessing equipment, clean utilities, cleanrooms, and facility systems in line with EU GMP and FDA standards.
Based at our Kiel, Germany site, you will serve as the on-site SME during audits and inspections, ensuring robust qualification of bioprocess equipment and utilities, while guiding root-cause investigations of excursions and ensuring regulatory
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Join us at GB01 Elanco UK AH Limited as our next Senior CQV Engineer: Biopharma Validation in Liverpool, England, United Kingdom.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior CQV Engineer: Biopharma Validation role in the description above.
We appreciate your interest in this position.