​Mantell Associates is partnered with a very exciting up and coming CDMO who are looking to bring in a Senior Validation Engineer to join their team.

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Senior Validation Engineer - Responsibilities:

• Support validation of cGMP facilities, equipment and processes

• The focus of this position will be on process validation, PPQ, and tech transfer.

• Some duties will include validation of laboratory systems, production equipment, manufacturing processes and utilities.

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Senior Validation Engineer - Requirements:

• 5 years of experience in a pharma, biopharma, and/or biotech manufacturing environment is preferred

• Knowledge of cGMPs for API facilities, pharmaceutical manufacturing processes, clean rooms, utility systems and packaging operations is preferred

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Sponsorship is also provided for this opportunity

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Mantell Associates is a specialist Pharmaceutical and Life Sciences headhunting firm. For more information on this role, please contact Christopher Gomez 786-245-8592 or Christopher.gomez@mantellassociates.com.