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.
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.
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
Sponsorship is also provided for this opportunity
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.email@example.com.