Senior C&Q Engineer - Biopharma GMP Validation Lead

MMR Consulting in Mexico is seeking a Sr. C&Q Engineer with over 12 years of experience in the pharmaceutical and biotech industries. The successful candidate will lead commissioning and qualification efforts for various systems, ensuring compliance with cGMP regulations. This role requires strong leadership and mentoring skills as well as a solid background in validating biopharmaceutical processes.

Candidates should hold an engineering degree and have experience with biotech process equipment. Travel may be required and TN Visa sponsorship is offered.