Biopharma CQV Manager: Lead Process Validation

A consulting firm in the pharmaceutical industry is seeking a CQV Manager to lead commissioning and qualification activities in bioprocess systems. The ideal candidate will have over 8 years of experience in the pharmaceutical/biotech sectors, strong leadership and project management skills, and a relevant engineering degree. This role requires direct management of a team and oversight of various validation projects to ensure compliance with industry standards.

Occasional travel may be required.
Step into the Biopharma CQV Manager:
Lead Process Validation role at MMR Consulting in Toronto, ON, Canada and grow with us. The position is based in Toronto, ON, Canada. This opportunity is part of our work in Bio & Pharmacology & Health. The advertised compensation is 95.. We aim to respond to suitable candidates as soon as possible.