Full-time
Biopharma CQV Manager: Lead Process Validation
Posted by MMR Consulting • toronto, on, Canada
About the Role
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.
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