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. #J-18808-Ljbffr
Biopharma CQV Manager: Lead Process Validation in Toronto employer: MMR Consulting
MMR Consulting is an exceptional employer located in the vibrant Rochester, NY area, offering a dynamic work culture that fosters collaboration and innovation in the medical device sector. Employees benefit from hands-on experience in a regulated environment, with ample opportunities for professional growth and development through diverse projects and cross-functional teamwork. The company values diversity and inclusivity, ensuring a supportive atmosphere where every team member can thrive and contribute meaningfully to impactful healthcare solutions.
