Job description

Are you an experienced CQV professional looking to contribute to critical pharmaceutical projects? We are currently seeking CQV Engineers to join our growing team in Toronto! If you're open to exciting new opportunities and thrive in fast-paced, highly regulated environments, we’d love to hear from you.

Responsibilities:

• Lead and execute commissioning, qualification, and validation (CQV) activities for pharmaceutical equipment, utilities, and systems.


• Prepare and review CQV documentation, including protocols (IQ/OQ/PQ), reports, and risk assessments.


• Ensure compliance with GMP, FDA, EMA, and other global regulatory standards.