Location
hamilton, on, Canada
Posted
July 04, 2026
Job Description
Join OmniaBio in Hamilton, ON, as an Associate I, focused on Commissioning Qualification and Validation in support of transformative biomanufacturing. Drive compliance and documentation processes in a dynamic role.
This position requires a detail-oriented candidate to assist with validation activities, including preparing documentation and ensuring compliance with GMP standards. Your expertise in CQV will be essential as you work with cross-functional teams to develop necessary SOPs and validation master plans, contributing to the efficiency of advanced therapy production.
Key Responsibilities:
• Support validation master plans and deliverable assessments
• Work with Science, Technology, Operations, and Quality Assurance teams
• Develop preventive maintenance and calibration SOPs
• Participate in internal audits as a subject matter expert
• Maintain thorough documentation and reporting
Requirements:
• 1+ years in a related CQV role in biopharma/pharmaceutical...
This position requires a detail-oriented candidate to assist with validation activities, including preparing documentation and ensuring compliance with GMP standards. Your expertise in CQV will be essential as you work with cross-functional teams to develop necessary SOPs and validation master plans, contributing to the efficiency of advanced therapy production.
Key Responsibilities:
• Support validation master plans and deliverable assessments
• Work with Science, Technology, Operations, and Quality Assurance teams
• Develop preventive maintenance and calibration SOPs
• Participate in internal audits as a subject matter expert
• Maintain thorough documentation and reporting
Requirements:
• 1+ years in a related CQV role in biopharma/pharmaceutical...