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...