Transform healthcare with AtomVie Global Radiopharma Inc. as a CQV Specialist (Lab). Focus on equipment qualifications, calibrations, and ensuring compliance in a GMP workplace.

This role reports to the Engineering Manager and is crucial for managing laboratory equipment qualifications and documentation in adherence to GMP practices. You will also lead third-party coordination, drive continuous improvement, and engage in troubleshooting activities on laboratory equipment.

Key Responsibilities: • Manage vendor calibration and preventive maintenance programs. • Execute HPLC and Gas Chromatography equipment qualifications. • Develop lab instrument SOPs and maintenance programs. • Support qualification documentation for equipment and software.



• Collaborate on calibration program implementation across teams.

Requirements: • College Diploma in a technical field or relevant experience. • 2-5 years in a GMP Pharmaceutical lab environment. • Strong knowledge of Health Canada and FDA regulations. • Ability to lift 50lbs and work in small spaces. • Excellent communication and technical report writing skills.

Bring your expertise in lab qualifications and regulatory compliance to elevate AtomVie’s mission in healthcare.

📌 CQV Specialist for Laboratory Equipment (Winnipeg)
🏢 AtomVie Global Radiopharma
📍 Winnipeg