Elevate your career with AtomVie Global Radiopharma as a CQV Specialist (Lab). This role involves laboratory equipment qualification and compliance with GMP practices in a collaborative work setting. As a CQV Specialist, you will support the Engineering department in executing calibrations, validations, and documentation.

Your expertise in quality control will drive improvements and ensure compliance with regulatory standards. You'll also coordinate with third-party contractors and lead troubleshooting efforts for equipment validation issues. Key Responsibilities:

- Manage calibration and preventive maintenance programs
- Perform equipment qualification for laboratory instruments
- Create operational SOPs and maintenance programs
- Support development of qualification documentation
- Investigate equipment and validation issues Requirements:
- College diploma in a technical field or relevant experience
- 2-5 years in GMP pharmaceutical lab settings
- Ability to lift 50 lbs and work in small areas
- Knowledge of Health Canada and FDA regulations
- Proficiency in Waters HPLC systems and report writing Utilize your skills in compliance and technical support to enhance patient outcomes at AtomVie.

📌 CQV Specialist Lab at AtomVie (Canada)
🏢 AtomVie Global Radiopharma
📍 Canada