Laboratory CQV Specialist at AtomVie

Advance your expertise as a CQV Specialist at Atom Vie Global Radiopharma based in Hamilton, ON. This onsite role is essential for managing equipment qualification and ensuring GMP compliance.

As a key member of the Engineering team, you will report to the Engineering Manager, overseeing calibration programs and conducting validation activities. You will also collaborate with various departments to troubleshoot equipment issues and ensure all processes align with cGMP standards. Continuous improvement initiatives within the engineering realm will be part of your contributions.

Key Responsibilities:

• Execute calibration and preventive maintenance programs

• Conduct HPLC and Gas Chromatography equipment qualifications

• Create lab instrument SOPs and maintenance records

• Support qualification documentation and training processes

• Address non-conformance and resolution tasks

Requirements:

• College Diploma in a technical field or equivalent experience

• 2-5 years of GMP lab experience, particularly in Metrology

• Ability to lift 50lbs and navigate tight spaces

• Knowledge of Health Canada and FDA regulations

• Proficiency in technical communication and report writing

Bring your passion for quality and compliance to the innovative team at Atom Vie.
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