CQV Specialist at AtomVie in Hamilton

Join AtomVie Global Radiopharma Inc. as a CQV Specialist in Hamilton, ON. Contribute to laboratory equipment qualifications and compliance with GMP practices while working onsite. In this role, you will report to the Engineering Manager, focusing on calibration, recertifications, and documentation execution.

Managing vendor programs and overseeing equipment validation activities like HPLC qualifications will be key responsibilities. Collaborate across teams to ensure compliance with cGMPs and troubleshoot CQV tasks effectively. Key Responsibilities: • Execute vendor and internal calibration maintenance programs • Perform equipment qualifications and validation activities • Develop lab instrument SOPs and maintenance programs • Lead the creation of qualification documentation • Investigate and troubleshoot CQV-related issues Requirements: • College Diploma in a technical field or relevant experience • 2-5 years of hands-on GMP lab experience • Ability to lift 50lbs and work in small spaces • Strong knowledge of regulations like Health Canada and FDA • Excellent communication and report writing skills Leverage your skills in quality compliance and technical troubleshooting at AtomVie to advance healthcare solutions. #J-18808-Ljbffr