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 programsPerform equipment qualification for laboratory instrumentsCreate operational SOPs and maintenance programsSupport development of qualification documentationInvestigate equipment and validation issuesRequirements:College diploma in a technical field or relevant experience2-5 years in GMP pharmaceutical lab settingsAbility to lift 50 lbs and work in small areasKnowledge of Health Canada and FDA regulationsProficiency in Waters HPLC systems and report writingUtilize your skills in compliance and technical support to enhance patient outcomes at AtomVie.

📌 Cqv Specialist Lab At Atomvie (Hamilton)
🏢 AtomVie Global Radiopharma
📍 Hamilton