Join AtomVie Global Radiopharma as a Manufacturing Systems CQV Specialist in Hamilton, ON. This full time position involves crucial equipment qualification and compliance activities.

As a CQV Specialist I, you will collaborate within the Engineering department to handle equipment validations, oversee qualification protocols, and ensure adherence to GMP standards. Your background in pharma or food manufacturing will enable you to streamline processes and make significant contributions toward continuous improvement.

Key Responsibilities:
• Lead equipment performance verification and qualification
• Review qualification protocols for completeness and accuracy
• Execute internal certification programs effectively
• Create equipment maintenance SOPs in CMMS
• Support troubleshooting and resolution of CQV issues

Requirements:
• College Diploma in a technical discipline or relevant experience
• 2-5 years of experience in a related technical role
• Capability to lift 50lbs and work in confined spaces

Leverage your skills to enhance AtomVie’s manufacturing processes while ensuring compliance in Hamilton.
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📌 Manufacturing Systems CQV Specialist (Ontario)
🏢 AtomVie Global Radiopharma
📍 Ontario