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Manufacturing Systems CQV Specialist
Job in
Hamilton, Ontario, E8H, Canada
Listed on 2026-07-31
Listing for:
AtomVie Global Radiopharma Inc.
Full Time
position Listed on 2026-07-31
Job specializations:
-
Manufacturing / Production
Validation Engineer, Pharmaceutical Manufacturing, Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below
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 Atom Vie’s manufacturing processes while ensuring compliance in Hamilton.
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