Contribute your skills as a QC Analyst at AtomVie, where quality control meets pharmaceutical excellence. Ensure product integrity through precise testing in a GMP-compliant environment.
This role focuses on maintaining the high standards of AtomVie’s products. As a QC Analyst, you’ll engage in analytical testing, documentation, and quality assurance under strict SOPs. Your work will help support the growth of the company's pharmaceutical portfolio and foster compliance with nuclear safety regulations.
Key Responsibilities:
• Conduct release and in-process testing of drug substances
• Prepare Certificate of Analysis and other technical documents
• Report deviations and assist in investigations




• Oversee laboratory equipment maintenance
• Ensure a safe working setting following AtomVie policies
Requirements:
• B.Sc. or College Diploma in related areas
• Experience with HPLC, GC, and microbiological testing
• Familiarity with data processing and documentation software
• Strong collaborative skills and safety focus
• Shift work and physical lifting capability required
Bring your analytical expertise to AtomVie and help build a safer future through quality drug development.
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📌 QC Analyst Role at AtomVie (Hamilton)
🏢 AtomVie Global Radiopharma
📍 Hamilton