Take on the role of QC Analyst at AtomVie, focusing on quality control testing while adhering to GMP and safety regulations. Contribute actively to drug development with your analytical skills.

As a QC Analyst, you will work with a variety of testing methods in a fast-paced lab environment. Your role will involve performing tests on drug substances and raw materials, adhering to SOPs, and documenting results meticulously. You'll also have responsibilities related to housekeeping and inventory management to support efficient lab operations.

Key Responsibilities:
• Perform comprehensive quality control testing
• Report on testing failures and implement corrective actions
• Maintain lab safety and compliance with all regulations




• Generate technical reports and document findings
• Assist in training and guiding other lab colleagues

Requirements:
• B.Sc. in Chemistry, Biotechnology, or related field
• 1-3 years' experience with HPLC, GC, and microbiology
• Familiarity with technical documentation and software
• Strong ability to work independently and in a team
• Physically capable of lifting heavy materials

Help advance AtomVie's drug portfolio through your robust quality control expertise.
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📌 QC Analyst Role in Pharma Industry (Ontario)
🏢 AtomVie Global Radiopharma
📍 Ontario