Join AtomVie as a Quality Control Analyst focused on GMP compliance and quality testing. Utilize your chemistry expertise to ensure high-quality drug products through rigorous testing and documentation.

As a QC Analyst, you will support their product portfolio by conducting quality control testing of raw materials and finished products. This position requires proficiency in analytical techniques and adherence to AtomVie SOPs. You'll be responsible for accurate reporting, maintaining lab equipment, and ensuring compliance with nuclear safety regulations.

Key Responsibilities:



• Perform quality control testing of drug products and materials • Document analytical data and generate technical reports • Conduct investigations for testing failures and implement corrective actions • Maintain laboratory equipment calibration and inventory • Assist colleagues in training and adhere to health and safety practices

Requirements: • College Diploma or B.Sc. in Chemistry or related field • 1 to 3 years in analytical chemistry techniques • Proficiency with Empower software and Microsoft Office • Solid communication skills in English • Ability to lift weights up to 23 kilograms

Bring your technical skills to AtomVie and ensure quality standards in drug development. #J-18808-Ljbffr

📌 Quality Control Analyst at AtomVie (Winnipeg)
🏢 AtomVie Global Radiopharma
📍 Winnipeg