Become a Quality Control Analyst with AtomVie, where you will support drug quality integrity by performing essential testing and documentation in compliance with GMP. Your analytical expertise will help shape product quality.

This position at AtomVie requires a keen attention to detail and a solid understanding of both analytical chemistry and microbiology. You'll be entrusted with performing various quality control tests on drug products and raw materials and ensuring all documentation meets regulatory standards. Your role will also include equipment maintenance and inventory management, making you a pivotal part of the team.

Key Responsibilities:
• Execute quality control testing on finished and raw products
• Maintain accurate records and documentation of testing




• Write Certificates of Analysis and other reports
• Oversee calibration and maintenance of testing equipment
• Cooperate with contract laboratories for testing coordination

Requirements:
• College Diploma or equivalent in Chemistry, Biotechnology
• 1-3 years in laboratory testing with relevant methodologies
• Skills in technical report writing and document management
• Excellent communication in English—both oral and written
• Ability to lift weights up to 23 kilograms

Apply your passion for quality control at AtomVie and contribute to advancing pharmaceuticals.
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📌 Quality Control Analyst in Quality Assurance (Ontario)
🏢 AtomVie Global Radiopharma
📍 Ontario