Join AtomVie Global Radiopharma as the Quality Assurance Director. Lead initiatives to ensure compliance with regulations such as Health Canada and FDA while driving a culture of quality across operations.

Reporting to the VP of Quality, you will spearhead the quality assurance program for AtomVie’s cutting-edge radiopharmaceutical products. This position includes collaborating with teams across Product Development and Manufacturing, enhancing robust quality management systems, and overseeing the transition from clinical to commercial GMP activities. Your efforts will support growth through world-class QA operations.

Key Responsibilities:
• Monitor day-to-day QA operations and implement improvements
• Conduct audits and provide oversight for sterile manufacturing




• Act as the QA contact for all client-related projects
• Host regulatory audits while coordinating corrective actions
• Maintain current knowledge of industry regulations

Requirements:
• Doctorate or Masters in relevant scientific discipline
• 15 years’ experience in pharmaceutical QA
• At least 5 years in a managerial role
• Strong experience in sterile manufacturing
• Proven track record of implementing quality systems

Utilize your extensive QA experience to elevate AtomVie’s commitment to healthcare excellence.
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📌 Quality Assurance Director Role at AtomVie (Ontario)
🏢 AtomVie Global Radiopharma
📍 Ontario