Job Description
Join AtomVie Global Radiopharma as a GMP Analytical Chemist, focusing on method validation and quality assurance of radiopharmaceuticals. This role demands expertise in both chemistry and regulatory compliance.
In this position, you will play a crucial role in analytical method development and validation to support our clinical and commercial drug products. Your responsibilities include conducting testing, managing documentation, and ensuring adherence to strict regulatory guidelines. Your work will significantly impact patient outcomes and advance healthcare initiatives.
Key Responsibilities:
• Conduct analytical method development and validation activities
• Perform quality investigations and manage corrective actions
• Write technical documents and prepare client presentations
• Participate in process improvement initiatives
• Maintain laboratory equipment and safety standards
Requirements:
• Relevant Bachelo...
In this position, you will play a crucial role in analytical method development and validation to support our clinical and commercial drug products. Your responsibilities include conducting testing, managing documentation, and ensuring adherence to strict regulatory guidelines. Your work will significantly impact patient outcomes and advance healthcare initiatives.
Key Responsibilities:
• Conduct analytical method development and validation activities
• Perform quality investigations and manage corrective actions
• Write technical documents and prepare client presentations
• Participate in process improvement initiatives
• Maintain laboratory equipment and safety standards
Requirements:
• Relevant Bachelo...
Ready to Apply?
Submit your application today and join our talented team at AtomVie Global Radiopharma Inc..
Submit ApplicationJob Details
- Location hamilton, on
- Job Type Full-time
- Category Engineering
- Posted Date June 01, 2026
- Application Deadline July 11, 2026