Ensure compliance in radiopharmaceutical production with AtomVie as a Quality Assurance Systems Associate. This role is focused on maintaining GMP standards and effective quality systems in Hamilton, Ontario.

As a key player in the Quality Assurance team, you will interact with various stakeholders to uphold regulatory requirements and internal procedures. You will manage non-conformances, conduct internal audits, and prepare quality performance reports. Your expertise will ensure that the quality systems adapt to meet current regulations effectively.

Key Responsibilities:
• Monitor compliance of quality systems with regulations
• Manage and track non-conformance and CAPA systems
• Lead job board meetings and internal audits
• Prepare monthly quality performance metrics
• Train new employees in GMP practices

Requirements:
• Post-Secondary Education in a related field
• 3 to 5 years’ experience in GMP envir...