Become a pivotal member of AtomVie Global Radiopharma as a Quality Assurance Associate Systems. Focus on GMP compliance and quality assurance tasks to enhance the production of life‑changing radiopharmaceuticals.

In this role, you will support quality assurance initiatives, ensuring compliance with internal and external regulations. Collaborating with various teams, you will oversee quality documentation, conduct audits, and lead training sessions to maintain high standards in radiopharmaceutical production and development.

Key Responsibilities

• Monitor ongoing compliance of quality systems
• Manage change controls and non‑conformance tracking
• Lead audits and compile performance metrics
• Support regulatory audits and follow‑up activities
• Mentor QA staff on compliance best practices

Requirements

• Post‑secondary education in a relevant field
• 3 to 5 years of GMP experience required
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