Contribute to critical quality assurance initiatives with AtomVie Global Radiopharma as a Quality Assurance Systems Associate. Focus on GMP compliance to elevate standards in radiopharmaceutical production.
In this key role, you will enhance quality assurance processes, ensure adherence to regulations, and oversee documentation. Collaborating with diverse teams, your responsibilities include conducting audits and providing training to uphold high production standards. Your expertise will be pivotal in supporting both internal regulations and compliance initiatives.
Key Responsibilities:
• Monitor compliance of quality systems effectively
• Manage change controls and track non-conformance
• Lead audits and compile crucial performance metrics
• Support regulatory audits and track follow-up actions
• Mentor QA team on compliance best practices
Requirements:
• Post-secondary education in a relevant field
• 3 to 5 years of GMP experience needed
• Familiarity...