Elevate your career as a Quality Assurance Associate at AtomVie Global Radiopharma in Hamilton, ON. This onsite role focuses on ensuring GMP compliance in radiopharmaceutical production.

As a key member of the team, you will interface with quality, regulatory, and production departments to uphold stringent compliance standards. The role necessitates monitoring quality systems, managing non-conformances, and leading audits. Your contributions will directly support the development of cutting-edge radiotherapeutics aimed at combating cancer and other diseases.

Key Responsibilities:
• Ensure compliance with regulatory GMP requirements
• Manage and track laboratory investigations and CAPAs
• Prepare quality performance metrics for management
• Lead internal audits and assist in regulatory audits
• Conduct GMP training sessions for new employees

Requirements:
• Degree in Engineering, Chemistry, or related field
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