Quality Assurance Systems Associate

Position: Quality Assurance Systems Associate Role
Become a key player at Atom Vie Global Radiopharma Inc. as a Quality Assurance Associate Systems. This position focuses on maintaining GMP compliance in the production of essential radiopharmaceuticals.

As a Quality Assurance Associate, you will be responsible for ensuring that quality systems align with regulatory standards and operational needs. Collaborating with stakeholders and leading audits will be essential in this role, allowing you to contribute significantly to the quality assurance efforts r expertise will help to uphold the company's commitment to providing high-quality radiopharmaceuticals.

Key Responsibilities:

• Ensure compliance of quality systems with regulations

• Conduct and participate in internal audits

• Manage non-conformances and CAPA resolutions

• Prepare and report on quality performance metrics

• Provide GMP training and guidance to staff

Requirements:

• Post-secondary degree in relevant discipline

• Minimum 3 years in a GMP setting

• Knowledge of quality systems and documentation

• Familiarity with Health Canada and FDA guidelines

• Strong organizational and teamwork capabilities

Elevate quality assurance practices at Atom Vie and support compliance in radiopharmaceutical production.
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