Quality Assurance Systems Associate at AtomVie

Elevate quality standards as a Quality Assurance Associate Systems at Atom Vie Global Radiopharma. Focus on GMP compliance and maintain robust quality systems in radiopharmaceutical production.

As a Quality Assurance Associate Systems, you'll play a pivotal role in upholding Atom Vie's high-quality benchmarks. Collaborate with stakeholders to manage critical systems like non-conformances and laboratory investigations. Your expertise will be vital for compliance with internal procedures and key regulatory standards.

Key Responsibilities:

• Monitor compliance of quality systems with regulations

• Manage non-conformances and laboratory investigations actively

• Lead change control committee meetings effectively

• Prepare quality performance metrics for management review

• Conduct and report on internal audits thoroughly

Requirements:

• Post-secondary degree in a relevant field

• 3 to 5 years experience in a GMP workplace

• Proficient in quality systems and audits management

• Solid knowledge of Health Canada and FDA regulations

• Excellent communication skills in English

Join Atom Vie to drive quality improvement and compliance initiatives in radiopharmaceutical production.
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