Ensure GMP compliance and maintain data integrity as a QA Data Reviewer Associate at Atom Vie Global Radiopharma. Contribute to the verification of analytical results and adherence to high standards in a collaborative setting.

Atom Vie is seeking a QA Data Reviewer Associate to uphold GMP compliances and data integrity principles in the Analytical Development and Quality Control labs. The role involves reviewing data from various laboratory equipment and ensuring adherence to protocols and Standard Operating Procedures.

Ideal candidates should possess a strong understanding of Good Documentation Principles and related regulations in the pharmaceutical field.

Key Responsibilities:

- Review analytical data from diverse laboratory equipment
- Verify the completeness and integrity of testing records




- Ensure compliance with test methods and SOPs
- Conduct periodic audit trail reviews of laboratory methods
- Guide laboratory staff on data integrity and GDP principles

Requirements:

- Post-secondary education in a related field
- Minimum 5 years' experience in analytical data review
- Experienced in a GMP environment
- Proficiency in written and spoken English
- Detail-oriented with excellent communication skills

Become a vital part of Atom Vie’s mission to transform healthcare through rigorous data review and compliance.

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📌 Associate QA Data Reviewer at AtomVie (Canada)
🏢 AtomVie Global Radiopharma
📍 Canada