Ensure GMP compliance and maintain data integrity as a QA Data Reviewer Associate at AtomVie Global Radiopharma. Contribute to the verification of analytical results and adherence to high standards in a collaborative environment.
AtomVie 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 AtomVie's mission to transform healthcare through rigorous data review and compliance.
Associate QA Data Reviewer at AtomVie in Hamilton employer: AtomVie Global Radiopharma Inc.
At AtomVie Global Radiopharma, we pride ourselves on being an exceptional employer that fosters a culture of innovation and collaboration. As the Director of Quality Assurance, you will not only lead critical quality initiatives but also benefit from our commitment to employee growth through continuous training and development opportunities. Located in a dynamic environment, our team is dedicated to making a meaningful impact on patient lives while enjoying a supportive workplace that values excellence and integrity.
Contact Details:
AtomVie Global Radiopharma Inc. Recruitment Team
