Apply GLP and GCP expertise as a Quality Control Reviewer supporting Sample Management documentation and audits. This position requires French and English fluency.
The Quality Control Reviewer oversees documentation quality within the Sample Management team at Altasciences. You will perform audits, address QA citations, and support compliant sample management and glass washing procedures. The work requires regulatory knowledge, careful organization, and strong written and oral communication.
Key Responsibilities:
- Perform 100% quality control on Sample Management documentation
- Conduct audits, execute reviews, and write audit reports
- Complete forms and documentation for deviations and non-conformance
- Archive records and respond to QA citations
- Review SOPs and training materials for accuracy
Requirements:
- High school diploma or higher in health sciences
- At least three years of relevant experience
- In-depth knowledge of FDA-GLP, GCP, and TPD regulations
- Fluency in French and English
- Strong organizational, leadership, and problem-solving skills
Bring detail-oriented quality control, regulatory knowledge, and bilingual communication to Altasciences Sample Management documentation and audits.
Quality Control Reviewer Sample Management in Laval employer: Altasciences
Altasciences is an exceptional employer that fosters a collaborative and passionate work environment, where every team member plays a vital role in advancing healthcare solutions. With a strong commitment to employee development, competitive benefits including health insurance and retirement plans, and a focus on diversity and inclusion, Altasciences offers meaningful career opportunities in the vibrant region of Quebec. Join us to make a significant impact on global health while enjoying a supportive workplace culture that values integrity and excellence.
