Join Teva as a Quality Assurance Specialist II, focusing on quality oversight for imported pharmaceutical products in Scarborough, Ontario.

Your role will involve critical assessments and collaboration with partners. This role requires a solid background in the pharmaceutical sector, with at least three years of experience in quality assurance. You will be responsible for leading investigations into quality deviations and approving documentation related to product launches. Your efforts will support compliance initiatives while maintaining robust relationships with stakeholders. Key Responsibilities:

- Conduct thorough reviews of stability reports and transfer protocols
- Evaluate and close change controls and deviations
- Collaborate with suppliers to ensure GMP compliance
- Prepare monthly and quarterly quality trend reports
- Manage quality-related documentation and annual product reviews Requirements:
- Bachelor’s degree in relevant scientific field
- Minimum of 3 years of QA experience
- Expertise in GMP-regulated environments
- Familiarity with quality management systems
- Excellent problem-solving and analytical skills Lead initiatives to maintain product excellence and regulatory standards at Teva.

📌 Teva Quality Assurance Specialist (Toronto)
🏢 Tevapharm
📍 Toronto