Job Description
Elevate pharmaceutical standards with Diteba as a Quality Assurance Associate, enforcing compliance with cGMP and GLP regulations in Mississauga. Play a crucial role in quality improvement and regulatory support.
In this position, you will ensure adherence to quality systems and applicable regulations while working in a collaborative workplace. Responsibilities include conducting inspections, preparing protocols, and managing documentation controls. Your expertise in laboratory operations will be vital for successful CAPA completion.
Key Responsibilities
- Enforce compliance with GMP, GLP, and ISO standards
- Conduct self-inspections and identify quality deficiencies
- Support during regulatory inspections and client audits
- Prepare protocols, reports, and review investigations
- Manage training curriculum and maintain records