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

Requirements