Elevate your career at Apotex as a QAIP Associate focused on sterile manufacturing oversight. This role entails proactive quality management and compliance with GMP in a pharmaceutical setting.

As a QAIP Associate at Apotex, you will provide critical quality oversight on the production floor to ensure adherence to Valuable Manufacturing Practices (GMP) and established Standard Operating Procedures (SOP). Your expertise in aseptic practices and contamination control will be essential in maintaining high production standards. With a focus on mentorship and collaboration, you will guide production staff and ensure compliance across operations.

Key Responsibilities:



• Provide real-time quality oversight on the production floor • Verify sterile manufacturing processes and line setups • Conduct routine inspections of production and packaging areas • Lead deviation investigations and implement CAPA • Review batch records ensuring data integrity

Requirements: • Bachelor’s degree or relevant diploma in a related discipline • 5+ years in the pharmaceutical industry • 3+ years in sterile manufacturing environments • Strong knowledge of GMP and FDA requirements • Effective communication skills in English

Advance your QAIP expertise and drive quality standards in sterile manufacturing at Apotex. #J-18808-Ljbffr

📌 QAIP Associate in Sterile Manufacturing (Richmond Hill)
🏢 Apotex
📍 Richmond Hill