Elevate your career as an Equipment Qualification Specialist at Apotex in Toronto. Focus on qualification activities, regulatory compliance, and training while supporting creative healthcare solutions.

In this specialist role, you will be pivotal in planning and executing qualification protocols for production equipment and facilities. Your expertise will ensure adherence to cGMP requirements, while you document specifications, develop tools, and lead training sessions. Collaborating with various departments, you will contribute to Apotex's mission of improving access to pharmaceuticals.

Key Responsibilities:
• Author qualification protocols for equipment and facilities
• Document critical parameters and maintenance requirements




• Coordinate Equipment and Facility Qualification activities
• Provide training on qualification topics to teams
• Participate in audits and improvement initiatives

Requirements:
• Degree in Engineering or Pharmaceutical Technology
• Minimum 5 years of pharmaceutical industry experience
• Robust knowledge of qualification concepts and GMP
• Excellent organizational and communication skills
• Proven experience with Microsoft Excel and Word

Utilize your skills to drive qualification processes and maintain compliance at Apotex.
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📌 Equipment Qualification Specialist At Apotex Ontario (Canada)
🏢 APOTEX
📍 Canada