Join Apotex as an Equipment Qualification Expert, focusing on planning and executing critical qualification activities for pharmaceutical manufacturing. Play a vital role in ensuring compliance with regulatory requirements and company standards.
In this vital position, you will be responsible for developing and executing installation, operation, and performance qualification protocols for diverse equipment and facilities. You are expected to coordinate qualification activities while training team members and authorship of comprehensive documentation that ensures objectivity and compliance.
Key Responsibilities:
• Develop qualification protocols compliant with regulatory standards
• Conduct training sessions on equipment qualification
• Manage and document equipment qualification verification




• Collaborate with cross-functional teams to achieve goals
• Review and initiate documentation changes as necessary
Requirements:
• Degree or equivalent in Engineering or pharmaceutical technology
• At least 5 years’ experience in pharmaceutical qualification
• Proficient in Microsoft Office Suite and validation tools
• Excellent problem-solving and communication abilities
• Solid understanding of cGMP and quality assurance processes
Contribute to the success of Apotex by enhancing equipment qualification processes and ensuring compliance.
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📌 Apotex Equipment Qualification Expert Role (Brantford)
🏢 APOTEX
📍 Brantford