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
Robust understanding of cGMP and quality assurance processes Contribute to the success of Apotex by enhancing equipment qualification processes and ensuring compliance.