Job Description & How to Apply Below
This coordinator position emphasizes the importance of Good Manufacturing Practices (GMP) and regulatory compliance in the pharmaceutical industry. With responsibilities including site licensing management and quality complaint handling, you'll play a crucial role in ensuring product integrity. Your background in quality assurance will enable you to drive compliance initiatives effectively.
Key Responsibilities:
• Coordinate updates for Drug Establishment and NHP licences
• Record and analyze product quality complaints
• Implement corrective action plans for quality improvements
• Support cross-departmental quality investigations
• Prepare for and participate in regulatory audits
Requirements:
• Bachelor’s Degree in Science or a related discipline
• 3-5 years in Quality Assurance or Quality Control
• Strong communication skills with regulatory agencies
• Knowledge of Health Canada and FDA standards
• Proficient in quality management systems
Apply your quality assurance knowledge at Sun Pharma to make a tangible difference in patient health.
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