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Monitors CSR’s performance on a daily basis, by taping, listening to, reviewing and evaluating calls...

• Support complex and higher exposure quality and compliance activities
• Provide guidance and risk assessment on GCP, GVP, MDR, and IVDR compliance issues
• Serve as advisor and subject matter expert for Quality and Compliance-related processes
• Lead deviation management and process management activities

• Support and assist PDRL colleagues to accomplish tasks in meeting deadlines to achieve the project, team and departmental goals
• Gradually assume responsibility for agreed tasks under supervised coaching and tutoring
• Prepare regulatory labeling packages in collaboration with the other teams

• Ensuring collection, reporting, and handling of safety information with high integrity
• Driving continuous improvement and simplification of Pharmacovigilance processes
• Collaborating with global experts and external vendors in a complex matrix environment