Lead regulatory quality oversight in Global Medical Affairs as an Associate Director at AstraZeneca. Your expertise in risk management and compliance will ensure adherence to high-quality standards.
In this critical role, you will oversee the governance, risk, and control program, focusing on regulatory quality within Global Medical Affairs. With over 10 years of experience in the pharmaceutical industry and a quality-related role for at least 4 years, you will engage with various functions, including Global Patient Safety and R&D Quality, to promote consistent quality execution across the board.
Key Responsibilities:
• Develop and enhance regulatory quality programs for Medical Affairs
• Represent the department in regulatory forums and inspections
• Foster communication about quality initiatives across functions
• Incorporate risk management processes with subject matter experts
• Ensure robust GxP training for Medical Affairs personnel
Requirements:
• 10+ ...