As the key figure overseeing product quality and harmonisation of our Quality Management System, you will play a pivotal role in ensuring our manufacturing processes meet the highest standards. Reporting directly to the Senior Director of Quality and
Accountable for setting and executing the site Quality Assurance strategy, ensuring sustained cGMP compliance, regulatory readiness, and a strong quality culture across manufacturing operations. This role serves as a senior member of the site leadership
Lead and oversee all Regulatory Affairs activities across the European Union, ensuring regulatory compliance, lifecycle management, and strategic regulatory support for existing and new products. Drive regulatory strategy, manage the team
You will provide senior statistical leadership across clinical and translational programs. This is a hands-on, high-autonomy role with strong matrix leadership: you will shape quantitative strategy, guide study design and analysis oversee complex
Leads and handles all Quality & Compliance related programs supporting manufacturing, testing and release. This includes the clinical and commercial manufacturing and testing in full compliance with all J&J and governmental environmental, health, safety,
The role is responsible for ensuring Gilead’s medical affairs activities comply with pharmaceutical regulations and laws and providing expertise on drug safety and medical topics. Provides medical expert advice to ensure accuracy of data to support