Bausch Health is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what we hope it will become.
The Regulatory Affairs – CMC Senior Director independently manages all regulatory CMC aspects of assigned Bausch Health Company products throughout their lifecycle. This includes Brand, Generics, OTC/Nutritionals, Dietary Supplements and Medical Devices. The Senior Director is responsible for the regulatory CMC strategy of submissions for all products under his/her responsibility as well as managing interactions with regulatory authorities on CMC issues.
Formulate, lead and drive CMC regulatory strategy for development and marketed products. Lead and drive all CMC submission activities (planning, authoring, reviewing, coordination, submission). Lead FDA or other Health Authority interactions on CMC issues.