Global CMC Regulatory Lead for Biologics Submissions

An established industry player is seeking a skilled regulatory professional with a strong background in CMC regulations and drug development. In this role, you will participate in the development of regulatory strategies for biologics submissions and prepare essential documentation for health authority interactions. Your expertise in FDA, EMA, and ICH guidelines will be crucial as you work on complex projects within cross-functional teams. This position offers the opportunity to make a significant impact in the pharmaceutical industry while developing your skills in a collaborative environment. If you are passionate about regulatory affairs and eager to contribute to innovative drug development, this is the perfect opportunity for you. #J-18808-Ljbffr