Executive Director, Regulatory CMC – London Area (Hybrid) Our client, a mid-sized pharmaceutical company, are looking for an Executive Regulatory CMC Director (Small molecule focus) with a passion for leadership, driving strategy, ensuring compliance with EMA and FDA regulations, whilst fostering innovation and operational excellence. The Client The company is based in the London area and cover a number of therapeutic areas in small and large molecule products. They are dedicated to developing cutting-edge therapies that improve lives, have a strong global footprint, and are committed to regulatory excellence and delivering high-quality products to patients worldwide. The Role As Executive Director of Regulatory CMC, you will: Lead CMC regulatory strategies for global submissions (EMA, FDA, and beyond). Oversee the preparation and review of regulatory submissions (IND, NDA, BLA, MAA), as well as post approval activities. Drive collaboration with cross-functional teams, ensuring compliance and efficiency in drug development. Provide strategic guidance on CMC regulatory matters, shaping the regulatory landscape for the company’s pipeline. Represent the company in regulatory agency interactions, influencing outcomes in alignment with business goals. Experience Proven leadership experience in Regulatory CMC within the pharmaceutical industry. Expert knowledge of EMA and FDA regulatory requirements. Strong background in small molecule drug development. Exceptional communication and stakeholder management skills. Ability to drive innovation while ensuring regulatory compliance. To apply, please contact me at rhi@greenlsr.com