Whether you’re a detail-oriented professional passionate about regulatory affairs and eager to contribute to successful document submissions, a seasoned Regulatory CMC professional with experience implementing CMC strategies for Biological and/or vaccines projects, we invite you to apply for this exciting opportunity on our team. […]
Play a crucial part in coordinating various Global regulatory submissions ie. INDs, IMPDs, BLA/NDS/MAA post-approval commitments, Annual Reports, and Responses to regulatory authority questions. […]
Support the team in conducting regulatory assessments of manufacturing...