Global CMC Regulatory Consultant (Senior)

A global pharmaceutical consultancy is seeking an experienced CMC Regulatory Affairs Senior/Consultant to join its Regulatory Affairs team. The role involves providing regulatory strategy input, preparing CMC documentation for submissions, and collaborating across functions to ensure compliance with global regulatory standards. The ideal candidate has 4–6 years of regulatory experience, excellent analytical skills, and a Bachelor's degree in Pharmaceutical Sciences. Preference will be given to candidates in the Eastern Time Zone. #J-18808-Ljbffr