Global CMC Regulatory Consultant (Senior)

A global regulatory affairs firm seeks a CMC Regulatory Affairs Senior/Consultant in Little Rock, Arkansas. The ideal candidate will provide regulatory strategy input for both small-molecule and biologic products and prepare necessary documentation for FDA and EMA submissions. With 4-6 years of experience preferred for Consultant roles and strong skills in regulatory documentation and process optimization, this position offers the opportunity to lead cross-functional collaborations and ensure compliance throughout product development. Candidates in the Eastern Time Zone are preferred. #J-18808-Ljbffr