Hybrid Regulatory Affairs I (CMC/CTD) – 6 Mo Contract

A reputable technology-solutions firm is seeking an individual for a 6-month hybrid role in North Chicago. Responsibilities include managing activities for marketed product variations, authoring regulatory documentation, and collaborating with internal departments. Candidates should have at least 1-2 years of pharmaceutical experience and a BA/BS in Chemical or Biological Sciences. This position requires excellent communication skills and the ability to manage multiple projects simultaneously. #J-18808-Ljbffr