Regulatory Bioprocess Technical Writer (GMP/Pharma)

A leading IT staffing company is seeking a detail-oriented individual to assist with regulatory documents and reports. The ideal candidate will have excellent communication skills and experience in technical writing, particularly in the pharmaceutical or bioprocess areas. You will support R&D teams, create regulatory drafts, and utilize document management systems. This position is primarily based in Andover, MA, with flexibility for Chesterfield, MO as a secondary location. #J-18808-Ljbffr