Regulatory CMC Technical Writer – Cell Therapy

A leading biopharma company in New Jersey is seeking a Technical Writer and Document Specialist to support regulatory submissions for a late-stage clinical cell therapy program. Responsibilities include co-authoring scientific content, managing submission logistics, and ensuring document clarity. Candidates should have a Bachelor's degree in Biology and experience in regulatory documentation. This role requires effective collaboration across technical teams and offers a contract position with a starting hourly rate of $38 to $41.96, with 50% onsite work required. #J-18808-Ljbffr