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.
We are looking to fill the Regulatory CMC Technical Writer – Cell Therapy position at Bristol Myers Squibb in Milltown, NJ, United States. If your experience matches this role, we encourage you to apply. All applications are reviewed carefully by our team. The position is based in Milltown, NJ, United States.