cGMP Technical Writer – Operations & Documentation

A pharmaceutical company in Nashville is seeking a Technical Writer to coordinate and complete technical documentation in a cGMP environment. Responsibilities include the revision of SOPs, management of change controls, and collaboration with Quality Assurance. The ideal candidate has 2+ years of experience, strong communication skills, and proficiency with technical writing in a fast-paced environment. This role supports R&D Scientists in product development experiments and requires adaptability to change. #J-18808-Ljbffr