Biopharma Technical Writer II — Regulatory Methods, Remote

A leading biopharmaceutical firm is seeking a Technical Writer to join their team. This role involves creating and reviewing technical documents to ensure compliance with regulatory standards. Candidates should have a BS/BA in Life Sciences or Engineering, with a preference for a Master's or PhD. A minimum of 2 years of experience in a cGMP laboratory environment is required. This is a remote opportunity, with a hybrid option available for local candidates in West Point, PA. #J-18808-Ljbffr