Analytical Method Writer – GMP QC Docs (Onsite, 3–6 mo)

A biopharmaceutical company in Bristol, PA, is seeking an Analytical Method Development Technical Writer for a contract role. Responsibilities include drafting analytical methods and QC protocols, collaborating with experts, and preparing documentation for reviews. Candidates should have a relevant scientific degree and at least 5 years of experience in a GMP environment. This position offers a competitive hourly rate of $35-$40 and various benefits, making it a great opportunity for skilled technical writers. #J-18808-Ljbffr