GMP Deviation Writer (3-6 Month Contract)

A leading biopharmaceutical contract development organization is seeking a Quality Control Deviation Writer for a 3-6 month contract. The role involves investigating, writing, and resolving GMP deviations while ensuring compliance with regulatory requirements. Candidates should have a Bachelor's degree in a scientific discipline and a minimum of 3 years' experience in technical writing or deviation investigation. Strong knowledge of GMP regulations and excellent communication and organizational skills are essential. Join a collaborative team in advancing medicine to save lives. #J-18808-Ljbffr