Senior GxP Deviation & Investigation Specialist

A biotechnology firm located in North Carolina is seeking a qualified individual to perform investigations and write deviation reports for its technical operations. Applicants should hold a Bachelor's degree and possess 3-5 years of relevant experience, preferably in a regulated GxP environment. Adeptness in technical writing and understanding of cGMP regulations are essential. Responsibilities include coordinating evaluation of discrepancies and updating standard operating procedures as needed. This position may require a 10-hour work schedule with overtime as necessary. #J-18808-Ljbffr