Sterile Operations Tech Writer - cGMP & Batch Records
Synerfac Technical Staffing
Synerfac Technical Staffing is seeking a Technical Writer, Sterile Operations for a pharmaceutical CDMO client in New Jersey. You will develop, revise, and maintain SOPs, FRMs, MBRs, and logs covering sterile processes from bulk formulation to autoclaving and cleaning, ensuring compliance with cGMP and DEA-adjacent requirements. The role collaborates with Operations, Quality, Validation, and Engineering SMEs; you will write clear investigative narratives for deviations, support CAPA activities, #J-18808-Ljbffr Synerfac Technical Staffing
Vacancy posted 1 day ago
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