PDT Process Research & Development

Role: Pharmaceutical Development Technician in Process Research & Development at Bristol Myers Squibb, supporting GMP-compliant lab activities related to active pharmaceutical ingredient manufacturing. Responsibilities include maintaining documentation, inventory management, safety compliance, calibration and maintenance of analytical and process equipment, and executing preparative and unit operations such as distillation, crystallization, and filtration. Qualifications: Associate Degree in science or equivalent; experience in a laboratory setting, especially with API manufacturing and cGMP, is highly desired. Skills: proficiency with lab instruments (HPLC, GC, UV systems), computer systems (SAP, DeltaV, MS Office), attention to detail, and strong communication. High-Value: focus on GMP processes, lab instrumentation, chemical/radiological/biological hazard handling, and compliance with safety and regulatory standards. Work setup: onsite, 7:00 am - 3:30 pm shift, hourly union position, safety protocols for handling hazardous agents, with a pay rate of $42.04/hr.