Pharmaceutical Development Technician
Bristol Myers Squibb
September 17, 2026
Full-time
On-site
New Brunswick, NJ
Operations
Role: Pharmaceutical Development Technician in the Kilo Lab at Bristol Myers Squibb, supporting manufacturing of Active Pharmaceutical Ingredients (API) and Antibody-Drug Conjugates (ADC) for clinical and non-clinical use. Responsibilities include maintaining clean and safe lab environments, setting up and operating process equipment (reactors, dryers, mills, etc.), executing unit operations such as reactions and filtrations, and collecting data per cGLP and cGMP standards. The position involves handling hazardous materials, working in containment areas, and ensuring compliance with safety and regulatory protocols. Qualifications: Associate Degree in science or equivalent, with practical lab experience, preferably in API manufacturing, and cGMP familiarity. Skills include operating manufacturing equipment, attention to detail, computer proficiency (SAP, DeltaV, MS Office), and effective communication. High-value biopharma specifics: focus on API and ADC production, adherence to GMP, and work within specialized containment environments. Work setup: On-site at New Brunswick, with a shift from 7:30 am to 4:00 pm; union position with pay rate of $42.04/hour; compliance with safety procedures regarding hazardous agents and PPE use.