Pharmaceutical Development Technician
Bristol Myers Squibb · New Brunswick, NJ
CMCFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Bristol Myers Squibb seeks a Pharmaceutical Development Technician for the Kilo Lab in New Brunswick, NJ. The role involves maintaining lab cleanliness, assisting scientists with material handling, operating manufacturing equipment, executing unit operations, and ensuring compliance with cGLP and cGMP regulations in API and ADC production.
What they're looking for
- Two-year Associate Degree in science or equivalent educational background
- Laboratory experience, preferably in Active Pharmaceutical Ingredient manufacturing
- cGMP experience in pharmaceutical industry highly desired
- Proficiency with computer systems including SAP, DeltaV, and Microsoft Office
- Strong attention to detail and commitment to safety and compliance
- Ability to work independently and collaborate effectively with scientists and teams
- Excellent oral communication skills and adaptability to learn new technologies
What you'll be doing
- Support Kilo Lab Operations team with process scale-up activities and manufacturing operations
- Set up, operate, sample, and clean process and utility equipment such as reactors and dryers
- Execute and document unit operations including reactions, filtrations, distillations, and drying
- Stage, store, and manage raw materials, intermediates, products, and hazardous waste
- Record data in compliance with cGLP and cGMP regulations and recognize abnormal operating conditions
Compensation$42.04 per hour
Privacy & handoff
This role links to Bristol Myers Squibb's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.