Pharmaceutical Development Technician
Bristol Myers Squibb
July 01, 2026
On-site
New Brunswick, NJ
Operations
Permanent – Pharmaceutical Development Technician, Analytical Research – 25 (ASO)
Shift: 7 AM–3:30 PM EST | Site: New Brunswick, NJ | Rate: $42.04/hour
Responsibilities
- Carry out assigned laboratory responsibilities, including tests/analysis.
- Assist in development, execution, and validation of analytical methods and routine sample analysis under supervision.
- Work independently on routine pharmaceutical development sample analysis.
- Follow written procedures and/or verbal instructions; execute safely and with quality.
- Prepare and label standards/samples/reagents (including HPLC mobile phases and dissolution media), sort/prepare glassware, collect waste solvents, and maintain lab housekeeping.
- Maintain GLP/GMP and safety-compliant laboratory documentation; make minor repairs/adjustments per IOPs.
- Report anomalies/irregularities; maintain lab notebooks (paper/electronic), capture raw data, calculate results, and submit for review/approval.
- Some projects require high containment work.
Required/Preferred Skills & Qualifications
- Two-year Associate Degree in Science related to pharmaceutical development (or equivalent).
- Proficiency with computer programs/systems.
- Demonstrated competency (after training) with analytical equipment including HPLC, GC, spectrophotometers, IR/Raman, fluorimeters, polarimeters, dissolution instruments, volumetric/gravimetric analyzers, balances, and pH meters, plus automated systems.
- Ability to maintain skills via internal/external training; complete interactive (on-the-job) competency modules and re-training if needed.
Benefits (if applicable)
- Medical/pharmacy/dental/vision; wellbeing support (Living Life Better, EAP); 401(k); disability and life insurance; supplemental health; business travel protection; survivor support.
Application instructions
- If the role doesn’t perfectly match your resume, encourage applying anyway.
Shift: 7 AM–3:30 PM EST | Site: New Brunswick, NJ | Rate: $42.04/hour
Responsibilities
- Carry out assigned laboratory responsibilities, including tests/analysis.
- Assist in development, execution, and validation of analytical methods and routine sample analysis under supervision.
- Work independently on routine pharmaceutical development sample analysis.
- Follow written procedures and/or verbal instructions; execute safely and with quality.
- Prepare and label standards/samples/reagents (including HPLC mobile phases and dissolution media), sort/prepare glassware, collect waste solvents, and maintain lab housekeeping.
- Maintain GLP/GMP and safety-compliant laboratory documentation; make minor repairs/adjustments per IOPs.
- Report anomalies/irregularities; maintain lab notebooks (paper/electronic), capture raw data, calculate results, and submit for review/approval.
- Some projects require high containment work.
Required/Preferred Skills & Qualifications
- Two-year Associate Degree in Science related to pharmaceutical development (or equivalent).
- Proficiency with computer programs/systems.
- Demonstrated competency (after training) with analytical equipment including HPLC, GC, spectrophotometers, IR/Raman, fluorimeters, polarimeters, dissolution instruments, volumetric/gravimetric analyzers, balances, and pH meters, plus automated systems.
- Ability to maintain skills via internal/external training; complete interactive (on-the-job) competency modules and re-training if needed.
Benefits (if applicable)
- Medical/pharmacy/dental/vision; wellbeing support (Living Life Better, EAP); 401(k); disability and life insurance; supplemental health; business travel protection; survivor support.
Application instructions
- If the role doesn’t perfectly match your resume, encourage applying anyway.