Pharmaceutical Development Technician – Chemical Process Development

Scorpion Therapeutics; New Brunswick (NJ); On-site; USD 45,000 - 65,000; Full time

Job summary

Bristol Myers Squibb is seeking a Pharmaceutical Development Technician in Chemical Process Development onsite in New Brunswick. The role focuses on performing analytical tests and assays for in-process samples using HPLC, GC, spectrophotometry, and Karl Fischer.

Responsibilities include sample prep, labeling, lab housekeeping, and maintaining GLP/GMP documentation while supporting method development and validation in potent compound areas.

Qualifications

• Associate degree in life sciences or 5+ years of chemical analysis experience.
• Proficiency with lab and analytical equipment and strong attention to detail.
• Team-oriented and able to work extended hours in a regulated environment.

Responsibilities

• Prepare samples, label reagents and standards, and maintain documentation in GLP & GMP compliance; support method development and validation in potent areas.

Skills

Analytical testing

Detail-oriented

Team player

Education

Associate degree in life sciences

5+ years chemical analysis experience

Tools

HPLC

GC

Spectrophotometry

Karl Fischer

GLP/GMP knowledge

Job description

Role

Pharmaceutical Development Technician in Chemical Process Development at Bristol Myers Squibb, focused on performing analytical tests and assays for in-process samples using techniques such as HPLC, GC, spectrophotometry, and Karl Fischer.

Responsibilities

• sample preparation, reagent and standard labeling, lab housekeeping, and maintaining documentation in compliance with GLP & GMP standards; supporting method development and validation, often in potent compound areas.

Requirements

• Associates Degree in life sciences or 5+ years related experience in chemical analysis within manufacturing or R&D, proficiency with lab and analytical equipment, high attention to detail, team-oriented, and able to work extended hours.

High-Value

work involves hazardous agents, operates within regulated GxP environments, and supports pharmaceutical development in a manufacturing/R&D setting.

Work setup

onsite in New Brunswick, with safety procedures to handle hazardous materials.