Pharmaceutical Development Technician – Chemical Process Development

Bristol Myers Squibb • New Brunswick, NJ

9d • Onsite

About The Position

The Pharmaceutical Development Technician (PDT) - Chemical Process Development performs tests and assays for in-process samples utilizing a variety of test equipment including High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), spectrophotometers, Karl Fischer apparatus, among others. Laboratory responsibilities include the preparation and proper labeling of standards, samples, reagents, glassware storage and cleaning, and general laboratory housekeeping. The PDT maintains laboratory documentation and equipment under strict compliance with GLP & GMP standards as well as federal, state and local regulations. The PDT also assists in the development and validation of analytical methods under the direct supervision of a scientist or laboratory supervisor. Some projects require working in potent compound/containment areas using established procedures.

Requirements

• A minimum of an Associates Degree in the life sciences (Chemistry, Biology, etc.) or 5 years related work experience in bulk fine chemicals, bulk API or petrochemical analysis in a manufacturing or R&D environment is required.
• Must be proficient in the use and operation of all related laboratory, analytical, and computer equipment.
• Must perform tasks with high degree of accuracy and attention to detail.
• Must be a team player who can work in a collaborative environment.
• Must be able to work extended work hours as requested.

Responsibilities

• Performs tests and assays for in-process samples utilizing a variety of test equipment including High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), spectrophotometers, Karl Fischer apparatus, among others.
• Prepares and properly labels standards, samples, reagents.
• Manages glassware storage and cleaning, and general laboratory housekeeping.
• Maintains laboratory documentation and equipment under strict compliance with GLP & GMP standards as well as federal, state and local regulations.
• Assists in the development and validation of analytical methods under the direct supervision of a scientist or laboratory supervisor.
• Works in potent compound/containment areas using established procedures for some projects.

Benefits

• Medical, pharmacy, dental and vision care.
• Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP).
• Financial well-being resources and a 401(K).
• Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree