Chemical Process Development Technician - Pharma Analytics

Bristol-Myers Squibb Co; New Brunswick (NJ); On-site; USD 50,000 - 66,000; Full time

Benefits offered by this job

Medical, pharmacy, dental and vision

Wellbeing program (Living Life Better)

401(K)

Disability & Life Insurance

Travel protection

Job summary

Bristol Myers Squibb is seeking a Permanent Pharmaceutical Development Technician for the New Brunswick site. The PDT will perform tests and assays on in-process samples using HPLC, GC, spectrophotometers and related lab equipment, while ensuring GLP/GMP compliance and proper documentation under supervision.

Qualifications include an Associate’s Degree in life sciences or 5 years of related experience, proficiency with lab equipment, and the ability to work extended hours.

Qualifications

• Minimum of an Associate’s Degree in the life sciences or 5 years related work experience in bulk fine chemicals, bulk API or petrochemical analysis.
• 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 using a variety of test equipment (HPLC, GC, spectrophotometers, Karl Fischer apparatus).
• Maintains laboratory documentation and equipment in compliance with GLP & GMP standards and regulations.
• Assists in development and validation of analytical methods under supervision.
• Some projects may require work in potent compound/containment areas following established procedures.

Education

Associate’s Degree in Life Sciences

Tools

HPLC

GC

Spectrophotometers

Karl Fischer apparatus

Job description

Bristol Myers Squibb is seeking a Permanent Pharmaceutical Development Technician for the New Brunswick site. The PDT will perform tests and assays on in-process samples using HPLC, GC, spectrophotometers and related lab equipment, while ensuring GLP/GMP compliance and proper documentation under supervision.

Qualifications include an Associate’s Degree in life sciences or 5 years of related experience, proficiency with lab equipment, and the ability to work extended hours.