QC Analytics Specialist - In-Process & Stability Testing

Bristol-Myers Squibb Co; Summit (NJ); On-site; USD 72,000 - 88,000; Full time

Job summary

Bristol Myers Squibb is seeking a Specialist, QC Analytical to support in-process, final product, and stability testing. The role emphasizes data review, GMP documentation, and collaboration with cross-functional teams in a fast-paced environment.

Responsibilities include method transfers, deviations investigations, CAPA, and ongoing improvements while training junior analysts. Shift is Wed–Sat, 1:30pm–11:30pm, located in Summit, NJ.

Qualifications

• Bachelor's degree or equivalent; science preferred.
• At least 2 years of analytical testing or QC experience in a regulated environment.
• Experience with cell and molecular biology techniques (e.g., flow cytometry, qPCR, ELISA) is a plus.

Responsibilities

• Perform routine QC testing of in-process, final product, and stability samples.
• Review data and GMP documentation; support method transfer/verification activities.
• Assist with deviations, investigations, CAPA, and continuous improvement tasks.
• Train analysts on general duties and ensure timely completion of tasks.

Skills

GMP knowledge

LIMS

ELN

Problem solving

Communication

Technical docs

Education

Bachelor's degree or equivalent

Tools

LIMS

ELN

Job description

Bristol Myers Squibb is seeking a Specialist, QC Analytical to support in-process, final product, and stability testing. The role emphasizes data review, GMP documentation, and collaboration with cross-functional teams in a fast-paced environment.

Responsibilities include method transfers, deviations investigations, CAPA, and ongoing improvements while training junior analysts. Shift is Wed–Sat, 1:30pm–11:30pm, located in Summit, NJ.