Quality Control Analytical Associate

1w1 week ago

Bristol Myers Squibb

Summit, US · Full-time · $72,000 – $88,000

About this role

Working at Bristol Myers Squibb means challenging, meaningful, life-changing work that transforms patients' lives and careers. As Quality Control Analytical Associate, support testing for in-process, final product, and stability samples. Assist with documentation, deviations, investigations, and continuous improvement efforts while reporting to QC management.

Perform routine testing of in-process, final product, and stability samples using analytical techniques. Review GMP documentation and perform data verification for accuracy. Support document revisions, projects, CAPAs, deviations, investigations, and continuous improvement tasks.

Operate in a fast-paced team environment, meeting deadlines and prioritizing work effectively. Communicate with peers and management on task completion, roadblocks, and needs. Train analysts on general job duties as required.

Grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. Enjoy balance and flexibility in the work environment with resources for personal and professional goals. Apply even if your background does not perfectly match the role.

Requirements

Ability to accurately and completely understand and follow procedures
Apply scientific principles to analytical testing and proper use of laboratory equipment
Communicate effectively with peers and management regarding task completion, roadblocks, and needs
Attention to detail and demonstrated organizational skills
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work
0-2+ years of relevant analytical testing or QC experience, preferably in a regulated environment
Demonstrated experience with basic laboratory techniques and safety practices
Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique) preferred