Associate, QC Analytical Cell Therapy - Summit West NJ
About The Position
The Associate performs testing of in-process, final product, and stability samples according to Bristol Myers Squibb policies, standards, procedures, and global regulatory and cGMP requirements. The role supports the Quality Control Analytical department at BMS’s CAR T Manufacturing facility in Summit, New Jersey. The Associate may also support data verification and GMP documentation review. The schedule is Wednesday through Saturday, 6:30 a.m. to 4:30 p.m. The position involves laboratory work, including frequent pipetting and work in a biological safety cabinet, handling laboratory materials and chemicals, and using required personal protective equipment. The Associate reports to a Manager or Senior Manager, QC Analytical.
Requirements
- Ability to accurately and completely understand and follow procedures.
- Ability to apply scientific principles to analytical testing and proper use of laboratory equipment.
- Ability to communicate effectively with peers and management about 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.
- Bachelor’s degree preferred in science; an associate degree with an equivalent combination of education and work experience may be considered.
- 0–2+ years of relevant analytical testing or QC experience, or an equivalent combination of education and experience; preferably in a regulated environment.
- Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.
- Ability to lift up to 45 lbs at floor and waist height (commonly under 20 lbs), lift up to 10 lbs overhead, and push or maneuver carts to transport materials.
- Ability to operate scissor lift carts requiring 15–20 lbs of initiation force.
- Ability to perform frequent pipetting and laboratory tasks within a biological safety cabinet, including prolonged seated work.
- Ability to independently don, doff, and wear required PPE during the work shift, including cryogenic gloves as needed.
- Ability to safely handle chemical disinfectants, flammable materials, and hazardous chemicals.
- Ability to use step stools to reach and handle materials.
Nice To Haves
- Prior experience in cell and molecular biology techniques, such as cell-based assays, flow cytometry, qPCR, or aseptic technique.
Responsibilities
- Perform routine testing of in-process, final product, and stability samples.
- May review GMP documentation and perform data verification.
- Support document revisions, projects, CAPA and deviation/investigation-related tasks, and continuous improvement efforts.
- May train analysts on general job duties.
- Perform other tasks as assigned.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
