Associate, QC Analytical Cell Therapy - Summit West NJ

Military Spouse Corporate Career Network•Summit West, NJ

3d•Onsite

About The Position

The Associate performs testing of in-process, final product, and stability samples in accordance with Bristol Myers Squibb policies, standards, procedures, global regulatory requirements, and cGMP requirements. The role supports the Quality Control Analytical department at the BMS CAR T Manufacturing facility in Summit, New Jersey. The associate may also support data verification and GMP documentation review as needed. The schedule is Wednesday through Saturday, 6:30 a.m. to 4:30 p.m. The role involves laboratory testing and handling biological materials, chemicals, and potentially liquid nitrogen. It requires wearing appropriate personal protective equipment and meeting the described lifting, handling, and laboratory-work demands. The position reports to a Manager or Senior Manager, QC Analytical.

Requirements

Ability to accurately understand and follow procedures.
Ability to apply scientific principles to analytical testing and proper laboratory equipment use.
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 in science preferred; 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 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 and handle 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; work may involve liquid nitrogen and other cryogenically cooled materials.
Ability to use step stools to reach and handle materials.

Nice To Haves

Prior experience with cell and molecular biology techniques, such as cell-based assays, flow cytometry, qPCR, or aseptic technique.
Bachelor’s degree in science.

Responsibilities

Perform routine testing of in-process, final product, and stability samples.
Review GMP documentation and perform data verification as needed.
Support document revisions, projects, CAPA and deviation/investigation-related tasks, and continuous improvement efforts.
Train analysts on general job duties as needed.
Perform other tasks as assigned.