At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.
Position Summary
Responsible for supporting QC testing for in-process, final product, and
stability samples, including data review/verification. May assist with
method transfer, documentation, deviations, investigations, and
continuous improvement efforts.
Shift: Wed – Sat, 1:30pm – 11:30pm
Duties/Responsibilities
Perform routine testing of in-process, final product, and stability samples.
Perform testing for method transfer/validation/verification.
Perform data verification, data review and review of GMP documentation for general methods.
May perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
Train analysts on general job duties.
Perform other tasks as assigned.
Qualifications
Specific Knowledge, Skills, Abilities:
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
Knowledge of LIMS, ELN and laboratory data analysis systems preferred.
Problem-solving ability/mentality, technically adept and logical.
Ability to communicate effectively with peers, department management and cross-functional peers.
Experience with writing technical documents preferred.
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
Education/Experience/ Licenses/Certifications:
Bachelor's degree or equivalent required, preferably in science.
2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated
environment.
Demonstrated experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, ELISA, and aseptic technique).
Job Safety Requirements & Essential Physical Demands
Ability to perform lifting tasks up to 20 lbs (9 kg) at floor and waist height. Ability to lift up to 10 lbs (4.5 kg) overhead as well as push or maneuver carts to transport materials between locations.
Ability to perform frequent pipetting and related laboratory tasks within a biological safety cabinet, including extended periods of seated work.
Ability to independently don, doff, and wear required personal protective equipment such as but not limited to lab coat/frock, gloves, safety glasses/face shield for prolonged periods while performing laboratory work.
Ability to safely handle and use chemical disinfectants, flammable materials, and hazardous chemicals.
Work may involve handling of dry ice, liquid nitrogen, and cryogenically cooled materials.
Ability to use step stools while reaching and handling materials.
Ability to work in a Biosafety Level 2 (BSL-2) environment.
The laboratory employee is responsible for performing work safely in accordance with EHSS procedures. This includes identifying and controlling risks, proper use of personal protective equipment (PPE), safe handling of chemicals and biological agents, compliance with waste and emergency procedures, and active participation in training and safety programs.
We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.
Compensation Overview:
Summit West - NJ - US: $34.82 - $42.19per hour
The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully…