Associate, QC Analytical, Cell Therapy

1010 Celgene - Summit (Corp); New Jersey; Presencial; USD 47.000 - 57.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible Time Off

11 paid holidays

Medical, dental, vision insurance

Disability insurance

Descripción de la vacante

Bristol Myers Squibb is seeking an Associate in Summit, NJ to perform testing of in-process, final product, and stability samples, ensuring compliance with cGMP and regulatory standards. The role engages in data verification and GMP documentation review to support the QC Analytical team in a cell therapy facility.

The ideal candidate has a science background, up to 2 years of analytical/QC experience, and familiarity with lab techniques.

Formación

• Bachelor's degree in science preferred; associate degree with relevant experience may be considered.
• 0-2+ years of analytical testing or QC experience in a regulated environment.
• Experience with basic laboratory techniques and GMP documentation is preferred.

Responsabilidades

• Perform routine testing of in-process, final product, and stability samples.
• May review GMP documentation and perform data verification.
• Support document revision, CAPA and deviation/ investigation tasks and continuous improvement.
• May train analysts on general job duties.
• Perform other tasks as assigned.

Conocimientos

QC testing

GMP documentation review

Data verification

Educación

Bachelor's degree in science

Herramientas

Basic laboratory techniques

Flow cytometry

Descripción del empleo

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

The Associate position is responsible for performing testing of in-process, final product, and stability samples in accordance with BMS policies, standards, procedures, and Global Regulatory and cGMP requirements to support the Quality Control Analytical department in the Bristol Myers Squibb (BMS) CAR T Manufacturing facility located in Summit, NJ. The candidate may also support data verification and GMP documentation review as needed.

Shift: Wednesday - Saturday, AM (6:30AM-4:30PM)

Duties/Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• May review GMP documentation and perform data verification.
• Support document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
• May train analysts on general job duties.
• Perform other tasks as assigned.

Job Safety Requirements & Essential Physical Demands

Ability to lift up to 45lbs at floor and waist height (commonly <20lbs), lift up to 10lbs overhead, and push or maneuver carts to transport materials. Ability to operate and handle scissor lift carts requiring 15–20lbs 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 (e.g., lab coat/frock, gloves, safety shoes, eye/face protection) during work shift, including cryogenic gloves as needed. Ability to safely handle chemical disinfectants, flammable materials, and hazardous chemicals. Work may involve handling liquid nitrogen and other cryogenically cooled materials. Ability to use step stools to reach and handle materials.

Specific Knowledge, Skills, Abilities

Ability to accurately and completely understand and follow procedures. Apply scientific principles to analytical testing and the proper use of laboratory equipment. Ability to 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.

Education/Experience/ Licenses/Certifications

Bachelor's degree preferred in science. Associates degree with equivalent combination of education and work experience may be considered. 0-2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment. Demonstrated experience with basic laboratory techniques and basic laboratory safety practices. Prior experience in cell and molecular biology techniques (e.g., cell based assays, flow cytometry, qPCR, aseptic technique) is preferred. We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume,

Compensation Overview

Summit West - NJ - US: $34.28 - $41.55 per 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 considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

Benefits

• Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).
• U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.
• Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.
• Depending on eligibility, employees may also have access to additional time‑off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs.
• Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.

How We Work

Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ For roles based in Washington State only: If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] the Job Title and Requisition number. Do not send application-related inquiries to this email.

R1608018 : Associate, QC Analytical, Cell Therapy Data Privacy Link

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.