New · posted Oct 16
Bristol Myers Squibb · Biotechnology
Specialist, QC Analytical
- Summit, NJ
- On-site
- Full-time
- Associate & Specialist
Closes Dec 31, 2026 · 77 days left
The role
The Specialist position is responsible for performing routine 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. Additionally, this role may support testing for method transfer, validation, and verification as well as document revisions and supporting investigation related tasks.
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.
Where you work matters – because collaboration, innovation and patient impact happen in many settings. 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.
What you need
Safety Requirements and Essential Physical Demands
- Ability to lift up to 45 lbs at floor and waist height (commonly <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 (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, 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).
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.
What you'll do
- Perform routine testing of in-process, final product, and stability samples.
- May 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.
Pay
$72,426 – $87,755 a year
Employer provided$34.82 – $42.19 an hour · yearly at 2,080 hours (40 a week)
How this comparesCompensation 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 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.
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.
U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits
Where you'll work
Summit, NJOn-siteOpen in Maps (opens in a new tab)
More jobs in Summit, NJSchedule and working conditions
Days
Hours
Equal opportunity, accessibility and legal noticesBristol Myers Squibb's statements, word for word
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 [email protected]. 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/
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 [email protected]with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.
R1607543 : Specialist, QC Analytical
Job intelligence
The context around this role
Live data · October 16, 2026
Salary intelligence
How the pay compares
This role's midpoint is 33% above the US median for Quality Control roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US104 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $72,426 | — | $87,755 |
| All US (middle half) | $49,375 | $60,000 | $76,625 |
This role: Bristol Myers Squibb's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 16, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 290 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Bristol Myers Squibb's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 28 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods8
- Collaboration and leadership5
- Documentation and SOPs4
- GMP and compliance3
- Investigations and CAPA2
- Validation and qualification2
- Quality systems and risk1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Bristol Myers Squibb on Regulatory Jobs
- 43
- Open roles
- 42
- Distinct roles
- 9
- Locations
By discipline
- Quality37 86%
- Regulatory6 14%
By level
- Senior & Principal18 42%
- Associate & Specialist11 26%
- Director7 16%
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Specialist, QC Analytical at Bristol Myers Squibb
Applications close December 31. $72K–$88K a year, employer provided.