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Salary
$76k – $92k per year
Location
In office (New Brunswick)
Employment
Full-Time
Overview
Company
Impact
Profile match
Bristol Myers Squibb is an American pharmaceutical company whose predecessors date to 1858 and 1887 and which took its present form in a 1989 merger. Its portfolio is concentrated in oncology, haematology, immunology and cardiovascular disease, including the checkpoint inhibitor Opdivo, the blood thinner Eliquis co-marketed with Pfizer, the cell therapies acquired with Celgene, and newer products such as the schizophrenia treatment Cobenfy. Headquartered in Princeton, New Jersey and listed on the New York Stock Exchange, it faces a heavy sequence of patent expiries and has been buying and licensing assets to replace them.

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.

Key Responsibilities:

  • Support Reference Standard and Critical Reagent (RSCR) operations across biologics and small molecule programs, including inventory management, laboratory activities, and project deliverables.

  • Partner with project teams and key stakeholders to support RSCR portfolio needs, project milestones, timelines, and operational priorities.

  • Maintain communication with stakeholders regarding material supply, project status, deliverables, and business expectations.

  • Prepare, review, maintain, and issue protocols, supporting data, reports, Certificates of Analysis (COAs), and related documentation in accordance with current procedures and quality requirements.

  • Execute routine inventory functions, including labeling, subdivision, aliquoting, material tracking, inventory reconciliation, and accurate inventory recordkeeping.

  • Support sample scheduling, material tracking, and coordination of project milestones while performing laboratory benchwork as needed.

  • Maintain compliance with GxP, EHS, site quality requirements, and established procedures.

  • Support reference standard qualification and requalification activities, including protocol execution, data review, testing coordination, purity calculations, and assignment of expiration dates.

  • Identify, document, communicate, and support the resolution of operational issues and risks, escalating concerns when appropriate.

  • Contribute to investigations, documentation activities, operational excellence, and continuous improvement initiatives.

Qualifications

Specific Knowledge, Skills, Abilities: General experience in biological and chemical Analytical techniques, Separation science, Instrumentation and Method Validation and or bioanalytical techniques and biologics development. Industry experience in biotech/biologics, specifically working with reference standards and/or critical reagents is also desirable

Education/Experience/ Licenses/Certifications: BS or MS in biological sciences, chemistry, or related scientific disciplines. 0 to 5 years of experience in the biotech or pharmaceutical industry.

Travel: This position requires up to 5% of travel

#LI-Onsite

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:

New Brunswick - NJ - US: $75,850 - $91,907

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.

U.S.-based job seekers can explore full benefit offerings athttps://careers.bms.com/benefits

How We Work

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.

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.

R1605988 : Scientist RSCR

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