Scientist, Analytical Development

Bristol-Myers Squibb Co; Cambridge (MA); On-site; USD 106,000 - 128,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid holidays

Comprehensive benefits

Job summary

Bristol Myers Squibb in Cambridge, MA is seeking a Scientist on the Analytical Development Potency team to advance analytical strategies and bring transformative therapies to patients. This hands-on role designs, develops, and executes complex potency cell-based assays, flow cytometry workflows, and immunoassays, leading method transfer and validation in GMP settings.

You will work with limited supervision in a cross-functional environment, mentoring junior scientists and contributing to project

Qualifications

• Master’s (PhD preferred) in immunology, molecular biology and cell biology.
• 4–6+ years of assay development or QC/cGMP experience.
• Proficient in JMP, SAS, or equivalent.
• Strong technical writing and cross-functional communication.
• Working knowledge of QbD, ICH guidelines.
• Proven ability to work independently and collaboratively within teams.

Responsibilities

• Lead method transfer, validation, and routine testing.
• Design, execute, and interpret potency cell-based assays.
• Develop robust, scalable analytical workflows with quality data.
• Collaborate across cross-functional teams and document results.
• Mentor junior scientists and train on methods.

Skills

Analytical development

Potency assays

Statistical analysis

Scientific writing

Regulatory guidelines

Program management

Education

Master’s degree

PhD preferred

Tools

JMP

SAS

Job description

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 As a Scientist on the Analytical Development Potency team at BMS, you will help advance analytical strategies that bring transformative therapies from the bench to patients. This hands‑on, autonomous role designs, develops, and executes complex potency cell‑based assays, flow cytometry workflows, and immunoassays. As a subject matter expert, you will lead method transfer and validation. Working with limited supervision in a cross‑functional environment, you will apply strong scientific judgment, communicate clearly, and contribute to project decisions and method implementation in GMP Analytical Development and Quality Control settings.

Key Responsibilities

• Scientific Expertise & Strategy Applies broad expertise in analytical development and working knowledge, including awareness of technical advances impacting the field, to advance analytical strategies and project objectives. Proficient in scientific/technical data review and writing, including regulatory documents, protocols, and literature assessments to solve complex problems.
• Experimental Design & Execution Independently designs, executes, analyzes and evaluates hypothesis‑driven experiments; and based on interpretation of results, defines appropriate next steps. Interprets and communicates study results, ensures conclusions are scientifically rigorous, well documented, and actionable.
• Troubleshooting & Problem Solving Identifies, investigates, and resolves technical and method‑related challenges of moderate to high complexity through systematic troubleshooting and sound scientific judgment. Makes timely, tactical, data‑driven decisions with little to no direction from senior team members, including assay optimization for robustness, throughput, and reproducibility, identifying new solutions or developing procedures where none exist.
• Documentation & Data Integrity Performs data verification, data review, and documentation reviews across multiple methods and/or products. Authors, reviews, and revises technical documents such as SOPs, development reports, method validation reports.
• Method Expertise & Quality Serves as subject matter expert (SME) supporting method transfer, validation, and routine testing of in‑process, final product, and stability samples. Cross‑trained on multiple complex analytical methods and/or products. Owns project, deviation/investigation and continuous improvement efforts.
• Continuous Improvement & Innovation Contributes to continuous improvement initiatives and evaluates innovative technologies, approaches, and workflows that enhance analytical capability, efficiency, and data quality. Proactively identifies and resolves technical challenges, identifies solutions and contributes to the development of new approaches where no established procedure exists with minimal supervision.
• Leadership & Collaboration Serves as a technical point of contact or SME. May represent the team in internal and external meetings clearly communicating recommendations, risks, and results. Represents Analytical Development on cross‑functional program teams, building effective partnerships, and contributing scientific expertise to shared objectives. Trains others on multiple methods, processes, and procedures; mentors junior scientists and contributes to the broader scientific strategy of BMS.
• Project Management Manages assigned work with limited supervision, balancing priorities, and delivering high‑quality results in alignment with project timelines.

Working Conditions Laboratory‑based role requiring the use of analytical instrumentation, biological safety cabinets, and cell culture facilities. Hands‑on work with biological materials, mammalian cell lines, and reagents requiring adherence to appropriate biosafety protocols. May require occasional flexibility in scheduling or traveling to support time‑sensitive studies or cross‑site collaboration.

Qualifications and experience

Master’s (Preferred PhD) in relevant scientific field i.e., immunology, molecular biology and cell biology

4-6+ years of relevant experience in assay(s) development or QC/cGMP experience.

Demonstrated experience in potency assay development and execution.

Proficient in statistical analysis tools such as JMP, SAS, or equivalent.

Strong technical writing and oral communication skills, with the ability to effectively convey project status, roadblocks, and needs to peers, management, and cross‑functional stakeholders.

Working knowledge of QbD, ICH guidelines, and global regulatory guidance.

Proven ability to work independently and collaboratively within multidisciplinary teams in a fast‑paced environment.

Strong prioritization and time management skills, with the ability to manage deliverables across multiple projects and meet deadlines.

Compensation Overview

Cambridge - MA - US: $106,010 - $128,462 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 at https://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 [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/

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. To check your application status, please login to your Candidate Home Account.

R1607272 : Scientist, Analytical Development 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.