Senior Associate Scientist, Analytical Development

Bristol Myers Squibb; Cambridge (MA); On-site; USD 94,000 - 114,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid company holidays

Vacation time

Job summary

Bristol Myers Squibb in Cambridge, MA seeks a Senior Associate Scientist with expertise in analytical method development to advance RNA therapeutics and lipid nanoparticle programs across discovery and development. You will design, qualify, validate, and transfer methods while coordinating with process development, formulation, and manufacturing teams.

The role requires 2+ years in CMC-related work, HPLC/UHPLC experience, and strong writing skills for regulatory submissions.

Qualifications

• 2+ years of relevant CMC-related experience
• Hands‑on experience with HPLC/UHPLC for RNA, lipid, and impurity quantitation
• Hands‑on experience with DLS, RiboGreen, ELISA, Raman, UV-Vis
• Ability to manage multiple projects in a fast‑paced environment
• Strong technical writing for reports, protocols, and regulatory documentation
• Familiarity with ICH/FDA regulatory expectations for analytical data

Responsibilities

• Independently design, develop, and optimize analytical methods for RNA therapeutics, lipids, and related components
• Support routine and platform analytical testing across safety, identity, content, purity/impurity, potency, and quality attributes for LNP-encapsulated RNA
• Lead method lifecycle activities including method development, qualification, validation, and transfer to CROs/CDMOs with SOPs and reports
• Collaborate with process development, formulation, research, and manufacturing teams to support analytical development and milestones
• Troubleshoot analytical challenges, interpret data, and improve assay performance and robustness
• Perform and oversee routine and non-routine analytical testing, data review, and interpretation to ensure data quality and compliance
• Operate, maintain, and troubleshoot analytical instrumentation
• Analyze and communicate complex analytical data in clear reports to inform leadership decisions

Skills

Analytical Chemistry

HPLC/UHPLC

Biophysical characterization

Technical writing

Regulatory knowledge

Project management

Education

B.S./M.S. in Analytical Chemistry or related

PhD considered with experience

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.

BMS at Kendall Square is seeking a highly skilled and motivated Senior Associate Scientist with strong expertise in analytical method development to support the advancement of novel RNA therapeutics. The successful candidate will leverage biophysical and separation techniques to design, develop, and execute analytical methods that enable comprehensive characterization of lipids, antibodies, and RNA-based modalities across discovery and development stages. This role will play a critical part in generating high-quality analytical data to support product understanding, process development, and CMC strategies.

Responsibilities:

• Independently design, develop, and optimize analytical methods to characterize RNA-based therapeutics, lipid nanoparticles, and related components.
• Support routine and platform analytical testing across safety, identity, content, purity/impurity, potency, and general quality attributes for LNP-encapsulated RNA.
• Lead phase-appropriate method lifecycle activities, including method development, qualification, validation, and transfer to internal and external laboratories (e.g., CROs/CDMOs), with authorship of SOPs, protocols, and technical reports.
• Collaborate cross-functionally with process development, formulation, research, and manufacturing teams to support analytical development, troubleshoot issues, and enable program milestones and timelines.
• Troubleshoot complex analytical challenges, interpret data, and provide scientifically sound recommendations to resolve issues and improve assay performance and robustness.
• Perform and oversee routine and non-routine analytical testing, including data review, verification, and interpretation to ensure data quality, integrity, and compliance with internal standards.
• Operate, maintain, and troubleshoot analytical instrumentation.
• Analyze and communicate complex analytical data, generating clear, concise reports and presentations to inform technical teams and leadership decisions undefined

Qualifications:

• B.S./M.S. in Analytical Chemistry, Biochemistry, or a related discipline with 2+ years of relevant CMC-related experience. PhD. candidates with appropriate experience will be considered for this position.
• Hands‑on experience with HPLC/UHPLC (IP-RP, RP, CAD detection) for RNA, lipid, and impurity quantitation.
• Hands‑on experience with biophysical/biochemical characterization techniques: DLS, RiboGreen, ELISA, Raman spectroscopy, light/confocal microscopy, UV-Vis spectrophotometry
• Ability to manage multiple projects and priorities in a fast‑paced environment
• Strong technical writing skills for reports, protocols, and regulatory documentation
• Familiarity with regulatory expectations (e.g., ICH, FDA) for analytical data and submissions

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’s perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

Cambridge - MA - US: $94,400 - $114,392

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 workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries [e-mail]. Visitcareers.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.