Associate Scientist, RNA Pilot Manufacturing

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

Benefits offered by this job

Flexible Time Off

Paid holidays

Wellbeing benefits

Job summary

Bristol Myers Squibb is seeking a professional to support RNA manufacturing operations in a fast-paced, matrixed environment. You will contribute to nonGMP activities, participate in agile development, and help ensure compliant, high-quality material delivery.

Qualifications include a degree in bio/chemical engineering or related field with 2–4+ years of science experience; MS with 1–2+ years is a plus. Strong emphasis on data analytics, KPI management, and mentoring others.

Qualifications

• Degree in Bio/Chemical Engineering, Bio/Chemistry, or related field required.
• BS with 2–4+ years in science-related disciplines; MS with 1–2+ years preferred.
• Experience with RNA manufacturing unit operations including bioreactors, chromatography, and filtration.
• Knowledge of technology transfer from PD to pilot and pilot to GMP manufacturing.
• Strong KPI management and production documentation experience.
• Experience compiling/interpreting RNA analytics and biophysical characterization (HPLC, CE, ELISAs).
• Past people management or mentorship experience encouraged.

Responsibilities

• Support and execute RNA manufacturing operations for nonGMP activities.
• Operate in an agile development manufacturing model for rapid material delivery.
• Ensure phase-appropriate execution balancing speed, compliance and rigor.
• Collaborate with analytical labs for sample submission and release of material.
• Provide technical problem-solving during campaigns and implement CAPAs.

Skills

People management

Independent work

Analytical thinking

Problem solving

Continuous improvement

Team collaboration

Education

Bachelor's degree in Bio/Chemical Engineering, Biochemistry or related

Tools

ELN workflows

Multivariate data analysis tools

HPLC

CE

RNA analytics techniques

Job description

Position Summary

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 and execute RNA manufacturing operations supporting nonGMP manufacturing activities.
• Work in an agile development manufacturing model in the RNA space capable of rapidly delivering material for various program needs.
• Ensure manufacturing operations are executed in a phase-appropriate manner, balancing speed, compliance, scientific rigor, and operational discipline.
• Partner with analytical testing laboratories to ensure sample submission, investigation support, and timely release of material.
• Enable technical problem-solving during manufacturing campaigns, including real-time escalation, root-cause analysis, and implementation of corrective and preventive actions.
• Maintain systems for tracking process performance using ELN workflows and multivariate data analysis tools.
• Ensure learnings from manufacturing activities are captured, communicated, and incorporated into future strategies.

Qualifications & Experience

• Degree in Bio/Chemical Engineering, Bio/Chemistry, or related field
• BS with 2-4+ years’ experience in science related disciplines
• MS with 1-2+ years’ experience in science related disciplines
• Experience in process unit operations relevant to RNA manufacturing including bioreactors, chromatography, and filtration.
• Knowledge and understanding of technology transfer from PD to the pilot facility and from the pilot facility to GMP manufacturing.
• Strong track record of utilizing standardized operations, KPI management, and production documentation systems.
• Experience with compiling and interpreting RNA analytics and biophysical characterization techniques for RNA such as HPLC, CE, ELISAs, and cell-based assays.
• Prior management and mentorship experience; passion for people management and development
• Ability to work independently as well as part of a team in a highly dynamic, fast-paced, matrixed environment with rapidly evolving priorities.
• Demonstrated continuous improvement mindset, driving efficiencies, process improvements across diverse initiatives.
• 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

• $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 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.

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.