Scientist, LNP Process Development

Bristol Myers Squibb; Cambridge (MA); On-site; USD 111,000 - 134,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid holidays

Job summary

Bristol Myers Squibb in Cambridge, MA is seeking a Senior Associate Scientist for the LNP Process Development team. The role focuses on developing, characterizing, and implementing robust preclinical and clinical manufacturing processes for lipid nanoparticles, spanning early development to clinical manufacturing support.

The successful candidate will plan and execute lab studies, contribute to protocols, reports, and regulatory documentation under senior guidance, with opportunities for growth

Qualifications

• Degree in Bio/Chemical Engineering, Bio/Chemistry, or related field.
• BS with 6+ years’ experience or MS with 4–6 years’ experience or PhD with 0–2 years’ experience.
• Experience with nanoprecipitation, filtration, and innovative separation processes.
• Strong DoE and multivariate data analysis fundamentals.
• Experience with process analytics and biophysical characterization (DLS, ribogreen, HPLC).
• Knowledge of cGMP, ICH, and QbD in clinical manufacturing.

Responsibilities

• Execute lab experiments for LNP process development and scale-up.
• Design experiments for optimization and characterization using QbD and DoE.
• Prepare protocols and reports for early- to late-stage development.
• Perform routine analytical testing for LNP characterization.
• Collaborate with R&D, analytics, and manufacturing to advance pipeline.

Skills

DoE principles

Multivariate data analysis

Statistical methods

Laboratory data interpretation

LNP process development

Education

BS in Bio/Chemical Engineering or related

MS in related field

PhD in related field

Tools

DLS

HPLC

RiboGreen

TFF/UF-DF

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

Bristol Myers Squibb is seeking a motivated and detail-oriented Senior Associate Scientist to join our LNP Process Development team in Cambridge, MA. The LNP PD team works to develop, characterize, and implement robust preclinical and clinical manufacturing processes to support Bristol Myers Squibb's exciting pipeline of products. This role is specifically focused on LNP process development, with responsibilities spanning early process development through clinical manufacturing support. This is an excellent opportunity for an early-career scientist to grow within a dynamic, fast-paced environment. The successful candidate will support planning and execution of laboratory studies and contribute to protocols, technical reports, and regulatory documentation under the guidance of senior team members.

Key Responsibilities

• Execute hands-on laboratory experiments focused on LNP process development and scale-up from bench to pilot scale
• Design and perform experiments for optimization and characterization of targeted lipid nanoparticles using structured approaches in both upstream and downstream unit operations (i.e. QbD principles, DoE)
• Contribute to the authoring and review of technical protocols, experimental reports, and batch records in support of early- to late-stage development activities
• Perform routine analytical testing to assess LNP characterization
• Analyze and interpret experimental results, present findings to senior scientists and project teams
• Collaborate with internal R&D, analytical development, and manufacturing to advance BMS's LNP pipeline
• Support interactions with manufacturing partners, including review of technical documents and participation in technology transfer activities as needed
• Maintain accurate and complete laboratory notebooks and documentation in compliance with internal quality standards

Qualifications & Experience

• Degree in Bio/Chemical Engineering, Bio/Chemistry, or related field
• BS with 6+ years’ experience in science related disciplines
• MS with 4-6 years’ experience in science related disciplines
• PhD with 0 - 2 years’ experience in science related disciplines
• Expertise in nanoprecipitation, filtration (TFF/UF-DF), and innovative separation unit operations
• Solid knowledge foundation of statistical design of experiments (DoE) and analysis of multivariate data
• Experience with performing process analytics and biophysical characterization techniques such as DLS, ribogreen, and HPLC
• Knowledge of cGMP, ICH, regulatory guidelines and QbD principles as they apply to risk management and clinical manufacturing
• Demonstrated background of providing technical support for clinical manufacturing processes, including support of process investigations, and implementation of proactive process modifications
• Knowledge of advanced mathematics, nucleic acid chemistry, lipid chemistry, and biology is a plus
• Knowledge of establishing and qualifying scale down models and mechanistic models for process characterization is a plus

Compensation Overview

Cambridge - MA - US: $110,810 - $134,281

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.

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.

R1606184 : Scientist, LNP Process Development