Associate Scientist

Bristol-Myers Squibb Co; New Brunswick (NJ); On-site; USD 90,000 - 109,000; Full time

Job summary

Bristol Myers Squibb in New Jersey is seeking a Kilo Lab Scientist to translate laboratory chemical processes into safe, robust manufacturing operations for GMP active drug substances in the New Brunswick Kilo Lab and beyond.

The role involves leading campaign design and scale-up, equipment selection, materials planning, safety review, and thorough process documentation, partnering with chemists, engineers, and analytical scientists to drive quality and efficiency.

Qualifications

• BS in Chemistry, Chemical Engineering, or related field with 1–3 years of experience.
• Ability to translate lab processes into scalable manufacturing procedures.
• Commitment to safe working practices and regulatory compliance (GMP).

Responsibilities

• Lead scale-up and execution of GMP active drug substance manufacturing in the Kilo Lab.
• Coordinate cross-functional teams across chemistry, engineering, and analytics.
• Plan campaigns, select equipment, plan materials, and document processes.
• Identify and resolve technical and operational scale-up challenges.

Skills

Strong problem-solving

Interpersonal skills

Communication skills

Education

BS in Chemistry or Chemical Engineering

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. Our Chemical Process Development group is a team of organic chemists, analytical chemists, and chemical engineers working together to design novel syntheses from raw materials to supply new medicines to patients. Our scientists focus on developing safe, economical, sustainable, and robust processes to support clinical trials and the launch of new medicines across various drug modalities including small molecules, peptides, oligonucleotides, and antibody drug conjugates. Our work combines innovative science, data-driven decision-making, and cross-functional collaboration to translate laboratory chemistry into reliable manufacturing processes. The scientific and process knowledge generated through development, scale-up, and manufacturing establishes the process understanding, design parameters, and control strategies needed to support regulatory filings and the delivery of new medicines to patients worldwide.

Job Summary

The Kilo Lab Scientist plays a key role in translating laboratory-developed chemical processes into safe, robust, and executable manufacturing processes within the New Brunswick Kilo Lab and beyond. Working hands‑on with multidisciplinary Chemical Process Development teams, the scientist is responsible for the preparation, scale‑up, and execution of processes supporting the manufacture of GMP active drug substance for pharmaceutical development. The scientist leads and coordinates manufacturing campaign activities, including process design and scale‑up, equipment selection and setup, materials planning, process safety evaluation review, recipe development, batch execution, equipment cleaning, process documentation, and post‑campaign assessment. The role requires a combination of scientific understanding, practical problem‑solving, and mechanical aptitude, with a strong commitment to safety, quality, and environmental compliance. Kilo Lab Scientists execute processes from laboratory scale through 200L and work directly with processing equipment throughout campaign preparation and manufacturing. The Kilo Lab also provides an environment for evaluating and implementing emerging manufacturing technologies and methodologies, giving scientists opportunities to contribute to the advancement of how new novel medicines are scaled and manufactured.

Responsibilities

Lead the implementation and scale‑up of chemical processes from the development laboratory into the New Brunswick Kilo Lab in support of clinical development and GMP active drug substance manufacturing. Work hands‑on with chemists, engineers, analytical scientists, and other cross‑functional partners to translate laboratory processes into safe, robust, and executable manufacturing operations. Plan, coordinate, and execute Kilo Lab manufacturing campaigns, including equipment selection and setup, raw material planning, process safety readiness, recipe preparation, batch execution, cleaning, and manufacturing documentation. Apply scientific and engineering principles to identify and resolve technical and operational challenges encountered during process scale‑up and manufacturing. Review process safety information and translate identified process requirements and operating boundaries into appropriate manufacturing practices. Monitor and assess process performance during manufacturing and document observations, deviations, learnings, and opportunities for process improvement. Ensure manufacturing activities are conducted in accordance with applicable safety, GMP, environmental, and procedural requirements. Collaborate with development teams before and after campaigns to incorporate scale‑up and manufacturing learnings into subsequent process development. Participate in the evaluation and implementation of new equipment, manufacturing technologies, and processing methodologies within the Kilo Lab. Contribute to a collaborative working environment through effective communication, knowledge sharing, and partnership across scientific and engineering disciplines.

Required Qualifications

• BS in Chemistry, Chemical Engineering, or a related scientific or engineering discipline with 1-3 years of experience.
• Demonstrated ability to apply scientific and technical principles to laboratory, process development, scale‑up, or manufacturing activities.
• Strong problem‑solving skills and the ability to manage multiple priorities in a dynamic laboratory and manufacturing environment.
• Ability and willingness to work hands‑on with chemical processing equipment and perform activities associated with setup, operation, and execution of manufacturing processes.
• Strong interpersonal and communication skills with the ability to work effectively across scientific and engineering disciplines in a matrix environment.
• Ability to work independently, exercise sound technical judgment, and manage assigned activities with appropriate levels of supervision.
• Commitment to safe working practices, quality, and regulatory compliance.

Preferred Qualifications

• Advanced degree in Chemistry, Chemical Engineering, or a related scientific or engineering discipline.
• Relevant industry experience in laboratory process development, chemical process scale‑up, pilot‑scale operations, or pharmaceutical/chemical manufacturing.
• Familiarity with chemical processing equipment and unit operations used in synthetic chemical manufacturing.
• Knowledge of GMP manufacturing principles and process safety practices.
• Experience translating laboratory procedures into larger‑scale manufacturing operations.
• Experience with emerging or intensified manufacturing technologies, including continuous or flow processing.
• Ability and interest in applying and expanding technical capabilities across process development and manufacturing, including supporting Development Engineering laboratory activities and Process Engineering activities associated with externally executed manufacturing campaigns.

Compensation Overview

New Brunswick - NJ - US: $89,660 - $108,644. 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.