Scientist

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. The Kilo Lab Scientist will be able to assume roles in Chemical Development Engineering to support the transfer scale‑up experience that strengthens the operational and equipment knowledge base, understanding of scale‑up risk and development of safe, scalable processes, and tech transfer skills through the organization. Responsibilities Independently lead the implementation and scale‑up of chemical processes from the development laboratory into Kilo Lab and pilot‑scale manufacturing. Serve as the technical and operational lead for process scale up manufacturing campaigns. 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. Evaluate and implement new equipment, emerging technologies, and improved processing methodologies. Contribute to a collaborative working environment through effective communication, knowledge sharing, and partnership across scientific and engineering disciplines. Required Qualifications PhD in Chemistry, Chemical Engineering, or a related scientific or engineering discipline with 0–2 years, MS with 2–4 years, or BS with 5–7 years of relevant process development scale‑up experience. Demonstrated experience in chemical process development, scale‑up, pilot‑plant operations, or pharmaceutical/chemical manufacturing. Working knowledge of chemical processing equipment and synthetic manufacturing unit operations. Demonstrated ability to troubleshoot technical and operational problems using sound scientific judgment. Ability and willingness to work hands‑on with chemical processing equipment and perform activities associated with setup, operation, and execution of manufacturing processes. Understanding of process‑safety principles. Strong knowledge and understanding of GMP requirements and manufacturing practice and principles. Ability to manage multiple priorities and coordinate complex activities across functions. 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, regulatory compliance and continuous improvement. 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: $104,300 - $126,391 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 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 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 View email address on click.appcast.io. 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. 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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. #J-18808-Ljbffr Bristol-Myers Squibb Co