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Associate Scientist

Job in New Brunswick, Middlesex County, New Jersey, 08933, USA
Listing for: Bristol-Myers Squibb Co
Full Time position
Listed on 2026-10-23
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research, Pharmaceutical Manufacturing, Chemical Manufacturing
  • Research/Development
    Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 89660 - 108644 USD Yearly USD 89660.00 108644.00 YEAR
Job Description & How to Apply Below

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…

Position Requirements
10+ Years work experience
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