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Associate Scientist, Automation Process Development

Bristol Myers Squibb
United Statesfull_timeVerifiedPosted 31 Mar 2026
💰 $107,151/yr($88,430/yr$107,151/yr)

About the role

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Position Summary:
The Associate Scientist will join the Automation Process Development team and support the development and qualification of scale down models for automated cell manufacturing suits (AMS) with focus on transduction process development. The role involves hands-on execution of experiments, including lentiviral vector titration and the development of bioreactor/automated processing system scale down models. The successful candidates will collaborate closely with cross-functional teams to advance process understanding and support technology transfer activities.

Key Responsibilities:

  • Develop, optimize, and qualify scale down models for bioreactor and automated cell processing systems, simulating large-scale manufacturing conditions.
  • Perform lentiviral vector titration assays to determine viral particle concentration and support process development activities.
  • Prepare cell culture media, reagents, and samples for experimental procedures.
  • Operate and maintain laboratory equipment used in cell therapy process development.
  • Collect, analyze, and interpret experimental data, document results in electronic laboratory notebooks.
  • Ensure all work is performed in compliance with safety guidelines, standard operating procedures, and regulatory requirements.
  • Collaborate with team members to design experiments, share findings, and support project goals.
  • Maintain accurate and detailed laboratory records in accordance with BMS policies and regulatory requirements.

Basic Qualifications:

  • MS or BS degree in Biomedical Engineering, Cell Biology, Immunology, or related field with relevant industry experience preferably in cell therapy, gene therapy, or bioprocess development (BS with 1+ years)
  • Hands-on experience with cell culture, viral vector handling, and bioreactor and/or automated processing systems.
  • Excellent written and verbal communication skills, including drafting study protocols and reports.
  • Excellent organizational, documentation, and communication abilities.

Preferred Qualifications:

  • Experience in developing, qualifying, and utilizing scale-down models for process development.
  • Knowledge of GxP regulations and regulatory requirements for cell therapy manufacturing is a plus.
  • Proven experience designing DOE and high-throughput process screening studies.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Seattle - WA: $88,430 - $107,151

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. 

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
 

Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the

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Company

Bristol Myers Squibb

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