Bristol Myers Squibb · 19 hours ago
Process Engineer
Bristol Myers Squibb is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines. The Process Engineer will be responsible for implementing cell therapy manufacturing technologies and process changes related to the life-cycle management of a commercial CAR-T Therapy, ensuring project advancement and communication of challenges within the manufacturing network.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Lead the commercial lifecycle plan for a cellular product, maintain oversight of process capability through data trending and statistical analysis of critical variables, ensure processes are robust, in a continued state of validation, and continuously improving
Develop and implement process improvement projects to improve robustness, scalability, and Cost of Goods (COGs) for cell therapy products
Develop product technical strategies including manufacturing requirements, process improvement plans, and ensure successful and timely execution working across functional groups
Provide technical content for significant documents such as validation activities, author content for regulatory submissions
Ensure technical and manufacturing requirements are addressed throughout lifecycle of new solutions
Provide necessary technical analysis to support impact assessments and investigations
Function as a subject matter expert for autologous T-cell therapies and manufacturing technologies
Provide technical input and requirements for design of future clinical and commercial manufacturing facilities
Present complex technical topics internally and externally
Share operational and process leanings with the rest of the manufacturing network
Qualification
Required
Bachelors or Graduate degree in Chemical Engineering, Biomedical Engineering or Life Sciences with more than 5 years of experience in Biotech industry
Ability to effectively work in cross functional teams, meet deadlines as an individual contributor, and prioritize responsibilities
Experience working in a self-driven, performance/results oriented, fast paced matrix environment
Experience assimilating large data sets in support of batch history sections for regulatory submissions
Excellent problem-solving skills, including issue resolution, root cause investigations and CAPAs
Ability to assess risk and develop contingency plans for process risks
Able to manage time and elevate relevant issues to project lead and line management
Detail oriented with excellent verbal and written communication skills
Strong interpersonal and leadership skills to work with teams in different functions and organizations
Preferred
Life Cycle Management Experience
Experience developing and implementing process improvement projects to improve robustness, scalability, and Cost of Goods (COGs) for cell therapy products
Familiarity with cell therapy processes and camps
Proficiency in data management/statistical analysis software, including Excel, JMP, and Spotfire
Company
Bristol Myers Squibb
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.
H1B Sponsorship
Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (213)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)
Funding
Current Stage
Public CompanyTotal Funding
$29.32BKey Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B
Leadership Team
Recent News
2025-12-30
BioWorld Financial Watch
2025-12-29
2025-12-25
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