Manufacturing Science and Technology Process Engineering; MSAT PE Co-Op
Summit, Union County, New Jersey, 07902, USA
Listed on 2025-12-10
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Engineering
Manufacturing Engineer, Process Engineer, Biotechnology
Manufacturing Science and Technology Process Engineering (MSAT PE) Co‑Op
Apply for the Manufacturing Science and Technology Process Engineering (MSAT PE) Co‑Op role at Bristol Myers Squibb.
Working with UsChallenging. Meaningful. Life‑changing. Those aren’t words that are usually associated with a job, but working at Bristol Myers Squibb is anything but usual. Every day, work happens in every department—from optimizing production lines to the latest breakthroughs in cell therapy. It transforms the lives of patients and the careers of those who do it. You’ll grow and thrive through opportunities uncommon in scale and scope with high‑achieving teams.
PositionSummary
The MSAT PE Co‑Op program is an excellent opportunity for aspiring engineers and scientists to gain hands‑on experience in the fast‑paced and evolving field of cell therapy manufacturing technology. This 6‑month co‑op program (July – December 2026) provides participants with valuable mentorship, executive exposure, and customized development opportunities that accelerate their ability to deliver impactful results. Co‑op participants will contribute to key initiatives while learning about cutting‑edge technologies.
Key Responsibilities- Lead and design experiments to characterize and evaluate the limits of cell therapy equipment and processes.
- Analyze experimental data and/or continuous process monitoring data to draw actionable conclusions and improve understanding of manufacturing processes and cell therapy drug product.
- Communicate experimental results and technical findings effectively through detailed technical reports and presentations to key stakeholders.
- Support the creation and revision of process support documentation, ensuring accuracy and compliance with industry standards.
- Develop and maintain electronic databases and dashboards to track experimental results and process performance metrics.
- Contribute to continuous improvement efforts by identifying opportunities for enhancement throughout the cell therapy product lifecycle.
- Work closely with a multidisciplinary team of engineers and scientists to support various technical projects and process improvements.
- Travel between BMS’s Warren and Summit sites and complete occasional remote work as necessary to support project activities.
- Currently enrolled in a Bachelor's or Master’s degree program in Biomedical Engineering, Chemical Engineering, Mechanical Engineering, Biotechnology, Biological Sciences, or a related field.
- Preference for students entering their junior or senior year, with a strong foundation in core scientific and engineering principles.
- All candidates must be authorized to work in the U.S. at the time of hire and for the duration of employment. Immigration or visa sponsorship is not available for this position.
- Familiarity with basic laboratory techniques (cell culture, pipetting, sterile technique) and preferred experience with equipment used in biotech settings.
- Basic understanding of statistical analysis and experience with data analysis software (Excel, MATLAB, R, Python, JMP).
- Strong analytical and problem‑solving skills, with the ability to break down complex issues and find practical solutions.
- Ability to think critically when designing experiments and analyzing data.
- Strong written and verbal communication skills, with the ability to clearly convey technical information to both technical and non‑technical audiences.
- Experience in writing lab reports or academic papers is a plus.
- Ability to work independently and as part of a cross‑functional team.
- Strong time‑management skills and the ability to manage multiple tasks and deadlines in a dynamic environment.
- Basic proficiency in Microsoft Office Suite (Word, PowerPoint, Excel).
- Familiarity with database tools or dashboards is a plus (but not required).
- Previous internship, lab, or co‑op experience in a related field (biotechnology, engineering, or manufacturing).
- Exposure to Good Manufacturing Practices (GMP) in a manufacturing setting.
The starting hourly compensation for this assignment is within the range of $23.00 to $42.00/hr final individual compensation will be determined by the employer of record and may vary based on demonstrated experience, location, and other factors.
Employment Type& Seniority Level
Employment type:
Full‑time. Seniority level:
Internship. Duration: 6 months (July – December 2026).
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