Specialist, Associate Operations Engineer, Cell Therapy in Devens, MA
Listed on 2026-01-12
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Engineering
Process Engineer, Manufacturing Engineer, Quality Engineering
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:
At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
Specialist,Associate Operations Process Engineer, Cell Therapy
The Specialist, Associate Operations Process Engineer, Cell Therapy provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment. Technical support includes troubleshooting process and equipment related issues that occur during the Manufacturing process, in facility. The Associate Operations Process Engineer works closely with the Manufacturing and Quality teams to determine immediate corrective actions for deviations, identifies root cause, and implements long‑term preventive actions.
Other responsibilities include participation in process tech transfer, supporting incoming process changes by communicating the changes to applicable departments, and participating in process improvement projects at the site. The process engineer works to identify and drive continuous improvements to the manufacturing process.
- 1 - Day Shift: 6am - 6pm, rotating schedule including holidays and weekends
- 3 - Night Shift: 6pm - 6am, rotating schedule including holidays and weekends
- Provides on-the-floor and on-site troubleshooting and technical support to Manufacturing and patient increase (RAMP) campaign support for variable shifts (Panama schedule, 0600 to 1800 or 1800 to 0600 variable shifting of days coverage)
- Facilitates deviation prevention and deviation closure through site quality systems
- Analyze and summarize manufacturing data to support impact assessments and investigations
- Owner of change controls for routine process and procedure changes
- CAPA owner for Manufacturing improvements
- Author and revise manufacturing SOPs and provide technical content and direction for electronic batch records
- Participates in technology transfer efforts for new processes and product implementation
- Train and support GMP operators on new procedures, processes, and changes
- Applies continuous improvement tools to identify and close procedural and compliance gaps
- Identify opportunities for process improvements and operational efficiencies, and lead implementation efforts.
- Interfaces with other functions such as Scheduling, Global MSAT, Supply Chain, Quality, and Facilities & Engineering
- Support equipment and systems validation activities, including review of equipment qualification documents, drafting user requirements, and participating on impact assessments
- Ability to perform gowning activities and enter the manufacturing plant. Exposure to strong magnetic fields is commonplace in the manufacturing areas.
- BSc and/or MSc degree in Science or Chem/Bio Engineering
- Minimum 1+ years of industry experience. cGMP and/or Cell Therapy manufacturing experience preferred
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply…
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