Devens Co-op Program; STEM
Listed on 2026-10-09
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Business
Regulatory Compliance Specialist
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.
Are you seeking an opportunity to gain hands‑on experience in Bio Pharma, develop your leadership skills, receive career mentorship, and make a meaningful impact? The 6‑month Co‑op program at Bristol Myers Squibb offers an exceptional career experience at our state‑of‑the‑art Biologics facility or our cutting‑edge Cell Therapy campus in Devens, MA. Join us and be part of the next generation of medicine!
The program includes formal and informal networking, development, and mentorship of participants with a focus on building and advancing professional skills in the Bio Pharma industry. Candidates will be matched with projects based on skills and interests to support projects and continuous improvement initiatives at the Devens Campus. Projects are associated with functional areas including:
Commercial Biologics Manufacturing – Engineering, Operations, Technology Transfer Cell Therapy Manufacturing Quality - Ensuring compliance with health authority regulations and internal standards All projects will be defined with key deliverables and provide candidates with opportunities to develop new skills and work directly on key aspects of the business. Example deliverables include process optimization, documentation and knowledge management updates, workflow or tool development, and continuous improvement.
This full‑time six‑month co‑op program will take place January through July of 2027. Please ensure that you can support a full‑time work schedule (40 hours per week, 5 days per week M-F) for these positions.
- Knowledge or understanding of biotech process such as cell culture and purification
- Support structured problem‑solving and continuous improvement efforts within a GMP‑regulated manufacturing environment
- Review, organize and/or maintain technical documentation
- Analyze data or trends to identify root causes and develop practical, actionable recommendations
- Collaborate cross‑functionally within Manufacturing, Quality, Engineering, Automation, and Supply Chain teams
- Explore and help pilot emerging tools and technologies
- Currently enrolled in a Science or Engineering Bachelor of Science, Masters, or Doctorate program (STEM)
- Interest and passion for biotechnology, specifically biologics/cell therapy processes
- Strong communication skills and attention to detail
- Experience working in highly collaborative environment, ability to work in a team
- Comfortable with Microsoft Office tools
- Strong analytical and problem‑solving skills as demonstrated through previous experiences which may include: laboratory experience, project design course(s), research projects, knowledge of programming/scientific software, and/or previous co‑ops/internships
- Willingness to gown into controlled manufacturing spaces when required
- All candidates must be legally authorized to work in the United States at the time of hire and for the duration of their employment
- Please note that visa sponsorship, including for student or temporary work authorization programs, is not available for this role
- Candidates must have work authorization that does not require sponsorship now or in the future
$24.00 to $45.00 Pay for this…
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