Scientist, Manufacturing Technology Devens - MA - US R1603924 Posted ago

Position: Scientist, Manufacturing Technology Devens - MA - US R1603924 Posted 8 minutes ago
## Scientist, Manufacturing Technology Devens - MA - USFind out how well you match with this job
** 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:  Bristol Myers Squibb’s Devens Manufacturing Science and Technology
- Manufacturing Technology team as a Scientist supporting commercial biologics manufacturing. In this role, you will serve as a process technical expert for large-scale cell culture and single-use manufacturing operations, providing science- and data-driven support to sustain GMP compliance, resolve complex process issues, and ensure reliable supply of life-changing therapies to patients. As a key member of the Manufacturing Technology
- Process Technical Operations team, you will serve as a technical lead for commercial biologics manufacturing, leading and supporting deviation investigations, root cause analyses, CAPA development, process monitoring, continuous process verification, change controls, regulatory inspection readiness, and lifecycle management activities. You will apply process knowledge, manufacturing data, and scientific judgment to identify trends, resolve complex process challenges, improve process robustness, and support reliable GMP execution.

In this role, you will collaborate closely with Manufacturing, Quality, MS&T, Validation, Analytical, Technical Product Teams, and site leadership to strengthen process performance, enable technology transfer, and advance continuous improvement across biopharmaceutical manufacturing. This opportunity is ideal for a technically strong, collaborative scientist who thrives in a fast-paced, data-driven environment and is motivated by solving complex problems that directly support BMS’s mission to deliver patient-focused therapies.

Major

Duties and responsibilities:

* Provide technical expertise and floor support for commercial biologics manufacturing operations, including investigation and resolution of process deviations, troubleshooting of process upsets, assessment of process performance, and identification of opportunities to improve process robustness, reliability, and efficiency.
* Lead and support root cause investigations for process deviations, including development of scientifically sound impact assessments, risk-based conclusions, and effective CAPAs to prevent recurrence and support timely batch disposition.
* Serve as a process subject matter expert for internal audits, regulatory inspections, technical discussions, and health authority interactions, including preparation of inspection-ready technical rationale, supporting documentation, and responses.
* Provide on-call technical support for 24x7 manufacturing support for large-scale cell culture and single-use biologics manufacturing operations, as needed.
* Demonstrate strong knowledge of cGMP expectations, BMS corporate standards, site procedures, regulatory requirements, and quality systems, and incorporate these expectations into investigations, change controls, technical assessments, and project deliverables.
* Support process technology transfer, process validation, process performance qualification, post-approval changes, and preparation or review of CMC documentation for regulatory filings and health authority responses.
* Lead and manage cross-functional technical projects that support process robustness, yield improvement, cost of goods…