Sr Specialist, Process Engineer, CTF Automated Manufacturing

Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsSr Specialist, Process Engineer, CTF Automated ManufacturingDevens - MA - US No longer accepting applications.Job IDR1604385Date posted07/12/2026DepartmentNot ApplicableAt 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.Process Engineers within the Automated Manufacturing Suite (AMS) Team provide technical leadership for automated manufacturing equipment at the Devens Cell Therapy Facility (CTF). This role focuses on the design, development, testing, installation, commissioning, and validation of automated workcells and supporting systems that enable next‑generation cell therapy manufacturing.Engineers in this role work closely with Manufacturing, MSAT, Digital Plant, IT, and Quality to ensure new automated platforms are robust, compliant, and operationally ready. The engineer serves as a technical owner, providing on‑the‑floor support, equipment monitoring, and lifecycle management to maintain high system reliability and support routine GMP operations.This position emphasizes proactive system performance, equipment readiness, and continuous improvement.Responsibilities:Key responsibilities for this role include:Contribute to equipment and workstation design, ensuring requirements meet manufacturing, quality, and digital system needs.Draft or support development of User Requirements (URS), Functional Specifications, design documentation, and interface definitions.Lead or support FAT, SAT, installation, commissioning, and qualification of automated systems and robotics used within AMS.Ensure systems integrate effectively with MES, automation layers, and digital infrastructure to meet business needs.Partner with Manufacturing to ensure automated systems are ready for operational use, including operator training, workflow optimization, and readiness assessments.Support manufacturing launch, providing on‑the‑floor troubleshooting during early operations.Serve as equipment / workstation owner for designated AMS units following commissioning.Lead or support continuous improvement initiatives to increase uptime, throughput, safety, and ease of use.Identify and implement process and automation enhancements that improve system robustness or operator experience.Collaborate with MSAT, Quality, Digital Plant, Scheduling, Supply Chain, and Facilities/Engineering to ensure reliable operation of automated manufacturing systems.Provide technical input for process transfers, new equipment introduction, and automation upgrades.Specific Knowledge, Skills, Abilities:Strong understanding of regulatory requirements, industry standards, and best practices for validation in pharmaceutical or biotechnology industries.Experience with equipment startup and validation.Experience with single-use technologies and closed systems.Experience within a cGMP manufacturing...