Bristol-Myers Squibb
Manager, Process Systems Engineer, Cell Therapy in Devens, MA
Bristol-Myers Squibb, Harvard, Massachusetts, us, 01451
Overview
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: careers.bms.com/working-with-us. 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. Position
The Manager, Process Systems Engineer provides input to the design and development for electronic Process systems including electronic batch records (MES), DeltaV, OSI Pi, and process monitoring systems. The Engineer works with Digital Plant, IT, Manufacturing Operations, and process subject matter experts to deliver process Changes. The position requires excellent project management skills and coordination with stakeholders, as well as leadership, enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The incumbent must be goal-oriented, flexible, and a subject matter expert in process systems. The Engineer reports to the Associate Director, Process Systems within the Manufacturing Sciences and Technology (MSAT) department. Shifts Available
Monday – Friday, Standard Working Hours Responsibilities
Apply manufacturing process expertise and process system technical knowledge during change management. Own User Requirements for process systems. Ensure consistent execution of system modifications and changes. Ensure adherence with governing documents related to change management. Works collaboratively with Manufacturing, Digital Plant, IT, Validation, Quality, and MSAT to ensure change initiatives are driven to closure and migrated to the production area in a timely manner. Owns the lifecycle of process system changes. Works with site functional teams, including manufacturing, engineering, warehouse, and quality assurance to gather user requirements for change development. Understanding of DeltaV and MES library objects. Use that understanding to direct changes to associated systems. Develop documentation to support the qualification of the DeltaV and MES recipes, including test scripts and User Requirements. Execute testing of the changes in the development environment to ensure functionality. Support Chain of Identity program and ensure it is maintained within the process systems. Manage User Acceptance Testing process for system qualification. Develop and deliver reports from reporting software. Able to use creative problem solving. Provides technical expertise to management and less experienced professionals. Provide technical support for manufacturing operations, investigations and change controls as a process system subject matter expert. Drive strong collaboration within the plant and across the network. Build trust and effective relationships with peers and stakeholders. Promote a mindset of continuous improvement, problem solving, and incident prevention. Perform other tasks as assigned. Knowledge and Skills
Strong project management skills are needed. Minimum of 1 year of experience with project coordination and cross-functional team leadership preferred. Minimum 1 year of experience support DeltaV, or other process automation software desirable; ability to use process historian and analyze data to assist troubleshooting. Knowledge of electronic batch records, preferably Syncade MES. Basic Requirements
Bachelor’s Degree in a related field from an accredited college or university required (science or engineering preferred). 5 or more years of relevant work experience required, preferably in the pharmaceutical, biotechnology, or cell therapy manufacturing industry. Knowledge of DeltaV and process automation is required. Syncade MES is a plus. Experience in cell therapy, biologics, or vaccine manufacturing support, tech transfer, and validation is required. Additional
BMSCART #LI-ONSITE GPS_2025 Compensation and Benefits
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview: Devens - MA - US: 103110 - 124939. The starting compensation range (for a full-time employee) may include additional incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills, location, work schedule, knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit careers.bms.com/life-at-bms. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include: Medical, pharmacy, dental and vision care; wellbeing programs; 401(K); disability, life insurance, and other benefits; paid holidays, vacation, volunteer time, sick time, and other leave options. Other perks may include tuition reimbursement and a recognition program. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science,” every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol and Accessibility
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role. Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite. Onsite presence is considered an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through accommodations and ongoing support in their roles. For accommodations, contact adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our Equal Employment Opportunity statement. BMS cares about well-being and recommends vaccination updates per company guidance. BMS will consider applicants with arrest and conviction records as required by law. If you live in or expect to work from Los Angeles County, visit careers.bms.com/california-residents/ for information. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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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: careers.bms.com/working-with-us. 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. Position
The Manager, Process Systems Engineer provides input to the design and development for electronic Process systems including electronic batch records (MES), DeltaV, OSI Pi, and process monitoring systems. The Engineer works with Digital Plant, IT, Manufacturing Operations, and process subject matter experts to deliver process Changes. The position requires excellent project management skills and coordination with stakeholders, as well as leadership, enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The incumbent must be goal-oriented, flexible, and a subject matter expert in process systems. The Engineer reports to the Associate Director, Process Systems within the Manufacturing Sciences and Technology (MSAT) department. Shifts Available
Monday – Friday, Standard Working Hours Responsibilities
Apply manufacturing process expertise and process system technical knowledge during change management. Own User Requirements for process systems. Ensure consistent execution of system modifications and changes. Ensure adherence with governing documents related to change management. Works collaboratively with Manufacturing, Digital Plant, IT, Validation, Quality, and MSAT to ensure change initiatives are driven to closure and migrated to the production area in a timely manner. Owns the lifecycle of process system changes. Works with site functional teams, including manufacturing, engineering, warehouse, and quality assurance to gather user requirements for change development. Understanding of DeltaV and MES library objects. Use that understanding to direct changes to associated systems. Develop documentation to support the qualification of the DeltaV and MES recipes, including test scripts and User Requirements. Execute testing of the changes in the development environment to ensure functionality. Support Chain of Identity program and ensure it is maintained within the process systems. Manage User Acceptance Testing process for system qualification. Develop and deliver reports from reporting software. Able to use creative problem solving. Provides technical expertise to management and less experienced professionals. Provide technical support for manufacturing operations, investigations and change controls as a process system subject matter expert. Drive strong collaboration within the plant and across the network. Build trust and effective relationships with peers and stakeholders. Promote a mindset of continuous improvement, problem solving, and incident prevention. Perform other tasks as assigned. Knowledge and Skills
Strong project management skills are needed. Minimum of 1 year of experience with project coordination and cross-functional team leadership preferred. Minimum 1 year of experience support DeltaV, or other process automation software desirable; ability to use process historian and analyze data to assist troubleshooting. Knowledge of electronic batch records, preferably Syncade MES. Basic Requirements
Bachelor’s Degree in a related field from an accredited college or university required (science or engineering preferred). 5 or more years of relevant work experience required, preferably in the pharmaceutical, biotechnology, or cell therapy manufacturing industry. Knowledge of DeltaV and process automation is required. Syncade MES is a plus. Experience in cell therapy, biologics, or vaccine manufacturing support, tech transfer, and validation is required. Additional
BMSCART #LI-ONSITE GPS_2025 Compensation and Benefits
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview: Devens - MA - US: 103110 - 124939. The starting compensation range (for a full-time employee) may include additional incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills, location, work schedule, knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit careers.bms.com/life-at-bms. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include: Medical, pharmacy, dental and vision care; wellbeing programs; 401(K); disability, life insurance, and other benefits; paid holidays, vacation, volunteer time, sick time, and other leave options. Other perks may include tuition reimbursement and a recognition program. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science,” every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol and Accessibility
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role. Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite. Onsite presence is considered an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through accommodations and ongoing support in their roles. For accommodations, contact adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our Equal Employment Opportunity statement. BMS cares about well-being and recommends vaccination updates per company guidance. BMS will consider applicants with arrest and conviction records as required by law. If you live in or expect to work from Los Angeles County, visit careers.bms.com/california-residents/ for information. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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