Bristol-Myers Squibb
Specialist, Associate Process 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 and Responsibilities
Specialist, Associate 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. The Associate 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, supports incoming process changes by communicating the changes to applicable departments, and participates in process improvement projects at the site. The process engineer works to identify and drive continuous improvements to the manufacturing process. Shifts Available:
TBD Responsibilities
Provides on-the-floor and on-site troubleshooting and technical support to Manufacturing 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. Basic Requirements
BSc and/or MSc degree in Science or Chem/Bio Engineering Minimum 0-3 years of industry experience. cGMP and/or Cell Therapy manufacturing experience preferred. Additional Information
This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management. BMSCART #LI-ONSITE GPS_2025 Compensation and Benefits
Devens - MA - US: $79,150 - $95,914 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related 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
care ers.bms.com/life-at-bms/. Benefits offerings are subject to the terms and conditions of the applicable plans then in effect and may include medical, dental and vision care; wellbeing programs; 401(k); disability, life insurance; travel protection; paid holidays; vacation; volunteer time; leave programs; and other perks. 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 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 BMS has an occupancy structure that determines where an employee is required to conduct their work. 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; site-by-design roles may be eligible for a hybrid model with at least 50% onsite; field-based and remote-by-design roles may require travel and occasional onsite presence as directed. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support. Applicants can request accommodations prior to accepting an offer. If you require accommodations, direct inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eoe-accessibility to access our Equal Employment Opportunity statement. BMS requires that employees be fully vaccinated for Covid-19 and stay up to date with boosters. BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws. If you live in Los Angeles County or work from there, visit care ers.bms.com/california-residents/ for additional 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 and Responsibilities
Specialist, Associate 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. The Associate 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, supports incoming process changes by communicating the changes to applicable departments, and participates in process improvement projects at the site. The process engineer works to identify and drive continuous improvements to the manufacturing process. Shifts Available:
TBD Responsibilities
Provides on-the-floor and on-site troubleshooting and technical support to Manufacturing 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. Basic Requirements
BSc and/or MSc degree in Science or Chem/Bio Engineering Minimum 0-3 years of industry experience. cGMP and/or Cell Therapy manufacturing experience preferred. Additional Information
This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management. BMSCART #LI-ONSITE GPS_2025 Compensation and Benefits
Devens - MA - US: $79,150 - $95,914 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related 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
care ers.bms.com/life-at-bms/. Benefits offerings are subject to the terms and conditions of the applicable plans then in effect and may include medical, dental and vision care; wellbeing programs; 401(k); disability, life insurance; travel protection; paid holidays; vacation; volunteer time; leave programs; and other perks. 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 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 BMS has an occupancy structure that determines where an employee is required to conduct their work. 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; site-by-design roles may be eligible for a hybrid model with at least 50% onsite; field-based and remote-by-design roles may require travel and occasional onsite presence as directed. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support. Applicants can request accommodations prior to accepting an offer. If you require accommodations, direct inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eoe-accessibility to access our Equal Employment Opportunity statement. BMS requires that employees be fully vaccinated for Covid-19 and stay up to date with boosters. BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws. If you live in Los Angeles County or work from there, visit care ers.bms.com/california-residents/ for additional 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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