Bristol Myers Squibb
Senior Manager, Benchtop IT Systems - Devens Cell Therapy Facility
Bristol Myers Squibb, Harvard, Massachusetts, us, 01451
Senior Manager, Benchtop IT Systems - Devens Cell Therapy Facility
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Senior Manager, Benchtop IT Systems - Devens Cell Therapy Facility
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Bristol Myers Squibb . Get AI‑powered advice on this job and more exclusive features.
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.
Position Summary The
Senior Manager, Benchtop IT Systems
at the Devens Cell Therapy Facility is responsible for leading the design, deployment, operation, and lifecycle support of laboratory and benchtop IT systems supporting advanced cell therapy manufacturing. This position plays a pivotal role in integrating digital technologies into GxP laboratory environments, ensuring robust compliance, reliability, and alignment with business objectives. The Senior Manager collaborates cross‑functionally with laboratory, manufacturing, quality, automation, and global IT teams to deliver solutions that enable scientific innovation and operational efficiency.
Key Responsibilities
Lead and manage the end‑to‑end lifecycle of benchtop and laboratory IT systems (LIMS, CDS, SDMS, ELN, bespoke instrument software) within the Cell Therapy Facility, including requirements gathering, design, implementation, validation, and ongoing support.
Oversee system integration with manufacturing, quality, and enterprise platforms, ensuring seamless data flow and strong information security.
Ensure strict adherence to GxP, FDA, and other applicable regulatory standards in system implementation, validation, and operations.
Partner with internal stakeholders (lab users, engineers, QA, manufacturing) to clarify user needs, recommend scalable solutions, and drive digital innovation at the bench level.
Direct vendor relationships and manage contractors supporting laboratory IT systems, including service level agreements and performance monitoring.
Monitor system performance and proactively resolve incidents, collaborating closely with global support teams.
Develop and maintain robust documentation, validation plans, SOPs, and change control records for laboratory IT systems.
Drive continuous improvement initiatives, including system upgrades, user training, cybersecurity enhancements, and lifecycle planning.
Effectively manage operational budgets, resources, and schedules, tracking and reporting progress to site leadership and global IT function.
Provide leadership, coaching, and mentorship to direct reports and cross‑functional project teams.
Required Qualifications
Bachelor's Degree (or higher) in Computer Science, Engineering, Life Sciences, or related field.
7+ years of experience managing laboratory IT systems in a GMP or GxP‑regulated pharmaceutical manufacturing or research environment.
Deep knowledge of laboratory informatics systems (e.g., LIMS, CDS, SDMS, ELN) and corresponding validation requirements.
Demonstrated experience leading complex IT or digital projects, preferably in biologics or cell therapy manufacturing.
Strong understanding of CSV (computer system validation), data integrity, and regulatory requirements in laboratory environments.
Proven leadership, people management, and cross‑functional project management skills.
Excellent communication, organizational, and stakeholder management abilities.
Preferred Qualifications
Advanced Degree (MS, PhD, or MBA) in a relevant discipline.
Experience delivering IT solutions for advanced therapy manufacturing/laboratories (cell, gene therapy, biologics).
Knowledge of data analytics, cloud platforms, cybersecurity, and modern automation tools as applied to laboratory settings.
Experience with global organizations and matrix reporting structures.
Compensation Overview Devens - MA - US $151,280 - $183,319
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.
Benefits Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://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 the following: Medical, pharmacy, dental and vision care, Wellbeing support such as the BMS Living Life Better program, employee assistance programs (EAP), financial well‑being resources and a 401(k), short‑ and long‑term disability, life insurance, supplemental health insurance, business travel protection and survivor support, parental, caregiver, bereavement, and military leave, family care services, 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 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 at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field‑based and remote‑by‑design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Accessibility and Reasonable Accommodations BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
COVID‑19 Vaccination Policy BMS strongly recommends that all employees be fully vaccinated for Covid‑19 and keep up to date with Covid‑19 boosters.
Background Check BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
California Residency Requirement If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https://careers.bms.com/california-residents/.
Data Privacy Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Information Technology; Pharmaceutical Manufacturing
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Senior Manager, Benchtop IT Systems - Devens Cell Therapy Facility
role at
Bristol Myers Squibb . Get AI‑powered advice on this job and more exclusive features.
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.
Position Summary The
Senior Manager, Benchtop IT Systems
at the Devens Cell Therapy Facility is responsible for leading the design, deployment, operation, and lifecycle support of laboratory and benchtop IT systems supporting advanced cell therapy manufacturing. This position plays a pivotal role in integrating digital technologies into GxP laboratory environments, ensuring robust compliance, reliability, and alignment with business objectives. The Senior Manager collaborates cross‑functionally with laboratory, manufacturing, quality, automation, and global IT teams to deliver solutions that enable scientific innovation and operational efficiency.
Key Responsibilities
Lead and manage the end‑to‑end lifecycle of benchtop and laboratory IT systems (LIMS, CDS, SDMS, ELN, bespoke instrument software) within the Cell Therapy Facility, including requirements gathering, design, implementation, validation, and ongoing support.
Oversee system integration with manufacturing, quality, and enterprise platforms, ensuring seamless data flow and strong information security.
Ensure strict adherence to GxP, FDA, and other applicable regulatory standards in system implementation, validation, and operations.
Partner with internal stakeholders (lab users, engineers, QA, manufacturing) to clarify user needs, recommend scalable solutions, and drive digital innovation at the bench level.
Direct vendor relationships and manage contractors supporting laboratory IT systems, including service level agreements and performance monitoring.
Monitor system performance and proactively resolve incidents, collaborating closely with global support teams.
Develop and maintain robust documentation, validation plans, SOPs, and change control records for laboratory IT systems.
Drive continuous improvement initiatives, including system upgrades, user training, cybersecurity enhancements, and lifecycle planning.
Effectively manage operational budgets, resources, and schedules, tracking and reporting progress to site leadership and global IT function.
Provide leadership, coaching, and mentorship to direct reports and cross‑functional project teams.
Required Qualifications
Bachelor's Degree (or higher) in Computer Science, Engineering, Life Sciences, or related field.
7+ years of experience managing laboratory IT systems in a GMP or GxP‑regulated pharmaceutical manufacturing or research environment.
Deep knowledge of laboratory informatics systems (e.g., LIMS, CDS, SDMS, ELN) and corresponding validation requirements.
Demonstrated experience leading complex IT or digital projects, preferably in biologics or cell therapy manufacturing.
Strong understanding of CSV (computer system validation), data integrity, and regulatory requirements in laboratory environments.
Proven leadership, people management, and cross‑functional project management skills.
Excellent communication, organizational, and stakeholder management abilities.
Preferred Qualifications
Advanced Degree (MS, PhD, or MBA) in a relevant discipline.
Experience delivering IT solutions for advanced therapy manufacturing/laboratories (cell, gene therapy, biologics).
Knowledge of data analytics, cloud platforms, cybersecurity, and modern automation tools as applied to laboratory settings.
Experience with global organizations and matrix reporting structures.
Compensation Overview Devens - MA - US $151,280 - $183,319
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.
Benefits Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://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 the following: Medical, pharmacy, dental and vision care, Wellbeing support such as the BMS Living Life Better program, employee assistance programs (EAP), financial well‑being resources and a 401(k), short‑ and long‑term disability, life insurance, supplemental health insurance, business travel protection and survivor support, parental, caregiver, bereavement, and military leave, family care services, 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 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 at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field‑based and remote‑by‑design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Accessibility and Reasonable Accommodations BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
COVID‑19 Vaccination Policy BMS strongly recommends that all employees be fully vaccinated for Covid‑19 and keep up to date with Covid‑19 boosters.
Background Check BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
California Residency Requirement If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https://careers.bms.com/california-residents/.
Data Privacy Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Information Technology; Pharmaceutical Manufacturing
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