Senior Manager, Project Engineer

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 .

The Engineer will support the delivery of capital and improvement projects for cell therapy manufacturing as part of the GoSolo Hypercell Team. This role is responsible for executing cross-functional projects that enable new capabilities, process enhancements, and technology deployments within the Devens Cell Therapy Facility.

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 life-cycle management to maintain high system reliability and support routine GMP operations.

Key responsibilities for this role include:

Project Execution & Delivery

• Support planning and execution of cell therapy capital and improvement projects from feasibility through implementation, commissioning, and qualification.

• Coordinate cross-functional project activities, schedules, and deliverables to ensure alignment with business, manufacturing, and quality requirements.

• Support development and execution of project documentation, including project charters, schedules, risk registers, and change management activities.

· Lead FAT, SAT, installation, commissioning, and qualification of automated systems.

Process & Technical Support

• Provide technical process support for cell therapy manufacturing operations, including hands-on engagement during implementation, start-up, and early operations.

• Partner with process, MSAT, and manufacturing teams to translate process needs into project and system requirements.

• Development and review of User Requirements (URS), functional specifications, design documentation, and commissioning/qualification deliverables.

Cross-Functional Collaboration

• Work across the Cell Therapy network to integrate advanced equipment and platforms into cell therapy manufacturing operations.

• Partner with Digital teams to ensure alignment with MES, data systems, and digital plant strategies.

• Collaborate with Quality to ensure projects meet GMP, validation, and regulatory requirements.

• Engage Manufacturing Operations to ensure solutions are operationally fit, supportable, and ready for routine use.

Start-up, Commissioning & Lifecycle Support

• Support FAT, SAT, installation, commissioning, and qualification activities for new equipment and systems.

• Provide on-the-floor support during project start-up and transition to operations.

• Support handover to sustaining teams, including documentation completion, training support, and issue resolution.

· Ensure systems integrate effectively with MES, automation layers, and digital infrastructure to meet business needs.

Continuous Improvement

• Identify opportunities to improve process robustness, project execution efficiency, and operational readiness.

• Apply lessons learned and standard practices across GoSolo and cell therapy project implementations.

Specific Knowledge, Skills, Abilities:

• Strong understanding of regulatory requirements, industry standards, and best practices for validation in pharmaceutical or biotechnology industries.

• Demonstrated experience delivering engineering or capital projects in pharmaceutical or biotechnology manufacturing.

• Working knowledge of cell therapy manufacturing processes and GMP operations

• Experience with equipment startup and validation.

• Experience with single-use technologies and closed systems.

• Experience within a cGMP manufacturing environment, including use of electronic records, electronic control systems, and ERP systems, such as Syncade MES, DeltaV, and SAP.

• Ability to develop and execute design, engineering, and validation strategies, including risk assessments, plans, protocols, and reports.

• Strong collaboration and communication skills, with ability to translate technical details into practical manufacturing guidance.

• Proficiency with data analysis to evaluate equipment performance and support continuous improvement.

• Excellent critical thinking skills and diligence.

Experience/ Licenses/Certifications:

Education

• Bachelor's degree in science or engineering, or a related discipline.

• Excellent critical thinking skills and diligence.

· Senior / Project Engineer Level: Minimum 4-6 years of industry experience with demonstrated experience delivering manufacturing or capital projects in biologics or cell therapy environments.

Travel:

· May require up to 10% travel to support vendor activities, FATs, or project start-up activities.

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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: $139,480 - $169,013

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

Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:

• Health Coverage: Medical, pharmacy, dental, and vision care.

• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).

• Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life benefits include:

Paid Time Off

• US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)

• Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

*Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the 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.

Supporting People with Disabilities

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 [email protected] . Visit careers.bms.com/ ( eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

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:

Data Protection

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Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [email protected] . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1600423 : Senior Manager, Project Engineer Company: Bristol-Myers Squibb

Req Number: R1600423

Updated: 2026-03-27 03:18:19.062 UTC

Location: Devens-MA

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.