
Senior Manager, Manufacturing Programs
- Bothell, WA
- $164,020-198,759 per year
- Permanent
- Full-time
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: .The Senior Manager, Manufacturing Programs plays a critical role in ensuring facility readiness and equipment reliability for CAR-T manufacturing operations. Reporting to the Senior Director of Manufacturing, this role leads key strategic programs focused on maintaining the facility in a state of GMP readiness, ensuring equipment availability, and supporting operational scalability. While this position has no direct reports, it requires strong cross-functional leadership, program ownership, and the ability to influence teams across engineering, facilities, maintenance, and operations.In addition to owning core manufacturing enablement initiatives, this role provides program and operations leadership to drive reliability improvements and ensure seamless execution of manufacturing priorities. The Senior Manager also leads project and change management efforts, developing and implementing structured plans that align stakeholders, remove barriers, and enable operational readiness for new products, processes, and site expansion.QUALIFICATION REQUIREMENTS (Knowledge, Skills and Abilities):Education:Bachelor’s or Graduate degree in Engineering, Life Sciences, or related field required.Experience:
- 7+ years of experience in a GMP-regulated environment, preferably in biologics or cell therapy manufacturing.
- Proven success in leading complex programs or projects across multiple departments.
- Strong understanding of equipment qualification, maintenance practices, and GMP facility operations.
- Experience in facility startup, technology transfer, or large-scale program execution preferred.
- Excellent communication skills, with ability to present clear, concise project plans and updates to leadership and stakeholders.
- Demonstrated ability to influence without authority and drive cross-functional collaboration.
- Strong project management, organizational, and problem-solving skills.
- Lead cross-functional programs to support facility design, equipment lifecycle management, and ramp readiness for current and future CAR-T operations.
- Champion reliability initiatives to reduce equipment downtime and improve turnaround time in support of manufacturing needs.
- Drive continuous improvement projects that enhance equipment performance, process robustness, and overall operational reliability.
- Serve as the primary liaison between Manufacturing and partner groups (Engineering, Facilities, Maintenance, MS&T, QA) to remove barriers to equipment and facility readiness.
- Represent Manufacturing’s priorities in site-wide forums and influence alignment across partner functions to enable operational success.
- Develop and manage clear, actionable project plans; track milestones and deliverables, and provide regular updates to key stakeholders and site leadership.
- Participate in strategic planning for site growth and support readiness activities for new product introductions, tech transfers, and expansion initiatives in strategic planning for site growth and support readiness activities for new product introductions, tech transfers, and expansion initiatives.
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 ProtocolBMS 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.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 . Visit to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.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:Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.