Job Information
Bristol Myers Squibb Senior Manager, Capacity & Drug Product Planning Lead in Seattle, Washington
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 rich in diversity. 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 Summary
The Sr. Manager in the mid/long term planning organization is an instrumental role in the CAR-T supply chain organization that will lead Cell Therapy network capacity and supply planning. This person will drive standardization of drug product supply planning amongst all products and ensure that a scalable robust process is built. While this role is an individual contributor, the role requires an ability to be able to influence across organizations to optimize and ensure sufficient capacity available for the Cell Therapy organization. The individual works closely with site and above-site counterparts to collate, quantify, and troubleshoot capacity plans and projections. Overall, this individual must have an internal drive to challenge the status quo, excellent organization, and analytical skills, as well as excellent written and verbal communication skills.
Key Responsibilities
Own and manage the monthly capacity planning cycle which includes partnering with sites and above-site supply chain on determining 3-year capacity plans.
Enable and support the semi-annual capacity planning cycle which includes partnering with sites and above-site supply chain on determining capacity projections for years 4-10 to enable Long-Term Supply Plan.
Analyze execution gaps to the capacity plans to continue to challenge the organization to drive more accurate planning.
Accountable for the cyclical execution of a 36-month rolling Supply Network Plan for Cell Therapy assets delivering global master schedule for all applicable manufacturing nodes.
Support and/or drive maintenance of digital planning systems (e.g. SAP IBP)
Maintain network supply planning rules and systems to enable on-time delivery of monthly plan.
Create scenario plans for what if scenarios and provide assessment on impact to demand vs. supply balance.
Own data gathering, analysis, insight extraction, recommendation generation, and material preparation in support of monthly stakeholder meetings such as Global Supply Review and Cell Therapy S&OP meetings.
Collaborate with global Business Process Owners and IT to identify, pilot, and implement advancements to digital planning tools(e.g. SAP IBP) to advance global master scheduling capabilities.
Perform ad hoc analysis and reporting to support business decisions.
Communicate insights concisely to a wide variety of stakeholders for purposes ranging from informative to need for approvals from executives.
Demonstrate advanced tactical and strategic thinking to form insights based on supply analyses.
Develop and review metrics and assess performance against targets to identify improvement plans to close gaps and increase accuracy.
Work cross-functionally to ensure that decisions are made and actioned which will allow our operations to run as effectively as possible
Build a collaborative environment that fosters decisive decision making and accountability
Lead as a change agent in a fast-paced environment to promote flexibility, creativity, and accountability to ensure project prioritization and adequate resource allocation
Create an environment of teamwork, open communication, and a sense of urgency.
Promote a mindset of continuous improvement, problem-solving and prevention
Build and maintain positive relationships with all functions across the Cell Therapy network, as well as with external customers and stakeholders.
Performs other tasks as assigned
Qualifications & Experience
Bachelor's degree in supply chain, engineering, life sciences, information systems, business management or related fields; advanced degree preferred.
8+ years' of related experience in GMP manufacturing and/or supply chain. Cell therapy experience preferred.
An equivalent combination of education, experience and training may substitute.
Demonstrates high degree of business acumen, with ability to deliver executive level presentations, challenge assumptions and drive decision making.
Flexible and comfortable working with ambiguity
Strong understanding of current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) and other regulatory requirements (EMA, TGA).
The starting compensation for this job based in Washington state is a range from $152,430 - $184,700, plus incentive cash and stock opportunities (based on eligibility).
The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. 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 our BMS Careers Site (http://careers.bms.com/) .
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 and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick
time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.
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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.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through scienceā¢ , 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 an inclusive culture, promoting diversity 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 a diverse 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 adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility 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: https://careers.bms.com/california-residents/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Company: Bristol-Myers Squibb
Req Number: R1589263
Updated: 2025-02-07 04:16:30.445 UTC
Location: Seattle 1000 Dexter-WA
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.
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