Working with UsChallenging. 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 inspired by a single vision - transforming patients' lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change.

We bring a human touch to every treatment we pioneer. Join us and make a difference. Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today.

With therapies only in their infancy and BMS's continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible. Position Summary: This role will be accountable for the end-to end management for drug product or viral vector value stream for our commercial cell therapy product. Reporting to the Global Product Leader, this role will be responsible for identifying and implementing strategies, governance, initiatives, metrics, and risk mitigations to optimize drug product/viral vector performance with a focus on supply continuity, improving quality attributes, capacity expansion, cycle time improvement, productivity and COGM improvement.

This role will lead a high visibility cross functional team with strategic and functional scope spanning across sourcing, network capacity, supply assurance, product line/indication extensions, product enhancements, process and method technical changes, robustness/quality and productivity projects and business continuity planning. Accountabilities may also include budget setting, talent management/succession planning including hiring, and training to retain the best workforce talent.The Drug Product/Viral Vector Value Stream Leader will be responsible for setting strategic direction and operational KPIs to maximize drug product performance and delivery, in alignment with overall Brand Strategies, Global Product Supply/Cell Therapy Operations objectives and Enterprise priorities, while maintaining highly productive clinical and commercial operations.

The incumbent will be responsible for establishing and driving a culture of collaboration and alignment between various CTO functions to deliver value to patients.Responsibilities include but are not limited to:Maintains an integrated multi-year life cycle management roadmap across the end-to-end value chain, prioritizing key projects and investments encompassing drug product enhancements, process and method technical changes, sourcing, launches, robustness/quality and productivity projects. Drive product performance through establishing critical drug product performance KPIs, rigorously monitor and escalate progress through appropriate tier reporting and keep critical stakeholders informed of key trending, risks, and progressProvides input, documents and maintains long-range physical and financial flows, strategic and operational inventory targets, and long-range capacity plans to meet global supply requirementsIdentifies, prioritizes, roadmaps, and captures year-on-year continuous improvement opportunities in alignment with sites and functions, including robustness and cycle time.

Support GPL to secure drug supply strategies endorsements, including relevant product sourcing decisions, and may own technical agenda endorsements at appropriate governance forums which reflect priorities and sequencing of changes Ensures CMC change plans are developed and coordinated across sites, functions, and markets within the product vertical. Support GPL to ensure budget critical projects are aligned and resourced across key functions and sites and ensures completion and value delivery aligned with overall brand objectives & prioritiesOversees supply risk assessments and mitigation planning deliverables, including Annual Business Continuity Plans.Manages risks and issues that escalate above single site or function level to the right stakeholders as necessaryDrive continuous improvement and foster an operational excellence culture to enhance productivity and efficiency of operations across all functions.

Implement innovative solutions which sets BMS as the leader of cell therapy manufacturing.Sponsor in-house expertise with Lean process improvement and promoting a Lean culture.Coach a matrixed team of direct and indirect professionals and enable their individual growth.

Mature functional vision and drive strategy development and deployment to ensure reliable, efficient, and effective supplyDevelop the Best Team: lead, coach, and mentor a high performing supply chain organization that is adaptable to meet the dynamic needs of the future and integrated with the broader BMS Cell Therapy networkBuilds positive working relationships across the network, can effectively motivate and influence cross-functional teams, partners, and executive management to resolve issuesQualifications & Experience: B.S. in Engineering or Life Sciences/Masters or higher degree in a biology, chemistry, engineering, or other related field eg, MBA preferred.12 + years of experience in pharmaceutical manufacturing operations in Cell Therapy Manufacturing and/or Biologics Manufacturing, manufacturing science and technology, manufacturing systems, and/or quality assurance with at least 3 years in senior management positions.

Work effectively with US FDA and other regulatory agencies. Substantial knowledge of QSR, GMP, FDA, GAMP, ISO and other applicable standards.Demonstrated experience in both CMC development and commercial manufacturing operations.

Superb ability to lead both direct reports and large cross-functional teams; strong situational leadership skills, ability to lead staff at all levels of the organization. Ability to coach, mentor, and develop staffEssential ability to distill complex information and tailor verbal and written communications in a concise, logical, and audience appropriate manner; strong background to understand and solve complicated supply and demand problemsProven leadership ability to carry out difficult decisions in a logical, rational manner, and demonstrated ability to engage and influence team members in a matrixed environment.Ability to embrace and effectively prioritize implementation of new technologies and other life cycle management activities to support manufacturing improvements.

Ability to collaborate cross functionally within site and across the Global Cell Therapy Manufacturing Network to establish harmonization of best practices, processes, systems and engrain values. The starting compensation for this job is a range from $202,000 - $254,000, 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 Career Site.

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.Why You Should ApplyAround the world, we are passionate about making an impact on the lives of patients with serious diseases.

Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.If you want to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here with our Cell Therapy team. Full of incredible and dedicated team members, those working on CAR-T and other forms of Cell Therapy are transforming patients' lives through science.

From studying individualized cell lines to making brand new discoveries, this bold and personal discipline allows you to grow your career while making a lasting impact on the field of medicine. Join us today.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.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or 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.BMSCARTyou 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 CareersWith 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 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

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