Bristol Myers Squibb Job Trends

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...

Bristol-Myers Squibb Company is hiring a(n) Senior Manager, Global MES Delivery (in Tampa, FL). Duties Collaborate with IT and Business teams to understand requirements and develop solutions for the Enterprise Manufacturing Execution Systems (EMES). Design, build, test, and deliver both standard and custom EMES capabilities across the global manufacturing network. Provide ongoing support to minimize disruptions to manufacturing operations and maintain product integrity. Support the administration of central EMES development and test systems, while overseeing site-specific development, test, and production environments. Contribute to the knowledge management strategy by creating content and mentoring team members. Identify and execute opportunities for continuous...

“Compensation Overview Tampa –FL - US $ 147948 - $157550 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. Duties Integrate data products from diverse source systems to ensure quality, performance and scalability using cloud platforms. Collaborate with business users to gather requirements...

Job Summary The Senior Specialist, Benefit Operations plays a central role in managing and coordinating the administration of all company-sponsored health and welfare benefits and wellness programs. This position is primary for Canada and also provides support for US and Puerto Rico. This position provides Tier 2 support and works collaboratively with internal People Services teams, including Payroll, Communications, HR Business Partners and Workforce Administration, as well as external partners such as benefit administrators, insurance carriers, vendors, and brokers. Ultimately, our goal is to provide an exceptional customer experience, ensuring our benefit programs are not only effective and efficient, but...

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...

The Clinical Veterinary Scientist I will support BMS’s AAALAC-accredited vivarium in Brisbane, CA by providing clinical veterinary care for laboratory rodents and promoting the research goals of BMS scientists through administration of the study support program. Key Responsibilities Provides daily clinical veterinary care (basic diagnostics and medical treatments) for laboratory rodents and maintains appropriate documentation. Coordinates study support program, including scheduling, pre-study planning, and providing direct clinical support on technical procedures for investigative staff. Serves as subject matter expert for relevant study support procedures and processes, including training staff, recommending procedure and process refinements as appropriate, and implementing change in...

Business Unit Overview Our Global Technical Services (GTS) organization is responsible for the safe, sustainable, and cost-effective construction, operation and maintenance of world-class facilities that enable the discovery, development and delivery of innovative medicines that help patients prevail over serious diseases. As part of GTS , t he Capital and Facilities Portfolio team oversees strategic capital and facilities across the portfolio , includ ing strategic site master planning , asset life cycle management, business case build and approval align ed to business and sustainability goals . In partnership with our Finance , Real Estate and executive stakeholders across BMS and...

Seeking a motivated and skilled Senior Scientist to join the Analytical Development team. The successful candidate must possess extensive scientific knowledge and hands-on experience in cell biology/immunology and/or RNA therapeutics. The candidate will collaborate with the research team, delivery team, process development, and other CMC groups to develop novel bioassays, including potency assays. The candidate will also conduct method transfer and qualification activities. Responsibilities Manage the development and pre-qualification work of multiple cell-based assays for RNA/LNP drug substance and drug product. Coordinate with other colleagues within analytical development and research group to transfer the phase-appropriate methods to external testing labs...

The WW Commercialization Learning Team plays a critical role in ensuring that healthcare providers are educated on the appropriate use of our medicines and have the information they need to improve outcomes for their patients. We develop learning strategies, scientific learning solutions and skill-based training to elevate the capability of customer-facing teams across the globe to compliantly engage in high quality scientific exchange with the healthcare community. The Sr. Manager, US Medical Learning - IMM embodies our medical mission by supporting our filed medical teams, i.e., Medical Science Liaisons, (MSLs). This role focuses on becoming the trusted partner of...

The Principal Scientist, LNP Process Development & MS&T plays a central role in enabling the success of batches in clinical development across multiple products. Connecting with both the larger LNP PD team and with research to develop clinical scale batches that are representative across scales and sites. The Principal Scientist is a scientific leader responsible for driving clinical manufacturing strategy, influencing cross-functional decisions, and delivering high-impact outcomes across an increasingly diverse portfolio. The Principal Scientist provides scientific leadership for bulk drug product programs spanning preclinical to early-stage development and leading the tech transfer and implementation of process into clinical...

The MSL role embodies our medical mission to be recognized as the trusted partner for internal stakeholders and the healthcare community, driving scientific exchange to enhance medical education, data generation, insight generation and patients’ access to medicine. The Medical Science Liaison (MSL) is responsible for identifying disease and product related medical needs in a defined geography. The primary role of the MSL is to develop and maintain relationships with Thought Leaders (TL) and Healthcare Providers (HCP) within their healthcare system. The purpose of their interactions is to engage in meaningful scientific exchange that will ensure patients have access to BMS...

Senior Associate Scientist (EG90 Lvl2), LNP Process Development Bristol Myers Squibb is on a mission to discover, develop, and deliver innovative medicines that help patients prevail over serious diseases. Guided by a commitment to rigorous science, integrity, and transformative innovation, BMS is a global biopharma leader dedicated to improving the lives of patients worldwide. In October 2025, BMS significantly expanded its RNA medicines capabilities through the acquisition of Orbital Therapeutics, bringing with it a powerful and differentiated RNA platform that combines circular and linear RNA engineering, advanced delivery technologies, and AI-driven design. This platform is accelerating BMS's efforts to pioneer...

This territory includes Atlanta, Augusta, Athens, Macon GA As part of the Oncology Field Medical organization, the Clinical Nurse Consultant (CNC) is a trusted clinical expert responsible for developing professional relationships and educating key Health Care Professionals (HCP) involved in the care of patients receiving BMS hematology and oncology products in a defined geography. The primary role of the CNC is to drive peer to peer interactions with customers that optimize patient outcomes by delivering end-to-end clinical exchanges that clarify the complexities of patient identification and management. The purpose of these interactions is to deliver a continuum of clinical education...

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...

When you join BMS, you are joining a diverse, high-achieving team united by a common mission. The Informatics and Predictive Sciences (IPS) mission is to Pioneer, Partner and Predict to drive transformative insights for patient benefit. IPS conducts applied computational research in areas that include genomic, structural and molecular informatics, computational and systems biology, patient selection and translational biomarker research, and broader fields including knowledge science, epidemiology and machine learning—across the full lifecycle of drug discovery and development and across all therapeutic areas at BMS. We do this in close partnership with scientific and clinical experts in the field, both...

1. PURPOSE AND SCOPE OF POSITION Process Engineers provide technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment. Technical support includes troubleshooting process and equipment related issues that occur during the Manufacturing process. Process Engineers work closely with the Manufacturing and Quality teams to determine immediate corrective actions for deviations, identifies root cause, and implements long-term preventive actions. Other responsibilities include participation in process tech transfer, supports incoming process changes by communicating the changes to applicable departments, and participates in process improvement projects at the site. Process engineers work to identify and drive continuous...

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...

Reporting to the Vice President, Cell Therapy Supply Chain, the Executive Director, Internal Site & ExM Supply Chain is accountable for the strategic development and operational execution of Cell Therapy Supply Chain across BMS's global internal drug product manufacturing sites and external manufacturing partners. This leader drives end-to-end supply chain execution — encompassing planning, scheduling, inventory, and materials management — while serving as the key Supply Chain representative across site and operations leadership forums, including Site General Managers, Site Leadership Teams as well as Cell Therapy Supply Chain leadership team. This role has direct leadership responsibility over a team of...

Duties/Responsibilities Lead the Campus IT Compliance and CSV team Promote a safe and compliant environment and mindset. Select, develop, coach, and manage the Devens Campus IT Compliance and CSV team. Set goals, objectives, and contributions of the Campus IT Compliance and CSV team. Drive continuous improvement of team productivity and KPIs. Ensure the team delivers critical projects on time. Act as a liaison between site stakeholders and enterprise/business application teams to ensure business continuity is maintained. Manage service providers and ensure alignment with contractual SLAs. Engage and support PBRG teams in support of the BMS culture. Act as the Computer...

The Executive Director, E2E Supply & Demand Planning, is a strategic leader responsible for establishing and governing the integrated supply chain plan across all planning horizons, including long-range, mid-term and short-term planning for Drug Product and Vector. This role leads the translation of commercial and clinical demand into a feasibly demand, supply and capacity network plan ensuring alignment between product strategy, operational and financial objectives. This position is responsible for scenario planning, capacity planning, inventory optimization, proactive identification of supply and demand risks and opportunities while ensuring reliable patient delivery by monitoring and ensuring adherence to TAT targets. Through leadership...

Position Medical Science Liaison, Cardiovascular Location Houston, South Texas & Louisiana The MSL role embodies our medical mission to be recognized as the trusted partner for internal stakeholders and the healthcare community, driving scientific exchange to enhance medical education, data generation, insight generation and patients’ access to medicine. The Medical Science Liaison (MSL) is responsible for identifying disease and product related medical needs in a defined geography. The primary role of the MSL is to develop and maintain relationships with Thought Leaders (TL) and Healthcare Providers (HCP) within their healthcare system. The purpose of their interactions is to engage in...

The Manager Quality Systems - Change Control and Quality Risk Management (QRM) is responsible for supporting ownership and oversight of assigned quality systems per established local and global standards. This position supports the overall compliance and performance of the Change Control and QRM processes as they apply to the site level, including periodic assessments of process performance and continuous improvement opportunities. Duties/Responsibilities Support oversight of the Devens Cell Therapy site Change Control system, including facilitation of site Change Control Review Board. Drive Change Control governance maturity plans to improve site performance through data-based analysis and integration of management review through...

Translational Development is part of the Global Research organization in BMS and leads late-stage clinical, pharmacological and translational research and development activities for the pipeline and supports late-stage portfolio for regulatory, translational development and life cycle management. Translational Development drives strategy across core therapeutic areas at BMS including hematology, oncology, immunology, cardiovascular and neuroscience. This group integrates laboratory science, clinical trial/biomarkers and asset development as well as disease research to maximize the potential of BMS current and future therapeutics. Incumbents with deep training and education in cardiovascular, or related disease areas, including but not limited to neurocardiac research. Key Responsibilities...

The Manager, Data & AI Analytics Engineering is a hands-on individual contributor responsible for designing, building, and delivering scalable data and AI-driven analytics solutions supporting Global Patient Operations (GPO). This role plays a critical part in advancing the GPO Analytics Hub, enabling standardized, high-quality data models, cross-platform data integration, and AI/automation use cases to drive operational insights and decision-making across patient operations, manufacturing logistics, scheduling, supply chain, and workforce analytics. Key Responsibilities Collaborate with cross-functional teams (SCLT, APH Ops, BI&T, Manufacturing, Supply Chain) to translate business needs into scalable data solutions Design, develop, and maintain scalable ETL pipelines and data...

As part of the Real-World Data Analytics team, you will get the opportunity to work with a collaborative team in an inclusive and supportive environment. Associate Director, is an individual contributor responsible for performing non-interventional research projects in support of key customer groups including Global HEOR, PV&E, medical, regional and local HEOR, medical teams, and others. Project work includes support of protocol development, identification of appropriate data sources, execution of protocol-related programming, analysis and summary of data, and collaboration with customers on presentation of results. In addition, this role will supply methodological expertise on non-interventional research methods to the Real-World...

The Director of Cell Therapy Network Orchestration leads enterprise-level Cell Therapy (CT) supply chain strategy, owning end-to-end network outcomes and decision-making. This role defines and drives AI/analytics strategy, standards, and frameworks for network orchestration, ensuring consistent, scalable, and data-driven operations across the organization. The Director of Cell Therapy Network Orchestration serves as a key enterprise thought leader, shaping not only Cell Therapy strategy but also influencing broader PDS and CTLT supply chain direction. This role integrates cross-functional inputs into actionable insights, while representing BMS externally through industry engagement, partnerships, and thought leadership. Key Responsibilities Network Strategy & Planning Develops CT...

Associate Director, US Oncology National Account Executive Position EG-140 – Associate Director, US Oncology National Account Executive Location Remote by Design Hiring Manager Kim Mueller Reports to Kim Mueller, Director - US Oncology National Account Executive Travel Approximately 50% overnight travel within the assigned geography Position Overview The Associate Director, US Oncology National Account Executive (ONC NAE) is responsible for leading strategic account management and market access initiatives across major oncology customers in Minnesota, Michigan, and Wisconsin. This role drives optimal product access, appropriate utilization, and sustained portfolio performance for both launch and inline oncology assets by engaging senior clinical,...

The Senior Manager, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. / Objective Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct May serve as Clinical Trial Lead for one or more trials May lead or support trial level activities for one or more trials with the necessary supervision May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members Position Responsibilities Collaborate and...

Reporting into the Executive Director of Strategy and Operations, this role dotted lines into and serves as the Chief of Staff for the VP, Rheumatology Marketing and Sales. This is an exciting time for the US Rheumatology team, with a strong in-line business and two potential upcoming launches, requiring a highly effective strategic and operational partner to help drive focus, alignment, and execution across the organization. As a director on the ICV S&O team, this individual will also help drive the evolution of Strategy & Operations capabilities by building new ways of working, enhancing organizational effectiveness, and contributing to a...

At BMS, digital innovation and Information Technology are central to our vision of transforming patients’ lives through science. To accelerate our ability to serve patients around the world, we must unleash the power of technology. We are committed to being at the forefront of transforming the way medicine is made and delivered by harnessing the power of computer and data science, artificial intelligence, and other technologies to promote scientific discovery, faster decision making, and enhanced patient care. If you want an exciting and rewarding career that is meaningful, consider joining our diverse team! This role will play a crucial part...

The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients. The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. The role builds and maintains strong professional credibility...

Manufacturing Associate Biopharmaceutical Manufacturing | Day Shift (Quad 1) | cGMP Cleanroom Environment About the Role The Manufacturing Associate is responsible for producing human blood-derived components in a controlled, cGMP cleanroom environment in accordance with Standard Operating Procedures (SOPs) and regulatory requirements. This role operates within a collaborative, shift-based team structure and plays a critical part in ensuring the quality, safety, and timely delivery of life-changing therapies. Shift Schedule Quad 1 — Sunday through Wednesday, 500 AM – 530 PM Start and end times are subject to change based on business needs. This position reports directly to the Manufacturing Manager...

Key Responsibilities Own site‑level quality oversight for Manufacturing and Laboratory IT systems, including support for deviations, investigations, and CAPAs, ensuring sustained compliance and inspection readiness. Accountable for IT Change Management governance, providing risk‑based oversight and acting as the primary site authority for IT change control. Act as a Validation Lead for Manufacturing IT and OT systems, accountable for approval and lifecycle compliance of CSV and SDLC deliverables. Maintain ongoing compliance accountability for IT systems, procedures, and training supporting CAR‑T manufacturing and laboratory operations. Lead the Site IT System Periodic Monitoring program, ensuring effective execution, documentation, and remediation of compliance risks....

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...

The Senior Director, Digital Integration & Execution, Cell Therapy Supply Chain , is accountable for driving standardization across planning systems and ensuring the delivery of integrated, system-enabled solutions aligned with business planning processes. This role spans key Cell Therapy sites—including Summit (NJ), Bothell (WA), Devens (MA), and Leiden (Netherlands)—with responsibility for ensuring alignment to Global Supply Chain (GSC) strategies and priorities. The scope includes leading master data strategy and execution, including critical data cleansing and remediation, advancing system-based planning adoption, and driving enhancements across both digital systems and business processes to enable a scalable, integrated supply chain. Lead Change the...

The Associate Director, US Policy Research & Economics leads the development, execution, and oversight of policy evidence strategies that shape federal and state healthcare policy landscapes. This role holds authoritative responsibility for high‑risk, complex projects and contributes directly to strategic direction‑setting across US policy, state and federal advocacy, and legislative engagement. The Associate Director provides senior‑level guidance, drives priorities for their area, and ensures evidence generation informs and influences external environments, policy decisions, and organizational strategy. Core functions include evidence strategy development, project design and management, distilling findings into policy-relevant messaging, and dissemination. Responsibilities Lead the design and execution of...

We are seeking a Associate Engineer, IT Laboratory Systems to support laboratory and manufacturing benchtop IT systems in a GMP-regulated environment. This role provides hands-on technical support, troubleshooting, and operational execution to ensure system availability and compliance across manufacturing and laboratory operations. The position primarily supports non‑standard business hours, including nights, extended hours, weekends, holidays, and scheduled site shutdowns. Flexibility to Support Core night and morning shifts 8pm-6am 9am-5pm 4x10 hr shift and 5x8 hr shift Sunday- Wednesday and Wednesday-Saturday The Associate Engineer serves as a critical off‑hours resource, providing independent issue resolution, escalation, and execution support to maintain continuity...

The Senior Consultant, Benefits Product Design (PDD) role focuses on implementing and supporting benefits projects and process improvement initiatives, with customer-centric, change management and compliance mindset. This position requires a blend of strategic planning, and operational excellence to ensure the delivery of benefits services align with organizational goals and employee needs. The Senior consultant will be responsible for data management, and enhancement of benefits offerings, working closely with the benefits operation teams. This role demands an interest in process improvement, standardization and automation. Detailed Position Responsibilities 1 . Product Design Assist in developing processes that align with business goals and...

As BMS Oncology evolves toward a more targeted, biomarker-driven portfolio, it is critical to maintain deep, sustained engagement across the global oncology ecosystem to inform and shape long-range portfolio strategy. The Senior Manager, Strategic Alliances is an important role within Global Medical Oncology Portfolio & Alliance Strategy (PAS), accountable for supporting and executing the external alliance vision that advances BMS Oncology’s portfolio ambition. This role will ensure partnership excellence for our strategic oncology alliances, leading academic institutions, external experts, and thought leaders across tumor types and modalities Key Responsibilities Reporting to the Senior Director, Alliance Strategy, you will be a...

The RNA Purification Process Development function plays a central role in designing efficient, robust, and scalable manufacturing processes. By combining deep scientific expertise with enabling technologies and strong cross-functional partnerships, RNA Process Development delivers transformative innovation across the pipeline. The Principal Scientist is a scientific leader responsible for driving RNA drug substance purification development strategies, influencing cross-functional decisions, and delivering high-impact outcomes across increasingly diverse portfolio. The Principal Scientist provides scientific leadership for drug substance programs spanning early- to late-stage development across circular and linear mRNA modalities. This role encompasses hands-on and technical leadership contributions, addressing critical challenges by driving...

Job Posting Senior Therapeutic Area Specialist, Cardiovascular Specialty - Detroit N, MI Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Detroit N, MI At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. The BMS Mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. 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....

The Principal Scientist, RNA Synthesis Process Sciences role plays a central part in collaborating with research and manufacturing to define early process conditions and scale down process development. By combining deep scientific expertise with enabling technologies and strong cross-functional partnerships, RNA Process Development delivers transformative innovation across the pipeline. The Principal Scientist is a scientific leader responsible for driving RNA drug substance synthesis and circularization strategies, influencing cross-functional decisions, and delivering high-impact outcomes across increasingly diverse portfolio. The Principal Scientist provides scientific leadership for drug substance programs spanning preclinical to early stage development across circular and linear mRNA modalities. This...

The Bioprocess Associate uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for the manufacture of therapeutic proteins used in medicines that are revolutionizing the treatment of serious disease. Shift hours are TBD Key Responsibilities Operate production equipment within an assigned functional area adhering to Good Manufacturing Practices (GMPs) and standard operating procedures (SOPs) Revise and create process documents and assist with process related investigations Train for proficiency in process automation and supporting business systems and in the operation of primary production equipment within the assigned functional area Lead in maintaining material and components inventory level...

Job Posting Senior Therapeutic Area Specialist, Cardiovascular Specialty - Toledo, OH Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Toledo, OH At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. The BMS Mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. 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...

Summary The Senior Director, Field Medical Analytics will lead the global strategy, development, and execution of advanced analytics capabilities that enable Bristol Myers Squibb’s Field Medical organizations to deliver data-driven insights and optimize decision-making across therapeutic areas. This role is accountable for defining the vision and roadmap for field medical analytics, integrating AI-driven solutions, and ensuring robust governance and compliance in all field analytics activities. As a senior leader, this individual will oversee the design and implementation of analytics frameworks that support field medical engagement, clinical trial performance, and medical insights. The Senior Director will partner closely with Medical Affairs,...

The Associate Director, Global Medical Mavacamten is a key medical contributor responsible for driving execution of the Global Medical plan for mavacamten across its lifecycle in hypertrophic cardiomyopathy (HCM), with a primary focus on enabling US medical execution. This role provides scientific and clinical leadership across global deliverables—including core content and scientific materials, congress planning support, medical education, and cross-functional scientific engagement—to ensure timely, high-quality support for US priorities and milestones. The Associate Director operates in a highly collaborative environment with a diverse matrix team and partners closely with US Medical, Regional Market Medical, Medical Communications, Clinical Development, Regulatory, Safety,...

What We Are Looking For The US Commercialization Learning team is seeking a highly organized and service-oriented Executive Associate to enable operational excellence across the US Commercialization Learning organization. The selected candidate will be responsible for coordinating the people, processes, vendors, budgets, and events that underpin a scalable, data-driven learning operation. This role requires discretion, strong interpersonal skills, and a collaborative mindset to support the team's mission of delivering impactful learning experiences across the US commercial organization. Who You Will Work With This position is a headquarters-based role reporting to the Executive Director, US Commercialization Learning. The Executive Associate will...

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...

The Senior Manager, US Medical Promotional Review (Oncology), plays a critical role in the Medical Communications team within Global Medical Affairs. As a member of this team, you will serve as a strategic, solutions-oriented partner focused on ensuring the medical accuracy and scientific validity of promotional and non-promotional materials, within an Oncology brand and disease area. This includes ensuring robust scientific evidence and compliance with US laws and regulations. Key Responsibilities Maintain therapeutic area and product knowledge through ongoing assessment of relevant published literature, treatment guidelines, internal resources, and data Provide strong medical guidance in interdisciplinary meetings and related initiatives,...

This territory includes Myrtle Beach, SC, Charleston, SC and Savannah GA The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients . The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients . To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience ( Cx ) through deeper scientific dialogue on and consistent with...

The Senior Director, Device Quality provides global strategic leadership and accountability for Quality across medical devices, drug device combination products, companion diagnostics (CDx), and precision medicine–enabling platforms, including CLIA certified laboratory operations supporting clinical trials and commercial diagnostics. This role ensures patient safety, robust regulatory compliance, and sustained inspection readiness across the full lifecycle—from early development through commercialization and post market surveillance. The Senior Director partners closely with Precision Medicine, R&D, Clinical Development, Regulatory Affairs, Global Manufacturing, External Manufacturing, and Commercial teams to embed quality by design into innovative, personalized medicine solutions. This role is a key strategic position within...

The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients. The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. The role builds and maintains strong professional credibility...

Chemical Process Development (CPD) is a team of organic chemists, analytical chemists, and chemical engineers working together to design novel syntheses from raw materials to supply new medicines to patients. CPD scientists focus on developing safe, economical, sustainable, and robust processes to support clinical trials and the launch of new medicines across various drug modalities including small molecules, peptides, oligonucleotides, and antibody drug conjugates. Our work is driven by innovative science, data-driven decision-making, and collaborative teamwork. The scientific knowledge package from the manufacturing process, design parameters, and control strategies enables regulatory filings to bring these novel medicines to patients worldwide....

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. The Manufacturing Associate, Cell Therapy brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The incumbent...

The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients. The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. The role builds and maintains strong professional credibility...

Summary The Senior Manager, GMP Maintenance, leads the 24/7 GMP Maintenance team that supports Devens Site Biologics Manufacturing Operations. This role is accountable for day-to-day management of the GMP Maintenance organization within the Devens Site Engineering Department and for ensuring that GMP manufacturing facilities, systems, and equipment are operated and maintained in a state of operational and inspection readiness. The Senior Manager develops and executes a strategic maintenance and reliability plan to maximize equipment and critical-utility availability and performance at an optimal cost, while meeting quality, safety, and environmental requirements. Major Responsibilities Serve as a member of the Site Engineering...

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...

Associate Director – Biomarker Data Scientist This is a new position . You will join a new cutting-edge Drug Development Data Science and Biomarker team to advance the global drug development process. We are looking for candidates with strong leaderships skills; strong computational, statistical, and biological capabilities; and a demonstrated track record of translating complex data into testable hypotheses and experience modeling multimodal (clinical, omics, real-world) data using the classical ML and Deep Learning algorithms. We are looking for hands-on state-of-the-art practitioners. What you’ll do Develop and apply novel or existing computational methods for patient segmentation from multimodal clinical and...

USRL, working on the Hematology and Oncology Strategy GRS Organization at BMS. In close partnership with the regional strategists / liaisons and/or GRL Team leader, develop strategic and operational plan for the development and the registration of assets across Therapy Area. Support marketing application submission teams for indications that are at the regulatory filing stage; helping to develop strategy and content for global dossiers. Develop contingency plans in conjunction with the GRL or Team Leader for achieving regulatory objectives with associated risks and mitigation strategies in conjunction with GRT Propose approaches to resolve regulatory issues and appropriately drive speed to...

We are looking for a dynamic and commercially savvy marketer to join the US Breyanzi Marketing team in the role of Senior Product Manager, US Breyanzi HCP Treater Marketing. This individual will be a key member of the US Cell Therapy Organization, responsible for driving the day-to-day execution of HCP-facing marketing strategies and tactics that advance the Breyanzi brand. They will serve as the primary lead for field insight gathering and synthesis, playing a critical role in ensuring that marketing execution is rooted in a deep understanding of the HCP landscape and translates meaningfully into the field. The ability to...

Support Devens site through review and approval of investigations and change controls. Provide Quality oversight and support for Technology Transfer, Automation, Cell Bank Disposition, Validation, Manufacturing Science and Technology, Master Data and Site Engineering programs. Assure the quality of manufactured products are in compliance with all applicable regulations and guidelines. May assist in preparing for and hosting of regulatory audits. Key Responsibilities Supports and provides quality oversight to technical transfer sub-teams and the review and approval of technology transfer documentation Maintains operating procedures for the site Quality Assurance programs to ensure consistent, high-quality materials are produced. Provides floor support to...

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...

The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients. The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. The role builds and maintains strong professional credibility...

Summary As a Senior Data Scientist within Bristol Myers Squibb's AI Venture Studio delivery team, you will be a hands-on senior individual contributor who helps convert ambiguous scientific and business opportunities into measurable AI product hypotheses, experiments, and working solutions. You will partner with AI Engineers, Data Engineers, App/Cloud Engineers, Frontend Engineers, product owners, and domain experts to build and evaluate AI systems across R&D, Commercialization, Manufacturing, and Enabling Functions. The role sits at the edge of applied data science and AI engineering you will design evaluation datasets, build analytical features, prototype models, test agent and retrieval performance, measure product...

The Executive Director, Microbiology Quality Sterility Assurance (MQSA) is a pivotal global leadership role within BMS's Corporate Quality organization. This position brings critical expertise in sterility assurance, microbiological controls, and contamination control strategy across BMS's internal and external commercial and PD manufacturing sites — spanning pharmaceutical, biopharmaceutical, cell therapy and radiopharmaceuticals. This role is responsible for defining, owning, and governing BMS's enterprise-wide Contamination Control Strategy (CCS) as a living, risk-based framework — ensuring alignment with EU GMP Annex 1, FDA, and all applicable global regulatory standards. The Executive Director serves as the global Single Point of Contact (SPOC) for all...

In conjunction with the Team leader; develop global regulatory strategy in development and through life cycle management taking into account all relevant guidance, commercial needs, and company objectives. Lead regulatory dossier submissions to global and/or FDA (IND, BLA, NDA, and supplements) utilizing internal and external resources; ensure appropriate quality controls in place for compliant submissions Work with cross-functional groups to define and manage contributions to submissions; Participate in or lead the regional Regulatory Sub-team for assigned product(s)/project(s); Writing regulatory documents (e.g. new INDs, briefing book content, BT Designation request, Priority Review Requests, ODD); reviewing core documents to support IND/BLA/NDA, in...

Summary Within the Nonclinical Discovery and Development Sciences (NDDS) organization at BMS, the Development DMPK Team provides ADME (absorption, distribution, metabolism, and excretion) and PK (pharmacokinetics) support for all pipeline assets throughout clinical development, from candidate nomination through registration and lifecycle management. The Development DMPK team is responsible for characterizing the ADME properties, and drug-interaction potential of drug candidates. Working closely with drug safety and clinical pharmacology, Development DMPK plays a critical role in IND submissions and marketing authorization applications. We utilize our deep expertise in ADME and PK to collaborate with peer R&D functions to identify and solve issues,...

Bristol Myers Squibb is seeking an Associate Director, Regulatory Excellence & Hematology/Oncology Operations to lead operational and business management activities within the Oncology/Hematology organization. This role serves as a strategic partner to leadership, driving execution of portfolio priorities, operational planning, compliance, and regulatory excellence initiatives across a team of approximately 45 professionals. The successful candidate will be recognized internally as a subject matter expert in regulatory operations and business management, exercising considerable latitude in shaping deliverables, leading initiatives of strategic importance, and developing solutions to highly complex, sometimes novel problems with broad impact across the department. The role requires anticipating...

Bristol Myers Squibb is on a mission to discover, develop, and deliver innovative medicines that help patients prevail over serious diseases. Guided by a commitment to rigorous science, integrity, and transformative innovation, BMS is a global biopharma leader dedicated to improving the lives of patients worldwide. In October 2025, BMS significantly expanded its RNA medicines capabilities through the acquisition of Orbital Therapeutics, bringing with it a powerful and differentiated RNA platform that combines circular and linear RNA engineering, advanced delivery technologies, and AI-driven design. This platform is accelerating BMS's efforts to pioneer a new generation of programmable RNA therapies across...

Associate Director, Global Regulatory Strategy, Hematology/Oncology Position Responsibilities as a Global and US Regulatory Lead In conjunction with the Team leader; develop global regulatory strategy in development and through life cycle management taking into account all relevant guidance, commercial needs, and company objectives. Lead regulatory dossier submissions to global and/or FDA (IND, BLA, NDA, and supplements) utilizing internal and external resources; ensure appropriate quality controls in place for compliant submissions. Work with cross-functional groups to define and manage contributions to submissions. Writing regulatory documents (e.g. new INDs, briefing book content, BT Designation request, Priority Review Requests, ODD); reviewing core documents...

Summary Executes preventive and corrective maintenance tasks following approved procedures and job plans to sustain asset functionality and compliance. Updates and closes work orders in CMMS system, maintains accurate records, and supports vendor escorting activities to ensure safe and compliant work execution. Shift Monday - Friday 200PM - 1000PM (second shift) MAJOR DUTIES AND RESONSIBILITIES Regulatory Compliance Follow internal policies, procedures, and recognized deficiencies while executing task. Support continuous inspection with execution by performing preventive and corrective task. Audit & Inspection Support Perform routine inspections and testing of assigned systems in accordance with established procedures; report observed deficiencies to supervisor....

The Oncology Thematic Research Center at BMS is a key research and early development engine, responsible for the discovery and development of novel oncology therapeutics for patients. Centered at our state-of-the-art research sites in Cambridge, scientists focus on novel targets and pathways for tumors that are refractory to current therapies. With a deep understanding of the causal human biology, we are leveraging our multiple modality platforms to best match the modality to the mechanism and desired outcome. We are a fully integrated drug discovery through translational and early clinical development organization which exploits state-of-the-art in vitro, in vivo and ex-vivo...

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. The Supply Chain Operator, Cell Therapy brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The...

KNOWLEDGE AND SKILLS REQUIRED BS in Science, Engineering, or technical related field. Five 5 years of experience in Engineering Department related matters in the biopharmaceutical industry. Knowledge of EOHSS, cGMP’s, local/Federal regulatory requirements, and documentation procedures pertaining to a biopharmaceutical manufacturing plant. Timely and effective decision making, and timely conflicts resolution skills. Computer literate with the ability to understand and use basic computer software packages like Excel, Word, Power Point, Internet, etc. Ability to read and interpret layout drawings, mechanical, pneumatic and electrical blueprints, is preferred Fluently in English/Spanish (Oral and Written) Strong interpersonal relationship skills with subordinates, peers,...

Summary The Associate Director, U.S. Health Systems Analytics will lead complex analytics and strategic decision-support workstreams that help Bristol Myers Squibb understand how U.S. pricing, payer, reimbursement, and health policy dynamics may affect portfolio planning, pricing, patient access, budget impact, and business decisions. This role will focus on high-priority U.S. pricing and access topics, including the Inflation Reduction Act, Medicare and Medicaid reforms, PBM reform, government payer and pricing dynamics, broader payer / reimbursement changes, and policy-driven access issues. The ideal candidate will bring a strong understanding of the U.S. health system, along with the ability to translate policy, payer,...

The Senior Director, Global Clinical Development serves as the Clinical Indication Lead for one or more indications of a given asset. This role is accountable for clinical strategy and execution in the given indication(s). This role leads a team of physicians and scientists in the design, execution, analysis, and interpretation of all clinical studies for respective indications of a given asset. Key Responsibilities Clinical Strategy & Asset Leadership Owns and drives clinical development strategy across given asset indications, aligned to overall asset strategy, Target Product Profile (TPP), and relevant disease area strategy. May lead the Clinical Development Team(s) for given...

Summary The Senior Manager, Health Systems Analytics will manage analytical workstreams that help Bristol Myers Squibb understand how changes in policy and market access may affect pricing, patient access, portfolio planning, and business decisions. This role will support high-priority work across emerging pricing and access topics, including the Inflation Reduction Act, Most-Favored Nation policy, Medicare and Medicaid reforms, PBM reform, government payer and pricing dynamics, and broader payer and reimbursement trends. Candidates do not need experience in all of these areas, but should have relevant experience in market access, pricing, health policy, payer dynamics, commercial analytics, or a related field....

This position plays a critical role in the development and execution of BMS' WW & US medical strategy within our Mavacamten (Camzyos®) cardiovascular portfolio. The Global Medical Mavacamten Medical Product Lead (MPL) is a strategic leader with a broad scope of responsibilities within the Worldwide Medical organization and a key leader of the cross-functional matrix, providing medical insights and interpretation of the evolving cardiomyopathy landscape and disseminating clinical data across the organization. The MPL has overall accountability to develop aligned medical strategies and execute core medical deliverables, including Integrated Evidence Plans, Scientific Narratives, and External Engagement and Advocacy plans as...

Reporting to the Sr Director, the Director, WW Cell Therapy Class Expansion & Solid Tumor (ST) Pipeline serves as a global medical leader responsible for driving CAR-T class expansion strategy across hematology and autoimmune disease and shaping early-stage solid tumor pipeline medical strategy. The role drives enterprise-level strategy, evidence generation, and cross-functional alignment to accelerate global impact of the cell therapy portfolio. Key Responsibilities Strategic Leadership of Portfolio CAR T Class Expansion Develop and execute global medical strategy for expanding the class of CAR-T cell therapy across diseases and settings Identify gaps/barriers and implement innovative solutions to improve delivery of...

Summary The Manager, Health Systems Analytics will support high-priority analytics that help Bristol Myers Squibb understand how changes in policy and market access may affect pricing, patient access, portfolio planning, and business decisions. This role will contribute to work across emerging pricing and access topics, including the Inflation Reduction Act, Most-Favored Nation policy, Medicare and Medicaid reforms, PBM reform, and broader payer and reimbursement dynamics. Candidates do not need experience in all these areas; the most important qualifications are strong analytical judgment, structured problem-solving, comfort with ambiguity, and the ability to translate complex inputs into clear business implications. The role...

Job Posting Senior Therapeutic Area Specialist, Cardiovascular Specialty - Pennsylvania Central Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Pennsylvania Central At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. The BMS Mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. 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...

Summary Lead GHEOR strategy and tactics for one or more indications within the Alzheimer’s Disease (AD) portfolio with input from key stakeholders such as Clinical, Medical, Marketing, Market Access, Statistics, and Regulatory Responsibilities Lead the development of an aligned strategy for GHEOR to demonstrate the value of neuroscience assets in one or more indications within Alzheimer’s Disease (AD). Integrate and align this HEOR strategy through establishing and maintaining cross-functional collaborative relationships with internal stakeholders including, but not limited to access strategy, clinical, medical affairs, and commercial. Give input into clinical trial design and endpoints aligned to value demonstration strategy. Lead...

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...

Director of Medical Evidence Generation in Medical Affairs, will lead strategy, development, and execution of robust evidence generation strategies for the Neuroscience portfolio through Clinical Research Collaborations (CRCs), Medical Affairs Sponsored Studies (MAST), and Investigator-Sponsored Research Studies (ISRs), designed to inform clinical development, support product value, and underpin medical strategy across the product lifecycle. This will be a scientific and strategic leader collaborating across internal functions (Medical Strategy, RWE/Epidemiology, Clinical Operations, Regulatory, HEOR, Access & Value) and with external stakeholders including key opinion leaders (KOLs), academic partners, and data collaborators. Responsibilities will include, but are not limited to, the following...

This is a high-impact strategy and operations role that sits at the center of one of BMS's most important growth priorities; the build-out of the US Neuroscience marketing organization. This role carries a dual mandate that is both enterprise-facing and brand-specific 1. US Neuroscience Portfolio Strategy & Operations Serve as the primary S&O partner to the VP, US Marketing, Neuroscience in building and operationalizing a growing commercial organization. This is a unique and highly visible opportunity to help shape how the Neuroscience team is structured, how it operates, and how it scales across cross-functional brand leadership teams. Responsibilities include establishing...

Summary Experienced medicinal chemist who is seeking to lead and contribute to the drug discovery portfolio in the Protein Homeostasis Thematic Research Center in our San Diego Discovery Chemistry group. We are seeking a talented and highly motivated individual with a strong background in medicinal chemistry to join our Global Discovery Chemistry, Therapeutic Discovery Sciences team in San Diego. The successful candidate will contribute and lead a team of scientists that engage in rational design of new agents for the potential treatment of diverse oncology indications. The individual will apply modern drug design principles to solve medicinal chemistry problems relevant...

Job Posting Senior Therapeutic Area Specialist, Cardiovascular Community - Seattle North, WA Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Seattle North, WA At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. The BMS Mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. 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....

The Immunology and Cardiovascular Thematic Research Center (ICV TRC) at BMS is one of the fundamental Research units delivering therapeutics to patients. Our mission is to create transformative medicines of tomorrow based on the cutting-edge science of today. We leverage BMS’s internal invention engine that includes industry-leading expertise in small molecule chemistry, protein biotherapeutics, cell therapy, protein degradation, nucleic acids, and other therapeutic modalities. We are seeking a translational scientist with a background in cardiovascular biology to identify and discover novel and existing biomarkers to support the progression of late-discovery programs to early phase clinical trials and beyond. As...

Sr Director, Global Regulatory Strategy, Neuroscience Will be a key member of the GRSP Extended Leadership Team to ensure the development, implementation, and alignment of regulatory strategies across projects and the Neuroscience therapeutic area. Acts as regulatory representative on various company-wide projects and initiatives. Support due diligence and business development assessments. Working with regional regulatory staff as Global Regulatory Lead and US Regional Regulatory Lead on assigned development assets and marketed products Develop global therapeutic regulatory strategies and operational plans for identified investigational and marketed products. Review/provide counsel on product development plans. Assemble the global regulatory plans for identified projects/products....

The Associate Director, Global Clinical Science reports through the Clinical Development function which provides scientific expertise necessary to design and deliver clinical studies and programs. / Objective Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial Lead for one or more trials Successfully leads, plans, and executes trial level activities for multiple trials with minimal to moderate level of supervision Provides scientific and clinical leadership to team of supporting Clinical Scientists (matrix leadership) Co-Leads study team meetings in partnership with GDO protocol manager; and collaborate with cross functional study team members May support...

Director of Medical Evidence Generation in Medical Affairs, will lead strategy, development, and execution of robust evidence generation strategies for the Neuroscience portfolio through Clinical Research Collaborations (CRCs), Medical Affairs Sponsored Studies (MAST), and Investigator-Sponsored Research Studies (ISRs), designed to inform clinical development, support product value, and underpin medical strategy across the product lifecycle. This will be a scientific and strategic leader collaborating across internal functions (Medical Strategy, RWE/Epidemiology, Clinical Development, Clinical Operations, Regulatory, HEOR, Access & Value) and with external stakeholders including key opinion leaders (KOLs), academic partners, and data collaborators. Responsibilities will include, but are not limited to,...

This territory includes s San Jose, San Francisco, Bakersfield, Monterey, Fresno, Oakland, San Luis Obispo, Pismo Beach, CA As part of the Oncology Field Medical organization, the Clinical Nurse Consultant (CNC) is a trusted clinical expert responsible for developing professional relationships and educating key Health Care Professionals (HCP) involved in the care of patients receiving BMS hematology and oncology products in a defined geography. The primary role of the CNC is to drive peer to peer interactions with customers that optimize patient outcomes by delivering end-to-end clinical exchanges that clarify the complexities of patient identification and management. The purpose of...

Senior Institutional Mental Health Account Specialist Therapeutic Area Neuroscience - COBENFY Locations Boston MA; Belmont MA/ Burlington MA/ Salem MA/ Cambridge MA Bristol Myers Squibb has a rich history in Neuroscience focused on developing innovative medicines to help people living with Neurodegenerative and Neuromuscular conditions. Bristol Myers Squibb currently markets a product in Neurology and has reentered the Psychiatry market with a focus on patients living with schizophrenia. BMS is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will...

The Americas Benefits Process and Product Design (Benefits PPD) is a pivotal role focused on implementing and managing comprehensive benefits programs with a customer-centric and successful vendor management approach. This position requires a blend of strategic planning, financial acumen, and operational excellence to ensure the delivery of top-tier benefits services that align with organizational goals and employee needs. The Americas Benefits PPD will be responsible for vendor management and ensuring compliance with regulatory changes. A strong emphasis is placed on data management, vendor relations, and budget oversight to maintain and enhance the effectiveness of benefits offerings. The role demands a...

The Associate Director, Global Clinical Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. / Objective Serves as a primary source of medical accountability and oversight for clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a high performing Study...

Key Responsibilities Independently lead initiatives end-to-end, acting as both the business partner and technical architect for ServiceNow solutions. Gather business requirements and translate them into Agile stories with clear acceptance criteria for the offshore development team. Design and architect scalable solutions within the ServiceNow platform across GRC, SecOps, and Legal Service Delivery modules. Manage relationships with process owners across GRC, SecOps, and Legal Service Delivery, handling day-to-day escalations. Partner with the OneTrust team to document current-state privacy workflows and translate them into ServiceNow Privacy Management requirements. Ensure feature parity, capture acceptance criteria, and support knowledge transfer during platform migrations. Coordinate...

The Senior Manager, Global Clinical Science function provides scientific expertise necessary to design and deliver clinical studies and programs. / Objective Will be r esponsible for design and execution of assigned clinical trial activities and w ork closely with clinical team members within the assigned project to execute activities associated with the conduct May serve as Clinical Trial Lead for one or more trials May lead or support trial level activities for one or more trials with the necessary supervision May co- lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members...

Bristol Myers Squibb is looking for people who align with our Mission and have a passion to help physicians and patients prevail over serious diseases and ensure appropriate access to our medications. We are looking for smart, professional, and passionate people, like you, who want to make a difference in the lives of patients. Bristol Myers Squibb has a personal stake in developing our people not only today but for the long term. We are looking to hire our future leaders and help you reach your potential while building a career that makes you proud. Please consider this opportunity to...

As part of the Market Access, Public Affairs and Patient Programs Leadership Team (MAPLT), oversees the strategy, evolution, and operations of our Patient Support Programs, services and associated innovative patient and health system solutions. Responsible for leading a team of Senior PSP Program Managers, who are accountable for a select number of PSPs and develop program strategy, manage program operations, oversee vendor performance and leverage insights to inform program evolution. The Associate Director works in full compliance with laws, regulations, business rules and BMS standards of Business Conduct and Ethics. Key Responsibilities Sets the vision, strategic direction and evolution...

Reporting to the Director, Enterprise Thought Leadership & Crisis & Issues Communications, the Senior Manager, Enterprise Thought Leadership & Crisis & Issues Communications plays a critical role in executing Bristol Myers Squibb’s global enterprise thought leadership strategy and supporting the company’s preparedness for and response to emerging issues and crises. This role is responsible for helping to identify, plan and execute thought leadership and visibility opportunities that enable BMS leaders to deliver a cohesive enterprise narrative. The Senior Manager partners closely with leader communicators and the broader corporate communications team including the coordination, logistics, briefing and messaging materials, and leader...

The Operations Scheduler is responsible for supporting manufacturing operations through maintenance-focused scheduling activities. This role primarily coordinates, tracks, and follows up on maintenance work with Site Engineering and Manufacturing. The Operations Scheduler serves as the primary operational interface to ensure maintenance activities are visible, coordinated, and aligned with manufacturing operations and supports day-to-day manufacturing scheduling changes as needed. Key Responsibilities Incorporate planned and unplanned maintenance activities into the manufacturing schedule. Coordinate closely with Site Engineering and Manufacturing to monitor maintenance execution, track status, and communicate schedule impacts. Submit and manage service requests for facilities, equipment, and project work, including extensions...

The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients. The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3. The role builds and maintains strong professional credibility...

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. Associate, Patient Materials Operations is responsible for handling patient material needs/requirements for CAR-T production per Standard Operating Procedures (SOPs) in controlled...

Senior Institutional Mental Health Account Specialist Therapeutic Area Neuroscience – COBENFY Territory Jackson MS; Tupelo MS, Biloxi MS, Monroe LA, Shreveport LA Bristol Myers Squibb has a rich history in Neuroscience focused on developing innovative medicines to help people living with Neurodegenerative and Neuromuscular conditions. Bristol Myers Squibb currently markets a product in Neurology and has reentered the Psychiatry market with a focus on patients living with schizophrenia. BMS is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will...

Senior Institutional Mental Health Account Specialist Therapeutic Area Neuroscience – COBENFY Territory North LA (Bakersfield, CA San Bernardino, CA/Covina, CA) Bristol Myers Squibb has a rich history in Neuroscience focused on developing innovative medicines to help people living with Neurodegenerative and Neuromuscular conditions. Bristol Myers Squibb currently markets a product in Neurology and has reentered the Psychiatry market with a focus on patients living with schizophrenia. BMS is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the...

The Executive Director, CASA, Portfolio & Forecasting AI is responsible for designing, building, and scaling AI-driven forecasting products and decisioning capabilities that power Bristol Myers Squibb’s portfolio planning, brand forecasting, and financial outlook. This role owns the end-to-end AI product roadmap for demand, inventory, and Gross-to-Net (GTN) forecasting—from data ingestion and model development to deployment, monitoring, and closed-loop learning—ensuring accuracy, transparency, and explainability across brands and markets. As a senior leader within the AI & Omnichannel organization, this executive partners closely with Finance, Commercial Operations, Market Access, Supply/Inventory, and BI&T to modernize the forecasting tech stack, embed predictive and generative...

The Director, Clinical Pharmacology is responsible for leading the planning, implementation, and execution of clinical pharmacology strategies across one or more development programs, reporting to the Senior Director, Clinical Pharmacology & Pharmacometrics. This role drives trial- and program-level activities, applying pharmacokinetics/pharmacodynamics (PK/PD) principles and model-informed approaches to support decision-making throughout drug development. The Director partners cross-functionally to shape and deliver integrated development strategies, contributes as a key member of Clinical Pharmacology leadership and program teams, and ensures the development and execution of robust Clinical Pharmacology & Pharmacometrics (CP&P) plans aligned with compound strategy. In addition, the role fosters a collaborative...

The AD, US Medical Learning (sometimes referred to as US Medical Trainer) embodies our medical mission by supporting our primary and complimentary learner populations. This role focuses on becoming the trusted partner of choice to a broad set of stakeholders, driving scientific exchange and collection of timely insights that can create measurable medical impact on patient outcomes, ultimately advancing science and enhancing patient access to our medicines. This position is based in NJ. The primary remit of the AD, US Medical Learning, is to have a thorough view of the training needs of medical colleagues with field facing responsibility. This...

People Consultant/ Generalist This role requires a balance of people-focused perspective and operational execution. The successful candidate will build strong partnerships across the business, apply sound judgment to complex workforce matters, and drive continuous improvement in People processes and employee experience. Success in this role depends on credibility, adaptability, and the ability to influence effectively across a diverse stakeholder group. The People Consultant serves as the primary point of contact for People Managers and is part of the People Services team. The role provides proactive support across the Americas Region, with specialist expertise in at least one of the...

The Senior Manager, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. / Objective Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct May serve as Clinical Trial Lead for one or more trials May lead or support trial level activities for one or more trials with the necessary supervision May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members Position Responsibilities Collaborate and...

The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients . The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients . To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience ( Cx ) through deeper scientific dialogue on and consistent with label , le veraging new ways of working and CE ^3 ....

The Oncology Thematic Research Center at BMS is a key research and early development engine, responsible for the discovery and development of novel oncology therapeutics for patients. Centered at our state-of-the-art research sites in Cambridge and Seattle, scientists focus on novel targets and pathways for tumors that are refractory to current therapies. With a deep understanding of the causal human biology, we are able to leverage our multiple modality platforms to best match the modality to the mechanism and desired outcome. We are a fully integrated drug discovery through translational and early clinical development organization which exploits state-of-the-art in vitro,...

The Director, Global Clinical Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. / Objective Serves as a primary source of medical accountability and oversight for multiple c linical trials Matrix management responsibilities across the internal and external network Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a high performing...

Leads the establishment and ongoing development of a Therapeutic Area (TA) team of scientific writers. Demonstrates in-depth expertise in the relevant TA and specific assets, enabling effective leadership in the creation of content libraries when warranted. Applies advanced regulatory documentation skills to guide and/or support the implementation of new processes, tools, and continuous improvements within the scope of departmental responsibilities. Demonstrates strong managerial, scientific, and customer-focused leadership skills. Applies regulatory documentation standards that enhance efficiency and ensure consistency across the entire development and life cycle management of TA assets, across geographic regions. Leads strategic planning for document automation and leads...

The Senior Manager of Biostatistics is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. These individuals develop collaborative relationships and work effectively with the Biostatistics Lead, and other cross functional team members. Key Responsibilities Collaborates in design of clinical study including methodology, data analysis & interpretation, and reporting of study results. Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, associated publications, and other study level specification documents with minimum supervision Performs and/or validates statistical analyses, advise ways to maximize...

The Associate Director, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. / Objective Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial Lead for one or more trials Successfully leads, plans, and executes trial level activities for multiple trials with minimal to moderate level of supervision Provides scientific and clinical leadership to team of supporting Clinical Scientists (matrix leadership) Co-Leads study team meetings in partnership with GDO protocol manager; and collaborate with cross functional study team members May support clinical development planning (collaboration with Clinical Development...

The Director, Global S&OP Capability Owner (GCO) designs, manages, and improves cross-pillar capabilities enabling BMS Global Supply Chain (GSC) to deliver on its strategic goals. The GCO has accountability for the continuous advancement and improvement of a horizontal business capability within the Global Supply Chain. The GCO collaborates with various stakeholders, including GSC Pillar leadership and functional teams, IT, finance, and other GCOs, to ensure consistent execution and drive towards best-in-class maturity of the assigned capability. The GCO leverages digital tools and technologies to streamline processes, enhance data accuracy, and drive innovation. Role & Responsibilities The GCO is responsible for...

The Senior Director, Global Clinical Development sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. CDLs are matrix leaders and managers who lead, develop, motivate and achieve results through teams; demonstrate a commitment to the development of a resilient attitude, embrace change and have an unwavering commitment to our People Strategy Serves as the clinical point of accountability for the Development Team and is responsible for the overall clinical development plan for asset(s) in one or more...

Summary The Senior Manager, Project Management will manage and/or support the aspects of initiating, planning, and executing complex, multi-disciplinary projects throughout Devens Biologics. With a breadth of hands-on project management experience in the Pharma/Biotech regulated environments, the Project Manager is expected to manage this critical initiative in support of specific site goals & objectives. The Project Manager will be responsible for using Devens PMO best practices, tools & templates and will be proficient in PMI program management standards, processes, procedures, and guidelines. The successful candidate must have a proven record of extensive professional experience and the drive to steer internal...

Position Summar y The Executive Director, PDS Digital Transformation & Fusion will report to the VP , PDS Chief of Staff and will lead the design and execution of a cross-functional operating model that embeds digital, data, AI, and advanced analytics capabilities into core business processes across Product Development & Supply (PDS). This role carries a clear executive mandate to lead and influence PDS wide transformation, shaping how the organization operates through product-based delivery, end-to-end workflow redesign, and data-driven decisioning. This leader represents PDS in enterprise governance forums and plays a central role in aligning digital and operational priorities to...

The Associate Director, Aseptic & Sterile Process Engineering will serve as a technical leader for aseptic and sterile processing strategy supporting an advanced, automated manufacturing platform for cell therapy. This role is responsible for defining, justifying, and sustaining aseptic processing strategies that support regulatory approval and long‑term commercial manufacturing. The position requires deep technical expertise in aseptic processing combined with strong cross‑functional leadership and the ability to influence outcomes in a matrixed environment. Duties/Responsibilities Aseptic Processing Strategy Serve as the technical authority for aseptic and sterile processing strategy for an advanced automated manufacturing environment. Lead the development of scientific and...

Are you ready to lead the next chapter of AI at BMS? The Tech Education & Adoption team within Enterprise IT educates and engages the BMS workforce so we have the “digital dexterity” required to thrive in a continuously evolving, AI-powered modern workplace. In this role, you’ll be instrumental in advancing our AI adoption strategy—supporting employees in building AI literacy, integrating AI into their workflows, and unlocking innovation across the enterprise. Your primary focus will be on the AIQ Champions program, AIQ Academy, and the adoption of BMS’s AI ecosystem, but will also include change management and adoption of other...

Summary This position is critical to maintaining quality oversight and ensuring GMP compliance in day-to-day manufacturing operations. The Senior Field QA Specialist is responsible for reviewing Manufacturing Batch Records (MBRs), performing real time on-the-floor exceptions reviews and logbooks, conducting GMP area walkthroughs, and supporting timely return-to-service (RTS) walkthroughs to confirm that manufacturing areas and equipment are properly cleaned, calibrated, and ready for production use. The role also working closely with Manufacturing Operations to investigate and resolve manufacturing issues as they arise. Additionally, this position contributes to authoring and revising quality SOPs, supporting the review and closure of no-impact manufacturing deviations,...

The Associate Director, GTS Reliability will be responsible for driving the adoption and execution of the BMS reliability vision and strategy in line with business expectations. This role oversees and collaborates with sites, functions, and the greater Reliability network to develop and implement strategies that drive a continuous improvement culture. This position is a key contributor to the development and execution of reliability initiatives, strategic scorecards and dashboards, best practices in business processes, operational excellence principles, and systems development and deployment. It will be critical that this position work with leaders across PDS to meet business objectives and build the...

Senior Therapeutic Area Specialist Therapeutic Area Neuroscience - Cobenfy Territory West LA, CA The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients. The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging...

Associate, Patient Materials Operations Bristol Myers Squibb | Cell Therapy | Onsite 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. The Associate, Patient Materials Operations is responsible for...

Position Equipment Engineer, ECQ Operations – Day Shift Location Summit West PURPOSE AND SCOPE The Equipment Engineer, Equipment Commissioning & Qualification (ECQ) Operations supports laboratory, clinical and commercial manufacturing operations at their home site. Working with minimum supervision, this individual executes routine tasks, applies analytical skills to solve problems, and may lead small to medium-sized projects. The incumbent will write deviations, support investigations, and assist with change control implementation. Must be available to support 8-hour day shift operations, 5 days per week. REQUIRED COMPETENCIES Knowledge of cGMP, GXP, GAMP, SDLC regulations, 21 CFR Part 11, computer systems validation, and...

This role is responsible for leveraging technical expertise to develop and deploy cutting-edge data science and machine learning solutions across all Forecasting applications, with focus primarily on Commercial Demand. This role is pivotal in transforming our enterprise forecasting capabilities, shaping strategies, and implementing advanced methodologies, processes, and technologies that will accelerate insight generation and enhance decision-making and planning across the organization. Key Responsibilities and Major Duties Contribution to Analytical AI Community Contribute as part of a dynamic group of data scientists, machine learning engineers, and forecasting SMEs. Help inspire and shape the organizational mindset to leverage forecasting as a strategic...

Reporting to the Senior Director, Global Media Relations , the Associate Director, Media Relations, is responsible for executing a global media relations strategy designed to advance Bristol Myers Squibb’s reputation among key audiences. The ideal candidate will bring sharp media judgment and strong storytelling ability, with the proven ability to navigate a fast-paced news environment and deliver impactful media outcomes while effectively managing scope, timelines and resources. Key Responsibilities Execute a global, top-tier media strategy aligned with corporate positioning to advance the company narrative and enhance reputation through proactive and opportunistic engagement across print, broadcast, and digital media. Drive continual...

The Director of Medical Evidence Generation in Medical Affairs will lead the strategic development and execution of a robust evidence generation plan for an important asset within the Oncology portfolio, focused primarily in gastrointestinal (GI) and genitourinary (GU) cancers, including Clinical Research Collaborations (CRCs), Medical Affairs Sponsored Trials (MAST), and Investigator-Sponsored Research Studies (ISRs), designed to Uncover new clinical development opportunities that will maximize the benefit our medicines can bring to patients Address important unmet needs that are gaps in the current clinical development plan This will be a scientific and strategic leader collaborating across internal functions (Medical Strategy, RWE/Epidemiology,...

Associate Director - Key Account Management Therapeutic area Neuroscience, COBENFY Location Kansas City We are seeking a strategic, results-driven and experienced individual to join our team as an Associate Director, Hospital Key Accounts Manager (KAM) – Neuroscience. This is a critical role in establishing Bristol-Myers Squibb as a leader in Neuroscience and our commitment to supporting the efforts of Neuroscience Healthcare Providers in improving patient outcomes. The Associate Director, Key Accounts – Neuroscience is a field-based strategic leader responsible for driving enterprise account strategy, access, and adoption across complex health systems and Integrated Delivery Networks (IDNs). This role...