Bristol Myers Squibb Job Trends

Position Senior Director, Workforce Operations & Finance Partnership Location Tampa As the Senior Director, Workforce Operations & Finance Partnership within People Services, you will serve as the primary HR strategic partner to Finance, ensuring seamless connectivity between People Services operations and enterprise financial systems. You will lead the design and execution of end-to-end HR operational processes that have downstream implications in our financial systems and processes — from workforce planning through Procure-to-Pay — ensuring that all people-related costs are accurately captured, automated, and reflected in financial systems with full transparency. In this role, you will act as the bridge...

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 a human touch to every treatment we pioneer. Join us, build your professional career within one of the most innovative bio-pharma companies, and make a difference. The TAS is...

Position Senior Therapeutic Area Specialist Therapeutic Area (TA) Psychiatry Location Reno, NV; Chico, CA/Yuba City, CA/Auburn, 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...

Position Senior Therapeutic Area Specialist Therapeutic Area (TA) Psychiatry Location Ventura CA; Santa Barbara, CA/Chatsworth, CA/Slymar, 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...

The Senior Counsel, Global Supply Chain & Trade serves as the lead legal advisor to the Global Supply Chain organization, which includes Customs & Trade. This individual will join the GSC leadership team and directly support the SVP, Global Supply Chain. This individual will provide regulatory, strategic and transactional support to the GSC organization. This individual should bring pharmaceutical legal experience with the ability to learn quickly, exercise excellent judgement, navigate complexity and be able to work with urgency and creativity across time zones, regulatory schemes, and stakeholders to advise on the successful resolution of legal and business issues while...

Position Senior Therapeutic Area Specialist Therapeutic Area (TA) Psychiatry Location San Francisco CA; Santa Cruz, CA/Palo Alto, 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...

The Director, Global Commercial Strategy, Thoracic/H&N will be a key member of the Oncology Global Commercial Strategy team, responsible for driving the strategic direction and commercial success of the Thoracic/H&N. This role will focus on maximizing asset value, shaping franchise growth, and ensuring strategic alignment across functions and geographies. The successful candidate will demonstrate strong strategic thinking, cross-functional leadership, and deep oncology market expertise. Key Responsibilities Lead the development and execution of global commercial strategies for Thoracic/H&N, in alignment with overall oncology portfolio objectives. Partner closely with Tumor Leads, Business Development, Medical, Market Access, and other stakeholders to drive integrated...

The Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations, including but not limited to Manufacturing, Quality Control laboratories, and Supply Chain/Warehouse Operations. This position will oversee and partner with operational areas to ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP. Shift NIGHT shift, 6 PM – 6 AM, Panama schedule (12-hour shift patterns with a 2-2-3 work cycle, including weekends and holidays) The Specialist, QA Shop Floor, is accountable to own quality decision making as it relates to unexpected events on the production floor, including deviation triage and determination,...

As part of our long-term strategy to elevate our Medical organization and transform the lives of million patients each year, we are seeking a Director, Professional Societies Cardiovascular within our Global Immunology & Cardiovascular teams.The position reports to the Executive Director, Portfolio Strategy Head within WW Medical Immunology & Cardiovascular (ICV) Global Medical Affairs. The Director, Professional Societies Cardiovascular is responsible for developing, leading and excetuing the strategic engagement plan for Worldwide Cardiovascular Professional Societies and Associations. This role works closely with the Portfolio Strategy Head and the Medical teams and additional key internal stakeholders to create and initiate innovative...

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. The Associate Engineer serves as a critical off‑hours resource, providing independent issue resolution, escalation, and execution support to maintain continuity of GMP operations. The role requires sound technical judgment, the ability to work with minimal supervision, and active participation in both...

Position The RWDR Sr Manager is an individual contributor responsible for performing non-interventional research projects in support of key customer groups including HEOR, PV&E, local HEOR teams, Medical and others. Project work includes identification of appropriate data sources, execution of protocol-related programming, analysis and summary of data and collaboration with customer on presentation of results. In addition, this role serves as a knowledge resource for the data development team and works with the RWDR Hematology Lead to coordinate therapeutic area support and communication. Position Responsibilities Conduct thorough and careful analysis of data, to effectively produce required information. Includes assisting...

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 role of Associate Director of US Commercial Regulatory Affairs requires the ability to apply complex scientific and expert regulatory advice and risk assessment for the development of promotional campaigns and materials for an assigned product/therapeutic area in order to help ensure the Company’s objectives are met. Individual will ensure materials are consistent with BMS guiding principles, PhRMA guidelines, FTC guidelines, and applicable FDA regulations and guidances. Responsibilities include Provides regulatory advice, risk assessment and mitigation strategies to Commercial Teams, Medical Affairs, Public Affairs, Value Access and Payment, and other internal groups, on all promotional materials, including concepts, disease awareness,...

This role is part of the Bothell Manufacturing Logistics & Services team and will focus supporting cGMP Manufacturing Operations for the BMS Bothell site, including the coordination, issuance, reconciliation, and management of production labels and records. Functional responsibilities include all batch label and documentation control activities for Cell Therapy Operations (CTO), including developing, performing, and maintaining a GMP compliant clinical and commercial batch documentation and label issuance and control process. The Manufacturing Labels & Issuance (MFG LI) Senior Specialist will work proactively to identify and address any batch record and label control compliance issues, own and update procedures within their...

The Global Information and Records Analyst is a key contributor to the Law Strategy & Operations Function, providing comprehensive Information Governance support across global business units. This role requires a strong analytical mindset, advanced project management, critical thinking and technical capabilities, to ensure compliance with legal, regulatory, and organizational requirements. Major Responsibilities and Accountabilities Lead and coordinate, develop, implement, and optimize all facets of the BMS Global Information and Records program, managing challenging projects while applying advanced analytical skills to assess program effectiveness and identifying opportunities for process improvement. Independently administer the Records Management System (Open Text/Content Manager), including the...

We are seeking to fill multiple Negotiation Governance Lead, Site Contracting roles in Princeton, New Jersey. As Bristol Myers Squibb ( BMS ) Negotiation Governance Lead, Site Contracting, you'll be the final word on complex, escalated contract and budget negotiations for global clinical trials. When site contracting gets difficult, legally, financially, or operationally, you're the person who resolves it. That's a level of influence and professional authority that's genuinely rare, and it comes with the scope, visibility, and support to match. If you've spent years building deep expertise in clinical site contracting and you're ready to lead at a strategic...

This position performs protocol-driven microbiological method validations and supports testing for the Clinical Supply organization and the BMS network of microbiologists. Testing will include but not be limited to bioburden, endotoxin, mycoplasma, minute virus of mouse, microbial identifications, sterility, container closure integrity testing. Position will keep track of data in electronic systems or notebooks, and will be expected to write or contribute to reports. This position is a 100% hands-on laboratory position, supporting new and existing products in BMS. This is a laboratory position, enabling the incumbent to develop laboratory skills and gain exposure to areas within an innovative company....

Position reports to the Executive Director of Global Medical Immunology & Cardiovascular, Medical Communications within Global Medical Affairs and lead a team across markets responsible for developing market level communication plans and execution of high quality, medical communications to ensure pull through of the Scientific Narrative. This role is responsible for the strategy and execution of BMS Medical Pulmonology Communications portfolio. The Director of Global Medical Pulmonology, Medical Communications will ensure the disclosure of the science of BMS products and research data to inform Healthcare Providers and Patients worldwide. Key Responsibilities Core member of Pulmonology Medical Communications Leadership Team, the...

The Associate Director of Site Contracting Governance & Strategy provides strategic leadership for the regional governance function, overseeing a highly skilled team responsible for direct site negotiations, complex budget and legal escalations, and the development of global contracting standards. This role serves as the strategic architect of regional site contracting approaches, driving policy development, portfolio‑level strategy, and enterprise alignment. The role ensures rigorous governance, consistent decision‑making, and executional excellence across all programs, partnering closely with operations team to ensure high‑quality delivery and seamless integration across the contracting lifecycle. Key Responsibilities Strategic Leadership & Governance Provide strategic direction for site contracting...

Werden Sie Expertin (m/w/d) für Kardiomyopathie und treiben Sie innovative Therapien dort voran, wo sie wirklich zählen! Beschreibung der Position Als Therapeutic Area Specialist, Cardiomyopathy (m/w/d) in dem Gebiet Berlin & Südbrandenburg bist Du verantwortlich für den Verkauf unseres innovativen kardiologischen Produktes in Kliniken und Praxen. Du entwickelst ein tiefgehendes Verständnis von Stakeholdern und Netzwerken Deiner Accounts und analysierst, welche Wege Patienten in Deiner Region von ersten Symptomen bis zur Diagnose und Therapieeinstellung durchlaufen und welche Bedürfnisse unsere Kunden haben. Du berätst Ärzte auf fachlich fundierter Augenhöhe und beherrschst das Spektrum moderner Verkaufstechniken, Omnichannel Strategien und digitaler Kanäle. Um ein...

Job Posting Senior Therapeutic Area Specialist, Cardiovascular Specialty - Portland, OR Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Portland, OR 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...

We are seeking an Associate Director to serve as a technology leader in an AI‑first, agile product team supporting Global Development Operations (GDO), specifically the Patient & Site Engagement Product Line. This role is accountable for technology direction and oversight in designing, building, and operating AI‑native products where large language models, agentic workflows, and data‑driven intelligence are the default approach to solving business problems—not an add‑on. The ideal candidate brings deep hands‑on engineering expertise and proven experience delivering production‑grade Generative and Agentic AI solutions in a regulated environment. This individual will shape how products are designed, developed, delivered, and continuously...

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...

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. As a Manufacturing Team Lead, you will Manufactures human blood derived components per Standard Operating Procedures (SOPs) in a controlled, cGMP...

Summary The Director, Customer Insights & Engagement will serve as a strategic leader within the Customer Insights & Engagement organization, driving the design and execution of advanced analytics and market research insights and capabilities that optimize engagement and performance across the US Thoracic business. This role is accountable for delivering end-to-end analytics and insights, ensuring alignment with brand objectives and enterprise commercial strategies. As a senior leader, the position will partner closely with cross-functional stakeholders—including Brand Tumor Leads, Sales, Finance, Medical and Access Leads—to integrate insights into broader go-to-market plans and enable data-driven decision-making. The Director will lead the development...

Reporting to the Executive Director, Policy, Purpose & Patient Communications, the Director, Purpose Communications , will own the enterprise purpose communications strategy for BMS to elevate our programs across population health and LMIC, patient advocacy and patient engagement, sustainability and social impact and corporate giving among key stakeholders. These communications efforts aim to enhance the company's reputation and underscore its purpose-driven mission to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. The Director, Purpose Communications will lead and set the strategic framework and priorities for purpose-driven communications across Corporate Affairs, working closely with the BMS...

The Senior Manager, , Sotyktu Forecasting PSO/PSA & Orencia plays a critical role within Worldwide Commercial Excellence by independently developing, maintaining, and delivering forecasts for one or more therapeutic areas. This role is responsible for generating high‑quality, objective forecasts that inform brand strategy, enterprise planning cycles, and cross‑functional decision‑making. The Senior Manager integrates insight streams (market research, competitive intelligence, chart audits), ensures assumptions are transparent and evidence‑based, and collaborates closely with Finance, MAx, Commercial, and Worldwide partners. At this level, the role focuses on hands‑on model execution, rigorous quality control, and the application of AI‑first forecasting tools through calibration and...

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,...

Job Summary Accomplished medicinal chemist aiming to lead and contribute to the BMS portfolio as an integral member of the Global Discovery Chemistry (GDC) organization, based in San Diego We are seeking a talented and highly motivated individual with a strong background in medicinal chemistry to join our Discovery and Development Sciences (D&DS) 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 to the...

The Cell Therapy Thematic Research Center is one of BMS’s differentiated research platforms delivering innovative therapies to patients. Our mission is to drive leadership in the use of cellular therapies to harness the power of the immune system in treating hematologic malignancies, solid cancers, and autoimmune disease. More specifically, our discovery and translational scientists are focused on developing next-generation, engineered cell-based therapies. The team is committed to discovering and developing transformative therapies that harness the power of the immune system to improve patient outcomes. We are seeking a highly skilled, collaborative, and detail-oriented scientist to join our Translational Research...

Our Associates perform a crucial role in driving our novel cell therapy programs by supporting routine manufacturing operations. We are searching for innovative, intellectually curious individuals with a general understanding of Good Manufacturing Practices (GMPs) to support routine manufacturing operations for Cell Therapy. Successful candidates must be goal-oriented and flexible, with the ability to work effectively and efficiently on a team while demonstrating safety, quality, and GMP compliance at all times. Key Responsibilities Learn and execute Cell Therapy Manufacturing operations compliantly Execute operations as outlined in Source Governing Documents (including but not limited to Standard Operating Procedures, Work Instructions, Batch...

Position Manager, Workforce Planning Partner Location Tampa A member of our People Services team, the Workforce Planning Partner is responsible for establishing a trusted relationship with Business Leads, Finance Leads and HR/TR Partners to understand organizational workforce strategies and plans during planning cycles (e.g. annual budget, projection forecasts, ad-hoc organizational changes). They use advanced skills and understanding of the entire worker life cycle to ensure data integrations are accurate throughout all human resources systems. Key Responsibilities Partners with Business Leads, Finance and HR/TR Partners to execute workforce planning actions against approved workforce plans Provides subject matter...

Role Summary The Senior Engineer I, serves as the system owner and lifecycle steward for integrated automation systems supporting analytical methods in late-stage and commercial cell therapy programs. This role is responsible for maintaining systems in a validated and inspection-ready state across GMP and non-GMP laboratories. The position drives governance of technology transfers from Analytical Development/QC into ASAT, oversees system validation activities, and provides operational ownership, end-user support, and training. The role works cross-functionally with Analytical Development, Quality Control, Quality Assurance, IT, and manufacturing stakeholders to ensure automation systems meet business needs while maintaining compliance with cGMP and data integrity...

The Director, Cell Therapy Quality Automation will play an important role in shaping the future of our organization's quality processes. This global position is responsible for the planning, execution, and implementation of next-generation quality processes to support high volume manufacturing processes. The Director will provide quality oversight of projects in supply chain, manufacturing, Quality Control, etc. The Director will be a core member of critical cross-functional teams which identifies the future state cell therapy value stream in conjunction with automated processing. This person will lead projects which integrate advanced technologies and methodologies, ensuring our quality systems are robust, efficient, and...

The Director of Fair Market Value (FMV) Operations within Strategic Risk Management at Bristol Myers Squibb will play a pivotal role in overseeing and managing all aspects of FMV operations, analytics, reporting, contracting, and governance. This leadership position is responsible for ensuring that all FMV activities are conducted in compliance with internal policies and external regulations. The ideal candidate will possess extensive experience in compliance, FMV operations, and analytics, with strong leadership skills and the ability to collaborate with various stakeholders across the organization. Key Responsibilities FMV Operations · Oversee and manage all FMV operations to ensure compliance with internal...

Summary The Executive Director, Global Market Research is responsible for setting the vision, strategy, and execution of Bristol Myers Squibb’s (BMS’s) global Market Research capability across all Therapeutic Areas and lifecycle stages. This role serves as a senior thought partner to Commercialization and Enterprise leadership providing strategic insight to inform pipeline prioritization, launch decisions, brand strategy, and in-market optimization. The Executive Director oversees a broad portfolio of Market Research capabilities, including performance tracking, demand and volume research, market mapping, brand positioning and messaging, market access research, early pipeline opportunity assessment, and patient- and consumer-focused research. This leader is accountable for...

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 Sr. Specialist of Manufacturing Science and Technology (MSAT) Manufacturing Systems Engineering and Operations (MSEO) - Labeling Operations brings enthusiasm, intellectual curiosity, scientific rigor, technical knowledge, and a desire to help drive novel programs to lead activities supporting labeling systems and operations for the Summit West Manufacturing Cell Therapy site. The Sr. Specialist is an individual contributor responsible for supporting the labeling operations intake and design, development, delivery, validation, operational support, continuous improvement, change management, and lifecycle for the site manufacturing execution system (MES) and associated boundary systems used in the labeling and packaging of personalized cell therapy products for...

Subject matter expert leading implementation of state-of-art automation solutions for QC bioanalytical methods and technologies in autologous and allogenic cell therapy programs. Work collaboratively with internal and external stakeholders to ensure automation designs meet compliance and business requirements. Build effective relationships/partnerships and work cross-functionally with internal and external stakeholders to implement novel integrated automated systems to streamline execution and analysis of cell therapy assays. Perform all functions related to automation technical transfer into the QC lab, including documentation associated with requirements gathering, development, IQ/OQ/PQ, and test method validation. Apply technical knowledge, regulatory requirements, and scientific principles to independently perform complex...

Position Senior Therapeutic Area Specialist, Neuroscience/MS (TAS) Location Field – Philadelphia North, PA 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,...

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...

Position Associate Director, Strategy & Operations, Customer Experience, Patient Access Liaison Reports to Executive Director, Strategy & Operations, Neuroscience Commercialization Location Remote/Field Company Overview At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology, and cardiovascular disease – and with one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contributes to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. The Associate Director, Strategy & Operations, Customer Experience,...

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 Scientist, Sterility Assurance, provides support to the CAR T manufacturing site. This role supports facility design/modifications, the aseptic process validation program, operator qualification, gowning certification, critical utilities, final product testing and adherence to the contamination control program for the site. The Scientist, Sterility Assurance is responsible to act as the SME during regulatory inspections. Duties/Responsibilities Support final product testing and release, incoming components and materials testing and release and monitoring of the critical utilities systems. Development and management of SOPs, forms, and methods required to ensure GMP compliance. Ensures the execution and support of the contamination control strategy for...

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,...

This position will prioritize the following Drug Development experience within a pharma/biotech organization Oncology experience; especially late phase PhD careers.bms.com/working-with-us Director of Biostatistics is a member of cross-functional team and contributes to development of compounds within Oncology. Drives the design of innovative and efficient clinical trials, including the selection of populations to study and endpoints to use. Develops trial designs that address study objectives that will support regulatory approval and market access. Contributes to Clinical Development Plans, submissions, and post-submission strategies, preparations, and defenses. Provides guidance and management to statisticians to ensure high quality and timely deliverables. Manages...

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 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 Director of Operational Excellence (OpEx) is primarily responsible for development and implementation of operational excellence systems and standards within...

Lead and manage Computer System Assurance (CSA) and IT qualification efforts for systems and applications in core GxP functions – primarily Research, Commercial and Cell Therapy functions. Supervise junior to mid-level team members assigned to IT and Compliance programs to ensure effectiveness, efficiency, consistency, quality of work and compliance with external regulations and internal procedures. Collaborate with cross functional and multi-location IT Delivery teams, business users and internal Global Quality compliance staff to ensure that CSA activities are planned and executed in accordance with internal procedures. Work with one-up manager and peers to propose effective and efficient quality strategies. Evaluate,...

The Senior MES Engineer is a strong technical subject matter expert (SME) responsible for the design, implementation, and support of Manufacturing Execution System (MES) solutions within the Devens Cell Therapy Facility. Leveraging deep expertise in Emerson Syncade MES and manufacturing systems, this role resolves complex challenges, enforces governance procedures, and drives the delivery of innovative digital solutions. The Senior MES Engineer collaborates across functions and the broader network to ensure operational consistency, regulatory compliance, and continuous improvement, while influencing the technical direction of MES initiatives. Duties/Responsibilities MES Business Analysis & Recipe Authoring Analyze MES requirements and implement recipe modifications to...

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 We are seeking talented and motivated M.S. synthetic organic/medicinal chemists who are passionate about joining a world-class group of scientists in the pursuit of innovative therapies at our San Diego, CA location. The successful candidate will be skilled in the art of organic synthesis and familiar with modern synthetic methods. The candidate will have demonstrated success in producing results, executing on synthetic routes to target molecules, analytical data interpretation, and troubleshooting reactions/purifications. The candidate will show an increasingly independent ability to design synthetic routes, understand medicinal chemistry concepts, and interpret biological data such that s/he is able to generate...

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 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...

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...

This territory includes Indianapolis, Terra Haute, Evansville, Bloomington, Kokomo, Richmond and Columbus, Indiana 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...

VP Finance, Research Highly visible finance business partnering role. The leader in this role will partner with BMS' Chief Research Officer and will be a member of the Global Research Leadership Team. The role reports directly to the SVP, R&D Finance and is a member of the R&D Finance Leadership Team. Influential and collaborative senior Finance business partnering role for a leader who operates with an Enterprise lens, and effectively shapes and drives the achievement of Research goals through Managing all aspects of the global Research P&L In close partnership with Research LT developing financial plans and goals grounded in...

The Executive Director, Early Differentiation & Pipeline (EDAP), Global Medical Neuroscience will lead the early‑stage medical strategy to differentiate pipeline assets and accelerate high‑value programs from discovery through key governance milestones. This role shapes integrated evidence strategies (clinical and real‑world), defines target product profiles (TPPs), advances biomarker/diagnostic and personalized care approaches, and drives cross‑functional portfolio decisions that maximize launch readiness, patient access, and long‑term lifecycle value across Neuroscience, with strategic alignment to Neuroscience portfolio. The leader will steward external scientific engagement, research collaborations, and scientific communications. while leading and coaching a high‑performing Early Asset Medical team. The Executive Director, Global...

Our Chemical Process Development group 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. Our 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. The 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...

Clinical Trial Physician, Rheumatology, Cell Therapy The Clinical Trial Physician, Rheumatology, is the primary source of medical accountability and oversight for one or more clinical trials within the Global Drug Development organization. This position will provide the candidate an opportunity to significantly change the treatment of autoimmune diseases such as lupus, scleroderma, inflammatory myositis and/or rheumatoid arthritis with CAR-T cell therapy. The incumbent will be accountable, alongside the Clinical Development Program Lead, for the development of differentiated and strategic CDPs from phase 2-3 and potentially through to registrational execution. They will be foundational in working with teams in Research, Early...

The Process Characterization Lab Scientist is a highly impactful and hands-on position within our global Parenteral Manufacturing Science & Technology organization, located in New Brunswick, NJ. The incumbent conducts product and process characterization studies; collaborates with research and development in drug product process development of sterile parenteral/biologics drug product and works with manufacturing sites to characterize, troubleshoot or optimize processes for late-stage to commercial and lifecycle products. The role touches many aspects of parenteral manufacturing including sterile filtration, formulation development/characterization, lyophilization, product compatibility and more. This gives the scientist the opportunity to contribute true scientific outcomes; enabling data driven decisions...

The Senior MES Engineer is a strong technical subject matter expert (SME) responsible for the design, implementation, and support of Manufacturing Execution System (MES) solutions within the Devens Cell Therapy Facility. Leveraging deep expertise in Emerson Syncade MES and manufacturing systems, this role resolves complex challenges, enforces governance procedures, and drives the delivery of innovative digital solutions. The Senior MES Engineer collaborates across functions and the broader network to ensure operational consistency, regulatory compliance, and continuous improvement, while influencing the technical direction of MES initiatives. Duties/Responsibilities MES Business Analysis & Recipe Authoring Analyze MES requirements and implement recipe modifications to...

This leader will shape the operational culture from the ground up, ensuring the site is staffed with exceptional talent, achieves operational readiness on an aggressive timeline, and continuously delivers operational excellence in a highly regulated, patient-centric environment. As the Associate Director of the Aseptic Observation Program, you will provide strategic leadership and direction for the team responsible for overseeing aseptic practices within Cell Therapy manufacturing cleanrooms and supporting environments. You will be accountable for ensuring that operators, verifiers, and support personnel consistently demonstrate proper aseptic techniques and behaviors, in line with the principles outlined in the Contamination Control Strategy. This...

The Director, Network Orchestrator , reporting to the Executive Director of GBU Services will play a pivotal role in overseeing and harmonizing supply chain operations across multiple Brand-focused value chain teams within the organization. This leader will ensure seamless supply planning, feasibility assessment, and resolution of capacity conflicts across internal and external manufacturing sites, covering Drug Substance, Drug Product, and Finished Packaged Goods across all modalities. Key Responsibilities This role is responsible for developing an integrated view of supply plans across the global manufacturing network, ensuring strategic alignment with corporate objectives, and driving execution excellence in support of patient supply...

Job Posting Senior Therapeutic Area Specialist, Cardiovascular Specialty - Bowling Green, KY Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Bowling Green, KY 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....

Reporting to the Executive Director, Policy, Purpose and Patient Communications, the Senior Director Policy Communications is responsible for translating the company’s policy messaging strategy into compelling, consistent strategic communication materials that reach and resonate with targeted external and internal audiences—including traditional and social media, influencers, and employees. Sitting within the Corporate Communications team, the Senior Director of Policy Communications will support the development of integrated communications plans that elevate our policy voice externally, build visibility for our positions, and support the company’s broader policy goals. The Senior Director will also be responsible for executing all communications activities in support of...

We are currently seeking a visionary Product Strategy Senior Manager to join our Drug Product Development Team, driving strategic product initiatives with a focus on integrating early commercial insights, fostering cross-functional collaboration, and ensuring a patient-centric approach. Key Responsibilities Early Commercial Insight Integration Collaborate closely with cross-functional teams to bring commercial insights into the R&D pipeline, enhancing the commercial viability of new assets from the early stages of development. Cross-Functional Collaboration Partner with internal teams across Commercial, Clinical, Regulatory, Product Development (e.g., formulation, packaging, devices), and CMC to define and execute product strategies. Partner with Business Development to identify strategic...

The Manager, Business Solutions Analyst, is a key member of the R&D Portfolio & Program Excellence product line within R&D Portfolio Operations BI&T. This role serves as the technical and analytical partner to product owners, program leaders, and IT delivery teams—turning business needs into scalable, high‑quality digital capabilities that enable effective portfolio governance, program management, RAID/risk tracking, and connected workflows across the R&D ecosystem. This role owns the end‑to‑end analysis and functional solution design lifecycle across R&D Project, Risk, and Resource Management capabilities and their integrations. The individual applies systems thinking, data fluency, and AI‑enabled analysis to design workflows that...

Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts. Duties/Responsibilities Perform method transfer/validation and routine testing of in-process, final product, and stability samples. Anticipate and perform routine troubleshooting and problem solving with minimal guidance. Perform data verification, data review and review of GMP documentation for general and complex methods. Perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts. Train and mentor others on QC test methods, processes and procedures. Perform other tasks as...

The Medical Evidence Generation (MEG) Lead in Oncology at Bristol Myers Squibb oversees evidence generation for the Oncology portfolio, including Clinical Research Collaborations (CRCs), Medical Affairs Sponsored Studies (MAST), and Investigator-Sponsored Research Studies (ISRs), ensuring alignment with internal strategies to accelerate pipeline development. Key responsibilities include fostering relationships with thought leaders, managing the lifecycle of CRCs and ISRs, and addressing evidence gaps by partnering with academic and professional networks. Responsibilities will include, but are not limited to, the following Facilitate collaborative exchange between BMS and thought leaders in community practice and academia, including scientific dialogue and representing BMS as a...

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 Executive Director, Technical Accounting, will play a pivotal role in leading the enterprise’s technical accounting function, ensuring global compliance with accounting standards, and driving excellence in financial reporting and governance. This leader will oversee the development, implementation, and continuous improvement of technical accounting policies and procedures, serve as a key advisor to senior leadership, and lead strategic projects that advance the organization’s accounting capabilities and transformation agenda. Key responsibilities include Lead the Technical Accounting, setting the vision and strategy for technical accounting governance, policy, and compliance across all regions. Ensure consistent application of US GAAP and other relevant accounting...

Summary The Manager, CSV Equipment and Instrumentation - Cell Therapy supports the successful implementation and support of manufacturing and laboratory equipment and local benchtop/standalone computerized systems at multi-use sites through interaction with internal customers and external service providers. With minimum supervision and given general instructions, this individual carries out routine tasks and functions, and uses strong analytical skills to recognize and solve common problems of various degrees of complexity and scope. As a developing team player, the incumbent interacts with their immediate supervisor and personnel within their own work group to achieve team goals while building trust and collaborative relationships...

Job Pos ting Title Senior Therapeutic Area Specialist, C ardiovascular Specialty - Frederick, MD Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Frederick, MD 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...

Summary The Senior Manager, MAx Strategy & Business Operations plays a critical role in enabling effective decision ‑ making, alignment, and operational excellence across the MAx organization. This role partners closely with the MAx core functional areas—including Global Market Access & HEOR, International Access, and Global Pricing—to drive consistent, high ‑ quality execution across strategic planning, business operations, and people strategy initiatives. Reporting to the Senior Director, MAx Strategy & Business Operations, this position serves as a trusted operational partner, ensuring strong governance, clear communication, and scalable infrastructure to support a complex, global, matrixed organization. The ideal candidate brings strong...

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 primary focus of this role is to support Bristol Myers Squibb (BMS) as the Associate Director, EHSS, Occupational Health &...

The Associate Director of Manufacturing Operations provides strategic leadership and operational oversight for multiple teams responsible for executing the end‑to‑end CAR‑T cell therapy manufacturing process, including Apheresis Receipt, Drug Product Packout, Cryopreservation, and Kitting. This role ensures that operations are carried out in compliance with cGMP requirements in both clinical and commercial settings. As a senior site leader, the Associate Director partners cross‑functionally with Global Manufacturing, Supply Chain, Quality, MS&T, EHS, and Operational Excellence to optimize business processes, enhance production capacity, strengthen compliance, and drive technical and organizational scalability. The role is responsible for developing front‑line leaders, setting strategic direction,...

The primary focus of the Quality Control Associate is to support QC testing for in-process, final product, stability samples and for supporting environmental and facility monitoring. May assist with documentation updates, deviations, investigations and continuous improvement efforts. Duties/Responsibilities Perform routine testing of in-process, final product and stability samples. Perform environmental/facilities monitoring and microbiological testing. May review GMP documentation and perform data verification. Perform document revision. Identify opportunities for continuous improvement. Support document revision, deviations, CAPA’s and investigations. May train analysts on general job duties. Perform other tasks as assigned. Qualifications Education and Experience Bachelor’s degree preferred in science. Associate degree...

The REMS Advisor Lead is responsible for building, developing, and leading a high-performing team of REMS Advisors who deliver exceptional REMS program education to certified prescribers and healthcare professionals. This role drives operational excellence by optimizing the prescriber and patient experience, collaborating with cross-functional BMS teams, and overseeing the development of REMS processes, materials, and technologies. We seek a dynamic leader who inspires their team to deliver superior service, fosters a culture of continuous improvement, and ensures REMS education is delivered with clarity, empathy, and impact. Responsibilities include, but are not limited to the following REMS Advisor Team Leadership &...

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,...

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...

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...

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 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. Our Manufacturing Associate, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled,...

The Clinical Trial 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 Delivery Team...

The Manager, REMS Advisor is a field-based position responsible for delivering exceptional education and support to healthcare professionals on REMS program requirements. Using data-driven insights, this role proactively engages with healthcare providers to enhance program understanding, minimize administrative burden, and prevent patient access barriers. The ideal candidate is a collaborative problem-solver who combines strong relationship-building skills with analytical capabilities to optimize the healthcare professional and patient experience. Occasional travel may be required. Responsibilities include, but are not limited to the following Healthcare Professional Education & Support Deliver comprehensive REMS program education to healthcare professionals through tutorials, on-demand training, and one-on-one...

Position summary The FP&A Lead, Germany plays a key leadership role in all FP&A activities for the German Commercial organization. This role is accountable for coordinating and executing the full financial planning and analysis cycle for the German market, ensuring high-quality budgets and projections, generating insights that enable strategic, data-driven decision making, and driving value creation and productivity initiatives. The FP&A Lead provides robust performance analysis and decision support and oversees operational excellence in FP&A delivery across both the local FP&A team and the Hyderabad Finance Hub. As a strategic business partner to the German Leadership Team, the FP&A Lead...

Senior Manager, Corporate Affairs Division/Department Global Corporate Affairs The Senior Manager, Corporate Affairs, will provide support for Puerto Rico (50%) & other commercial communications needs for the region (50%). He/She is responsible for designing and executing communications and corporate engagement strategies that will help support BMS growth and priorities in Puerto Rico and across the region. He/she is a seasoned Corporate Affairs leader, with strong strategic and operational ability to support the function. The Senior Manager, Corporate Affairs reports to the Associate Director of Communications for LATAM and will work closely with the General Manager for Puerto Rico and...

Job Posting Senior Therapeutic Area Specialist, Cardiovascular Community - Los Angeles W, CA Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Los Angeles W, CA 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...

Summary The East Regional Director, Cell Therapy Field Market Access is responsible for leading the East Cell Therapy customer-facing team for BMS’s Cell Therapy Market Access and Patient Access Support Services. This role communicates, implements, and oversees the strategic and operational plans for patient access to Bristol Myers Squibb’s cellular therapy portfolio, managing the daily performance of the Cell Therapy Field Market Access Team across the Eastern Region. The East Region Director will work closely with the Cell Therapy Field Market Access Leadership Team on all strategies and objectives outlined in this position summary. The field team is responsible for...

Summary The Associate Director, Commercial AI Product Owner is responsible for leading the transformation of advanced analytics into durable, scalable, and AI-powered solutions that directly accelerate commercial decision-making across the enterprise. You will collaborate across global teams—including BI&T, Data Science, and the engineering/analytics group—to deliver high-quality, production-grade analytics platforms, tools, and automation that embed actionable intelligence into everyday workflows for Marketing, Field, and Market Access stakeholders. This role enables the shift from project-based analytics to platform-enabled, always-on decision intelligence. You will operate within a hub-and-spoke model, setting standards, governance, and reusable components that empower therapeutic area-aligned teams while driving enterprise-wide...

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. Senior Specialist, Robotics Process Engineer, CTF Automated Manufacturing provide technical leadership for automated and robotic manufacturing equipment at the Devens Cell...

Independently and proactively leads a matrixed cross-functional medical project team within Cell Therapy Medical. This role will be a strategic and operational portfolio partner for the medical lead and team in identifying, planning, risk identification/mitigation and delivering on portfolio priorities and workstreams. Examples Asset Indication Medical meetings, medical planning, budget management/planning, congress activities, Ad Board planning, and portfolio governance/decision making. The role will partner across matrix functions (Medical Evidence Generation, finance, development teams, corporate giving, advocacy, professional societies, business operations, etc.) to support One BMS, prioritization and decision making. The individual would lead with passion, innovation, speed and accountability. Key...

Summary Creates and executes the overall GHEOR plan for cardiovascular asset with input from key stakeholders such as Clinical Medical, Marketing, Market Access, Statistics, Regulatory and other relevant stakeholders Responsibilities Lead global health economic and outcomes research in cardiovascular therapeutic area Develop and execute innovative GHEOR plans including real world evidence generation, economic modeling, and patient-reported outcomes assessment Identify opportunities and lead studies to differentiate and enhance value propositions of BMS assets Direct efforts to support market access activities Build relationships with key BMS groups to maximize opportunities Maintain and develop strong relationships and visibility with external key opinion leaders...

Summary As a Senior Data Engineer in Research IT, you will play a critical role supporting Bristol Myers Squibb's Foundational Data Products , including CoreReg, Substance Mart, DARE, and Asset Mart . You will be responsible for designing, developing, and maintaining scalable data pipelines, ensuring data quality, and enabling data-driven decision-making that accelerates our research and development mission. Working at the intersection of cutting-edge technology and life-changing science, you will collaborate closely with data scientists, researchers, and IT professionals to deliver solutions that matter. Key Responsibilities Data Pipeline Development Design, develop, and maintain robust and scalable data pipelines supporting Foundational...

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 ....

As Principal AI Engineer within Bristol Myers Squibb’s AI Engineering and Enablement team, you will lead the architecture, design, and implementation of scalable Enterprise AI applications. Drive the technical strategy for Gen AI solutions, ensuring robust integration, security, and performance across the organization. Key Responsibilities Enterprise GenAI Solution Development Architect, design, and build end-to-end GenAI applications Define solution architectures for leveraging cloud platforms (AWS, Azure, GCP) for scalability, reliability, and security. Present and propose technical solutions that fit requirements. Plan and coordinate project deliveries to ensure timelines and business needs are met. Hands-On Engineering Leadership Develop core features and infrastructure;...

Summary Associate role supporting the Global Policy Research, Analytics & Economics team within Global Policy & Government Affairs. The role performs highly diverse and complex administrative functions, including proactive calendar management, meeting scheduling, domestic and/or international travel arrangements, expense reporting, and preparation and editing of PowerPoint presentations. The Associate supports internal & external engagement activities and interfaces with a broad range of internal and external stakeholders. Responsibilities Proactively manage calendars and schedule recurring and ad hoc meetings for leaders, direct reports, and internal and external stakeholders. Coordinate meeting logistics with matrix partners and external stakeholders, including global organizations, trade associations,...

Job Summary The Senior Data Engineer is responsible for designing, developing, and optimizing robust data platforms and solutions that enable scalable, high-quality data delivery across the enterprise. This role leverages advanced engineering principles, emerging AI technologies, and strong collaboration skills to drive innovation and operational excellence—without formal people management responsibilities. Key Responsibilities Advanced Data Engineering & Platform Enablement Develop, optimize, and maintain robust data pipelines and frameworks (including basekits and unified portals). Support migration and integration of legacy systems into modern, AI-powered platforms. Agentic AI & GenAI Integration Apply agentic frameworks and GenAI solutions to enhance data engineering capabilities. Lead...

Bristol Myers Squibb is seeking a strategic and experienced Associate Director to lead our Leave & Absence Product and Process Design function. This high-impact leadership role is responsible for driving the strategic vision, operational excellence, and compliance framework for all company leave and absence programs globally. In this role, you will oversee leave program design, process improvement, vendor partnerships, and leave and benefit systems management. This role will also provide strategic oversight of global benefits administration system capabilities (e.g., eligibility, enrollment, integrations, and employee self-service), ensuring aligned, scalable processes and an optimized employee experience. You will serve as the subject...

Job Pos ting Title Senior Therapeutic Area Specialist, C ardiovascular Community - Los Angeles E, CA Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Los Angeles E, CA 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...

The Associate Director, Cell Therapy Network CQV , is responsible for the network strategy for equipment/facility/utility Commissioning, Qualification, and Validation. The scope encompasses the internal CT manufacturing sites and engagement with external CMOs via Virtual Plant Teams. This role will partner cross-functionally with site CQV leads, site equipment owners, Cell Therapy network Digital Plant leaders, the BMS QMS Qualification Global Process Owner, and CTTO Global Equipment Owners. Key Responsibilities Establish strategy and deliver optimized and harmonized CQV approaches across the Cell Therapy network. Work collaboratively with Cell Therapy network Digital Plant and BMS enterprise qualification L2 to synthesize guidance in...

The Regional Associate Director (RAD) is responsible for managing a team of Medical Science Liaisons (MSLs) trained in the area of Pulmonary Fibrosis/Interstitial Lung Disease (ILD). The RAD oversees their regional team to ensure disease and product related medical needs in the region are being identified. Oversight of the MSL primary responsibilities which includes establishing frequent and timely interactions with Thought Leaders (TLs) and other Health Care Providers (HCPs) aligned with medical strategies to discuss safe and appropriate use of approved products. RADs are responsible for ensuring the MSLs respond to unsolicited questions on current medical and scientific issues, healthcare...

Job Pos ting Title Senior Therapeutic Area Specialist, C ardiovascular Community - Madison, WI Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Madison, WI 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...

Execute the systems and asset lifecycle strategy, to ensure high reliability of assets, minimizing downtime and maximizing production capabilities. Asset induction and Preventive Maintenance administration and compliance in CMMS (BMRAM to MAXIMO) Key Responsibilities Develop, maintain, and ensure the accuracy and safety of job plans for maintenance execution in a bio-pharmaceutical manufacturing environment. Support the creation and modification of documentation such as Maximo Job Plans, Data Sheets, and Work Instructions. Apply operational excellence principles to maintenance activities, including cost-benefit analysis and the review or creation of metrics and KPIs related to maintenance execution. Collaborate with project engineering on small capital...

The BI&T Development Data Scientist Analyst position at Bristol Myers Squibb, as part of the Development Data & Analytics team offers a dynamic and meaningful career focused on advancing patient care through innovative data science solutions. The role involves designing and deploying advanced analytics, collaborating with stakeholders, and applying predictive modeling and machine learning to large and diverse datasets. The Development Data Scientist Analyst will play a crucial role in supporting study clinical operational analytics across Drug Development to ensure products continue to serve most pressing DD analytics needs, with opportunities to build new advanced analytics capabilities such as predictive...

Global Program Leads within the HOCT (Hematology, Oncology & Cell Therapy) Global Program Leadership organization are strategic-thinking, problem-solving, and action oriented scientific leaders who bring drug development and commercialization insights to drive a sustainable pipeline of innovative medicines. GPLs serve as the “point of accountability” for their assets and are respected, matrix leaders, overseeing multi-disciplinary teams typically responsible for the development of assets from later stage Discovery (pre-GT2) through commercialization. They will foster a high performing, highly collaborative, truth-seeking team environment aimed at developing and implementing compelling, integrated asset strategies to achieve ambitious near- and long-term portfolio objectives. Each leader...

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...

This territory includes Cincinnati, Dayton, and northern KY. 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 a human touch to every treatment we pioneer. Join us, build your professional career within one of the most innovative bio-pharma companies,...

Summary This role is accountable for strategic and functional leadership of a team responsible for accurate and timely Managed Care Commercial and Medicare Part D rebate processing and payments, data stewardship and compliance in connection with matrix team’s financial reporting (GTN, projections and budgets) as well as all aspects with evaluating implications of and reporting Managed Care data required for U.S. and Puerto Rico government pricing calculations. Responsibilities Lead and develop a team responsible for systems and processes that collect, process, monitor and use Managed Care data for financial, business or government pricing calculation purposes including but not limited to...

The Director, Global Cell Therapy (CT), Strategy & Operations (WW Commercial) will act as a critical and trusted thought partner to the CT Vice President, Global Commercial, Cell Therapy, Hematology, the Global Brand leads and their teams. Cell therapy has proven to be transformational in hematological malignancies, and BMS is the only company to have two FDA approved therapies against two distinct targets on the market and four assets in clinical development. As an industry leader, we are exploring opportunities to bring the promise of cell therapy into new frontiers, including autoimmune diseases and solid tumors. Abecma, Breyanzi and arlo-cel...

The primary focus of the Quality Control (QC) Micro Specialist, role will be to perform GMP testing to support product release, in-process testing and transfer/validation activities. This role will also provide technical support and method troubleshooting for microbiological tests. Responsibilities will also include projects, deviations/investigations/CAPA, and continuous improvement efforts. Duties/Responsibilities Ability to understand, follow, interpret and apply Global Regulatory and cGMP requirements accurately and completely. Perform Microbial Identifications of environmentally isolated organisms using Maldi-TOF technology. Knowledge of LIMS, ELN and laboratory data analysis systems preferred. Problem-solving ability/mentality, technically adept and logical. Ability to communicate effectively with peers, department management and...

The Regional Associate Director (RAD) is responsible for managing a team of Medical Science Liaisons (MSLs) trained in the area of Pulmonary Fibrosis/Interstitial Lung Disease (ILD). The RAD oversees their regional team to ensure disease and product related medical needs in the region are being identified. Oversight of the MSL primary responsibilities which includes establishing frequent and timely interactions with Thought Leaders (TLs) and other Health Care Providers (HCPs) aligned with medical strategies to discuss safe and appropriate use of approved products. RADs are responsible for ensuring the MSLs respond to unsolicited questions on current medical and scientific issues, healthcare...

The Content Specialist (m/f/d) acts as a critical BMS link between German brand teams, Agencies of Record (AORs), Business Insights & Technology (BIT), Commercialization AI Strategy & Analytics (CASA), and Mosaic to ensure BMS Germany’s content libraries are accurate, searchable, compliant, and activation-ready. This role is accountable for upholding content integrity and as such owns the local implementation of metadata /taxonomy standards, is responsible for tagging accuracy, seamless asset transfer, and building well-structured content libraries that enable GenAI-driven content creation and content reuse across the European region. This role ensures adherence to BMS metadata standards, supports BMS claims management, drives...

Medical Science Liaison, Neuropsychiatry Location Colorado, Utah, Wyoming, Nebraska, Las Vegas The Medical Science Liaison (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 MSL/Senior MSL is responsible for identifying disease and product related medical needs in a defined geography. The primary role of the MSL/Sr. MSL is to develop and maintain relationships with Thought Leaders (TL) and Healthcare Providers (HCP) within their territory. The purpose of their interactions is to engage...

Position Medical Science Liaison, Camzyos Location Field - NC,SC 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...

As part of the Real-world data Research team, you will get the opportunity to work with a collaborative team in an inclusive and supportive environment. This position includes management and scientific methodological responsibilities ensuring the delivery of high-quality real-world studies. This role will be responsible for engagement with functional leads to provide consultation and may include summarizing book of work across the team. This role also involves managing timelines and deliverable quality, maintaining organizational alignment with BMS customers and external stakeholders (vendors, research support). Additionally, it encompasses the advancement of organizational knowledge and capabilities through scientific and managerial development and...

The Associate Director, US Iberdomide will be a key scientific and strategic contributor to the Global Medical Affairs team supporting iberdomide, an investigational therapy being developed for the treatment of multiple myeloma. Reporting to the Director, US Iberdomide, this role will support the development and execution of global medical strategy across the asset lifecycle, with a strong emphasis on scientific engagement, field partnership, and insight generation. The Associate Director will collaborate closely across the matrix to ensure high-quality scientific exchange and effective execution of medical priorities. This role is well ‑ suited for a Medical Affairs professional with hematology experience...

Summary The Director, Omnichannel Engine Business Product Owner is responsible for owning Bristol Myers Squibb’s omnichannel orchestration and “next best engagement” engine as a business product. This role defines and executes the product roadmap for the decisioning and automation capabilities that determine which actions, messages, and channels to deploy for each customer and when. The Director will translate brand and Therapeutic Area strategies into the data, rules, and algorithms that power scalable, N=1 engagement across Oncology, Cardiovascular, Neurology, and HIV portfolios. They will partner closely with the CRM/Marketing Automation and Taxonomy & Tagging teams, as well as Business Insights and...

Job Pos ting Title Senior Therapeutic Area Specialist, C ardiovascular Specialty - San Diego, CA Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location San Diego, CA 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...

The Sr Director, Quality Systems and Compliance, is a full-time position located at the BMS Bothell Manufacturing Plant (JuMP) located in Bothell, Washington. The primary focus for this role is to lead the Quality Systems and Compliance teams to ensure site level Quality Systems (Deviation, CAPA, Change Control, Complaints, Data Integrity, Quality Risk Management, and Document Control) are appropriately designed, implemented, and measured for cGMP compliance and effectiveness. This position is also responsible for ensuring site compliance to health authority regulations and current good manufacturing practices ensuring site inspection readiness. The position leads the management of health authority (surveillance and...

The Associate Director, Audit Strategy and Vendor Quality supports the development and execution of risk-based audit strategies across Therapeutic Areas, R&D processes, and external vendors. This role focuses on operationalizing risk-based audit plans, delivering effective audit execution, supporting quality investigations and CAPA management, as well as proactively identifying and escalating quality risks. The Associate Director will lead and support maintaining and applying the vendor quality management framework such as vendor oversight plans, quality agreements, and governance metrics and supports inspection readiness and product submission activities through consistent, risk-based quality execution in partnership with RDQ Development Quality and business stakeholders. R&D...

The Executive Director, U.S. HCP Marketing, COBENFY Psychiatry will serve as the leader accountable for maximizing the commercial potential of COBENFY, while improving the lives of as many patients as possible with Schizophrenia (SCZ) and Bipolar Disease (BPD), if approved by the FDA. This position is responsible for leading a team of direct reports focused on HCPs, care partners, and customer experience while being a critical member of other cross-functional teams including but not limited to R&D, Medical, MAx, and Global Commercial. The ED of U.S HCP Marketing, COBENFY Psychiatry will drive the achievement of both short and long-term business...

The Associate Director, Audit Strategy and Vendor Quality supports the development and execution of risk-based audit strategies across Therapeutic Areas, R&D processes, and external vendors. This role focuses on operationalizing risk-based audit plans, delivering effective audit execution, supporting quality investigations and CAPA management, as well as proactively identifying and escalating quality risks. The Associate Director will lead and support maintaining and applying the vendor quality management framework such as vendor oversight plans, quality agreements, and governance metrics and supports inspection readiness and product submission activities through consistent, risk-based quality execution in partnership with RDQ Development Quality and business stakeholders. R&D...

The Associate Director, Audit Strategy and Vendor Quality supports the development and execution of risk-based audit strategies across Therapeutic Areas, R&D processes, and external vendors. This role focuses on operationalizing risk-based audit plans, delivering effective audit execution, supporting quality investigations and CAPA management, as well as proactively identifying and escalating quality risks. The Associate Director will lead and support maintaining and applying the vendor quality management framework such as vendor oversight plans, quality agreements, and governance metrics and supports inspection readiness and product submission activities through consistent, risk-based quality execution in partnership with RDQ Development Quality and business stakeholders. R&D...

Reporting to the Executive Director, Research & Early Pipeline Communications, the Associate Director, Research Communications, Informatics, Computational & Discovery Sciences, supports the execution of research and early pipeline communications across BMS’ Informatics and Predictive Sciences, Therapeutic Discovery Sciences, and Computational Sciences platforms. This role implements communications strategies that elevate BMS’ scientific leadership in data-driven discovery, advanced analytics, computational biology, and translational sciences. Responsibilities include supporting external scientific collaborations, data and regulatory milestones, partner announcements, medical congresses, and speaking opportunities for research leaders. The Associate Director contributes to earned, owned, and paid media initiatives with a focus on high-quality execution, creative...

Reporting to the Executive Director, Research & Early Pipeline Communications, the Senior Director, Research Communications, Neuro, ICV, & Integrative Sciences, will lead research and early pipeline communications efforts across BMS’ Neuroscience, Immunology & Cardiovascular (ICV), and Integrative Sciences portfolios. Additionally, the Senior Director will ensure a consistent and differentiated communications approach for external scientific collaborations and platform innovations aligned with enterprise and business priorities. Responsibilities include leading communications around early asset data and regulatory milestones, partner announcements, medical congresses, scientific forums, and speaking opportunities for research leaders. The role will drive earned, owned, and paid media strategies with an emphasis...

The Protein Homeostasis Thematic Research Center (PH TRC) advances BMS’s protein degradation and homeostasis strategies from discovery into early clinical development to address tumor‑intrinsic vulnerabilities and resistance mechanisms—enabling action on targets previously considered undruggable. As the Brisbane-based Senior Director of Translational Research, you will provide strategic scientific and organizational leadership in a cross-functional, cross-site environment, setting translational vision and standards and shaping and executing end-to-end translational strategies across a portfolio of early programs (pre-IND through Phase 1).You will influence portfolio-level decisions and ensure integration of preclinical biology with clinical biomarker strategy to drive patient enrichment, proof-of-mechanism, and decision-grade data in...

R&D Quality, Audit Strategy Operationalize and execute the risk-based audit and quality strategy across Therapeutic Areas, R&D processes, investigator sites, vendors, and digital health aligned with ICH E6(R3), regulatory expectations, and company objectives Lead the planning, conduct, and reporting of audits and assessments, ensuring consistency, quality, and timely delivery, in partnership with Clinical Auditing team, Development Quality and business stakeholders Identify, assess, and escalate quality risks, contributing to trend analysis, metrics, and evidence-based insights Support continuous improvement initiatives by translating audit and inspection findings into actionable corrective and preventive actions, monitoring audit trends and identifying emerging risks Support implementation of...

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,...

The Director, GCP Audit Strategy and Vendor Quality is accountable for designing and executing a global, risk-based audit strategy to ensure compliance with Good Clinical Practice (GCP) requirements. This role will drive robust vendor quality oversight across all clinical trial service providers in close partnership with Development Quality. Key responsibilities include leading strategic planning for audits, managing vendor-related quality investigations, CAPA development, and ensuring timely resolution of quality issues. The Director will establish and maintain a comprehensive vendor quality management framework for CROs and other external partners. This includes oversight of vendor quality programs and collaboration with cross-functional teams within...

As a Senior Scientist, you will combine high‑level scientific expertise with operational ownership. You will independently design and execute complex analytical studies, drive method readiness for process work and serve as a subject matter expert (SME) for key chromatographic and electrophoretic methods. You will also act as an Operations Manager—owning weekly task assignment and coordination to ensure clear priorities, balanced workload, and reliable coverage for the PA lab. Role & Responsibilities Analytical leadership Independently design, execute, interpret, and report complex analytical studies supporting process characterization, and investigations. Serve as an SME for assays such as CE‑SDS, SEC, RP‑HPLC/peptide mapping, iCIEF,...

Global Program Leads within the Hematology-Cell Therapy Global Program Leadership organization are strategic-thinking, problem-solving, and action oriented scientific leaders who bring drug development and commercialization insights to drive a sustainable pipeline of innovative medicines. GPLs serve as the “point of accountability” for their assets and are respected, matrix leaders, overseeing multi-disciplinary teams typically responsible for the development of assets from early development (pre-ID3) through commercialization and post-marketing lifecycle management. They will foster a high performing, highly collaborative, truth-seeking team environment aimed at developing and implementing compelling, integrated asset strategies to achieve ambitious near- and long-term portfolio objectives. Each leader is...

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 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. Key Responsibilities The Regional Oncology MSL role is field-based, and it is anticipated that the majority of their time will be spent in the field with external customers. Serves as an educational resource for external Oncology stakeholders in the Community. Primary responsibility is to...

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. Key Responsibilities The Regional Oncology MSL role is field-based, and it is anticipated that the majority of their time will be spent in the field with external customers. Serves as an educational resource for external Oncology stakeholders in the Community. Primary responsibility is to...

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. Key Responsibilities The Regional Oncology MSL role is field-based, and it is anticipated that the majority of their time will be spent in the field with external customers. Serves as an educational resource for external Oncology stakeholders in the Community. Primary responsibility is to...

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. Key Responsibilities The Regional Oncology MSL role is field-based, and it is anticipated that the majority of their time will be spent in the field with external customers. Serves as an educational resource for external Oncology stakeholders in the Community. Primary responsibility is to...

The Director, GCP Audit Strategy and Vendor Quality is accountable for designing and executing a global, risk-based audit strategy to ensure compliance with Good Clinical Practice (GCP) requirements. This role will drive robust vendor quality oversight across all clinical trial service providers in close partnership with Development Quality. Key responsibilities include leading strategic planning for audits, managing vendor-related quality investigations, CAPA development, and ensuring timely resolution of quality issues. The Director will establish and maintain a comprehensive vendor quality management framework for CROs and other external partners. This includes oversight of vendor quality programs and collaboration with cross-functional teams within...

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. Key Responsibilities The Regional Oncology MSL role is field-based, and it is anticipated that the majority of their time will be spent in the field with external customers. Serves as an educational resource for external Oncology stakeholders in the Community. Primary responsibility is to...

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. Key Responsibilities The Regional Oncology MSL role is field-based, and it is anticipated that the majority of their time will be spent in the field with external customers. Serves as an educational resource for external Oncology stakeholders in the Community. Primary responsibility is to...

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 Senior Manager, Senior Process Engineer provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP...

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,...

Summary The Director, Market Access Foresight is a pivotal strategic role within Global Pricing & Health Systems Analytics, embedded in the Market Access Intelligence & Innovation team. In this strategic role, you will build and lead a capability that delivers timely, high‑quality US and International market access intelligence—empowering BMS to anticipate disruption, respond with clarity, and make confident, forward‑looking decisions. You will design and evolve dynamic intelligence frameworks and outputs—such as dashboards, executive briefings, and scenario planning—that shape high‑stakes decisions across the enterprise. Acting as BMS’s rapid‑response and early‑warning engine, you will translate fast‑moving market, policy, and competitive developments into...

Functional Area Description The Senior Clinical Trial 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 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...

As a Director of Product Sciences , this energetic and motivated individual will lead a group of immunologists and cell therapy experts responsible for T cell characterization using established and novel technologies. The team designs, executes, and interprets complex studies to inform and optimize cell therapy process development. They also collect and utilize T cell characterization data to discover predictive measures of clinical outcomes. This individual must possess a profound understanding of cell therapy biological mechanisms, as well as foundational knowledge of analytical methodologies to measure genotype, phenotype and function of CAR-T cells. The dynamic leader will drive the achievement...

Clinical Trial Physician EMPLOYEE JOB PROFILE (EJP) – Date Modified 25-February-2020 Job Title Clinical Trial Physician (CTP) Division R&D / Global Drug Development Functional Area Description The Clinical Trial 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...

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...

The Quality Assurance (QA) Manager II is a frontline people leader responsible for managing QA Shop Floor teams at the BMS Bothell, WA cell therapy facility. This role drives end-to-end quality execution, from material receipt to final product release, in an expanding, fast-paced biotech manufacturing environment. You will lead teams providing real-time quality decision-making, batch record review, and deviation management in direct partnership with Manufacturing, Quality Control, and Supply Chain. Success requires deep technical expertise in cGMP requirements, robust knowledge of Risk and Quality Management Systems, and a proven ability to lead high-performing teams in a regulated environment. This role...

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. Our Manufacturing Associate, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled,...

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 Director, MAx Strategy & Business Operations provides strategic leadership and operational oversight across Global Market Access, Pricing, and Value Demonstration (MAx). This role partners closely with MAx Leadership Team members to drive alignment, operational excellence, and execution of high‑impact initiatives that support business growth. The Director oversees priority strategic initiatives and core business operations, enabling effective decision‑making across a highly matrixed, global organization. The ideal candidate has strong project management skills, executive-level communication abilities, and experience leading in a heavily matrixed environment are essential. A foundational understanding of the MAx function, along with demonstrated experience influencing without...

QA Shop Floor Lead is a frontline quality operations Lead responsible for coordinating and executing day-to-day QA operations to support clinical and commercial cell therapy manufacturing. This role ensures shift readiness, real-time oversight, and timely resolution of quality events while fostering a culture of cGMP compliance and operational excellence. The Lead serves as a key point of contact for internal escalations, owns critical documentation and deviation processes, and drives cross-functional alignment through proactive communication. In addition to mentoring QA team members, the Lead contributes to strategic initiatives and provides leadership continuity during manager absences and positively influences team culture as...

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 a human touch to every treatment we pioneer. Join us, build your professional career within one of the most innovative bio-pharma companies, and make a difference. The TAS is...

Medical Science Liaison, Neuropsychiatry Location South Texas (Houston) The Medical Science Liaison (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 MSL/Senior MSL is responsible for identifying disease and product related medical needs in a defined geography. The primary role of the MSL/Sr. MSL is to develop and maintain relationships with Thought Leaders (TL) and Healthcare Providers (HCP) within their territory. The purpose of their interactions is to engage in meaningful scientific...

Clinical Pharmacology & Pharmacometrics plays a key role in the drug development process such that we plan, design and execute clinical pharmacology studies while maximizing the potential for model-informed drug development to drive decisions that inform the course of the clinical development program. The vision for Sr. Research Investigators in the group is to be able to function in a blended role that includes both classical clinical pharmacology skillsets combined with quantitative analysis skills. Given the breadth of the portfolio, Sr. Research Investigators in this group would have the opportunity to serve as the clinical pharmacology & pharmacometrics leader on...

The Associate Director, Global Process Owner - Vendor Master role is responsible for managing the ownership of vendor data process and acts as the key liaison / subject matter expert between the Global Process owners, Business Stakeholders including Clinical, Sourcing, ARIBA Supplier Enablement Team, BCP, Accounts Payable and IT personnel (who are responsible for development and maintenance of Enterprise systems). This role is expected to ensure that the outcomes delivered by BMS managed service provider for Procurement Operations are aligned to set expectations. Overall, the objective is to maintain and manage BMS vendor data and data quality within our Vendor...

The Associate Director, Requisition to Pay (R2P) Service Desk role is responsible for defining and leading the global strategy, governance, and performance of the R2P Service Desk, providing end‑to‑end support for both internal BMS users and external suppliers across the requisition‑to‑pay lifecycle. This role serves as the global process owner for the R2P Service Desk experience, acting as the primary liaison between Global Process Owners, Global Financial Services Operations, IT, Finance, and managed service providers. This role is a cornerstone of the R2P operating model, directly influencing how BMS employees and suppliers experience our processes every day. It combines process...

Position Principal Compliance Engineer, ECQ Location Summit West, NJ Purpose and Scope of Position The Principal Compliance Engineer, Equipment Commissioning & Qualification (ECQ), supports the successful operation of facility, laboratory, and business functions at Summit, NJ. This role involves interaction with internal team members, peer-level customers, and external service providers. The Principal Compliance Engineer will lead a team of contract or full-time personnel responsible for performing periodic reviews of equipment, policies, and procedures to ensure they remain in a validated state. Responsibilities include performing gap analyses, and leading small and large-scale projects to achieve departmental objectives. Required Competencies Knowledge,...

The Director, Global Trial Lead (GTL) is accountable for the strategic leadership and operational excellence of global clinical trials, driving delivery across all phases and therapeutic areas. This role sets the vision for successful trial execution, influences organizational strategy, and ensures alignment with business objectives, regulatory standards, and quality benchmarks. As a senior leader within Global Development Operations (GDO), the Director GTL is responsible for critical decision making, risk management, and fostering a culture of innovation and continuous improvement. Works closely with internal and external stakeholders, identifying, defining and executing meaningful and targeted process improvement initiatives, supporting strategic planning efforts....

Position Overview The Senior Business Analyst in the Invivo and Non-Clinical Safety team will bridge scientific research needs and IT solutions, with a primary focus on Electronic Laboratory Notebooks/Laboratory Information Management Systems (ELN/LIMS) and the responsible adoption of Generative AI tools. This hands-on role partners with researchers, lab personnel, and IT to gather requirements, design solutions, and ensure effective implementation and support of ELN/LIMS capabilities, instrument connectivity, and GenAI-enabled workflows that improve data quality, speed of insight, and compliance. If you want an exciting and rewarding career that is meaningful, consider joining our diverse team! Desired Candidate Characteristics Strong commitment...

The Director, Digital Health Strategy & Operations is a strategic leadership role responsible for shaping, operationalizing, and governing the enterprise Digital Health portfolio at BMS. Reporting to the Vice President, IT Digital Health, this role acts as the strategic integrator and execution engine for a single, enterprise-wide Digital Health organization serving all of BMS. The role ensures that Digital Health initiatives, that span early diagnosis, patient engagement, AI-enabled evidence generation, and digital biomarkers, are prioritized, funded, governed, and executed with rigor. The role will have particular focus on ensuring the deployment of digital solutions at scale in clinical care environments....

Reporting to the US Commercialization Lead, Neuroscience, this is a critical leadership role within the Neuroscience organization. This position is charged with ensuring the U.S. performance of Cobenfy in Schizophrenia (SCZ) meets or exceeds our goals, and with the successful U.S. commercialization of Cobenfy in Bipolar Disease (BPD,) if approved by the FDA. This leader will be responsible for ensuring strong matrix collaboration across Brand, Global Commercial Strategy (GCS), Medical, Market Access, Sales, Legal and Business Insight & Analytics in line with the Neuroscience objectives. We are looking for a dynamic, performance-driven leader who cultivates a team-based, collaborative, customer/externally focused...

Senior Counsel, Cell Therapy & Biologics - Innovation Law Bristol Myers Squibb (BMS) is seeking a Senior Counsel, Innovation Law, based at our R&D center in Seattle, WA or San Diego, CA. The attorney will support clients across multiple functional areas to build and leverage BMS’ intellectual property interests, with a focus on cell therapy and biologics. Excellent communication skills and the ability to work well across functions and geographies are a must. Key Responsibilities Provide comprehensive IP legal support for cell therapy and biologics programs, including CAR‑T and next‑generation modalities. Prepare and prosecute patent applications, including drafting, filing, and...

Position Medical Science Liaison, Oncology, Lung & GU Tumors Location Central & North Texas/Oklahoma The primary role of the Medical Science Liaison (MSL) is to engage in meaningful peer-to-peer scientific dialogue with healthcare system leaders such as Regional Thought Leaders (RTLs), National Thought Leaders, and Healthcare Professional (HCPs) within a defined geography to translate science into patient care. MSLs will also engage the top HCPs in high-disease burden hospitals. The MSL captures medical insights and acts as a clinical & scientific advisor to cross-functional partners. Ensures applicable interactions are aligned with enterprise and medical strategies and ultimately serve to...

We are seeking a Senior Manager, Full Stack engineer, to serve as a technical leader in an AI first, agile product environment supporting Global Regulatory Sciences (GRS) technologies. This role is accountable for the end-to-end build and run of AI-native technology assets supporting Global Regulatory Sciences, ensuring solutions are reliable, accessible, secure, compliant, and cost-effective. The Senior Manager designs, builds, and operates AI native products where large language models, agentic workflows, and data-driven intelligence are the default paradigm—not an addon. The role blends hands-on full-stack engineering, AI product thinking, and operational ownership, with responsibility for both delivery and long-term‑ sustainability...

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 a human touch to every treatment we pioneer. Join us, build your professional career within one of the most innovative bio-pharma companies, and make a difference. The TAS is...

Context Bristol Myers Squibb is an integrated global biopharmaceutical company engaged primarily in the discovery, development and commercialization of novel therapies for the treatment of cancer, cardiovascular and inflammatory diseases. BMS R&D is at a critical and exciting phase of development. As it expands and integrates its portfolio, there is an opportunity for a dynamic and resourceful individual to lead our oncology efforts in Translational Development at our sites in New Jersey or Cambridge, MA. Translational Development at BMS Translational Development is part of the Global Research organization in BMS and leads late stage translational research and development activities for...

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...

About RayzeBio RayzeBio is a clinical-stage biopharmaceutical company focused on developing innovative radiopharmaceutical therapeutics for cancer patients. Leveraging advanced technology, RayzeBio aims to improve the lives of people with difficult-to-treat cancers through unique, targeted therapies. The company’s pipeline features several promising candidates, and its team is passionate about scientific excellence, collaboration, and patient impact. RayzeBio seeks a patent attorney to assist in developing global IP strategies and managing day to day intellectual property efforts to support multiple programs in pre-clinical/clinical development. The desired candidate will be responsible for a wide range of intellectual property related matters with an emphasis on...