Bristol Myers Squibb Job Trends

Schedule Wednesday-Saturday 200PM to 1200AM Responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts. Duties/Responsibilities Perform routine testing of in-process, final product, and stability samples. May review GMP documentation and perform data verification. Support document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts. May train analysts on general job duties. Perform other tasks as assigned. Qualifications Specific Knowledge, Skills, Abilities Ability to accurately and completely understand and follow procedures. Apply scientific principles to analytical testing and the proper use of...

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...

PRINCIPAL OBJECTIVE OF POSITION Provides strategic leadership and operational oversight for the Parenteral Vial (PVA), Parenteral Syringes (PSA), or Parenteral Vial Liquid Area (PVLA) manufacturing areas—including Preparation, Formulation, Filling, Lyophilization, Capping, and Sanitization—to ensure the consistent production of high-quality sterile pharmaceutical products. The Manager serves as a key supervisory figure, guiding teams and processes to meet production targets, quality standards, and compliance expectations. This role requires adherence to all applicable Environmental Health and Safety (EHS) regulations, Security protocols, regulatory requirements, and current Good Manufacturing Practices (cGMP). The position also fosters a culture of continuous improvement, operational excellence, and team development....

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...

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...

The Protocol Management Office (PMO) at Clinical Center of Excellence (CCoE) ensures scientific rigor and quality of clinical documents within Drug Development (DD). A critical component of the CCoE responsibilities is the oversight of the TA-aligned Protocol Review Committee (PRC) within DD. As an integral member of the PRC team, the PRC Lead helps achieve these objectives through leading the Therapeutic Area (TA) PRC process and supporting clinical teams through the process steps. The PRC Lead will drive implementation of the PRC process, work collaboratively with key stakeholders to strive for the highest quality output and audit compliance documentation. In...

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...

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 collaborative and detail-oriented scientist with deep expertise in immunology, molecular/cell...

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 ....

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...

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...

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 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...

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;...

Cell Therapy Analytical Development (CTAD) is seeking a highly skilled and experienced Principal Engineer to join the Assay and Data Automation team. This role will lead the design, development, and implementation of state-of-the-art automation solutions for a variety of analytical methods and technologies supporting cell therapy programs. The Principal Engineer brings hands-on expertise in assay automation and possesses a strong technical background in automation design, development, and deployment within both GMP and non-GMP labs. This individual will foster effective partnerships and collaborate cross-functionally with internal and external stakeholders—including CTAD functions and CTDO departments—to build analytical automation solutions to enhance sample...

Summary Bristol Myers Squibb is seeking a highly motivated individual to manage operations of our new state-of-the-art electron microscopy suite featuring a Titan Krios G5 as part of the Structural Biology team in San Diego, CA. The candidate will support a collaborative group of protein scientists, structural biologists, computational scientists, and interdisciplinary collaborators across a range of research programs. A strong background in protein sciences or molecular biology is essential for effective communication and program impact. Candidates must have robust expertise in biological cryoEM workflows and structural biology, with proven ability to coordinate complex projects in an industry setting....

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...

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...

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...

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,...

Project Coordinator, ICV US FM This position will report to the National Director, Rheumatology. The primary role of the Project Coordinator is to support the function of Field Medical, working within the ICV therapeutic area and across the multiple field teams. Individual will be responsible for performing a diverse set of administrative duties. Must be able to work independently and have successfully demonstrated an ability to work collaboratively within a large team environment. Responsibilities include but are not limited to ensuring that Field Medical Leads/Region Directors respond in a timely fashion to senior leadership requests, organizing team responses for leadership...

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, Pipeline Forecasting, Neuroscience, 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 Director 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 structured improvements. This position is...

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 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...

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 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...

Schedule Wednesday - Saturday 2PM to Midnight Responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts. Duties/Responsibilities Perform routine testing of in-process, final product, and stability samples. May review GMP documentation and perform data verification. Support document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts. May train analysts on general job duties. Perform other tasks as assigned. Qualifications Specific Knowledge, Skills, Abilities Ability to accurately and completely understand and follow procedures. Apply scientific principles to analytical testing and the proper...

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...

Position Senior Auditor, Global Internal Audit & Assurance Location Princeton, New Jersey At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. Across oncology, hematology, immunology, neuroscience, and cardiovascular disease, with one of the most diverse and promising pipelines in the industry, each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. The Senior Auditor in GIA will work in a team environment to plan and execute dynamic risk-based audits and identify value-added...

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...

As Senior Manager in the Project Office, you will lead high-impact functional and technical projects and drive continuous improvement across the People Organization. You will optimize processes, enhance efficiency, and ensure that HR initiatives are executed in alignment with organizational goals. This role is ideal for a proactive, detail-oriented leader who thrives in a fast-paced, collaborative environment and excels at managing complex, cross-functional projects from concept to completion. Key Responsibilities Project Leadership Lead and deliver HR projects from initiation to completion, ensuring timely and on-budget execution. Collaborate with cross-functional teams to define scope, objectives, and deliverables. Develop and manage comprehensive...

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...

Position Senior Princip al Scientist, Manufacturing Technology Location Devens, MA The Senior Princip al Scientist is a subject matter expert and process/project owner for biologic drug substance commercial technical transfers, process validations and project portfolio at Bristol Myers Squibb, Devens. The position will serve as lead or critical support for commercial biologics technical transfers and will engage cross-functionally across multiple stakeholder functions. The role will ensure processes are designed and validated per applicable current good manufacturing practices (cGMPs), site procedures, and that processes are defined consistent with regulatory guidance. The role will also be responsible for driving process...

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...

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 Team Lead, Product Logistics Cell Therapy is responsible for providing on the floor supervision and participate in materials management...

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,...

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...

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, R&D Quality Intelligence & Transformation leads the strategy, build, and adoption of data-driven quality capabilities and innovation across R&D Quality (RDQ). This role accelerates RDQ’s move from reactive, transactional activities to proactive, risk‑proportionate oversight by fusing high‑value analytics, automation, and digital solutions into core quality processes and practices. The Director partners across RDQ, Global Quality (GQ) and where needed with business functional teams to enable faster, smarter decisions that protect patients, strengthen compliance, and improve business delivery. This role will also facilitate budget planning and prioritization of the above strategies and is responsible for roadmap and delivery in...

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...

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...

Our Clinical Supply Operations is responsible for the supply of drug product administered to patients in clinical studies worldwide. In Global Product Development and Supply the team works closely with our partners to deliver quality products safely, efficiently and on time while operationalizing the innovative technologies that will deliver the transformative medicines of tomorrow. As a member of our team, you will get the chance to play a pivotal role to positively impact patients’ lives while developing professionally to achieve your own career goals. Role & Responsibilities Subject Matter Expert on all issues relating to Warehousing, Inventory Management and the...

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...

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,...

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...

Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. May assist with method transfer, documentation, deviations, investigations, and continuous improvement efforts. Schedule Sunday-Wednesday 600AM to 400PM Duties/Responsibilities Perform routine testing of in-process, final product, and stability samples. Perform testing for method transfer/validation/verification. Perform data verification, data review and review of GMP documentation for general methods. May perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts. Train analysts on general job duties. Perform other tasks as assigned Qualifications Specific Knowledge, Skills, Abilities ...

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...

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 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 Senior Director, Strategic Risk Enablement & Integration is responsible for building, operating, and continuously improving the enterprise risk operating backbone within Strategic Risk Management (SRM). This role enables consistent, high-quality risk execution across business units and risk domains by coordinating Enterprise Risk Committee (ERC) activities, integrating cross-functional risk efforts, and providing shared risk services, tools, guidance, and learning. The position ensures that enterprise risk processes are coherent, scalable, and decision-useful , while preserving clear ownership of risk execution within the business and risk domains. The role acts as the primary facilitator and integrator of SRM’s operating model—connecting people, processes,...

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...

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, AMS IT provides strategic, technical and hands on leadership for the Automated Manufacturing Suite, supporting GoSolo's digital manufacturing transformation. This role is accountable for building strategic roadmaps, architecting, building, and integrating the technology systems that enable scalable, reliable manufacturing operations—including MES platform modernization, recipe execution environments, DeltaV automation integration, and manufacturing scheduler capabilities. The Director, AMS IT leads a team of technical architects, engineers, and integration specialists by balancing workload, resolving technical conflicts, and achieving operational excellence through hands-on execution and accountability. This leader partners closely with cross-functional teams including Manufacturing, MS&T, Quality, IT PMO, GxP, and vendor...

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...

Key Responsibilities Create, maintain and review master data/static data in current/future lab systems by executing the appropriate change management process to ensure accuracy of the configured analytical workflow to support laboratory testing activities and to ensure business, project and/or investigation/CAPA timelines are met. Support review of change controls associated with lab systems, identify system impact, and develop appropriate change actions required to support implementation of the change, including impact to interfacing systems. Execute and document appropriate change control and/or verify changes executed by a team member are accurate associated within the lab system. Review method/specification changes and work with appropriate...

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...

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

Bristol Myers Squibb (BMS) is seeking an experienced Senior Counsel, Patent Litigation to join our growing Innovation Law / Patent Litigation team. This role will report directly to BMS’s Head of Patent Litigation and will play a critical role in protecting the company’s innovations, leading global patent litigation efforts, and aligning litigation strategy with business objectives. Success in this role requires expertise in pharmaceutical patent litigation, strong judgment and business acumen, and the ability to work collaboratively and effectively in a highly matrixed global organization. Key Responsibilities Lead and manage significant U.S. patent litigations, including under the Hatch‑Waxman Act and...

Drive transformation as an Agile HR Business Partner (m/f/d), delivering strategic HR execution where it matters most! Mission As part of the People Organization, the Associate Director, Agile HR Business Partner (m/f/d) contributes to organizational growth and employee engagement by delivering strategic execution and project-based HR support across markets, regions and functions. By design, the role will be focused on Germany as a priority and available to support other International markets and/or cross functional initiatives. This role will report directly Director, Strategic HR Business Partner Germany. Summary of this Role Assigned to provide strategic support and guidance to the...

Power Platform Senior Engineer Job Summary We are seeking an experienced Senior Power Platform Engineer to lead digital transformation and automation initiatives across the organization. This role is responsible for designing, developing, and deploying enterprise-grade solutions using Microsoft Power Platform technologies, including Power Apps, Power Automate, Power BI, Power Pages, and Microsoft Fabric, to optimize business processes, enhance productivity, and enable data-driven decision-making. A key aspect of this role is establishing and operating robust Power Platform governance and ALM practices, ensuring secure, scalable, and compliant adoption across the enterprise while enabling innovation and citizen development. Key Responsibilities Design and build...

SUMMARY The Government Market Access Account Executive is responsible for driving strategically aligned, fiscally responsible access outcomes across prioritized government payer accounts. This role serves as the primary strategic liaison to Medicaid Fee-for-Service customers and leads cross-functional efforts to advance timely patient access to Bristol Myers Squibb medicines. This role will cover the South territory consisting of South Carolina, Georgia, Florida, Tennessee, Alabama, Arkansas, Missouri, Texas, Louisiana, Oklahoma, and Mississippi. RESPONSIBILITIES Achieve targeted formulary and coverage outcomes within prioritized access accounts in a timely and financially responsible manner Develop and execute data-driven, strategically aligned account plans that support enterprise access...

The Senior Manager, Marketing Operations reports to the Director of Strategy & Operations for the US Hematology Franchise. This role supports multiple Hematology brand teams by coordinating the prioritization, scheduling, and planning of promotional materials through the PReP (MLR) review process, with input from brand champions. The Senior Manager interfaces with agencies and marketing stakeholders to ensure materials meet operating principles, timelines, and PReP requirements. The primary responsibility is to manage the digital content supply chain and facilitate the Promotional Review Process, ensuring efficiency and continuous improvement to meet evolving brand and organizational needs. Key Responsibilities 1. MLR/PReP Transformation &...

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,...

Senior Therapeutic Area Specialist Therapeutic Area Neuroscience - Cobenfy Territory MEMPHIS - JACKSON, TN; Jackson, TN/Cordova, TN 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 New Product Introduction (NPI) Engineer – Equipment Validation is responsible for supporting and executing equipment validation activities to support the successful introduction of new products into manufacturing. This role ensures that production and test equipment are properly specified, installed, qualified, and validated in compliance with internal procedures, quality system requirements, and applicable regulatory standards. The NPI Engineer partners cross-functionally with R&D, Manufacturing, Quality, and Suppliers to drive robust validation strategies, mitigate risk, and ensure equipment readiness for launch, scale-up, and sustained production. Key Responsibilities Work closely with internal Manufacturing, Quality Control, and Equipment Validation teams, as well as external...

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. This position is responsible for leading the Heartland Region, which covers TX, OK, KS, MO, LA, AR, KY in driving sales for Eliquis and Camzyos. The Heartland RBD reports to the VP, US...

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 Position Responsibilities In this role as a Scientist, Non-Viral Gene Editing Platforms, the ideal candidate Spends...

The Director, 340B Policy will help lead and support Bristol Myers Squibb’s policy strategy related to the 340B program across federal and state levels. Reporting to the Senior Director of U.S. Policy & Research, this role will serve as a policy partner in shaping and advancing BMS’s approach to 340B policy amid a dynamic legislative, regulatory, and litigation environment. The Director will act as a strategic advisor and subject-matter expert, supporting enterprise policy direction by monitoring developments, translating complex policy issues into actionable business insights, and helping drive coordinated advocacy and engagement strategies aligned with BMS’s patient access, affordability, and...

Power Platform Engineer Job Summary We are seeking a motivated and technically proficient Power Platform Engineer to design, develop, and maintain enterprise-grade applications and automation solutions using Microsoft Power Platform. This role will focus on building and enhancing Power Apps, Power Automate flows, and Power BI reports to improve operational efficiency and enable data-driven decision-making. The ideal candidate will work closely with business users, IT teams, and citizen developers to deliver impactful solutions aligned with enterprise standards. Key Responsibilities Develop and maintain Power Apps (Canvas and Model-Driven) to meet business requirements. Build and optimize automated workflows using Power Automate. Design...

Bristol Myers Squibb Cloud Engineering is seeking a Senior Cloud Architect with deep expertise in Microsoft Azure infrastructure and advanced cloud networking. Based in Lawrenceville, NJ, this role is responsible for architecting, securing, automating, and operating global cloud platforms that power AI services, data analytics pipelines, financial systems, and scientific computing workloads across the enterprise. Azure is the primary platform, but the organization also leverages AWS and GCP, and multi-cloud experience is highly desirable. This position offers the opportunity to design foundational cloud architectures that directly support life-saving scientific and medical innovations within a mission-driven organization. Key Responsibilities Design, architect,...

This position plays a critical role in the development and execution of BMS’ global & US medical strategy within our Thoracic/H&N portfolio. The Global Medical Oncology IO Thoracic/H&N Medical Lead is a strategic leader with a broad scope of responsibilities across within the Global Medical organization in leading a team to drive the cross-functional matrix to deliver on the global and US medical plan for assets in scope. The successful candidate will have oversight to develop aligned medical strategies and execute core medical deliverables, including Integrated Evidence Plans, Scientific Narratives and External Engagement and Advocacy plans, as well as a...

Senior Manager, Computer Systems Validation (CSV) – Cell Therapy Location Summit, NJ Department Equipment Commissioning and Qualification Organization The Senior Manager, Computer Systems Validation (CSV), Equipment Commissioning & Qualification supports design, development, delivery, validation, maintenance, and support of GMP computerized systems at multi-use sites. This individual interacts with internal team members, peer-level customers, and external service providers, supporting multiple projects and ongoing activities to ensure regulatory compliance. The Senior Manager supervises contract and/or full-time staff to facilitate departmental deliverables and directly supports CTDO Summit. Key Responsibilities Management Lead a team of up to 9 people. Interview and hire internal/external...

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 Manufacturing Associate II, Cell Therapy within Manufacturing brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel...

Summary The Sr. Director, Quality Technical Operations, Cell Therapy Manufacturing is responsible for leading the day-to-day quality review and approval of investigations, CAPA, Change Controls with associated documents and the oversight of the Quality Engineering team responsible for qualifications and validations of computerized systems, software, enterprise systems, equipment, methods, and manufacturing processes. The Sr. Director, Quality Technical Operations will serve as a primary delegate and proxy for the Head of Quality, Cell Therapy Manufacturing at Summit, and is as a champion for quality principles and compliance within the organization. Duties and Responsibilities Responsible for QA oversight of cGMP operations deviations,...

PURPOSE AND SCOPE OF POSITION The Sr. Process Engineer provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment. Technical support includes troubleshooting process and equipment related issues that occur during the Manufacturing process. The Sr. Process Engineer works closely with the Manufacturing and Quality teams to determine immediate corrective actions for deviations, identifies root cause, and implements long-term preventive actions. Other responsibilities include participation in process tech transfer and incoming process changes, communicate the changes to applicable departments, and lead the process improvement projects at the site. The Sr. Process engineer works to...

The Agile Sourcing Director of Corporate Functions & Services (CFS) and International plays a critical role in driving the execution of global category strategies for the CFS procurement categories and ensuring best practices, continuous improvement, and data-driven outcomes. This role is responsible for leading the Agile Sourcing (Source to Contract) program and the International CoE for Contracting, enabling the Category Management program across a diverse range of CFS categories and supporting end-to-end contracting process across multiple markets. The Director drives resource allocation for Agile Sourcing employees and outsourced providers supporting this function. This role is responsible for developing resource allocation...

This Senior Manager position is a headquarters-based position and reports to the Director, US Cardiovascular Commercialization Learning. In this role, the Senior Manager will work collaboratively across a fast-paced and complex matrix organization, which includes the Cardiovascular Commercialization Teams, the US Field Enablement Team, WW Centre of Excellence, and Enterprise Learning Services. Specifically, the Senior Manager will work in close partnership with colleagues from several functions (e.g. Sales, Marketing, Sales Operations, Medical, Legal, Compliance, etc.) to strategically address business needs and ensure that we deliver on our objective of demonstrating value to both customers and patients. In addition to the...

The Precision Medicine Program Manager works directly with the Precision Medicine teams to lead internal and external Biomarker Strategy and Companion Diagnostic development activities for multiple therapeutic areas including Solid Tumor, Hematology, Immunology, Neuroscience, Cardiovascular, Fibrosis, as well as Digital solutions. The team integrates scientific and business insights from multiple stakeholder functions to deliver innovative diagnostic strategies and solutions that will make precision medicine a reality for the patients and health care providers we serve. The Precision Medicine Program Manager (Companion Diagnostics, CDx) is accountable, with the Precision Medicine Lead to support BMS therapeutic product Development Teams (DT) to successfully...

The Medical Evidence Generation (MEG) Lead in Immunology & Neuroscience at Bristol Myers Squibb oversees evidence generation for the I&N 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 Provide medical/clinical accountability and oversight for the various medical affairs-led sponsored studies (interventional and non-interventional), in alignment with the...

This Senior Manager position is a headquarters-based position and reports to the Director, US Cardiovascular Commercialization Learning. In this role, the Senior Manager will work collaboratively across a fast-paced and complex matrix organization, which includes the Cardiovascular Commercialization Teams, the US Field Enablement Team, WW Centre of Excellence, and Enterprise Learning Services. Specifically, the Senior Manager will work in close partnership with colleagues from several functions (e.g. Sales, Marketing, Sales Operations, Medical, Legal, Compliance, etc.) to strategically address business needs and ensure that we deliver on our objective of demonstrating value to both customers and patients. In addition to the...

The primary responsibility of a Senior Manager in Commercial Regulatory Affairs is to provide expert and strategic regulatory advice and risk assessment on promotional issues with guidance from management to ensure that BMS implements product promotion consistent with BMS policies, PhRMA guidelines, FTC guidelines, and applicable FDA regulations and guidance’s. Responsibilities include Provide regulatory advice and risk assessment on concepts and final advertising/promotional materials, sales training materials, and external communications for marketed products, as assigned. Assure full regulatory compliance of all promotions with approved labeling and FDA guidance. Maintain up-to-date knowledge of laws, regulations and policies enforced by the Federal...

The Senior Director, Program Management Lead (individual contributor) is assigned to high priority development asset(s). They operate as a strategic partner to the Global Program Lead (GPL), to shape and deliver the Target Product Profile (TPP) and Integrated Development Strategy (IDP) for the assigned asset(s) and associated product indications. Responsible for the rigorous execution of the IDP through matrix or line management of Program Management team members. Duties/Responsibilities Program Management SME delivering as a key partner to the GPL. Serves as the strategic thought partner to the GPL / GPT and core to establish a high performing team environment Responsible...

Title Sr Therapeutic Area Specialist Therapeutic Area Oncology Territory Allentown,Bethlehem, Danville, Dunmore, Easton, Lebanon, Muncy, Pottsville, Reading, Sayre, Scranton, Wilkes-Barre, Williamsport Key Responsibilities Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas Prepares and successfully implements comprehensive territory and account plans. Proactively uses...

The Manager, External Engagement is responsible for supporting the development and execution of a coordinated approach to engaging external partners across the Greater Boston area. This role serves as a key liaison between the Cambridge Site Leadership Team and external organizations, including academic institutions, non-profit organizations, biotech incubators, entrepreneurs, and industry partners. The position supports scientific collaboration, community engagement, early career development, and site visibility initiatives that align with broader site and enterprise strategies. This role works cross-functionally with Government Affairs, University Relations, HR, and other internal stakeholders, supports the management of outreach-related budgets, and coordinates planning and execution of...

The Senior Manager, Procurement, Capital Engineering & Indirect Services position is a key leadership role within the Biotechnology Procurement network. Reporting into the Site Procurement Lead, this position will oversee site operational procurement activities and lead a team responsible for sourcing capital equipment, benchtop equipment, indirect goods, and engineering-related services across the Devens site and broader regional footprint. The role ensures strong alignment with the Biotechnology manufacturing network strategy, working closely with site leadership, engineering, operations, and global procurement teams to deliver best value, supplier reliability, governance, and operational excellence. The role requires outstanding communication, influential leadership, and a strong...

Background RayzeBio is a dynamic biotechnology company headquartered in San Diego, CA. Launched in late 2020 and recently acquired by Bristol Myers Squibb (BMS) as a wholly owned subsidiary, the company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio operates as a standalone entity within the BMS organization, maintaining its biotech culture with the opportunity to leverage the best-in-class oncology capabilities of BMS. RayzeBio is developing innovative drugs against targets of solid tumors. The lead asset, RYZ101, is in Phase 3 testing for patients with gastroenteropancreatic neuroendocrine tumors (GEP-NETs), as well...

The Associate Director Program Management (PM) will be assigned as a Program Manager and work under the matrix leadership of a Program Management Lead (GPT PM) and/or as a Program Management Lead. As a Program Manager, this team member is assigned at the asset and/or indication level to deliver integrated cross-functional planning, oversee execution and administrate the PM sub-team(s). If assigned as Program Management Lead, they will also operate as a strategic partner to the Global Program Lead (GPL), to shape and deliver the Target Product Profile (TPP) and Integrated Development Strategy (IDP) for the assigned asset(s) and associated product...

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 Specialist, Investigations, Cell Therapy provides investigation leadership to the Devens Cell Therapy Facility. The Senior Specialist will perform root...

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

Expected Areas of Competence Identify accurately the sales potential of all customers Sell / Promote awareness of the Oncology product range to achieve planned sales objectives Continually monitor and analyse new business opportunities within the defined territory. Develop and maintain effective new and existing business relationships through regular contact and liaison, including local medical organizations and key university and hospital departments. Identify, in conjunction with Manager, appropriate trade displays/exhibits to attend or conduct. Assist in / organize meetings and seminars to promote company image and/or product awareness to achieve sales objectives. Ensure effective management of territory by efficient time management,...

Position Senior Manager, Quality Assurance Shop Floor 2nd Shift Location Devens, MA The Senior Manager, Quality Assurance Shop Floor (QASF) 2nd Shift is a key people leader. The incumbent manages front line managers, and their teams, and will play a pivotal role in ensuring the highest quality standards in our cGMP Cell Therapy processes. The QASF organization is responsible for quality oversight of shop-floor activities at the Devens Cell Therapy Facility (CTF) including the manufacturing, release testing, and packaging of autologous drug product. The incumbent will be at the forefront of our night shift operations, fostering a culture...

The Director of TA-Portfolio Strategy will be responsible for helping to shape and execute portfolio-level strategies as well as Therapeutic Area (TA) strategies and facilitate active TA-level portfolio management. This position reports to the Vice President, Portfolio Strategy, but will support TA-aligned Portfolio Strategy Leaders, working closely with them to create strategies and facilitate portfolio management. This individual will demonstrate cross-functional business acumen and have demonstrated experience in strategy development, execution and managing decisions/choices across a portfolio. Additionally, this individual will work closely with other team members across Enterprise Strategy (e.g., Portfolio Analytics, Competitive Intelligence, Enterprise Governance) to drive analytics,...

The Senior Manager, Benchtop IT Systems at the Devens Cell Therapy Facility is responsible for leading the design, deployment, operation, and lifecycle support of laboratory and benchtop IT systems supporting advanced cell therapy manufacturing. This position plays a pivotal role in integrating digital technologies into GxP laboratory environments, ensuring robust compliance, reliability, and alignment with business objectives. The Senior Manager collaborates cross-functionally with laboratory, manufacturing, quality, automation, and global IT teams to deliver solutions that enable scientific innovation and operational efficiency. Key Responsibilities Lead and manage the end-to-end lifecycle of benchtop and laboratory IT systems (LIMS, CDS, SDMS, ELN, bespoke...

Summary The Associate Director, R&D BI&T Portfolio Delivery Lead, is responsible for leading the delivery and management of the R&D BI&IT project portfolio, ensuring alignment with strategic priorities and optimal resource utilization. This role will oversee project execution, financial management, and stakeholder engagement to drive successful outcomes for BMS’s R&D objectives. The Associate Director will maintain portfolio governance, resource allocation, risk management, and continuous improvement, with a strong focus on Agile principles to support successful Portfolio execution. Key Responsibilities Lead the management and delivery of the R&D IT project portfolio, ensuring alignment with the prioritized Book of Work (BOW) and...

The Material Handler is responsible for providing material movement and logistics support to internal and external customers at our research laboratories in Seattle. As part of the Supply Chain group, the Material Handler will help facilitate the safe receipt, storage, retrieval, and timely dispatch of goods with our laboratories located in Seattle. If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview Seattle - WA $30.94 - $37.49per hour The...

The Senior Material Handler is responsible for providing material movement and logistical support to internal and external customers in support of cellular therapeutic manufacturing at the Juno Manufacturing Plant (Jump) during process transfers, routine production, and technology improvements that support manufacturing operations per Standard Operating Procedures (SOPs). The Senior Material Handler will coordinate across multiple cross-functional departments and adheres to regulatory requirements and company policy while performing job functions. Duties/Responsibilities Coordinates internal and external customer requests across multiple unit operations during their shift to include personnel, material, and logistical needs. Working with production planning, the Sr. Manufacturing Associate, and other...

The Associate Director, Global Medical Affairs, SLE is a core member of the Global Medical SOTYKTU and Lupus team. This individual plays a pivotal role in developing and executing global medical and launch strategies, supporting scientific evidence generation, medical education, and congress initiatives. The Associate Director will report to the Global Medical Director, SLE and collaborate broadly across internal and external stakeholder groups. Key Responsibilities Therapeutic Area Rheumatology, SLE Contribute to the development, execution, and continual enhancement of global medical education and congress strategies for rheumatology, leveraging traditional, digital, and omnichannel approaches. Develop and oversee tactical initiatives including exhibits, symposia,...

Bristol Myers Squibb (BMS) is seeking a world-class physician-executive to serve as Senior Vice President, Worldwide Head of Immunology & Cardiovascular (ICV) Medical Affairs. This leader will define and drive the global medical vision, strategy, and execution across one of BMS’s most scientifically complex and strategically critical portfolios—spanning immunology, inflammation, cardiovascular disease, and cardiometabolic conditions . This is a mission-defining enterprise role for a highly credible leader who operates seamlessly across early development through lifecycle maturity , shaping evidence, influencing global practice, and ensuring BMS delivers practice-changing, equitable impact for patients worldwide . As the senior-most medical leader for ICV...

The TAS is 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 be accountable for the appropriate adoption of BMS assigned Rheumatology portfolio and generate demand. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deep scientific dialog. The role builds and maintains strong professional relationships with selected National Thought Leaders (NTLs) and focus on regional thought...

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. BMS Cell Therapy Manufacturing is seeking a Senior Manufacturing Associate, Cell Therapy that brings enthusiasm, intellectual curiosity, scientific rigor, and a...

Summary The Director of Pricing and Access Strategy Neuroscience will be responsible for the worldwide market access strategy for advancing pipeline assets in the neuroscience portfolio. The PASL will provide input to the Development and Commercial Strategy organization on access and pricing approaches globally. They will sit on multiple cross-functional teams, providing input into the development and commercialization strategy from a market access perspective, and assist the markets through product launch.The position is part of a highly matrixed organization. The PASL will partner with the cross-functional GMAx teams as well as with the extended team (commercial, medical, regulatory, development, advocacy,...

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. BMS is seeking a Manager of Cell Therapy Manufacturing for a manufacturing facility in Devens, MA. The Manager will support the...

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. BMS Cell Therapy Manufacturing seeks a Specialist, Lead Manufacturing Associate Cell Therapy that brings enthusiasm, intellectual curiosity, scientific rigor, and a...

Position Region Director, US Field Medical Hematology, MM/Lymphoma The Field Medical organization 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 Field Medical (FM) Region Director role is a field-based role focused on leading a team of Field Medical professionals. Direct reports will include field-based Medical Science Liaisons across the US. The FM Director will be responsible for oversight of MSLs in support of BMS Oncology medicines. This position will focus on Multiple Myeloma...

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 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. BMS Cell Therapy Manufacturing is seeking a Senior Manufacturing Associate, Cell Therapy that brings enthusiasm, intellectual curiosity, scientific rigor, and a...

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 Clinical Manufacturing Associate brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The Senior...

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

Position Medical Science Liaison, Cardiovascular - Milvexian Location Field - NE, MN, IA, WI, ND, SD 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...

We are currently searching for a candidate who can drive project management, strategic planning, and excellence in the execution of the Asset/Indication Medical Strategy team (AIMS). AIMS drives the medical strategy and execution for a specific asset and/or disease area (indication), ensuring its deliverables address critical unmet needs of patients and healthcare systems worldwide. We are seeking a highly organized and detail-oriented professional to join our team. The Senior Manager, Medical Project Manager (MPM) will work with the AIMS Medical Product Lead to manage AIMS operational excellence. The Senior Manager MPM plays an important role in organizing, managing, and communicating...

The Associate Director, Forecasting, US & WW Multiple Myeloma, 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 Associate Director 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...

The Senior Manager, Finance, R&D Global Drug Development position is a key financial position in the R&D Finance organization with responsibility for the financial management of HOCT ( Hematology, Oncology, and Cell Therapy), Neuroscience and Immunology & Cardiovascular (ICV) functional budgets managing spend of $0.3B and 600 headcount . The role will partner extensively with functions leadership teams to provide sound financial advice and decision support. The role includes leading functional budget and projection processes, monthly close activities, P&L analyses, strategic thought partner for LT members and achieving financial goals. Major Responsibilities and Accountabilities Lead HOCT, Neuro & ICV Budget...

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. Shift A2 Sunday - Wednesday 2PM - 12AM Key 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...

The Associate Director , Forecasting, Inline Solid Tumors 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 Associate Director 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...

The Director, Forecasting, WW Global, 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 Director 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 structured improvements. This position is...

The Senior Manager, Supply Chain External Manufacturing is the bridge / interface between the CMO and the wider BMS Supply Chain team. They are accountable for ensuring effective communication of supply chain information to and from the CMO & VPT and within BMS Supply Chain. The Supply Chain lead is also accountable for driving Supply Chain improvements with the CMO. Key Responsibilities Maintaining/developing strong relationships with supply chain counterparts at CMOs and internal BMS stakeholders to facilitate continuous performance improvement. Participate in Virtual Plant team meetings, CMO face to face meetings & lead supply chain related meetings with CMO as...

The Associate Director, Reblozyl Forecasting, 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 Associate Director 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 structured improvements. This position...

Scientist, Bioassay Development – Potency and Impurity Analytical Development Our Biologics Development team is responsible for development and transfer of safe, efficient, and approvable biologics drug substance manufacturing processes and analytical methods for all of BMS’ biologics portfolio. We work closely with other BMS units to support our clinical pipeline through to late stages of clinical development. Innovation is at the core of what we do, with an intense focus on efficiency, speed, robustness, and approvability of our processes and methods. Here, you’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, pursue innovative ideas,...

The Associate Director, Forecasting, Portfolio / Early Assets Transition Lead, 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 Associate Director 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...

The Executive Director, CASA, Commercial US & WW Forecasting TA Lead , is a senior leader that serves as a trusted, collaborative advisor to Commercial and Finance leadership team CLT & FLT) , providing strategic guidance and delivering a holistic, unbiased perspective on their portfoli o through data-driven insights to maximize the commercial potential . R esponsible for delivering robust, insight-driven forecasts across short-term (Year 1), mid-term (Year 3), long-term (Year 10), and business development (BD) horizons. This role is pivotal in shaping strategic decisions for the therapeutic area by integrating market insights, actual performance, and advanced analytics into comprehensive...

The Executive Director, CASA, Commercial US & WW Forecasting TA Lead , is a senior leader that serves as a trusted, collaborative advisor to Commercial and Finance leadership team CLT & FLT) , providing strategic guidance and delivering a holistic, unbiased perspective on their portfoli o through data-driven insights to maximize the commercial potential . R esponsible for delivering robust, insight-driven forecasts across short-term (Year 1), mid-term (Year 3), long-term (Year 10), and business development (BD) horizons. This role is pivotal in shaping strategic decisions for the therapeutic area by integrating market insights, actual performance, and advanced analytics into comprehensive...

The Executive Director, Global Commercial Strategy will lead the development and execution of global commercial strategies for key oncology assets across breast and other solid tumors. This role will be instrumental in shaping the long-term vision, lifecycle management, and launch readiness of pipeline and inline products, ensuring alignment across global markets and cross-functional teams. Key Responsibilities Strategic Leadership Develop and lead global commercial strategies for breast and other tumor indications, ensuring alignment with R&D, Medical Affairs, Market Access, and regional commercial teams. Drive asset strategy from early development through launch and lifecycle management. Cross-Functional Collaboration Partner with Global Product Teams...

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

Translational Development Overview 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. Key Responsibilities Designs and implements program-specific late development biomarker/translational plans, responsible for aiding in creation of...

The Senior Director, Forecasting, Sr. Director, Pipeline, Oncology, is an enterprise leader within Worldwide Commercial Excellence who sets the strategy, standards, and vision for forecasting across multiple brands and therapeutic areas. This role elevates forecasting as a strategic decision‑support capability by shaping enterprise methodologies and assumptions frameworks , advancing AI‑first forecasting platforms, and ensuring outputs are accurate , transparent, comparable, and decision‑useful across planning horizons. The Senior Director partners with senior leaders across Commercial, Finance, MAx , Medical, Pricing, Worldwide/Regional markets, Supply/GPS, and Investor Relations to drive assumption alignment and support portfolio and investment decisions. The role leads a multi‑level...

Position Medical Science Liaison, Cardiovascular - Milvexian Location Field - South TX 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...

Expected Areas of Competence Identify accurately the sales potential of all customers Sell / Promote awareness of the Oncology product range to achieve planned sales objectives Continually monitor and analyse new business opportunities within the defined territory. Develop and maintain effective new and existing business relationships through regular contact and liaison, including local medical organizations and key university and hospital departments. Identify, in conjunction with Manager, appropriate trade displays/exhibits to attend or conduct. Assist in / organize meetings and seminars to promote company image and/or product awareness to achieve sales objectives. Ensure effective management of territory by efficient time management,...

The Senior Facilitator plays a critical role in delivering an industry-leading contract facilitation capability for Bristol Myers Squibb. This hands-on position manages complex contracts from intake through execution, ensuring compliance with company standards and regulatory requirements. The successful candidate will demonstrate exceptional communication skills and the ability to manage relationships across diverse stakeholders, ensuring clarity, collaboration, and timely resolution of issues. Responsibilities 1. End-to-End Contract Facilitation in English & Spanish Perform due diligence, select templates, and draft agreements. Redline and negotiate contract terms using fallback language and escalation protocols. Draft commercial terms and defend legal terms on internal templates or...

Reporting to the SVP, Neuroscience Commercialization, the U.S. Brand Lead, KarXT, Alzheimer’s Disease Psychosis (ADP), is a critical leadership role within the Neuroscience organization. This role is charged with ensuring U.S. launch readiness and the U.S. commercialization of KarXT in ADP, 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. What we are looking for? We are looking for a dynamic, performance-driven leader who cultivates a team-based, collaborative, customer/externally focused environment which...

SENIOR DIRECTOR POSITION As a key leader of the Data Science and Advance Analytics (DSAA) organization in drug development is part of a cross-functional team of drug development scientists and data scientists focused on providing hands on skills, expertise, and tools to facilitate access, integration, visualization, and exploratory analysis of complex and diverse data in support of clinical development activities and decisions. The Data Science Lead will drive execution of exploratory analysis (hypotheses generating and hypotheses generated questions) for scientific considerations related to drug development and clinical study design. Through practical hands-on work, the Data Science Lead will define approaches,...

Summary The Content Strategist acts as a critical BMS link between brand teams, Agencies of Record (AORs), Mosaic Data Hub, BIT, and Commercialization AI Strategy & Analytics (CASA) to ensure BMS’s Strategic Asset Management AI (SAMai) platform and marketing content libraries are accurate, searchable, compliant, and activation-ready. This role is accountable for upholding content integrity and as such owns metadata /taxonomy standards, is responsible for tagging accuracy, seamless asset transfer, and building well-structured content libraries that enable GenAI-driven content creation and strategic content reuse. This role ensure adherence to BMS metadata standards, supports BMS claims management, drives BMS content quality...

Summary This role is a senior leader responsible for shaping and executing advanced analytics strategies that optimize patient support services, access strategies, and field resource engagement across multiple brands and disease areas. This role drives the integration of access and engagement analytics into enterprise-wide initiatives, delivering actionable insights for fulfillment performance, PAL/FRM engagement effectiveness, and access strategy reporting. The Director partners closely with Market Access, Patient Support teams, Field Operations, and cross-functional stakeholders to champion innovation, establish governance standards, and foster adoption of advanced tools and methodologies. By translating complex data into strategic recommendations, this leader empowers decision-making, improves patient...

The Vice President, U.S. Customer Insights & Engagement is a senior commercial leader responsible for shaping how Bristol Myers Squibb engages with healthcare professionals (HCPs) across the U.S., leveraging both personal and digital channels. This executive partners closely with U.S. Business Unit and brand leads to identify strategic opportunities, serving as a trusted advisor in developing commercial strategies and building the capabilities required for success. Leading a team of engagement and insights professionals, the VP translates data, customer insights, and market intelligence into actionable strategies that drive growth and competitive advantage. The role also collaborates with Business Insights and Technology...

Summary The Associate Director is responsible for shaping and executing advanced analytics strategies that optimize patient support services, access strategies, and field resource engagement across multiple brands and disease areas. This role drives the integration of access and engagement analytics into enterprise-wide initiatives, delivering actionable insights for fulfillment performance, PAL/FRM engagement effectiveness, and access strategy reporting. The Associate Director partners closely with Market Access, PSS teams, Field Operations, and cross-functional stakeholders to champion innovation, establish governance standards, and foster adoption of advanced tools and methodologies. By translating complex data into strategic recommendations, this leader empowers decision-making, improves patient access, and...

SENIOR COUNSEL – LITIGATION AND GOVERNMENT INVESTIGATIONS The Senior Counsel, Litigation & Government Investigations, will be responsible for independently managing various litigation, government investigation, and other legal matters faced by the Company. Responsibilities include · Managing a variety of litigation matters, including, but not limited, to antitrust, commercial, consumer protection, product liability, and securities actions, as well as other potential disputes faced by the Company. · Managing domestic and international internal and government investigations. · Effectively managing outside counsel representing the Company to achieve positive outcomes. · Collaborating closely with other Law Department colleagues and functional support groups to provide...

Summary BMS is in process of rewiring our marketing approach and moving toward a best-in-class, AI-driven commercialization model. AI will play a key role in increasing our speed, relevance, and impact of our insight driven strategic choices, our customer-facing content, and our omnichannel and measurement plan empowering our marketers to deliver exceptional and transformative customer experiences. Achieving our AI-driven marketing vision requires a full transformation of our capabilities, processes, and tools. We are looking for a leader of our End-to-End (E2E) AI Marketing Integration Leads to drive collaboration with our Commercialization AI Strategy& Analytics (CASA) Leadership Team members, our Marketing...

This position is a senior level technical individual contributor on the Process Automation Team within the Devens Cell Therapy Facility. This individual will be responsible for complex tasks within the group and operate autonomously with minor guidance and direction. This individual will maintain, configure, administer, and troubleshoot the DeltaV, PI, BAS, and integrated process equipment. Responsibilities Subject matter expert for the process automation systems and equipment. Lead complex technical efforts, such as large scope changes or difficult integrations Integrate with cross-functional teams throughout the site to perform qualification and validation. Provide troubleshooting and guidance support to automation systems in support...

Summary The Senior Director, Marketing AI Enablement, Commercialization AI Strategy & Analytics (CASA) will be pivotal in advancing BMS’s Rewire Marketing approach, championing the strategic development and requirements for a best-in-class, AI-driven commercialization model. As the primary business owner and strategic connector, this leader will ensure business and marketing requirements are captured and partner closely with IT, as the technical product owner, to drive the process and implement the marketing capabilities and technologies needed to realize our AI Commercialization Vision. Reporting to the CASA VP, Marketing AI Capabilities and Experience, the role requires a unique blend of commercial acumen and...

This position is a senior level technical individual contributor on the Process Automation Team within the Devens Cell Therapy Facility. This individual will be responsible for complex tasks within the group and operate autonomously with minor guidance and direction. This individual will maintain, configure, administer, and troubleshoot Aveva PI Systems. This individual will also provide support for the DeltaV and BAS systems. Responsibilities Subject matter expert for the Aveva PI and Data Historian Systems. Lead complex technical efforts, such as large scope changes or difficult integrations Integrate with cross-functional teams throughout the site to perform qualification and validation. Support audits...

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

This position is a lead level technical individual contributor and technical project lead on the Process Automation Team within the Devens Cell Therapy Facility. This individual will be responsible for a significant function within the group and operate autonomously. This individual will maintain, configure, administer, and troubleshoot the DeltaV, PI, BAS, and integrated process equipment. Responsibilities Technical lead and subject matter expert for the process automation systems and equipment. Lead substantial technical efforts, such as major system version upgrades or new process introductions. Integrate with cross-functional teams throughout the site to perform qualification and validation. Provide troubleshooting and guidance support...

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...