Bristol Myers Squibb Job Trends

This is a highly visible leadership position within the R&D Finance organization with responsibility for the financial management of Neurology early and late development studies across the Company, managing a budget of $0.6B . The successful candidate will be an influential and collaborative finance professional who leads beyond the role and effectively interacts and influences at all levels of the organization. The role will partner extensively with Neurology R&D leadership to provide sound financial advice and strategic decision support, to fully understand the development plans, key study drivers, and operational execution so that cost estimates and study accounting is properly...

Sr. Commercial Field Operations Manager (East), US Cell Therapy is a key member of the US CELL THERAPY National Account Team. This individual is responsible for supporting the US Cell Therapy East Region Director in execution of brand and franchise strategy to include the development and implementation of the business and account planning process. In addition, this individual serves as a home office liaison to specific operational functions including BI&A, Compensation and Marketing. This individual will work closely with the Sr. Commercial Field Operations Manager in the West, the Associate Directors of Field Strategy and Reporting as well as home...

The Director, Program Management, is assigned to early and/or late development stage 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 individually or in partnership with assigned 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 for the...

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, and advance professionally alongside some of the brightest minds...

The Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy for biomarkers and diagnostics, focusing on early-stage development through proof of concept and supporting registrations. This role establishes scalable frameworks for investigational assay development, ensuring timely, compliant submissions that support patient stratification in Phase I/II studies. As a key member of the Translational Medicine CLIA Laboratory Steering Committee, the director drives coordinated early-stage drug-diagnostic strategies and health authority engagement to accelerate access to precision therapies. The position demands deep scientific and regulatory expertise (US, EU, Canada, PMD, TGA or Global Devices/IVD preferred), cross-functional leadership, and a commitment to...

The QA Specialist within the Quality Assurance Shop Floor organization provides quality oversight for routine clinical and commercial cell therapy operations, ensuring adherence to current Good Manufacturing Practices (cGMP). This role serves as a subject matter expert (SME) in cGMP, Good Documentation Practices (GDocP ), and Data Integrity/ALCOA+ principles, supporting quality risk management and right-first-time execution on the Shop Floor at BMS Bothell. Shift Sun-Wed 0600-1630 Duties / Responsibilities Perform real-time review of executed batch records to ensure compliance with procedures; collaborate with manufacturing teams to resolve discrepancies. Quality Operator/Verifier for on the floor operations such as packaging, material receipt...

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

Summary This role serves as a strategic business partner to the Oncology Global Commercial Strategy team, driving ongoing commercialization efforts. The position is recognized as a trusted advisor, embedding customer and market insights into critical business decisions. It collaborates with key stakeholders to inform strategic and tactical choices through market research, forecasting, and secondary data analytics. By executing comprehensive business analyses, the role enhances value for patients through deep market understanding, subject matter expertise, and practical application. Responsibilities Delivers integrated insights across various analytical functions such as forecasting, market research, secondary data analytics to address key business questions and drive...

The Regional Associate Director (RAD) is responsible for managing a team of Medical Science Liaisons (MSLs) trained in the area of Cardiovascular diseases. 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 advances, treatment trends,...

BMS is actively seeking a dynamic and experienced Senior Manager, Software Development Engineer (Full Stack) to join our team, focusing on cutting-edge Cloud technologies. Based in our Seattle, WA location, you will play a key role in crafting innovative solutions and contributing to the advancement of our cloud infrastructure. As a Software Development Engineer, you will engage in diverse tasks, ranging from writing efficient Lambda functions to developing full-scale web applications (both front-end and back-end). You'll be an integral part of our team, contributing not only to code development but also to standard cloud infrastructure operations. Automation is at the...

BMS is actively seeking a dynamic and experienced Senior Manager, Software Development Engineer (Full Stack) to join our team, focusing on cutting-edge Cloud technologies. Based in our Seattle, WA location, you will play a key role in crafting innovative solutions and contributing to the advancement of our cloud infrastructure. As a Software Development Engineer, you will engage in diverse tasks, ranging from writing efficient Lambda functions to developing full-scale web applications (both front-end and back-end). You'll be an integral part of our team, contributing not only to code development but also to standard cloud infrastructure operations. Automation is at the...

The Associate Director, Field Strategy & GTM Solutions will play a critical role in shaping the commercial go‑to‑market model and designing future‑fit field deployment strategies across therapeutic areas. This role will lead the development of innovative structural solutions, coverage frameworks, and scenario planning that enhance customer engagement effectiveness. The individual will partner closely with cross-functional leaders to ensure that the field model is optimally configured to support brand priorities, organizational strategy, and evolving marketplace dynamics. This position is strategic in nature and does not include operational execution responsibilities. Key Responsibilities Lead enterprise-level GTM strategy development, including field structure recommendations, deployment...

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...

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...

At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team. The Associate Director, Supply Chain, New Product Introduction is accountable for leading and overseeing the successful integration of new products and...

Summary The Mechanical Technician is responsible for the installation, maintenance, and repair of pumping systems, including motors, centrifugal pumps, condensate pumps, fans, and any other mechanical systems requiring repair or replacement at the BMS Devens site. Their role is to ensure that all mechanical equipment operates efficiently and reliably to support critical manufacturing processes and comply with regulatory standards. The technician will work closely with engineering, facilities, and quality teams to ensure that mechanical systems meet stringent safety and product quality requirements. Duties/Responsibilities Participates in a detailed training program to develop expertise and train a cross functional team in mechanical...

The Legal Operations Analyst works with the BMS Law Department globally to help define and support operational and strategic approaches to ensure business success by managing, sustaining and continuously improving Legal Operation processes. The Legal Operations Analyst plays an integral role in the planning stages of project and program development for the BMS Law Department, and will monitor and deliver program and project metrics. The position will report to the Associate Director of Legal Operations in addition to liaise with other BMS Enabling Functions including Information Technology, Finance and Global procurement and other key stakeholders to support the Law Department...

The CMMS Administrator at the Devens Massachusetts site will be responsible for processing requests in support of the CMMS master data. This person will act as a gatekeeper in both processing requests but also enforcing data integrity and compliance. Key Responsibilities Ensure data integrity and alignment of processes of master data with the CMMS system within established service level agreements. Primary gatekeeper of the master data change request lifecycle. Primary executor of change management requests working with required stakeholders. Secondary provider of data extracts in support of data management bulk requests. Enforce data management request integrity ensuring all required fields...

RayzeBio is a dynamic biotechnology company headquartered in San Diego, CA with additional sites in Princeton, NJ and Indianapolis, IN. Launched in late 2020 and now a wholly owned subsidiary of Bristol Myers Squibb (BMS), the company is focused on improving survival for people with cancer by harnessing the power of targeted radioisotopes. RayzeBio operates as a standalone entity within BMS, maintaining its entrepreneurial biotech culture while leveraging world-class oncology and commercialization expertise. The company’s lead asset, RYZ101, is an actinium-based radiopharmaceutical therapy currently in Phase 3 development for patients with gastroenteropancreatic neuroendocrine tumors (GEP-NETs). In addition, RayzeBio has the...

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

Manager I, Manufacturing Cell Therapy Summary Lead and manage a team to execute cell therapy manufacturing processes (CAR-T) using cGMP standards. Drive daily operations, troubleshoot issues, oversee compliance, and implement process improvements. Foster a culture of safety, collaboration, and innovation in support of BMS values. Key Responsibilities Supervise and coach manufacturing staff; promote teamwork and accountability Oversee daily production, resource assignment, and compliance with SOPs Ensure documentation accuracy and training completion Support troubleshooting, investigations, and process improvement initiatives Drive safety and inspection readiness standards Hire, mentor, and develop staff; conduct performance reviews Communicate operational updates and coordinate with cross-functional teams...

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...

Cell Therapy Network Lead investigator will support the commercial and late stage clinical cell therapy network for complex trend investigations stemming from deviations and SAEs. The lead investigator will assemble and lead cross functional matrix teams necessary to close complex trend investigations. He/she will participate in strategic discussions, anticipate bottlenecks, technical risks, and address issues proactively, while fostering an environment of teamwork. The person will collaborate with SMEs, user groups, quality groups, and other stakeholders to complete complex trend deviations and CAPAs Key Responsibilities Serve as lead investigator for global trend investigations and global SAE events. Support site based investigators...

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 District Business...

Responsible for developing and managing the capital budget, purchasing lab equipment and supplies, overseeing external manufacturing contracts , creating purchase orders , reconciling invoices, and driving cost-saving initiatives. Partners with Finance, Site Engineering, and laboratory teams to ensure timely, cost-efficient procurement and budget alignment across Cell Therapy Development & Operations. Key Responsibilities Capital Equipment Purchasing Collaborate with laboratory staff to understand equipment specifications and budget constraints. Proactively engage with vendors and auction houses to identify the most competitive pricing options, ensuring alignment with budget goals and maximizing cost-saving opportunities. Request and review supplier quotations, proposals, and product demonstrations to support...

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology, and cardiovascular disease – and with one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contributes to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. We are seeking a highly skilled Senior Scientist to join our Protein Analytics team. This role is primarily bench-focused, supporting the analytical characterization of large molecule therapeutics including monoclonal antibodies, antibody-drug conjugates...

Key Responsibilities Subject Matter Expert (SME) and / or Local Process Owner (LPO) for Vendor Qualification and Management. Manage lifecycle activities of qualification and routine oversight of GMP and GDP vendors. This includes assessing new vendors, developing and revising Quality Agreements, providing input to the vendor risk assessment and audit program, and maintaining accurate data within the Approved Vendor List in the electronic Supplier Quality Management system. Subject Matter Expert and / or Local Process Owner for Material Qualification and Management. Manage the lifecycle activities of materials used for the manufacture of drug substance, which involves material qualification, maintenance /...

We are seeking strategic, results-driven and experienced individuals to join our team as Hospital Key Account Manager (KAM) – Neuroscience. This is a critical role in establishing Bristol-Myers Squibb as a leader in Neuroscience and our commitment to supporting the efforts of Neuroscience Healthcare Providers in improving patient outcomes. This is a field-based role that will report directly to a KAM Director. The Key Account Manager is responsible for developing a comprehensive and integrated stakeholder engagement strategy within targeted key accounts to optimize access, educate on COBENFY value proposition at the account-level, and support overall adoption of COBENFY. As such,...

Bristol Myers Squibb is an organization dedicated to bringing innovative medicines to patients in need. Chemical Process Development (CPD) is a world-leading chemical development organization, located within GPS-Product Development. Through innovation in chemical development, we invent the chemical processes that take small molecule and synthetic assets from development to launch in collaboration with CMC partners. Our team of innovative, passionate, and dedicated scientists strive to bring our company mission to life, for our patients, through the discovery of highly creative and impactful chemical processes, while nurturing a culture of scientific excellence, collaboration, and meaningful career development. The Process Chemistry function...

Summary The Senior Project Manager is responsible for end-to-end management of cross-functional teams coordinating all aspects of multi-departmental and/or multi-site projects. This includes planning, execution and finalizing projects per established scope, timeline and budget criteria. Working with project teams, the incumbent identifies and facilitates resolution of issues to minimize impact on project plans. The Senior Project Manager is also responsible for planning and leading key strategic programs impacting the Phoenix Manufacturing organization. The Senior Project Manager supports the development and continual improvement of project and program management competencies. Responsibilities Employ strategic visioning and planning to align program goals and benefits...

The Medical Director, US Medical, Multiple Myeloma will report to the Senior Director, US Medical Multiple Myeloma Lead. He/she will be headquarter based, and will provide medical leadership for a novel CELMoD asset and support for the overall Multiple Myeloma portfolio of products. This individual will be involved in integrated strategic planning within Global Medical Affairs under the direction of the US Medical Multiple Myeloma lead and Global Multiple Myeloma disease lead as well as in close partnership with the US Commercialization organization, Clinical Research and Development, HEOR, Market Access, Translational Development, and Regulatory, and will lead the US Medical...

Summary At Bristol Myers Squibb, we are inspired by a single vision—transforming patients’ lives through science. Across oncology, hematology, immunology and cardiovascular disease, our colleagues advance innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Position Overview The Senior Business Analyst in the LIMS ELN and Entity Registration Platforms 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...

RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals. RayzeBio, a Bristol Myers Squibb company, is looking for a Senior Associate II, Analytical Development at their Indianapolis manufacturing site. The person will be responsible for method development and implementation, method validation, verifications, or transfer, as well as stability...

Summary The Senior Engineer, IT Computer System Validation, Cell Therapy Devens role will provide support to the Digital Plant team at the Devens Cell Therapy Facility (CTF) through managing the computerized system validation (CSV) activities / major projects and supporting deviations and change controls related to computerized systems. This position work closely with the Digital Plant (IT/Automation) subject matter experts and other key stakeholders, such as Manufacturing Science and Technology (MS&T), Quality Engineering (QE), and Manufacturing Operations. Major Duties & Job Responsibilities Gain a thorough understanding of computer systems deployed at Devens CTF. Act as CSV Subject Matter Expert (SME)...

Position Fall 2026 Co-Op Undergraduate Hematology Translational Development Location Cambridge Crossing, MA The Hematology Translational Development group seeks a talented and highly motivated undergraduate student interested in a co-op that offers hands-on translational research experience in a team-oriented, fast paced environment. The student, working closely with a mentor, will be assigned an exciting translational project to understand how various biomarkers from hematological clinical trials help understand mechanisms of action and resistance, biology of disease and inform clinical development. During the 6-month co-op, the student will analyze biomarkers, develop critical thinking and presentation skills, and learn more about drug development...

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 purpose of the Manufacturing Manger role is to manage and provide oversight of a Work Centered Team (WCT) whose primary...

The Associate, Equipment Commissioning & Qualification (ECQ) Delivery supports the successful implementation of equipment, utilities, facility, and lab instruments at multi-use sites through interaction with internal customers and external service providers. The person in this role will support commissioning and qualifying new equipment, facilities and utilities, as well as maintaining equipment systems in a qualified/validated state according to established policies and procedures. With minimum supervision and given general instructions, this individual carries out routine tasks and functions and uses basic analytical skills to recognize and solve common problems of limited scope. As a developing team player, the person in this...

Key Responsibilities and Major Duties This role is part of Business Intelligence & Reporting Solutions team, responsible for global commercial portfolio reporting and related analytics/insight services, tools and platform, to serve the needs from HQ executive, Worldwide brand/therapeutic team, regional and country commercial leads, and the broader BI&A community around the globe. The role will also lead the commercial performance workstream for upcoming brand/indication launches readiness to ensure launch success. HQ Executive and Worldwide Brand Performance Management Ensures appropriate service delivery to Executives and Worldwide Brand Team as defined by stakeholder needs and Performance Management leadership direction. Facilitate business performance...

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 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 Executive Director, HRBP, Global Medical & RDMC Effectiveness will be a pivotal force in shaping the future of our organization. This role partners with the functional Leadership Team and their global counterparts to drive a forward-thinking people strategy. By spearheading workforce planning, organizational design, talent management, team effectiveness, and change management, this position ensures our company remains agile and competitive. The Executive Director will collaborate across multiple BMS locations and geographies, aligning closely with People Org and functional leadership to seamlessly integrate our talent strategy. Responsibilities Serve as a strategic HRBP delivering tailored support to key business areas. Forge...

This territory includes Portland, OR; Salem, Bend, Eugene, Beaverton, Lakewood The Senior 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 Senior 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...

Schedule Wed- Sat 2pm- 12 midnight Responsible for supporting QC testing for in-process, final product, stability samples and for supporting environmental and facility monitoring. May assist with documentation, deviations, investigations, and continuous improvement efforts. Key Responsibilities Perform routine testing of in-process, final product, and stability samples. Perform environmental/facilities monitoring and microbiological testing. May review GMP documentation and perform data verification. 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 & Experience Specific Knowledge, Skills,...

Bristol Myers Squibb (BMS) seeks an innovative, results-oriented leader to serve as the Pumitamig M edical P roduct L ead , Global Medical Oncology . This critical role leads the Global Medical vertical for P umit a mig , a single-asset, mission-focused team designed to accelerate clinical evidence generation, recruitment, education, and external advocacy for international markets in one of the most competitive therapeutic areas in BMS history. The MPL will drive a unified strategy, high-velocity execution, and end-to-end ownership across all Global Oncology , ensuring best-in-class medical engagement for Pumitamig in th is critical pre-launch phase . The role...

Responsible for leading QC deviation, laboratory investigations, CAPAs and change control. May provide support during health agency inspection Shift Available Tuesday- Saturday, Hybrid Evening Shift 300 p.m. to 1130 p.m. Duties/Responsibilities Lead and author QC deviation, laboratory investigations, CAPAs and change control. Work with QC SMEs to conduct root cause analysis. Ensure timely and compliant closure of investigations, deviations, CAPAs and change controls. Perform document revision, project, CAPA and deviation/ investigation, change mgmt. actions, related tasks and/ or continuous improvement efforts. Train and mentor others on deviation, investigation, CAPA and change control process/ procedures. May support health agency inspection as...

Summary The Executive Director, Customer Experience will lead a team focused on evolving patient and care partner customer experience, identifying, developing, and implementing external strategic alliances, executing local market initiatives, and preparing for our future in neuroscience. The primary focus of this role is to help patients start and stay on medication they’ve been prescribed. This will be accomplished by leading a team to deliver exceptional solutions at the national and local level and to identify and create new pathways to engage and enroll in these solutions. This role will involve a significant amount of internal collaboration with cross-functional leaders...

The Safety Centre of Excellence (S-CoE) is a team of technical subject matter experts, whose role is to develop, deliver and oversee innovative, best-in-class, and risk-based solutions to minimize risk, reduce complexity, ensure compliance, and drive bench-mark performance and cultural improvement in Safety across the global BMS organization (incl’ research, commercial, manufacturing & capital projects). Key Responsibilities Global Safety Strategy Support the development and execution of the company’s global safety strategy, ensuring alignment with overall business objectives and regulatory requirements. Safety Programs & Initiatives Lead and/or support the development, implementation and continuous improvement of comprehensive, risk-based, enterprise-wide safety programs and...

The Associate Director , HRBP Corporate Function provides strategic p eople p artnership t o senior leaders across our Business Insights & Technology Organization and Law & Policy department . Additionally, this role will serve as the Strategy & Operations leader for the Corporate Functions, working closely with counterparts in the People Organization as well as the relevant Centers of Expertise (CoEs) , driving alignment, strategy and consistency across the Corporate Functions . This role provides HR leadership in driving the people strategy, workforce planning, organizational design, talent management, team effectiveness, and change management Position Responsibilities Provides strategic HR Business...

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

At Bristol Myers Squibb, we are 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...

Description In support of Commercialization Strategy, the Sr. Manager of US Predictive Customer Engagement team develops and delivers analytical assessment, solution design and modeling capability relating to US customer experience and engagement across the portfolio, to drive competitive advantage and analytically informed decision making Key Responsibilities and Major Duties Hands-on data scientist or machine learning engineer that will be expected to ideate, design, develop, model and deploy advanced solutions Hands-on use of cutting-edge analytics and machine learning to understand and predict next best actions to improve US based customer experience and engagement using a variety of data sources to...

The Senior Director, HRBP for Neuroscience (NS) Commercialization provides strategic people partnership to senior leaders across the US Commercialization organizations. Additionally, this role will serve as the commercialization lead for a one of the critical RDC capabilities and will work in close partnership with counterparts in the Research and Development HR functions as well as the relevant Centers of Expertise (CoEs). This role provides HR leadership in driving the people strategy, workforce planning, organizational design, talent management, team effectiveness, and change management. The client group may be present in multiple BMS locations/geographies/global functions, requiring close alignment with the People Org...

The VP, US Cobenfy Sales, Neuroscience role will be responsible for leading BMS’ field sales team to support the US commercialization of Cobenfy, which is the first ever treatment to target muscarinic receptor circuits in schizophrenia. This role reports to the SVP, Neuroscience Commercialization. This role will provide strategic leadership to a team of ~450 including Region Business Directors, District Business Managers, Therapeutic Area Specialists, and have dotted oversight to the Sales Operations team. This leader will be responsible for advancing brand objectives and driving performance at various life-cycle stages. This includes developing, leading, and executing sales & pull through...

Job Pos ting Title Senior Therapeutic Area Specialist, C ardiovascular Community - Portland, OR Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Portland, OR At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. The BMS Mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful...

Position Medical Science Liaison, Rheumatology Location Field - Los Angeles, CA/HI 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. Key Responsibilities The Medical Science Liaison (MSL) is a member of a field-based team who function as an extension of the US Medical Affairs organization. MSLs are responsible for developing and enhancing professional relationships with medical thought leaders involved in various phases of product development. MSLs provide medical information through scientific...

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...

The Senior Director, HRBP for Immunology & Cardiovascular Commercialization (ICV) provides strategic people partnership to senior leaders across the US Commercialization organizations. Additionally, this role will serve as the commercialization lead for a one of the critical RDC capabilities and will work in close partnership with counterparts in the Research and Development HR functions as well as the relevant Centers of Expertise (CoEs). This role provides HR leadership in driving the people strategy, workforce planning, organizational design, talent management, team effectiveness, and change management. The client group may be present in multiple BMS locations/geographies/global functions, requiring close alignment with the...

The Senior Director, HRBP for Oncology Commercialization provides strategic people partnership to senior leaders across the US Commercialization organizations. Additionally, this role will serve as the commercialization lead for a one of the critical RDC capabilities and will work in close partnership with counterparts in the Research and Development HR functions as well as the relevant Centers of Expertise (CoEs). This role provides HR leadership in driving the people strategy, workforce planning, organizational design, talent management, team effectiveness, and change management. The client group may be present in multiple BMS locations/geographies/global functions, requiring close alignment with the People Org and...

RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals . Summary Lead the company’s radiopharmaceutical commercial/clinical manufacturing facility in Indianapolis, IN and associated operations. Accountable for manufacturing operations, departmental budgets, talent management/succession planning including hiring, training, and developing engagement strategies to retain the best workforce talent for radiopharmaceutical...

Responsibilities The Collaborative Research Director, is a field-based position with two main responsibilities, lead the research initiatives for the field HEOR team and lead the clinical engagement with select access customers in a field-facing role. Lead, manage, and advise on Field HEOR Research Offerings (RAPID, ORCHID & CUPID) Partner with Field HEOR to execute ORCHID & CUPID Studies Oversee and manage sourcing and procurement support for fHEOR projects Development and updating of customer research capability repository Lead and manage the research planning and review process for field tool development (Pre-Advisement & CARSE) Participate in customer research discussions with field research...

The Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations, including but not limited to Manufacturing, Quality Control laboratories, and Warehouse Operations. This position will oversee and partner with operational areas, to ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP. Shift NIGHT shift available, Panama schedule ( 12-hour shift patterns with a 2-2-3 work cycle including weekends and holidays) 6 pm to 6am Duties/Responsibilities Provide routine Quality on-the-floor oversight and triage unexpected events with Manufacturing, Quality Labs, and Supply Chain operations. Able to interpret problems and effectively prepare surrounding...

The Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations, including but not limited to Manufacturing, Quality Control laboratories, and Supply Chain Operations. This position will oversee and partner with operational areas, to ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP. Shift NIGHT shift available, Panama schedule ( 12-hour shift patterns with a 2-2-3 work cycle including weekends and holidays) 6pm to 6am Duties/Responsibilities Provide Quality on-the-floor oversight to Manufacturing/ QC/ Supply Chain Operations & responding to minor issues or escalating to senior members. Perform and document operational verification...

This position collaborates directly with the leadership of Corporate Functions and their global teams, which includes multiple BMS LT members. Located in our Lawrenceville, New Jersey location, this role provides HR leadership support to the global Law & Policy organization, including developing and implementing the people strategy, workforce planning, organizational design and development, talent management, team effectiveness, and change management. Position Responsibilities Provides strategic HR Business Partner leadership to Corporate Functions LT members and their respective teams to maximize business performance and foster cooperation across the enterprise through an aligned People Strategy. Translates business strategy and organizational needs into contemporary...

Job Pos ting Title Senior Therapeutic Area Specialist, C ardiovascular Community - Youngstown, OH Therapeutic Area (TA) Cardiovascular Primary Location Field – United States Primary Job Posting Location Youngstown, OH At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. The BMS Mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful...

The Global Purchasing Senior Specialist plays a crucial role in coordinating and leading financial and vendor management in a multi-country environment for HR. Build and Maintain Supplier Governance with assigned HR function and/or geographic region. Provide continuous improvement within Global Vendor Management Processes to enhance stakeholder’s experience and align business strategy/requirements. Provide Subject Matter Expertise with BMS Policy and Procedures for purchasing and payment processing. Collaborative with internal and external parties to problem solve with an understanding of end-to-end processes and knowledge of impacts to decisions. Key Responsibilities Proactively executing and coordinating the "Purchase to pay" process for People Organization,...

This individual will lead a team of engineers who design and execute experiments, evaluate data, and draft technical reports in support of process improvements, investigations, and manufacturing process changes. The primary focus of the Associate Technical Director will be to oversee testing and support implementation of operational improvements and resolve manufacturing process investigations at BMS cell therapy GMP manufacturing facilities. The Associate Director will manage a team tasked with assessing, planning, executing, and communicating a variety of process related projects, from process improvements, to manufacturing investigations, and/or run the business process changes. Included in this scope is the management of...

As the Senior Director, HRBP for Global Drug Operations, you’ll be a trusted advisor and thought partner to senior leaders, shaping the future of Drug Development through bold, transformative people strategies. This is more than partnership—it’s leadership at the intersection of talent, organizational effectiveness, and business innovation. You’ll architect cutting-edge organizational designs, drive enterprise-level workforce planning, and ignite talent strategies that accelerate performance and agility. Your work will enable teams to thrive, foster collaboration across geographies, and embed a culture of adaptability and excellence. In this role, you’ll lead change—not just manage it. You’ll champion dynamic transformation initiatives that position...

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...

The Clinical Development Program Leader 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. The Clinical Development Program Leader will set the clinical development strategy for assets or indications The Clinical Development Program Leader will directly supervise the work of multiple Clinical Development Leads who will in turn supervise individual Clinical Trial Physicians unless otherwise indicated This role will include above disease / indication strategy work (i.e. supervising Broad Clinical Development teams across several Development teams, as...

This territory includes Seattle, WA, Everett, WA and Anchorage, AL 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...

PRINCIPAL OBJECTIVE OF THE POSITION Support Devens site through review and approval of investigations and change controls. Provide Quality oversight and support for Technology Transfer, Automation, Cell Bank Disposition, Validation, Manufacturing Science and Technology, Master Data and Site Engineering programs. Assure the quality of manufactured products are in compliance with all applicable regulations and guidelines. May assist in preparing for and hosting of regulatory audits. Major Duties and Responsibilities Supports and provides quality oversight to technical transfer sub-teams and the review and approval of technology transfer documentation Leads and provides quality oversight to automation forums. Provide review and approval of...

SUMMARY The Specialist, Validation Engineer I supports the successful implementation of manufacturing, and laboratory equipment alongside facilities and utilities at multi-use sites through interaction with internal customers and external service providers. T he incumbent is tasked with qualifying new equipment, facilities, utilities and maintaining equipment systems in a qualified / validated state a cco r ding t o established policies and pr o cedures. The i ndividual participates in proj e cts an d ongoing wor k activities of l ow to moderat e complexity. With minimum supervision and given general instructions, this individual carries out routine tasks and functions,...

We are seeking a highly motivated professional to join the Cell Therapy Analytical Development team, specializing in cell line engineering and potency method development for viral vector applications. The ideal candidate will contribute to the optimization and qualification of cell-based viral vector transduction assays measured by flow cytometry and luminescent reporter genes. This position demands a strong foundation in cell culture, keen attention to detail, and enthusiasm for solving scientific challenges in a fast-paced, collaborative environment. Successful candidates will demonstrate competency in these areas and contribute to breakthrough developments in cell therapy. Key Responsibilities Generate monoclonal cell lines and establish...

As the trusted People Partner to the Senior Leader of the function, you’ll architect and activate a people strategy that fuels innovation and accelerates performance across a global footprint. In this role, you’ll lead with influence—driving workforce planning, organizational design, and talent strategies that enable agility and growth. You’ll be the catalyst for team effectiveness and cultural alignment, ensuring our organization is positioned to deliver on bold ambitions. Change management isn’t a task here—it’s a discipline you’ll master to help leaders and teams thrive through transformation. Your client group spans multiple geographies and functions, requiring a global mindset and seamless...

The Associate Director, Clinical Supply Program Leader strategizes direction for clinical supply chain planning activities for assigned programs in the R&D Portfolio. Proactively recognizes and address any technical and regulatory issues associated with the ability to meet the requirements of the clinical development program and Project Team objectives. Considered a subject matter expert on all information regarding the global use of investigational material in clinical studies Key Responsibilities Provides strategic direction for clinical supply chain planning activities for assigned programs in the R&D Portfolio. Serve as primary Clinical Supply Services point of contact on Development and Project Teams. Lead Clinical...

Summary The overall focus of this resource will encompass the following laboratory and manufacturing instrument PC support and application administration, local support and liaison for global laboratory and quality systems, and administrator for local laboratory and quality systems. The resource will integrate information from the end user and in collaboration with matrix teams within BMS to understand opportunities for investigating and implementation of existing and emerging technology in accordance with applicable regulations and BMS approved policies and procedures. Responsibilities Execute, update, and support staff on documentation for the support of benchtop equipment and lab and quality systems to ensure assets...

At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team. The Associate Director, CAR-T Process Engineering, Systems, & Technology Support leads a team of scientists and process and/or systems engineers that...

The MES (Manufacturing Execution System) engineer will support the MES for the Bristol-Myers Squibb Devens biologics manufacturing facilities, including recipe authoring and system support for both GxP operations and new projects. Key Responsibilities Support the operation of all GMP manufacturing systems (Manufacturing Execution System) in the Manufacturing facilities in Devens, MA. Provide troubleshooting support and guidance of Manufacturing Execution Systems in support of Manufacturing. Investigate the root cause of MES problems and propose solution to prevent recurrence. Lead or manage Manufacturing Execution Systems small size projects Support the configuration, testing and implementation of process control solutions to a variety of...

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 Material Handler, CAR-T Warehouse Operations manages material needs/requirements for CAR-T production per Standard Operating Procedures (SOPs) in controlled and/or classified...

Summary The Field HEOR team is a member of the US Health Economics & Outcomes Research (HEOR) organization. The Field HEOR Scientist works within a field matrix team to engage Access organizations and decision-makers within their assigned territory. They combine the technical knowledge of HEOR with the knowledge of the U.S. healthcare system’s business models to effectively engage, deliver and generate impactful data to support medication access decision-making. The Field HEOR Scientist is a field-based position and covers territories in the West region which includes CA, OR, WA, MT, ID, NV, AZ, UT, WY, CO, NM. Responsibilities The Field HEOR...

The Executive Director, Privacy Law and Compliance is responsible for leading the organization’s global privacy strategy, governance, and compliance programs under the NextGen Privacy Program framework in partnership with Business Insights and Technology (BI&T). This role sits in the newly formed AI, Data and Privacy Law and Compliance department and ensures adherence to international data protection laws and internal standards while enabling responsible data use across all business units. The position requires strategic vision, operational excellence, and strong leadership to manage privacy risks, foster a culture of compliance and trust, and drive technology-enabled solutions for scalability. Key Responsibilities Strategic Leadership...

Aufgabengebiet Als Senior Medical Science Liaison Manager (m/w/d) für den Bereich Cardiovascular betreuen Sie das Gebiet Kiel , Rostock , Greifswald , Berlin und sind erster wissenschaftlicher Ansprechpartnerin für Entscheidungsträgerinnen in Universitätskliniken und Studienzentren. Sie schaffen vorzügliche Kontakte und vertreten unsere medizinische Kompetenz nach außen. Fachärzteinnen stehen Sie bei tiefergehenden medizinischen oder pharmazeutischen Fragen zur Verfügung und recherchieren deren Bedarf an Fortbildungsprogrammen und wissenschaftlichen Austausch. Für klinische Studien identifizieren Sie geeignete Institutionen und begleiten die Studienzentren, Prüfärzteinnen und Site Managerinnen bei der Durchführung. Darüber hinaus erstellen Sie medizinisch-wissenschaftliche Präsentationen, die Sie dann vor Fachpublikum persönlich halten und identifizieren geeignete Referenteninnen...

The Senior Director, AI Governance, Law, and Compliance is responsible for defining, implementing, and leading the organization’s global AI governance strategy in partnership with Business Insights and Technology (BI&T). This role sits in the newly formed AI, Data and Privacy Law and Compliance department and ensures that AI technologies—including generative AI and high-risk systems—are developed and deployed in compliance with evolving international laws, ethical standards, and technical safeguards. The position drives enterprise-wide accountability for responsible AI, harmonizing regulatory requirements (EU AI Act, U.S. OMB M-24-10, OECD Principles, ISO/IEC 42001) and fostering innovation while minimizing legal, operational, and reputational risks. Key...

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...

This position will work under the oversight of the Executive Director, Policy and Research and will be a Washington, DC or Princeton, NJ based role . The Associate Director will support policy and reimbursement initiatives and strategies to ensure optimal patient access to BMS medicines. This role will work closely with crossfunctional partners in global policy and government affairs, policy analytics, and commercial functions to identify policy challenges and track risks impacting BMS pipeline and future innovation. This role will also support analytics projects across the federal policy team and requires subject matter expertise in Medicare coverage and reimbursement and/or...

Downtown Seattle, Tacoma, Olympia, Wenatchee, Yakima, Silverdale 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....

As a key member of the Congress Excellence Team, the Senior Manager, Congress Engagement supporting Neuroscience will be instrumental in shaping and guiding the overall direction of the company's congress initiatives. This role drives cross-functional collaboration and budget management. Additionally, the role supports the strategic planning and coordination of specific components within the congress ecosystem, including sponsorship strategy, thought leader engagement execution, exhibition booth-build and content, educational activities, and pre- and post-congress deliverables. The Senior Manager, Congress Engagement is responsible for championing effective execution across these diverse components, ensuring best practices are maintained, continuous improvement is achieved through congress metrics,...

Key Responsibilities Serve as SME for SharePoint Online, OneDrive, and Microsoft Teams within Microsoft 365. Design, implement, and optimize governance models, lifecycle management processes, and automation frameworks to enhance operational efficiency and effectiveness. Administer and enhance AvePoint Cloud Governance, including policy enforcement, automation, and reporting. Identify and deliver process improvements and automation opportunities to reduce manual effort and improve service efficiency. Lead data migration and modernization projects using tools such as ShareGate, AvePoint, and native Microsoft migration utilities. Drive the remediation and retirement of InfoPath solutions, migrating forms and workflows into Power Apps and Power Automate. Develop and maintain PowerShell...

We are seeking a WWMO Medical Communications Director with a deep understanding of the relevant disease states, medical education, scientific customer experience and communication within WWMO. In this exciting role you will be responsible for creating scientific communication strategic plans for the specific disease areas, publication tactics, materials for scientific exchange, scientific narrative and platform, and external communication tools in alignment with the business needs within Medical Affairs and Clinical Development. The Director will be responsible for building and fostering relationships across the alliance partners and ensuring alignment and pull through of the strategy across the medical communication plans. Position...

Position Medical Science Liaison, Oncology, Lung & GU Tumors Location Field - Northern California, San Francisco 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...

Nonclinical Safety (NCS), within Nonclinical Research and Biotherapeutics, is responsible for designing and implementing overall nonclinical safety strategy to support the development and eventual marketing approval and post-marketing safety for the breadth of the BMS portfolio in oncology, hematology, cardiovascular disease, fibrosis, immunology and neurology. Located in any of our sites (New Brunswick, Lawrenceville, Princeton, NJ; San Diego, Brisbane, CA; Cambridge, Mass; Seattle, WA) NCS members work with discovery and development colleagues, as well as health authorities across the country and the world, to bring innovative and impactful medicines to patients around the globe. Level dependent on experience. Position Overview...

The Director, Site Supply Chain & Logistics, is responsible for all supply chain functions at the Bothell Cell Therapy manufacturing facility (CAR-T Therapies) and reports directly to the Site Head. The role oversees a team managing patient supply, production planning, material planning, materials management, inventory control, product tracking, import/export permits, shipping/receiving, and cold chain logistics for cell therapies manufactured at the Bothell commercial and clinical site. As part of the site leadership team, the candidate contributes to establishing strategic direction for the facility in alignment with corporate objectives, including transitioning the site to commercial operations and launching new products. The...

The Senior Specialist in the Cross Study Operations and Specimen Management (CSO & SM) Product Line in Global Development Operations IT (GDO IT) will play a key role in bridging the gap between Clinical operations needs and IT solutions, primarily focusing on Clinical Study Design and Orchestration. This is a hands-on role where the successful candidate will work closely with clinical scientist, clinical center of excellence, clinical operations leads, and global biometric and data science teams to gather requirements, design prototypes, work with Product Manager to develop and support the technology solutions throughout its lifecycle. Proven ability to use AI...

Manufactures human blood derived components per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. This position is for Quad 1, 5 am-530 pm, Sunday through Wednesday. Start and end times are subject to change based on business demands. Start and end times are subject to change based on business demands. Duties/Responsibilities Oversee set-up and operation...

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 Associate Director, Site Operations will have oversight of the planning and operations support for the Greater Seattle Area in order to deliver on the stated purpose of the Greater Seattle LT (GSLT). To make Bristol-Myers Squibb (BMS) Seattle a place where employees thrive, by shaping local culture, building community (internally and externally), creating cross-functional and cross-site alignment, and connecting with the broader BMS organization. The position will report to the Seattle site head, the Vice President of CTD, currently Allison Bianchi. Key Responsibilities Work with the Site Lead and the GSLT to set site priorities and achieve site goals,...

The Manager, QC Reagents Materials Supply Planning , leads the CAR-T Global Materials Management team, overseeing the planning and coordination of QC reagents and materials across the global Cell Therapy (CT) network. This role is accountable for ensuring continuous and efficient delivery of reagents to meet patient demand, while driving strategic initiatives, process harmonization, and team development. Key Responsibilities Provide strategic input for QC reagents and materials supply planning across all CT network sites, ensuring alignment with global business objectives. Oversee the development and execution of precise forecasts and material requirements planning (MRP), ensuring robust inventory management and adherence to...

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...

Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations Department Value Stream CAR-T Manufacturing Operations Location Summit West, NJ (US) – S12 Join our team manufacturing human blood-derived components for CAR-T therapies in a controlled, cGMP cleanroom environment. You’ll work under the supervision of Manufacturing Management, strictly adhering to regulatory requirements and Standard Operating Procedures (SOPs). Job duties are performed within a team and according to an assigned production shift schedule. Production deviations must be communicated and you will assist with quality investigations as needed. Shift Structure Day Shifts (Quad 1 or Quad 3) 500 AM – 530 PM, Sunday–Wednesday or Wednesday–Saturday...

Bristol Myers Squibb has a rich history in Neuroscience focused on developing innovative medicines to help people living with Neurodegenerative and Neuromuscular conditions. Bristol Myers Squibb currently markets a product in Neurology and has reentered the Psychiatry market with a focus on patients living with schizophrenia. BMS is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, and spirit of independence and love of...

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 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 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...

We are seeking a dynamic and visionary Worldwide Medical Lead to oversee our Cell Therapy Autoimmune programs. This role involves shaping and executing the global medical strategy across disease areas within rheumatology and neurology as well providing oversight of other areas of development for our growing Cell Therapy portfolio. This leader will ensure scientific excellence and collaborate closely with the US Cell Therapy Medical organization as well as cross-functional teams across the enterprise, including Research & Development, Commercial, and Market Access, to maximize the value of our cell therapy portfolio in these disease settings. This position reports to the VP,...

Director, Global Customs & Trade Compliance Location New Brunswick, NJ We are seeking a Director of Global Customs & Trade Compliance to lead our customs strategy and ensure adherence to international trade regulations. This leadership position is responsible for driving global alignment, optimizing duty savings, and managing compliance across all our operations. You'll work closely with regional teams to develop and implement effective trade strategies that support our global supply chain. Responsibilities Strategic Leadership Influence and execute the strategic direction for global customs compliance. Process Optimization Partner with Regional Compliance Leads to standardize and optimize global trade activities, policies, and...

The GPS Business Operations Role is accountable for 1) Leading and coordinating key business, including annual planning cycles, process improvements, change management, communications and performance tracking across GPS 2) Driving data analytics and visualization strategies by collaborating with cross functional teams to collect, process, and analyze data from diverse sources delivering actionable insights to key stakeholders 3) Overseeing the development, documentation, and evolution of business processes, governance frameworks, and best practices 4) Conducting internal and external benchmarking to ensure operational relevance and identify opportunities for continuous improvement. Key Responsibilities Establish, document, maintain, evolve, and facilitate GPS and Chief of Staff...

Senior Therapeutic Area Specialist, Neurology – Atlanta South Position Senior Therapeutic Area Specialist, Neurology (TAS) Location Field Territory Atlanta South 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...

Position Senior Specialist, QC Analytical, Cell Therapy 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. 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...

The Therapeutic Area Specialist (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...

Position Sr. Manager, ServiceNow Location Princeton, NJ Location Tampa, FL 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 plays a key role in designing and maintaining ServiceNow. The person in this role will be responsible to deliver...

The Senior Manager, EHSS Performance Enablement supports the execution of EHSS performance monitoring, ensuring that EHSS systems and processes deliver accurate, reliable data for decision-making and lay the foundation for future predictive analytics capabilities. The role supports the maintenance and operational improvement of EHSS data and reporting systems, including performance measurement frameworks, maintaining data quality, and enabling analytics and visualization though data science to track EHSS performance. This role executes daily performance enablement activities, ensuring data accuracy and reliable reporting. The Senior Manager delivers on core EHSS analytics initiatives to meet departmental goals and operational objectives, partnering with internal stakeholders...

Position Senior Therapeutic Area Specialist Therapeutic Area (TA) Psychiatry Location Philadelphia PA; Sharon Hill, PA/Cheltenham, PA The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients. The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent...

The Senior Engineer I, Tech Transfer is responsible for supporting the production of personalized cell therapy products for both global clinical trials and commercial supply at the BMS Manufacturing Facility in Bothell, WA. The Senior Engineer I, Engineering/Process will be a site subject matter expert on the cell therapy allogeneic product and the aseptic filling process within the Cell Therapy Lifecycle Management team under the Bothell Manufacturing Sciences and Technology (MSAT) department. The Senior Engineer I, Tech Transfer oversees and participates in a variety of cross-functional teams that support strategy, development and implementation of new allogeneic systems, critical reagents, and...

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 Clinical Development Lead 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 CDLs are matrix leaders and managers who lead, develop, motivate and achieve results through teams; demonstrate a commitment to the development of a resilient attitude, embrace change and have an unwavering commitment to our People Strategy Serves as the clinical point of accountability for the Development Team and is responsible for the overall clinical development plan for asset(s) in one or...

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 B2 Wednesday - Saturday 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 test methods,...

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

Key Responsibilities Perform independent review and approval of initial Commissioning, Qualification, and Validation (CQV) lifecycle documents and subsequent changes. Review and approval of periodic reviews, re-qualification, decommissioning and retirement and plans, protocols, and summary reports. Review and approval of Standard Operating Procedures, Work Instructions, Deviations, CAPAs and Change Controls related to facilities, utilities, equipment, instruments, and systems. Provide instruction and guidance on CQV quality issues during regulatory agency inspections, deviations, and CAPA discussions. Support the Contract Service Providers program. Provide reports to management related to timely deviation completions, CAPA implementations or other issues related to CQV and CSV activities. Support...

Principal Objective of the Position Provide Quality oversight during Clinical Supply Operations drug product and packaging and labeling manufacturing activities, and other GMP support areas. Provide Quality on the floor in-Process support during manufacturing operations. Assure the quality of manufactured products complies with all applicable regulations and guidelines. Performs QA manufacturing floor support activities within the Clinical Supply Operations areas to ensure compliance with all principle of current Good Manufacturing Practices (cGMP). Support material and component release for clinical drug product manufacturing. Key Responsibilities and Major Duties Performs QA Manufacturing Support Program activities and upholds the program’s principles and initiatives....