Bristol Myers Squibb Job Trends

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 Lead Associates perform a crucial role in driving our novel cell therapy programs by supporting routine manufacturing operations. We are...

Key Responsibilities Strategy & Direction US Oncology Commercialization strategic narrative including leading presentations for Board of directors, BMS LT, and investor relations. Partnering with finance and BIA on development of business updates to leadership Developing US Oncology Commercialization LT key strategic imperatives and priorities. Monitoring success vs. priorities Designing innovative business models and solutions across the function. Identifying and leading key strategic projects to drive business forward including projects within US Oncology and across the BUs as required. Lead partnership with respective US Oncology Commercialization Strategy and operations leads, ensuring communications of key strategies and tactics to the business, and...

Bristol Myers Squibb (BMS) is driven by its vision to transform patients’ lives through science. The Global Product Development and Supply (GPS) division plays a crucial role in advancing this vision . GPS is responsible for developing, manufacturing, and supplying quality clinical and commercial medicines to patients worldwide. This role is part of the BI&T team supporting GPS and will report to the Associate Director of Knowledge Management. This role is part of a small team dedicated to developing and operationalizing a comprehensive data information model to support downstream GPS use cases, such as AI deployment and self-service analytics. The...

Due to the ongoing growth and successful integration of our Tax Hub, which has been centralizing and streamlining tax operations to support the Latin America region, we are seeking a proactive, self-motivated, and collaborative professional to join our team in Tampa, Florida. This newly created role reflects our commitment to innovation and operational excellence across LATAM markets. You will oversee tax operations, leverage best practices and external experience, and champion technology-driven improvements for sustainable growth. Key responsibilities include documenting tax compliance, preparing tax returns, meeting both internal and jurisdictional deadlines, and enhancing compliance routines with advanced technology. You will work...

The Director, Global Commercial Strategy Oncology, BioNTech/Solid Tumor will be a key member of the Oncology Global Commercial Strategy team, responsible for driving the strategic direction and commercial success of the BioNTech and solid tumor portfolio. This role will focus on maximizing asset value, shaping franchise growth, and ensuring strategic alignment across functions and geographies. The successful candidate will demonstrate strong strategic thinking, cross-functional leadership, and deep oncology market expertise. Key Responsibilities Lead the development and execution of global commercial strategies for BioNTech and solid tumor assets, in alignment with overall oncology portfolio objectives. Partner closely with Tumor Leads, Business...

Key Responsibilities The candidate will work in the cellular phenotype group to support development, validation, and transfer of flow cytometry based analytical methods. Perform hands-on experimental work for development of flow cytometry analytical methods Execute flow cytometry panels for detecting low level marker expression (ex. knockouts, knockdown) Support execution of phase appropriate validation and method transfer experiments designed to measure parameters such as precision, LLOQ, LOD, detection range, and repeatability Support routine critical reagent qualification for method development, phase appropriate validations, and transfers Support method optimization and robustness assays to test method reliability and performance Support cell culturing and cell...

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

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 Quality Assurance Shop Floor (QASF) organization has responsibility for quality oversight and responsibility for advising and assuring quality operations at...

Summary The Sr. Manager, Clinical Program Management is responsible for the oversight, planning and delivery of assigned clinical study(ies) within the RayzeBio programs, including oversight and management of the study Clinical Research Organization (CRO) and Vendors according to and in compliance with corporate and program Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines and other applicable federal (FDA) and state regulations, in order to achieve established study goals within timelines and budget and of the highest quality. Job Responsibilities Essential duties and responsibilities include the following. Other duties may be assigned. Manage global clinical study...

A position is available for an Sr Principal/Principal Scientist in Discovery Toxicology (DT) within the Pharmaceutical Candidate Optimization (PCO) organization at Bristol Meyers Squibb. The incumbent will have responsibilities to identify and address toxicology issues across discovery programs that inform on program advancement, optimization of lead candidates and progression into development. The candidate will have demonstrated experience leveraging computational toxicology tools and big data analytics to generate mechanistic insights and guide decision making in safety assessment. Scientists in DT work with biology, chemistry and biotherapeutics representatives along with integrating across the other disciplines in PCO, namely drug metabolism and pharmacokinetics...

We are seeking an individual with a track record of strong leadership, compliant execution, and a winning mindset to join the Neuroscience Sales Strategy & Operations team to support the continued success of the launch of Cobenfy. This role will be instrumental in driving operational excellence across our organization at a national level. In addition to national-level responsibilities, this individual will partner with the West Region Sales Leadership Team to pull-through business-related functions by providing dedicated in-region strategic and operational support to help enable execution excellence and ensure execution is aligned with broader national strategy. The selected candidate will have...

Position Associate, QC Analytical, Cell Therapy (2) Schedule B2 Wed- 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. Key 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 & Experience Specific Knowledge, Skills, Abilities Ability to accurately...

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 Training is seeking a Training Specialist, Cell Therapy Manufacturing brings enthusiasm, intellectual curiosity, strong technical background, and...

At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team. As an Associate Scientist, Product and Analytical Sciences within Cell Therapy Analytical Development, this energetic, collaborative and motivate individual will...

Position Associate, QC Microbiology, Cell Therapy (2) 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,...

The Cell Therapy Analytical Development group at BMS is seeking a motivated individual to perform routine functional characterization of CAR-T and gene edited cells used in cell therapy. The ideal candidate will have a strong understanding of flow cytometry and cell biology as well as an enthusiastic attitude and desire to work collaboratively. Key Responsibilities Routine analysis of cell product for quality attributes using flow cytometry and cell-based assays. Design, plan, execute, and analyze lab experiments. Manage inventory of samples and materials and ensure proper handling and storage Maintain proper documentation of experimental results using an electronic lab notebook Summarize...

Senior Director, Real-World Data Strategy Job Summary Real-World Data Research / R&D IT / Business Insights & Technology The Senior Director, Real-World Data Strategy leads the delivery of BMS’s global development and translational medicine RWD strategy and research platforms. This role oversees a global team of data strategists and scientists, directs the development of RWD assets and partnerships, and connects BMS’s R&D and commercial priorities with emerging data opportunities. The position requires deep expertise in clinical and genomics real-world data, the RWD compliance landscape, global RWD opportunities both within BMS and externally, and a strong orientation to the application of...

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. We are looking for an experienced Oncology Commercial Director who is looking to join RayzeBio in rapidly advancing our commercial presence in radiopharmaceuticals. Individuals with commercial radiopharmaceutical experience is required. This individual will also partner with our colleagues at...

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 Patient Planning Manager, Planning & Scheduling, Cell Therapy is accountable to manage supply chain and logistics planning duties for the...

Serve as a lead associate in the manufacture of human blood derived components per Batch Records and Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment. Lead Manufacturing Associate adheres to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Support the quad manager for communication of production deviations, review of executed batch records and assistance with quality investigations are required, as applicable. The Lead Manufacturing Associate works closely with the Quad Manager and serves to supervise the shift when the manager is not available. The Lead Manufacturing...

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...

The Executive Associate II will provide high-level administrative and operational support to the Senior Vice President of Global Medical Immunology & Cardiovascular. This role requires exceptional organizational skills, attention to detail, and the ability to manage multiple priorities in a fast-paced, global environment. The role will serve as a key liaison, ensuring seamless communication and coordination across internal and external stakeholders. This individual will perform highly diverse administrative and project focused duties, which by nature of the position may involve high level contacts and exposure to confidential material necessitating the use of tact, diplomacy, discretion and judgment. The ideal candidate...

As a Global Payroll Process Engineer, you will lead and support the design, optimization, and implementation of payroll processes across our international operations. Your primary responsibility will be to ensure that payroll systems are efficient, compliant, and scalable, delivering timely and accurate compensation for employees around the world. By collaborating closely with cross-functional partners and leveraging process improvement methodologies, you will harmonize payroll workflows, drive automation, and enhance overall employee experience. Your analytical mindset and technical expertise will enable you to identify opportunities for improvement, resolve process challenges, and support a culture of continuous innovation. In this critical role, you...

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 Manager, Cell Therapy Clinical Manufacturing supports the clinical operations of the facility. The Manager will be responsible for the people...

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 The Senior Manager, QA for QC is responsible for quality oversight of the Quality Control (QC) Analytical and Quality Control Microbiology laboratory operations at the RayzeBio facility in Indianapolis in accordance with RayzeBio policies, standards, procedures and global...

As the Director, Process & Design Engineering for Payroll, you will lead the strategic design, oversight, and optimization of payroll processes across global operations, ensuring that systems are highly reliable, compliant, and cost-effective. You will set the vision for payroll service excellence by establishing robust standards, procedures, and service level agreements to deliver predictable, high-quality outcomes. In this leadership role, you will partner with HR, legal, benefits, and technology stakeholders to drive special initiatives and continuous improvements, mitigate risks, and elevate the employee experience. Your expertise in process and design engineering, payroll operations, and automation will shape the future of...

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 The Senior Specialist, External Manufacturing Quality Assurance is responsible for quality oversight of the Contract Manufacturing Organization (CMO) operations for Radiopharmaceutical products in accordance with business agreements, regulatory standards, and RayzeBio procedures. The scope includes clinical and commercial...

" We are looking for an experienced, results-oriented, and strategic marketer to join our strong team in the role of Associate Director, Targeted Therapies Marketing within the US Oncology Marketing organization. This individual will be a key member of the US Oncology Thoracic team and will assist in the development and implementation of brand strategic planning, marketing programs, strategic positioning, and tactical implementation for BMS's targeted therapy portfolio in the thoracic space. Data and insights will be used to assess market potential, identify opportunities and barriers, shape strategy, and foster collaboration with cross-functional partners. This role offers the opportunity to...

We are seeking an experienced marketer to lead development of the strategy and tactics for oncology patient marketing for the GI/GU portfolio. This includes leading the patient-focused work in key strategic areas such as market research / patient insight development, messaging, promotional asset development, and media management. Primary Responsibilities Individual will play an active role in evolving the vision and strategy for the patient channel across the GI/GU portfolio. Individual will assist with many aspects of consumer-related activities including message development/refinement, campaign evolution, strategic /tactical evolution of unbranded work, marketing plan development and business/channel analytics. Individual will serve as patient...

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...

Are you looking for an opportunity to gain experience in BioPharma while gaining leadership exposure, career mentorship, and making an impact on work that matters? The 10-week internship program at Bristol Myers Squibb’s growing state of the art Biologics campus in Devens, MA is the ultimate career experience! The program includes formal and informal networking, development, and mentorship of participants with a focus on building and advancing professional skills in the BioPharma industry. Candidates will be matched with projects based on skills and interests to support projects and continuous improvement initiatives at the Devens Campus within the Biologics Development organization...

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 ....

Position National Director, US Field Medical Cardiovascular - Milvexian Location Field The Field Medical organization embodies our medical mission to be recognized as the trusted partner for internal stake holders and the healthcare community, driving scientific exchange to enhance medical education, data generation, insight generation, and patients’ access to medicine. The National Director, Field Medical (FM) Cardiovascular (CV) - Milvexian role is a field-based role and focused on leading a team of Field Medical professionals. Direct reports will include field-based Regional Associate Directors (RADs) and Region Directors (RDs) who manage a team of field-based Cardiovascular Medical Science Liaisons (MSLs)...

The Clinical Trial Manager (CTM) is accountable for end-to-end study operational oversight and delivery at country level, ensuring adherence to timelines, budget and quality standards. Acts as the primary point of contact at a country level for both internal and external stakeholders, ensuring clear communication, effective coordination, and successful project execution. Key Responsibilities Acts as the main point of contact for a country with global study team members and accountable for the coordination with local country cross functional teams. Implements the local country and site feasibility process, including proposal and validation of country study targets, as endorsed by country leadership....

Summary The Director of Global HEOR - Oncology is responsible for planning and leading the health economics and outcomes research (HEOR) evidence generation strategy, as well as executing studies for one or more assets and/or indications within the BMS Oncology portfolio to support global markets, including the US. As an HEOR Subject Matter Expert, the Director is proficient in most, if not all, areas of evidence generation activities. This includes designing, conducting analysis for, and interpreting findings from interventional studies, conducting non-interventional research and evidence synthesis studies, and developing, validating, and analyzing health economic models and clinical outcomes assessment measures....

The Senior Program Manager, Promotional Education position partners with U.S. Marketing and Sales teams to develop Promotional Education Program (Peer-to-Peer / P2P) strategies and tactics in alignment with business priorities. The Senior Manager is responsible for the effective planning and execution of Product Theater programs to support best-in-class HCP customer engagement. This person will contribute to performance excellence and continuous improvement for P2P marketing programs/tactics. Major Responsibilities and Accountabilities Channel Strategy Maintains an understanding of promotional education trends and BMS business priorities in order to identify opportunities to drive business impact. Provides recommendations to US Brand and Sales matrix teams...

The Associate Director, HCP Marketing –will serve as a key architect of the Reblozyl brand’s healthcare professional (HCP) engagement strategy—owning the development of core messaging, creative campaigns, and measurement frameworks that drive consistent, data-informed execution across channels. This role will combine strategic insight, creative excellence, and digital fluency to ensure Reblozyl’s value proposition is communicated with clarity and impact. The ideal candidate thrives in a matrixed environment, connecting insights to action and translating brand strategy into integrated, measurable, and high-performing HCP campaigns. Key Responsibilities Lead the development, refinement, and pull-through of the Reblozyl HCP core messaging platform, ensuring alignment with...

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. The Sr Regional Business Director leads the West Cell Therapy Region in the delivery of Cell Therapy products customers. This role reports to the Executive Director, US Cell Therapy Sales. Key Responsibilities Achieve...

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...

Position Associate, QC Analytical, Cell Therapy (3) Schedule Wed-Sat 2pm-12am Responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts. Key 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 & Experience Specific Knowledge, Skills, Abilities Ability to accurately and completely understand and...

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 Principal Scientist, QC Automation, Cell Therapy is the subject matter expert leading implementation of state-of-art automation solutions for QC bioanalytical...

Join our team as the Sr. Director of Enterprise Talent Processes, where you will play a pivotal role in advancing how we select, develop, and grow our workforce. As the leader of subject matter experts, you will drive the strategic direction and execution of a simplified and integrated set of enterprise talent practices, including but not limited to talent assessment, development, succession and talent planning, and performance management. You will be charged with shifting from manual processes to a tech-enabled and easily adoptable set of integrated experiences that our workforce and people managers can easily adopt. In this role, you...

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 . The Principal Scientist, Medical Physicist, will be responsible for applying their expertise in radiopharmaceutical (RPT)-specific modeling to the research and development of new drugs and therapies. Their focus will be on radiopharmaceutical dose modelling and analyzing data from...

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 . This position will be responsible for conducting research, experiments, and analysis in the field of radiochemistry. This role involves radiolabeling of diagnostic and therapeutic radioisotopes of peptides, small molecules, and/or antibodies as well as quality testing for in...

Senior Therapeutic Area Specialist Therapeutic Area Neuroscience, Cobenfy Location Charleston, SC; Florence, SC/Statesboro, SC/Myrtle Beach, SC The Sr. 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...

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 . The Principal Scientist, Medical Physicist, will be responsible for applying their expertise in radiopharmaceutical (RPT)-specific modeling to the research and development of new drugs and therapies. Their focus will be on radiopharmaceutical dose modelling and analyzing data from...

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...

Bristol Myers Squibb is looking for an experienced transactional attorney who will be responsible for providing legal advice, guidance and support for Business Development (i.e., licensing and collaborations), Corporate Development (i.e., mergers and acquisitions), and Alliance Management. The position will report to the Assistant General Counsel, Business Development Transactions Law. Key Responsibilities Lead drafting, negotiating, and structuring of transactions, including licensing, co-development/co-commercialization agreements, mergers and acquisitions, divestitures and equity investments. Identify and resolve critical legal and business issues in transactions, including managing legal due diligence. Collaborate with Corporate and Business Development to ensure strategic alignment and escalate material issues as...

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

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. Duties/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...

As a Senior Manager, State and Local Tax Compliance you will be a critical member of the team responsible for US state and local tax compliance. In this role, you will be supporting all compliance activities, including the timely filing of state and local tax returns, management of state notices and audit inquiries, tax technical research and analysis, monitoring tax legislation and state tax audit support, and aspects of state and local tax planning and reporting. The Senior Manager will work closely across the entire tax reporting and compliance teams and with colleagues across finance, treasury and legal, and will...

__________________________________________________________________________ The following positions will require the employees to work with chemical, radiological, or biological agents that may be hazardous to health if mishandled (including Agents which may potentially affect reproduction or the fetus). Employees will be required to follow all safety procedures and use personal protective clothing/Equipment where specified. Inquires for further information should be directed to the hiring manager. __________________________________________________________________________ Permanent Position – Clinical Packaging Operator Technician – 25 – CSO Shift 7 AM - 330 PM EST Site New Brunswick, NJ Bldg #107 (non-excluded) Rate $40.81 / hour Works under direction of supervision and follows established...

Assigned to oversee Oncology therapeutic area portfolio execution. The Oncology portfolio is the largest BMS development portfolio including several priority assets. The ED PM Portfolio Lead is accountable for PM team member delivery per defined roles and responsibilities as a Program Management Lead (GPT) or Program Manager (asset indication). They are expected to operate as a key business partner to the Global Franchise Leads and the Therapeutic Area Head as required (directly and in partnership with Portfolio Strategy and Operations Leads). Provide line management leadership, coaching and development for Program Management (PM) team members and line managers to deliver and...

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, Quality Assurance Investigations at the Cell Therapy Facility (CTF) in Devens, MA will be responsible for providing quality...

The Senior Director, PM Systems and Infrastructures is responsible for developing, implementing, and sustaining an enterprise-wide Program Management (PM) Systems and Infrastructure ecosystem that enables operational efficiency, strategic visibility, and data-driven decision-making across all program and portfolio levels. This role leads the vision and execution of the Enterprise Program Management (EPM) environment, ensuring that program managers and PM Leadership are supported by integrated, scalable, and fit-for-purpose tools and processes. The Senior Director oversees key platforms—including ePlan (Planisware) for the development plan per project, Microsoft Project / Planner for bottom-up planning of near-term deliverables, and the Global Program Team (GPT) collaborative...

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...

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. We are seeking a highly experienced and strategic Safety & Occupational Health (S&OH) Manager with a strong background in the pharmaceutical...

Senior Account Executive, Market Access, Policy, Specialty and Retail Pharmacy Location Guaynabo, P.R. Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther...

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 Manager for the QA Sterility Assurance group is a n individual contributor responsible for quality oversight of the site contamination control strategy, including Environmental Monitoring (EM). Duties/Responsibilities include, but not limited to Quality oversight and support for contamination control programs such as environmental monitoring, cleaning and disinfection, gowning, access and flow, facility modifications, qualifications, disruptions, and shutdowns. Quality oversight and support for Microbiology QC Testing Methods. Review and approve associated document revisions, protocols, reports, testing plans, Review and approve investigations/ CAPAs / effectiveness checks associated with the manufacturing site including but not limited to environmental monitoring excursions (EME), aseptic...

The Material Operations Specialist, Lead will support the Site Supply Chain organization through the development and execution of supply for BMS's autologous clinical and commercial products. The Material Operations Specialist, Lead is responsible for on the floor leadership, task and priority coordination, adherence to Site Supply Chain GMP processes, and support of various projects within the Supply Chain department, ensuring established procedures are routinely reviewed and updated for compliance, driving Continuous Improvement initiatives, developing departmental metrics and KPls, driving change management execution, and implementing new processes that support the overall mission of the Bothell manufacturing site. As a member of...

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...

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

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 Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations, including but not limited...

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 Sales Advisor will be in responsible for the sales of defined territory in Delhi NCR & Out stations in Northern India. Identification of potential customers, potential mapping of accounts and customers, promoting awareness about therapy area and promoting products as per company’s objectives, meeting doctors, pharmacists, purchase managers, hospital authorities to ensure smooth execution of marketing strategies and achievement of Organization’s sales objectives for the assigned territory, HCP engagement in scientific activities, timely submission of sales data and various reports. Key responsibilities Driving sales in the assigned territory as per organization’s objectives . Potential mapping of doctors and...

Enhancing Canadian Healthcare Efficiency and Capacity through Strategic Collaboration The Health System Partnership Manager is a central figure in the evolving landscape of Canadian healthcare, tasked with transforming access and efficiency across provincial and national systems. Operating at the intersection of patient need, institutional priorities, and innovative therapeutic solutions, this role exists to bridge gaps, unlock systemic capacity, and foster enduring partnerships that benefit both patients and the broader health ecosystem. Empowering System Efficiency and Capacity The Vision At its heart, the Health System Partnership Manager's mission is to facilitate access to cutting-edge therapies for Canadian patients by dismantling systemic...

The Director, EHSS Management System leads the strategic design, deployment, and continuous improvement of BMS’s global EHSS management system, ensuring alignment with internationally recognized standards and enterprise objectives. This role drives consistency, compliance, and performance by leading the development of a global EHSS risk framework, global documentation oversight, directing training development and delivery, and leading execution of management system operating mechanisms. The Director serves as a subject matter expert and strategic partner, supporting both global and site-level teams in implementing effective EHSS practices. Key Responsibilities Lead the design, deployment, and sustainment of the EHSS management system across global and site-level...

The Director, EHSS Audit & Assurance leads the global strategy and execution of BMS’s EHSS internal audit program, ensuring alignment with the EHSS management system and driving continuous improvement, risk mitigation, and compliance assurance. This role provides strategic oversight of audit planning, delivery, and reporting, while advancing audit methodologies through digital innovation and systems thinking. The Director partners with global stakeholders to deliver insights that strengthen EHSS governance and performance across the enterprise. Key Responsibilities Lead the global EHSS internal audit program, including strategic planning, scoping, execution, and reporting, aligned with internal standards and business priorities. Oversee annual audit goal-setting,...

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 Therapeutic Area...

The Medical Communications manager is accountable for the following Medical Communications Strategy Leads across the BMS matrix to develop and timely delivery of strategically aligned medical publications, scientific content, medical information, medical education, training content, and congress presentations. Ensures endorsement of medical communications plans by relevant governance bodies prior to execution, and continuously develops and maintains plans in conjunction with scientific landscape and in alignment with Local Market Medical, Global Medical and medical market-level strategy Serves as the Medical Communications point of contact between medical and other matrix partners Provides medical communications management oversight Understand the communication needs and own...

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 Director, EHSS Performance & Systems Innovation provides strategic leadership for driving EHSS performance and enabling systems innovation across the enterprise. This role is responsible for enhancing EHSS performance measurement and analytics capabilities, including data quality, forward-looking metrics, and predictive insights that support a proactive, risk-based EHSS culture. In parallel, the Director defines and leads the long-term vision for a unified EHSS systems strategy, ensuring platforms deliver accurate, actionable insights aligned with BMS’s internal management system requirements. The role governs and prioritizes all EHSS systems and applications, partnering with BI&T and business stakeholders to integrate emerging technologies and optimize digital...

The Sr. Manager, Sustainability Enablement at Bristol Myers Squibb will advance the company’s environmental commitments by operationalizing sustainability initiatives and fostering employee engagement. This role leads the global strategy for the Go Green employee sustainability network and oversees the implementation of the My Green Lab program, driving innovation and environmental stewardship across BMS. Responsibilities include designing engagement programs, developing communications, analyzing activity metrics, and using data to inform continuous improvement. Key Responsibilities Develop and execute the global strategy for BMS’s employee-led sustainability network, Go Green, in alignment with enterprise sustainability goals. Refresh the strategy annually, incorporating employee feedback and external...

The Senior Manager, EHSS Systems Implementation is accountable for operational performance and successful delivery of EHSS system initiatives, ensuring results impact departmental efficiency, compliance, and overall effectiveness. This role ensures systems are aligned with EHSS business processes and contribute to compliance, risk management, and performance improvement. Working closely with the Director, EHSS Performance & Systems Innovation and cross-functional partners, the Senior Manager supports EHSS systems governance activities, continuous improvement, effective use of EHSS systems across the enterprise and enhances stakeholder experience through training, guidance, and process optimization. The role also supports implementation of new system capabilities, contributing to a unified...

The Director EHS, External Manufacturing is the Environmental, Health & Safety (EHS) Lead for BMS’s global Third-Party Risk Management (TPRM) program and acts as the primary point of contact for EHS relating to the third-party supplier (TPS) network. In this key role, the Director of EHS (ExM) is responsible for integrating EHS requirements into all stages of the TPRM lifecycle to ensure third-party suppliers comply with local EHS regulatory requirements and meet BMS EHS performance expectations. The role will work closely with multiple teams and functions, including Global EHS, BMS External Manufacturing teams (A&I, Biologics, CTO, etc.), Product Development, Product...

The Director EHS – Operations Support provides environment, health & safety (EHS) leadership, direction and support to the BMS internal manufacturing network, serving as a strategic and operational partner across the Global Product Development & Supply (GPS) organization. The role is a critical interface between Corporate EHS, Business Unit, and site operations, ensuring that global EHS strategies are effectively implemented, risks are proactively managed, and performance continuously improves across all manufacturing locations. Reporting to the Executive Director EHS – GPS and S-CoE, The Director EHS – Operations Support works closely with Business Unit and site leaders, global and local EHS...

The Associate Director, Industrial Hygiene is a key member of the BMS Safety Center of Excellence (S-CoE) and is responsible for supporting the development, implementation, and continuous improvement of our corporate Industrial Hygiene (IH) programs across our global network, ensuring compliance with BMS standards, regulatory requirements and industry best practices, aligned to company goals. At BMS, our industrial hygiene programs are used to anticipate, recognize, evaluate, and control environmental factors in the workplace that may lead to injury or illness and encompass areas such as Air Contaminants, Chemical Exposure, Physical Hazards (Noise, Radiation, etc.), Ergonomics and Biosafety. While this role...

The Director, Industrial Hygiene is a key member of the BMS Safety Center of Excellence (S-CoE) and is responsible for overseeing the development, implementation, and continuous improvement of our corporate Industrial hygiene programs across our global network, ensuring compliance with BMS standards, regulatory requirements and industry best practices, aligned to company goals. At BMS, our industrial hygiene programs are used to anticipate, recognize, evaluate, and control environmental factors in the workplace that may lead to injury or illness and encompass areas such as Air Contaminants, Chemical Exposure, Physical Hazards (Noise, Radiation, etc.), Ergonomics and Biosafety. Reporting to the Executive Director,...

Position reports to the Director of Thoracic, H&N Medical Communications within WWMO, Global Medical Affairs and is responsible for the strategy and execution of medical communication plans. This role will ensure the disclosure of the science and health economic value of BMS products and research data to inform Healthcare Providers, Patients, and Payers in accordance with local regulations. Key Responsibilities The Associate Director of Medical Communications is accountable for the following Medical Communications Strategy Establishing a clear, viable and compelling strategy for the Medical Communications, aligned with overall Medical vision, strategy and objectives, and ensure delivery of timely and high-quality...

The VP, US Field Medical Oncology Commercialization will provide executive leadership and strategic direction to our US Hematology / Oncology Field Medical organization and will be responsible for leading a team of MSLs. This leader will be responsible for driving strategic medical planning and execution in the US Market for our Hematology / Oncology pipeline, including medical tactics and medical evidence g eneration to support appropriate use and adoption of medicines. In collaboration with cross - functional partners, they will also contribute to the planning and development of regional data generation, life cycle management initiatives and support the learn ing...

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 The Radiopharmaceuticals Production Operator will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As the Production Operator, you will play an active role in daily operations, striving to ensure each batch is...

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

Working within Cell Therapy Development Organization (CTDO) the individual will become part of the Product and Analytical Sciences group, part of CTAD (Cell Therapy Analytical Development function) based in Warren, NJ. The incumbent will contribute to the IND and BLA clinical laboratory component of early and late-stage studies contributing to biological product knowledge and analytical characterization of CAR T pipeline assets. The incumbent will work with other scientists and teach junior technical staff as needed to complete pipeline development projects. Key responsibilities of this role are to lead from the bench for the laboratory support of asset programs through design...

The Senior Manager is responsible for supporting the production of personalized cell therapy products for both global clinical trials and commercial supply at the Bristol Myers Squibb Cell Therapy Manufacturing Plant in Bothell, WA. The Senior Manager oversees an investigational function of the Compliance and Investigations (C&I) team under the Bothell Manufacturing Sciences and Technology (MSAT) department. The Senior Manager oversees a team of full time BMS employees and contractors performing product and/or process impacting root cause analysis investigation and assessment activities. The Senior Manager develops and enables technical excellence and advanced root cause analysis techniques to ensure thorough investigations...

The Senior Manager in Business Solutions & Reporting for Payroll is a critical role within Bristol Myers Squibb’s Global Process Ownership (GPO) team, ensuring the accuracy, compliance, and optimization of payroll processing and reporting across all regions. This role oversees the monitoring in governance of payroll operations, supports system and process improvements, and serves as a key escalation point for technical and compliance issues. The Senior Manager will bridge payroll outputs with finance and accounting, support audit and regulatory requirements, and drive data-driven decision-making through advanced analytics and reporting. The position requires strong cross-functional collaboration, stakeholder engagement, and a commitment...

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

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 Therapeutic Area...

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...

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

Patent Counsel/Patent Agent - Innovation Law Location Princeton, NJ; Cambridge, MA; San Diego, CA Bristol Myers Squibb (BMS) is seeking an experienced patent attorney or agent to join our headquarters in Princeton, New Jersey, or one of our research centers in Cambridge, MA, or San Diego, CA. The patent practitioner will support clients across multiple functional areas to provide strategic counsel to key stakeholders. Responsibilities will primarily include internal preparation and prosecution of patents as well as providing strategic counsel, including freedom to operate, business development diligences, and client counseling. The patent practitioner will work closely with clients in...

Summary The Director, Worldwide Omnichannel Excellence Insights and Data will be responsible for co-leading the implementation of a robust data foundation for BMS’s omnichannel marketing initiatives, with a strong focus on third-party (NPP) data integration, governance, and optimization. This role will oversee analytics and reporting resources within the GCC and drive the enterprise vision for unified, AI-powered measurement frameworks, advanced dashboards, and actionable insights. The Director will champion agentic AI adoption, ensuring both technical rigor and business relevance, while managing cross-functional partnerships and aligning analytics initiatives with global brand and commercial priorities. Responsibilities Vision & Strategy Develop and execute a...

The Manager, Quality Systems is responsible for supporting the ownership and oversight of Devens Cell Therapy quality systems, such as CAPA, Investigations per established local and global standards. This position supports the overall compliance and performance of Devens Cell Therapy Quality Systems Management as it applies to the site level, including periodic assessments of process performance and continuous improvement opportunities Duties/Responsibilities Review and approve complex site quality system deliverables and risk assessments associated with all aspects of manufacturing process including incoming, manufacturing, laboratory, facility, and utility systems. Ensure quality system deliverables are robust and adequately address requirements and risks, by...

Summary The Director, Pricing and Economics will be responsible for driving pricing analytics and strategic insights across the BMS Portfolio. Responsibilities Provide leadership and expertise to prepare for items needing US Pricing Committee approval Consolidate Brand Budget and LTFP Gross and Net Price projections for senior pricing leadership Provide strong guidance and support for the development and implementation of US and/or Global pricing strategies for key products in partnership with Global MAx teams inclusive of pricing strategy teams. Evolve pricing and economics for brands in response to new indications/clinical data, updated competitive environment, new product launches / dosing or any...

At BMS, the Medical Engagement Excellence (MedEngageX) team is positioned within the Medical Excellence (MedEx) organization. MedEngageX plays a critical role in ensuring that healthcare professionals are educated on the appropriate use of our medicines and have the information they need to improve outcomes for patients. We develop strategies, tools, and guidance to empower our Field Medical (FM) teams and Medical Engagement Leads (MELs )) around the globe to ensure that they are aware, informed, engaged, and equipped with the knowledge and skills to perform their roles effectively and compliantly. Our Associate Directors within MedEngageX serve as strategic partners across...

Position Technician II QC Sample Management, Cell Therapy Manager Manager, QC Sample Management Responsible for handling of test samples throughout the sample lifecycle from receipt to disposal. Prepares and ships material to offsite locations. Maintains inventory and coordinate distribution of QC sample and materials to appropriate functional groups as scheduled or requested. Key Responsibilities Handle test and retain samples throughout the sample lifecycle receipt, storage, distribution, transfer, and disposal. Facilitate cold chain transfers of samples. Prepares and ships material to off-site locations. Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling and chain of...

, Manager, GPS Learning Partner Locations Princeton NJ, Madison NJ, Devens MA, Dublin IE, or Boudry CH The Learning Partner is responsible for liaising with site/functional areas to deliver learning in alignment with Bristol Myers Squibb (BMS) policies, standards, procedures, and global current Good Manufacturing Practices (cGMPs). In this capacity, the incumbent will foster trust and cultivate a collaborative environment with key stakeholders both locally and globally. Key responsibilities include Stakeholder Engagement Establish and maintain strong relationships with key stakeholders to ensure alignment and support for learning initiatives. Training Delivery Deliver effective and relevant training to learners at sites/functional...

Position Associate, QC Microbiology, Cell Therapy 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,...

Position Specialist, QC Analytical, Cell Therapy 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. Key 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 & Experience Specific...

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, RayzeBio focuses on improving survival for people with cancer by harnessing the power of targeted radioisotopes. The company operates as a standalone entity within BMS, maintaining its biotech culture while leveraging best-in-class oncology capabilities. RayzeBio is developing innovative drugs targeting solid tumors, with its lead asset, RYZ101, in Phase 3 testing for gastroenteropancreatic neuroendocrine tumors (GEP-NETs) and earlier-stage testing for small cell lung cancer (SCLC). The company is led by a...

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...

Position Associate, QC Microbiology, Cell Therapy (3) 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,...

Position Technician II QC Sample Management, Cell Therapy Responsible for handling of test samples throughout the sample lifecycle from receipt to disposal. Prepares and ships material to offsite locations. Maintains inventory and coordinate distribution of QC sample and materials to appropriate functional groups as scheduled or requested. Key Responsibilities Handle test and retain samples throughout the sample lifecycle receipt, storage, distribution, transfer, and disposal. Facilitate cold chain transfers of samples. Prepares and ships material to off-site locations. Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling and chain of custody records in accordance with...

Position Technician II QC Sample Management, Cell Therapy Responsible for handling of test samples throughout the sample lifecycle from receipt to disposal. Prepares and ships material to offsite locations. Maintains inventory and coordinate distribution of QC sample and materials to appropriate functional groups as scheduled or requested. Key Responsibilities Handle test and retain samples throughout the sample lifecycle receipt, storage, distribution, transfer, and disposal. Facilitate cold chain transfers of samples. Prepares and ships material to off-site locations. Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling and chain of custody records in accordance with...

Position Associate, QC Analytical, Cell Therapy (3) Responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts. Key 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 & Experience Specific Knowledge, Skills, Abilities Ability to accurately and completely understand and follow procedures. ...

Position Associate, QC Analytical, Cell Therapy Manager QC Analytical Manager, A1 shift, Cell Therapy Responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts. Key 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 & Experience Specific Knowledge, Skills, Abilities Ability to accurately...

Position Associate, QC Microbiology, Cell Therapy 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,...

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 Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations, including but not limited...

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 . We are seeking an experienced Clinical Medical Writer with strong project management capabilities to join our growing clinical development team. This hybrid role combines the scientific writing of key clinical and regulatory documents with oversight of medical writing...

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 and mentor others on QC test methods, processes and procedures. Perform other tasks...

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. Key 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 & Experience Specific Knowledge, Skills, Abilities Ability to accurately and completely understand, follow, interpret and apply...

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 works a Monday to Friday schedule, Day shift. This position will oversee and partner with operational areas to ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP. In the capacity of Shop Floor QA, the Senior Specialist shall serve as one of the Shop Floor Representatives interacting with Manufacturing, Supply Chaing, Quality Control and other supporting teams. The Senior Specialist, Shop Floor QA, is accountable to monitor...

The Scientific Advisor (SA) in Hematology/Oncology plays a strategic leadership role in driving medical excellence, cross-functional integration, and business-informed scientific engagement across key therapeutic areas. This role goes beyond tactical execution to serve as a critical scientific voice in the matrix, collaborating closely with commercial, access, HEOR, and global medical teams to ensure that scientific strategies translate into tangible patient and business impact. With a strong command of business acumen, The Hematology/Oncology Scientific Advisor provides strategic scientific leadership and expertise to advance hematology, cell therapy and oncology programs. This role supports clinical trial execution, cross-functional collaboration, and scientific engagement with...

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, cell therapy, immunology, neuroscience 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. The RWE Director is a key member of cross-functional teams and RWE-CoE within GBDS. This role will be responsible for developing the strategic direction and leading execution of statistical and...

Position Executive Director, Technical Accounting Department Global Finance Reports To VP Financial Reporting & Chief Accountant Position The Executive Director, Technical Accounting COE, will play a pivotal role in leading the enterprise’s technical accounting function, ensuring global compliance with accounting standards, and driving excellence in financial reporting and governance. This leader will oversee the development, implementation, and continuous improvement of technical accounting policies and procedures, serve as a key advisor to senior leadership, and lead strategic projects that advance the organization’s accounting capabilities and transformation agenda. Key responsibilities include Lead the Technical Accounting COE, setting the vision...

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. Background 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...

Senior Therapeutic Area Specialist Therapeutic Area Neuroscience, Cobenfy Location Dayton, OH 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...

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

This position provides global docket services for the Innovation Law Patent Group, ensuring integrity and accuracy of the data and deadlines entered into an IPMS (Intellectual Property Management System). Candidate must have IP docketing experience in global jurisdiction docketing. This position plays a vital role in ensuring the protection of the company's intellectual property rights by managing statutory deadlines and formal requirements effectively. Key Responsibilities Responsible for organizing and maintaining records, deadlines and documents, and communicating actions and deadlines to all stakeholders Analyzes, interprets, and dockets correspondence correctly per respective countries' laws and regulations Ability to create specialty reports based...

Job Summary Responsible for technical leadership and project management for introduction of printed components used at BMS manufacturing sites. Supports design, development, and implementation of labeling and packaging for commercial and clinical cell therapy programs within BMS. Key Responsibilities Manage artwork for clinical and commercial printed materials for cGMP use Support life cycle management changes of L&P components Coordinate with artwork and label vendors to ensure key project milestones are met Identify gaps in the process and update policies/procedures as necessary Proactively mitigate and communicate issues between relevant functional areas Support Cell Therapy manufacturing sites in L&P related packaging deviations...

This district covers LA East, LA West and Fresno We are building our talent pipeline in Oncology/Hematology Sales and we are looking for smart, professional and passionate people, such as yourself, who want to make a difference in the lives of patients. As part of our Hematology Sales team, you will be a part of a growing and dynamic sales organization that has a strong heritage and continues to be at the forefront of bringing new and innovative cancer therapies to the market, such as immunotherapies in multiple tumor types. Our Oncology/Hematology pipeline is one of the best in the...

Summary We are seeking a SharePoint Online Subject Matter Expert (SME) with hands-on experience in AvePoint Cloud Governance and Microsoft 365. The candidate will lead collaboration initiatives, manage secure and scalable SharePoint environments, and drive governance, automation, and process improvements. This role plays a key part in strengthening lifecycle management and improving user experience across Microsoft 365. Key Responsibilities Serve as SME for SharePoint Online, OneDrive, and Microsoft Teams within Microsoft 365. Design and optimize governance models, lifecycle management processes, and automation frameworks. Administer and enhance AvePoint Cloud Governance, including policy enforcement and automation. Identify and implement process improvements that...

The Associate Director, CV Accounts & Customer Engagement, reports to the Director, CV Accounts & Customer Engagement and will work cross-functionally with matrix teams, both in the field and at the home office, to ensure tactical execution aligns with the overall brand strategy. By collaborating with teams focused on reimbursement, REMS, access, brand, and field operations, the Associate Director will support business goals and drive the effective implementation of strategic initiatives to achieve organizational objectives. Key Responsibilities Key Account Management Deliver all access, value, PHM, quality, and unbranded messages and tools with population health decision makers or C-suite individuals. Support...

The FP&A Director will be responsible for FP&A activities for the European Markets Commercialization organization, including financial oversight to drive improved business performance and facilitate timely decision making. Additionally, the FP&A Director will lead the European Markets HQ Commercialization FP&A team. The FP&A Director will be recognized as an influential and collaborative Finance business partner who leads beyond the role and effectively interacts at all levels of the organization to deliver financial planning & analysis. The role reports to the Executive Director, Commercialization FP&A Center of Excellence. Key Responsibilities Lead and own the financial planning processes and timelines (Budget, Projections...

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 Structured Benefit-Risk Assessment (SBRA) Lead will report into the Structured Benefit-Risk Assessment Head within Safety Evidence and Sciences and will be accountable to lead structured benefit-risk assessments for assigned assets from early clinical development through late-stage and post-marketing. This role requires close cross-functional collaboration with relevant departments across the organization, including medical safety assessment, clinical development, global regulatory, epidemiology and others. The SBRA Lead will drive functional alignment on key benefits and risks of BMS assets and establishment of company position on the product benefit risk balance through the application of benefit-risk assessment framework, tools and methodologies. Duties/Responsibilities Product...

The Associate Director, Supply Planning will drive the Sales & Operations Planning Process (S&OP) including the Production Scheduling process in support of the Devens Biologics Manufacturing Site. The role will lead a team that maintains and drives adherence to the site production schedule in collaboration with the manufacturing, global supply chain and material planning groups. This role will also oversee the introduction and maintenance of the relevant master data for the site. Key Responsibilities Leads site planning and manufacturing scheduling process and ensures schedule adherence. Develops, models and implements strategies to improve scheduling capability and adherence. Utilizes scheduling and modeling...

Summary We are seeking a highly skilled and motivated Medical Content IT Product Manager to support our Veeva Vault Medical platform. This role will be critical in ensuring effective implementation, integration, governance, and performance of Veeva Vault Medical. The Product Manager will partner with cross-functional teams, including Medical, Commercial, and IT, to drive efficiency and innovation within the platform to support our medical communications and content management needs. Key Responsibilities Own and articulate the product vision, strategy, and multi‑release roadmap for Veeva Vault MedComms and adjacent Medical content capabilities. Lead product discovery with Medical/MI stakeholders and field users; translate insights...

Summary The Director, ICON MAx, International Market Access, is a strategic leader responsible for driving market access and pricing strategies across several geographies in MEA, LatAm, and Brazil. Reporting to the Head of ICON MAx (Market Access), this role ensures alignment between local Intercon Market Access teams and Global Market Access, supporting the entire BMS portfolio and pipeline. Will collaborate with global and local MAx leaders, Global Policy, Medical, and Commercial teams to communicate the value of BMS therapies to government authorities, Private Payers, and HTA organizations. The Director will develop in collaboration with Local and Regional teams innovative access,...

Location New Brunswick, NJ 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...

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

At BMS, we believe business functions and Compliance & Ethics are equally accountable for both company success and ethical behavior. Our Compliance & Ethics team is committed to enabling well-informed, risk-based decisions that get more medicines to more patients, faster. You will lead a cross functional team whose remit is global in impact and that ensures the efficient, expedite and compliant operations of Events & Meetings (E&M) both internally and with external vendor partners. This is a key role within the Events and Meetings Leadership team and is accountable for ensuring the implementation, exemplary execution and alignment of the Events...

Responsibilities Develop worldwide health economic & outcomes research strategy to support BMS oncology products strategy and value proposition across early development to post launch lifecycle Design and execute HEOR studies with study concept, protocol, analysis plan, study report, data dissemination, for research including but not limited to systematic literature reviews, disease burden, patient reported outcomes, real-world treatment patterns and outcomes, economic modeling, prospective observational studies and comparative effectiveness studies in the oncology therapeutic area Engage and collaborate with oncology asset level matrix teams, including market access, clinical development, medical affairs, regulatory, biostatistics to ensure full alignment and integration HEOR evidence...

Position Senior Therapeutic Area Specialist, Immunology (TAS) Location Field - New Orleans 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...

Summary The Executive Director of Intelligence & Innovation (I&I) sits within the Global Pricing & Health Systems Analytics team, as part of the Market Access organization. This critical role leads a high-performing team to (1) Curate intelligence on the evolving market access and pricing landscape and drive internal awareness, understanding, and thought leadership, providing strategic perspectives on market changes to the organization and rapidly responding to senior leadership queries, (2) Strategically incubate innovative and transformative access and pricing approaches and solutions for BMS in anticipation of industry shifts and evolving business needs, (3) Shepherd the market access organization’s digital transformation,...

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 Senior Enterprise Learning Manager is a strategic and hands-on leadership role responsible for driving the design, development, and implementation of enterprise-wide Skills-Based Learning Pathways and the Learning Professional Excellence Program. Reporting to the Head of the Leadership Development Center of Excellence (CoE), this leader will accelerate BMS’s capability evolution by embedding future-ready cross-cutting skills, delivering best-in-class development journeys, and establishing standards of excellence for Learning Professionals across the organization. This role requires a blend of instructional design expertise, adult learning theory, project management acumen, and business partnership skills to ensure learning solutions are relevant, scalable, and aligned to the...

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

At Bristol Myers Squibb, we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team. The Associate Specialist, Value Stream Cryo Operations is responsible for the Cryopreservation, movement, storage, control of manufacturing patient materials, and support...

The Protein Homeostasis Thematic Research Center (TRC) in San Diego, CA aims to discover and develop revolutionary medicines for cancer patients with unmet medical needs. Comprised of scientists across multiple disciplines, we are responsible for delivering novel cancer therapeutics by engaging E3 ubiquitin ligases for targeted protein degradation. The Protein Homeostasis TRC is highly committed to supporting local STEM initiatives that give individuals the opportunity to participate in diverse aspects of the drug discovery process and to contribute to the goal of bringing novel therapeutics to cancer patients. To further this cause, we are excited to introduce the 2026 Summer...

Senior Manager – Analytical AI, Clinical Development Job Aligned with Bristol Myers Squibb's mission to advance clinical development through data-driven innovation, the Senior Manager – Analytical AI in Clinical Development will play a key role in designing and deploying machine learning pipelines to optimize clinical trial operations. This individual will engage with cross-functional stakeholders to deliver impactful AI-based solutions and ensure their seamless integration into business processes, driving efficiency and enhancing decision-making across the drug development portfolio. Key Responsibilities and Major Duties 1. Develop and Deploy Machine Learning Pipelines Apply expertise in machine learning to create, implement, and optimize...

The Senior Director for Milvexian Global Medical Strategy will provide deep disease state knowledge in thrombosis, leadership and direction to the Global and US Medical team; work with the medical matrix to focus on strategy, planning, development, and implementation of the medical plan. The Director will report to the Executive Director, Thrombosis Disease Area Head. Key Responsibilities Support the execution of Global medical plan that is both product and disease specific, translating commercialization and medical strategies into effective milvexian medical launch plans and life cycle management plans. Works with cross-functional matrix and alliance partners on a variety of projects, provides...

Associate Director, Clinical Data Management Department Biometrics Location San Diego, CA or Lawrenceville, NJ FLSA Status Exempt Reports to Director, Clinical Data Management Summary The Associate Director, Clinical Data Management, will play a crucial role in our data management efforts, ensuring the accuracy, consistency, and integrity of clinical data. This position involves leading and overseeing all aspects of data management, from planning and coordination to execution and quality control. The successful candidate will be responsible for managing relationships with external partners and collaborating across cross-functional teams to ensure data deliverables and expectations are met. Job Responsibilities Provide data management leadership,...

The Protein Homeostasis Thematic Research Center (TRC) in San Diego, CA aims to discover and develop revolutionary medicines for cancer patients with unmet medical needs. Comprised of scientists across multiple disciplines, we are responsible for delivering novel cancer therapeutics by engaging E3 ubiquitin ligases for targeted protein degradation. The Protein Homeostasis TRC is highly committed to supporting local STEM initiatives that give individuals the opportunity to participate in diverse aspects of the drug discovery process and to contribute to the goal of bringing novel therapeutics to cancer patients. To further this cause, we are excited to introduce the 2026 Summer...

RayzeBio 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. Located at our Indianapolis, IN Facility, the Sr. Warehouse Associate will be responsible for warehousing support related to domestic and international shipping and distribution of clinical trial and commercial products for RayzeBio programs. In this role, the Sr. Warehouse Associate shall provide tactile...

The Protein Homeostasis Thematic Research Center (TRC) in San Diego, CA aims to discover and develop revolutionary medicines for cancer patients with unmet medical needs. Comprised of scientists across multiple disciplines, we are responsible for delivering novel cancer therapeutics by engaging E3 ubiquitin ligases for targeted protein degradation. The Protein Homeostasis TRC is highly committed to supporting local STEM initiatives that give individuals the opportunity to participate in diverse aspects of the drug discovery process and to contribute to the goal of bringing novel therapeutics to cancer patients. To further this cause, we are excited to introduce the 2026 Summer...

Serves as the Chief of Staff and strategic thought partner to the ICV Development Head. Develop engagement plans (e.g., Town Halls, LT meetings), support business operations (e.g., budget, resourcing, business reviews), plan leadership communications, and prepare change messaging. Supports early and late Drug Development portfolio prioritization & management processes, in partnership with other P&SO Leads, PI&R, Commercial, BI&T. Key Responsibilities Strategy & Operations Manages ICV Development Head LT meetings. Helps develop yearly objectives and priorities for ICV Development organization, translate objectives into actionable functional plans, track progress, ensure ongoing risk mitigation and contingency planning for each objective. Plans workshops, manages...

At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team. The Manufacturing Associate, Cell Therapy brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The incumbent...

The 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...

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 RayzeBio is seeking a highly organized and detail-oriented Radiopharmaceutical Planner to join our on-site team in Indianapolis, IN. This entry-level role is pivotal in ensuring the efficient and compliant production and distribution of radiopharmaceuticals for our clinical trials....

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...

The primary responsibility of the Director for IO Lung Cancer in Global Medical, with a focus on the US, is to develop and implement the US Medical strategies and objectives for assigned tumors. This role is responsible for integrating and aligning tumor strategies by establishing and maintaining cross-functional collaborative relationships with key stakeholders, including, but not limited to, US Commercialization, Global Medical, Clinical Development, and Medical Capabilities teams. Key Responsibilities Collaborate with Medical Product Lead for US medical plan that is both product and disease specific in alignment with US Commercialization (USC) and Global Medical, translating strategies into effective US...

Summary The Associate Director US Pricing Strategy Cell Therapy Role on Cell therapy Max team evaluates the strategic implications of channel dynamics and ecosystem changes and uses these insights to identify value-creating opportunities and develop innovative pricing strategies for Hematology brands over their entire product life cycle. This role works closely with the Cell therapy access team to ensure implementation of value-creating pricing strategies and activities. The AD utilizes a deep understanding of BMS' Cell therapy portfolio, profitability objectives, health economics outcomes research, customer profiles, as well as financial and market data to analyze pricing scenarios and formulate innovative pricing...

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 Specialist, Lead Clinical Manufacturing Associate, Cell Therapy that bring enthusiasm, intellectual curiosity, scientific rigor,...

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

Position Senior Manager Cleaning Validation Location Devens, MA Key Responsibilities Provide strategic oversight and management of the cleaning validation program, ensuring alignment with regulatory requirements and industry best practices. Develop, write, and execute cleaning validation protocols, reports, and risk assessments. Establish acceptance criteria and sampling plans for cleaning verification and validation. Delegate tasks and coordinate the execution of cleaning studies, ensuring timely and effective completion. Optimize and update cleaning validation strategies and procedures to reflect current industry standards and regulatory expectations. Perform swab and rinse sampling, cleanability, degradation and sampling recovery studies reviewing analytical results against acceptance limits. Support...

This role will serve as the Chief of Staff to the VP, Global Milvexian and CV and will play a critical part in the future of Milvexian and CV in general. As Milvexian prepares for launch, the S&O Director will lead the preparation for governance presentations at BMS and across the J&J Alliance. In addition, this individual will lead global market engagement, LCM, and launch tracking. Beyond Milvexian, this individual will support the CV Early Asset and BD teams on CV strat plan and other important initiatives. Key Responsibilities Serve as Chief of Staff to VP, Global Milvexian and CV...

At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team. As a Principal Scientist with Cell Therapy Analytical Development, this energetic, collaborative, and motivated individual will establish and lead Non-Viral...

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 Manager, Global Trade Operations, Cell Therapy will ensure the import and export compliance for BMS North American operations. This...

Antibody Drug Conjugates are revolutionizing oncology. Here are BMS, we are excited to have a strategic alliance to co-develop and co-commercialize a potential first in class EGFRxHER3 bispecific ADC, iza-bren in US, and outside of China. The Global Medical Director, for Iza-bren will serve as the strategic and operational leader for the global medical strategy of the Iza-bren asset, with a focus on certain key indications under the leadership of the Medical Product Lead (MPL). As Iza-bren program expands into multiple tumor types, in a rapidly evolving oncology landscape, this role is pivotal in shaping the medical vision, driving execution...

Position Senior Manager Validation Engineering Location Devens, MA Key Responsibilities Lead functions within the Validation Engineering group responsible for the qualification lifecycle of facility, utility and processing equipment systems. Leads functions responsible for installation, operational and performance qualification (I/O/PQ) of systems arising from projects and change controls. Leads the site Periodic Assessment and Requalification program by establishing procedures aligned with BMS directives and industry guidance. Ensures execution of program to predefined schedule. Establish validation project plans commensurate with the level of risk and manage the execution of validation projects whose scope, regulatory visibility, schedule requirements, and complexity require coordination...

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...

The TAIP TA Lead is a senior leadership role reporting directly to the Head of the TAIP unit within Bristol Myers Squibb’s Trial Analytics, Insights, and Planning (TAIP) organization—an internal consulting team that drives clinical development excellence through data-driven insights, feasibility modelling, and strategic trial planning. As the analytics lead for a therapeutic area (TA), you will be responsible for the full portfolio of trials within that TA—owning analytics strategy, resource planning, and delivery oversight. You’ll provide strategic direction, hands-on support, and quality control across studies while coaching study-level analytics leads and coordinating cross-trial priorities. You will act as a...

Summary 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! Reporting to the Executive Director, Business Insights...

Working With Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. What we are looking for The...

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

Summary The Legal eDiscovery Specialist position will work with eDiscovery and cybersecurity stakeholders to manage the efficient and defensible eDiscovery and data lifecycle in support of legal, security, and compliance investigation matters. This position requires expert analytical and project management skills as well as in-depth expertise with technologies such as MS office suite, Relativity server and RelOne Legal Hold platforms. This role involves daily triage, interaction, and collaboration with various business functions which requires the Legal eDiscovery Specialist position to possess stellar interpersonal prowess and communication capabilities. Responsibilities will include, but are not limited to, the following Oversight and administration...

Business Unit Overview Our Global Facilities Operations team is responsible for the safe, sustainable, and cost-effective operation and maintenance of world-class facilities that enable the discovery, development and delivery of innovative medicines that help patients prevail over serious diseases. We deliver safe, effective, and strategically aligned facilities and services around the world. This includes day-to-day operations and maintenance, employee convenience services, laboratory services, and asset and document management. In close partnership with stakeholders to manage the contracts and service agreements for integrated facilities management, and other vendors. Here, you’ll get the chance to grow and thrive through opportunities uncommon in...

Senior Corporate Counsel, Quality Law Position summary The Senior Corporate Counsel role will have the opportunity to join the dynamic Global Manufacturing, Supply and Corporate Transactions Law team at BMS. In part, the team provides critical support and partnership to the Company’s Global Product Supply & Development organization, helping to deliver on our mission to serve patients in need. The team provides comprehensive legal support for the Company’s manufacturing operations, supply chain, import/export, customs and trade, facilities and engineering, product development, EHS and Occupational Health matters, and Quality. The Senior Corporate Counsel will support the Global Quality organization. Primary...

Bristol Myers Squibb es un empleador que brinda igualdad de oportunidades. Las personas que apliquen para cualquier vacante, y que estén calificadas para la misma recibirán consideración para el empleo sin distinción de raza, color, religión, sexo, orientación sexual, identidad de género, nacionalidad, edad, discapacidad, condición de veterano protegido, embarazo, ciudadanía, estado civil, expresión de género, información genética, afiliación política o cualquier otra característica protegida por la ley Responsabilidades clave y deberes principales Garantizar la ejecución de los análisis de control de calidad en el laboratorio Fisicoquímico y Microbiología cumpliendo con las políticas corporativas y requerimientos regulatorios. Documentar adecuadamente las...

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

Summary The Associate Director will serve as the critical conduit between our internal stakeholders – especially brand, omnichannel marketing teams – and GenAI Content Hub. This role will be especially critical over the course of a brand’s integration, as well as a times of critical changes for those stakeholders at times after integration, such as when the content hub is launching an important new capability. Success in this role means that the content hub is well-represented with our stakeholders, but also that the needs of our stakeholders are well represented to the content hub, laying the foundation for long-term partnership....

Summary The Senior Manager- Legal eDiscovery position will work with various internal stakeholders including, but not limited to Litigation & Government Investigations, Internal Investigations, HR Law, Innovation Law, Business Development, and Corporate security stakeholders to manage critical eDiscovery and data lifecycle programs. This position requires expert eDiscovery, eData, and project management skills as well as in-depth knowledge of the eDiscovery landscape in regulated industry. Knowledge of Relativity server and RelOne Legal Hold platforms are vital. This role involves daily triage, interaction, and collaboration with various business functions which requires the Senior Manager, Litigation eDiscovery position to possess stellar interpersonal prowess...

Functional Area Description Clinical Data Management key focus is to ensure data quality, integrity & completeness of all data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database lock. The Senior Manager, Clinical Data Management is a leadership role considered essential to the sustainability and success of the BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, Clinical Data Management This is an office-based in BMS New Jersey locations. Position Responsibilities Responsibilities will include, but are not limited to Project Management and Leadership Provides clinical data management...

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. We are seeking a highly-motivated candidate to join our analytical team in advancing reaction monitoring capabilities using Online Liquid Chromatography (LC). The successful candidate will play a key role in developing and demonstrating innovative analytical workflows...

SENIOR MANAGER, OCCUPATIONAL HEALTH The Occupational Health Senior Manager will oversee and provide nursing services including medical surveillance and fitness for duty examinations, travel assessments, occupational injury / illness care, case management (e.g. medical accommodations, workers compensation), and acute care for episodic non-occupational injuries/illnesses at Bristol Myers Squibb Washington locations. This position is responsible for managing a comprehensive occupational health program for the BMS Washington (Seattle and Bothell) sites. In this position the Senior Manager will manage a team of occupational health nurses / nurse practitioners and will closely collaborate with the Senior Medical Director. This program complies with BMS...

This territory includes Birmingham, Huntsville, Montgomery, and Tuscaloosa. 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...

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

The Associate Director, Hematology Regional Marketing (RMK) role is a senior in-market position within the US Hematology/Cell Therapy commercial organization that will focus on commercial Thought Leader (TL) engagements to gain insights into regional opportunities, provide a bridge between regional markets and headquarters, regionally support the brand strategy, support promotional Speaker training and development, the execution of peer to peer educational programs, and support regional congress activity. Regional Marketer (RMK) will liaise with other field-based professionals, within approved SOPs, including but not limited to Field Medical, Sales (DBM & RBDs), and US Value, Access & Payment, in addition to home...

The Director of Federal Government Affairs is accountable for shaping health care policy to benefit patient access, affordability, and innovation. The Director will be responsible for initiating and executing comprehensive strategies around policy proposals in Washington that will support BMS Enterprise priorities to bring innovative treatments to patients. The individual will be responsible for implementing an outreach strategy with Members of the United States Congress that align with BMS’ patient focused principles. The Director will monitor and analyze policies, trends and activities in Washington, DC and will be responsible for communicating the business impact to key external and internal stakeholders...

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...

The Director of Federal Government Affairs is accountable for shaping health care policy to benefit patient access, affordability, and innovation. The Director will be responsible for initiating and executing comprehensive strategies around policy proposals in Washington that will support BMS Enterprise priorities to bring innovative treatments to patients. The individual will be responsible for implementing an outreach strategy with Members of the United States Congress that align with BMS’ patient focused principles. The Director will monitor and analyze policies, trends and activities in Washington, DC and will be responsible for communicating the business impact to key external and internal stakeholders...

The Immunology and Cardiovascular Thematic Research Center (ICV TRC) at BMS is one of the fundamental Research units delivering therapeutics to patients. Our mission is to create transformative medicines of tomorrow based on the cutting-edge science of today. We leverage BMS’s internal invention engine that includes industry-leading expertise in small molecule chemistry, protein biotherapeutics, cell therapy, protein degradation, nucleic acids, and other therapeutic modalities. Located at the Cambridge Crossing site in Cambridge, MA, Bristol Myers Squibb is seeking a Senior Scientist, In Vivo Pharmacology, who will be conducting vivo research in the field of autoimmune diseases. This individual will...

Position Associate Director, US Medical Promotional Review Scientist, Immunology/Cardiovascular Location Princeton, NJ (Hybrid role) The Associate Director, US Medical Promotional Review Scientist (Immunology and/or Cardiovascular), plays a critical role in the Medical Communications team within Global Medical Affairs. As a member of this team, you will serve as a strategic, solutions-oriented partner focused on ensuring the medical accuracy and scientific validity of promotional and non-promotional materials. This includes ensuring robust scientific evidence and compliance with US laws and regulations. This role reports to the Executive Director or the Director of Global Medical Immunology/Cardiovascular, Medical Communications within Global Medical Affairs....

Responsibilities Partners with Access matrix team and home office HEOR on Cross-TA initiatives, communications, and business needs to assist in the development of strategy and plans for fHEOR scientific and access capabilities. Ensures training plan for fHEOR & Account Executive teams is organized, working with market access to execute individual team trainings, marketing touchpoints, and ad-hoc sessions. Participates in the development of training plans for prioritized launch products and RWE methods. Conducts certifications for fHEOR to enhance development of expertise in therapeutic and RWE methods areas in anticipation of prioritized launches and HEOR/Access initiatives. Understands the evolving US healthcare landscape...

The Director, Cell Therapy Drug Product Operations Risk Management , is responsible for delivering improvements in commercial cell therapy product supply reliability by leading risk assessments, prioritizing risk mitigations, and managing the resulting project portfolio. The scope encompasses suppliers, process, and analytics across the DPO manufacturing network. As a key member of the Proactive Risk Management team, this role will partner cross-functionally with Cell Therapy Technical Operations, Analytical Science & Technology, Quality, Regulatory-CMC, Supply Chain, and Product Strategy to holistically assess and mitigate risks to supply reliability. Key Responsibilities Assess risks/vulnerabilities which impact our ability to reliably supply product on-time...

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 We are seeking a highly motivated Sr. Scientist to lead the development and optimization of radiopharmaceutical drug products and radioisotopes. This position plays a pivotal role in driving preclinical development of innovative drug products aimed at treating various...

The Clinical Development Program Leader (Executive Director) 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...

Senior Director of Research Engineering Location Remote or Hybrid in Cambridge, Lawrenceville, San Diego, Brisbane, or Seattle sites (strong preference for Cambridge MA) The Senior Director of Research Engineering is a service-oriented, forward-thinking team leader who is responsible for overseeing a team engaged in the collaborative design, development and implementation of scientific use-case driven, experimental, innovative, scientific data management and analytical platforms, within the Informatics and Predictive Sciences (IPS) department at Bristol Myers Squibb (BMS). This role leverages deep scientific and technical expertise, close collaboration with scientific researchers, and knowledge of modern best practices in cloud-based scientific application development...

The Senior Statistician / Principal Statistician is a core team member of the global statistics group, responsible for providing statistical support for drug substances, APIs, and drug products across the BMS global internal and external manufacturing network. The position resides in Manufacturing Sciences and Technology within Bristol Myers Squibb’s Global Product Development and Supply (GPS). Role & Responsibilities Apply statistical techniques to facilitate better decision-making and improve business operation. Regularly interact with management of different levels in strategy meetings. Contribute to strategic planning to ensure statistically optimized non-clinical development plans and assist in the creation of strategic objectives for regulatory...

This position plays a critical role in the development and execution of BMS’ global medical strategy for 1) set of assets within our Oncology early development portfolio & 2) input to translational medicine plans across the oncology portfolio. The WWM EDAP Lead is a strategic leader within Worldwide Medical organization, accountable to the EA Development teams. The Lead will support development plans via interpretation of evolving pre-clinical & clinical data, develop a sustainable Integrated Evidence Plan & engage with TLs (researchers & clinicians) early and often during pre-POC phase of asset lifecycles. This individual will hold accountability for advancing scientific...

The MBA Finance Associates Program (FAP) has been in place for over 30 years, recruiting top MBA candidates for dynamic careers in Finance. The Finance Associates Program Internship is a 10-week, paid opportunity based in central New Jersey that offers representative experience of the full-time program. Assignments may encompass the development of operating budgets, R&D portfolio allocations, financial forecasting for developmental compounds, analysis of operating performance, and evaluation of returns on capital expenditures. Interns benefit from guidance provided by finance leaders, participate in professional development workshops, and establish a strong professional network throughout the organization. Top-performing interns will receive strong...

Summary The Director, Clinical Program Management, reporting to the Head of Clinical Operations, is accountable of on-time and on-budget delivery of assigned clinical study(ies) within the RayzeBio portfolio at the highest quality standards. The role will oversee all operational aspects of the clinical program according to and in compliance with corporate and program Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines and other applicable federal (FDA) and state or regional regulations, in order to achieve established corporate goals within timelines and budget. Job Responsibilities Essential duties and responsibilities include the following. Other duties may be...

We are looking for a motivated and detail-oriented Paralegal/Legal Coordinator to join our dynamic legal team. The successful candidate will support the Trademark Department with various administrative and project-oriented tasks. The ideal candidate is self-motivated, efficient, and a team player, with excellent organizational and accountability skills. Key Responsibilities Responsibilities for this position include, but are not limited to Perform a variety of complex project oriented, administrative matters and responsibilities on behalf of Trademark Department, both internally and externally. Support practice area on multiple day-to-day responsibilities and administrative tasks. Work independently and serve as a key team contributor for special...

The Associate Director, Hematology Regional Marketing (RMK) -role is a senior in-market position within the US Hematology/Cell Therapy commercial organization that will focus on commercial Thought Leader (TL) engagements to gain insights into regional opportunities, provide a bridge between regional markets and headquarters, regionally support the brand strategy, support promotional Speaker training and development, the execution of peer to peer educational programs, and support regional congress activity. Regional Marketer (RMK) will liaise with other field-based professionals, within approved SOPs, including but not limited to Field Medical, Sales (DBM & RBDs), and US Value, Access & Payment, in addition to home...

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

As part of our long-term strategy to elevate our Medical organization and transform the lives of million patients each year, we are seeking a Director Portfolio Strategy & Business Development within our Global Immunology & Cardiovascular teams. As such, the Director, Portfolio & Business Development will be critical in translating global strategy to fearless execution. The position reports to the Executive Director, Portfolio Strategy Head within Global Medical Immunology & Cardiovascular (ICV) Medical Affairs. The Director, Portfolio & Business Development – ICV plays a pivotal role in shaping and executing the early medical and scientific strategy across the Immunology &...

The Global Biometrics and Data Sciences (GBDS) Executive Associate provides support to members of the GBDS leadership teams Biostatistics, CSDIA, Strategy and Business Operations, and Data Sciences. Position Responsibilities Execute a wide range of sophisticated administrative responsibilities, such as proactive calendar oversight, effective coordination with fellow executive assistants, arranging both domestic and international travel, ensuring the manager is well-prepared for meetings by assembling necessary materials and pre-reads, and overseeing departmental SharePoint management. Demonstrates advanced organizational and communication abilities. Effectively maintains and coordinates office operations and procedures, including processing expense reports, handling purchase orders, and providing administrative services as required. Ensure...

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, Value Steam Cryo Operations, is tactically leading execution for a team of Specialists responsible for the cryopreservation, movement,...

Position Manager, Electrical Engineer Location Devens, MA Key Responsibilities Provide engineering support, system ownership and subject matter expertise for electrical infrastructure including but limited to Utility Electrical infrastructure, substations, Uninterruptible Power Supplies, generators, motor control centers, distribution panels, transformers, motors, transfer switches, lighting, grounding and lightning protection, heat race, etc. Provide guidance and oversee preventative maintenance of electrical equipment. This includes Job Plan development and maintenance. Oversee electrical elements of new projects including development of Scope of Requirements, Basis of Design, Detailed Design, installation, commissioning, as-built documentation, and turnover of equipment. Evaluate impact to site operations from applicable activities...

Location Remote Preferred location IL, IN, OH, MI 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 will operate 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...

Location Remote Preferred location WA, OR, UT, CO 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 will operate 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...

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