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At Texas Roadhouse, we are a people-first company that just happens to serve steaks. Legendary Food and Legendary Service is who we are. We’re about loving what you’re doing today and preparing you for what you’ll be doing tomorrow. Are you ready to be a Roadie?Texas Roadhouse is currently looking for a legendary Local Store Marketer (LSM) who can help build sales at the local level through establishing relationships within the community and increasing guest loyalty. If you have a passion for networking and being creative, apply today!As a Local Store Marketer your responsibilities would include:<ul><li>Assisting the Managing Partner and management team with the creation, development, and implementation of local store marketing programs that build guest loyalty, guest counts, check average, and overall sales</li><li>Helping promote all Texas Roadhouse in-house promotions (Great Steak, Rib Fest, Gift Cards, etc.)</li><li>Building relationships during food and bread runs with businesses, hotels, radio stations, etc.</li><li>Helping establish positive and ongoing business relationships with neighboring retailers, hotels, civic groups, etc.</li><li>Helping develop and execute ongoing charitable and community events that position Texas Roadhouse as a community leader and build brand awareness</li><li>Assisting in all public relation efforts including cooking segments, media releases, and publicity events that promote Texas Roadhouse</li><li>Communicating frequently with the Managing Partner, management team, and all employees (through Alley Rallies, etc.) about ongoing programs, plans, and results</li></ul>At Texas Roadhouse, our Roadies are the heart and soul of our company. We have a fun culture with flexible work schedules, discounts in our restaurants, friendly competitions, recognition, formal training, and career growth opportunities.Our Roadies are paid weekly. In addition, we offer one of the industry’s most competitive total rewards packages after one year of service to Roadies that meet our benefit eligibility requirements.The total rewards package includes, but is not limited to, the following:<ul><li>A choice of medical plans that are best in class</li><li>Dental and Vision Insurance</li><li>Tuition Reimbursement up to $5,250 annually</li><li>Paid vacation time</li><li>Short-Term Disability</li><li>Life, Accident, and Critical Illness insurance</li><li>Identity Theft Protection</li><li>Employee Assistance Program</li><li>Business Travel Insurance</li><li>Annual holiday bonus</li></ul>We are proud to be an equal opportunity employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, age, gender, pregnancy, gender identity, disability, veteran status, sexual orientation, citizenship, national origin, or any other legally-protected status. We encourage and welcome all applicants to apply.

Texas Roadhouse

Local Store Marketer

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. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.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 System Innovation, GoSolo Site Deployment will play a pivotal role in helping to design and execute the future of our organization's autologous drug product manufacturing capability. This position is responsible for quality partnership in the design and implementation of next-generation technologies which support the need to reach a wider patient population through improved cost while sustaining our commitment to excellence. This role will also own the implementation of future state Quality System processes. This person will lead projects which integrate advanced technologies and methodologies, ensuring our systems are robust, efficient, and aligned with industry best practices.Shift Available:Monday – Friday, Standard Working Hours, HybridResponsibilities:<ul><li>Manage Quality System Deployment: Lead the implementation and maintenance of next generation Quality System processes in collaboration with the GoSolo and HyperCell teams, ensuring alignment with organizational goals.</li><li>Monitor and Improve Quality Systems: Evaluate the effectiveness of current quality systems post-deployment and propose improvements or corrective actions as needed to enhance performance.</li><li>Cross-Functional Collaboration: Coordinate with QC, Manufacturing, Regulatory, and IT teams to facilitate the integration and operationalization of quality system processes and technologies.</li><li>Ensure Regulatory Compliance: Ensure compliance with industry standards and regulatory requirements, focusing on operational performance and quality assurance.</li><li>Cultivate Continuous Improvement: Foster a culture of continuous improvement by leveraging existing technologies and methodologies within the quality team.</li></ul>Basic Requirements:<ul><li>Bachelor's degree in a relevant field (e.g., Engineering, Life Sciences); advanced degree preferred.</li><li>Significant experience in Quality Systems management, typically achieved through 8+ years of experience, with a proven track record of leading initiatives and driving innovation.</li><li>Strong knowledge of industry standards and regulatory requirements related to quality systems.</li><li>Demonstrated understanding and application of Quality Risk Management and lean manufacturing principles</li><li>Demonstrated capability in leadership, communication, and project management skills.</li><li>Ability to work collaboratively with cross-functional teams and influence stakeholders at all levels of the organization.</li><li>Demonstrated ability challenge status quo and implement disruptive solutions.</li></ul>BMSCART#LI-HYBRIDGPS_2025If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol Myers Squibb

Senior Manager, Quality System Innovation, GoSolo Site Deployment

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. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.The Associate Director, Quality Assurance, GoSolo Site Deployment will play a pivotal role in helping to design and execute the future of our organization's autologous drug product manufacturing capability. This position is responsible for quality partnership in the design and implementation of next-generation technologies which support the need to reach a wider patient population through improved cost while sustaining our commitment to excellence. This role will also own the implementation of future state Quality System processes. This person will lead projects which integrate advanced technologies and methodologies, ensuring our systems are robust, efficient, and aligned with industry best practices.Shift Available:Monday – Friday, Standard Working Hours, HybridResponsibilities:<ul><li>Manage Quality System Deployment: Own the deployment of Next Generation Quality System processes in collaboration with the GoSolo and HyperCell visioning teams</li><li>Monitor and Improve Quality Systems: Monitor and evaluate the effectiveness of next generation quality systems after deployment, implementing enhancements and corrective actions as needed.</li><li>Cross-Functional Collaboration: Drive collaborate with cross-functional teams, including QC, Manufacturing, regulatory, and IT as the quality partner to implement next generation technologies</li><li>Ensure Regulatory Compliance: Drive the adoption of industry best practices and regulatory requirements, ensuring compliance and enhancing overall quality and business performance, with a focus on technology and artificial intelligence (AI)</li><li>Cultivate Continuous Improvement: Emphasizes innovation and continuous improvement within the organization by leveraging existing and innovating on new technologies.</li></ul>Basic Requirements:<ul><li>Bachelor's degree, preferably in a life science field; advanced degree preferred.</li><li>Deep subject matter experience in Quality Systems management, typically achieved through 10+ years of experience, with a proven track record of leading initiatives and driving innovation.</li><li>Strong knowledge of industry standards and regulatory requirements related to quality systems.</li><li>Demonstrated understanding and application of Quality Risk Management and lean manufacturing principles</li><li>Excellent leadership, communication, and project management skills.</li><li>Ability to work collaboratively with cross-functional teams and influence stakeholders at all levels of the organization.</li><li>Demonstrated ability challenge status quo and implement disruptive solutions.</li></ul>BMSCART#LI-HYBRIDGPS_2025If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Associate Director, Quality System Innovation, GoSolo Site Deployment

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. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.The Senior Specialist, QC Materials Management is responsible for the management of materials used in the analytical and microbiology QC laboratories in the Devens CTF, ensuring the availability of all QC laboratory supplies. This includes, but is not limited to, managing the lifecycle activities of QC laboratory materials, supporting onboarding of new materials through document creation and change control, collaborating with QC network functions and site functions such as QC lab, supply chain and other departments for the management of QC materials. The QC Material Management Senior Specialist will also serve as the QC Material Management SME, supporting training, document revisions, projects, CAPA, and related tasks and/or continuous improvement efforts.The QC Materials Management Senior Specialist role is stationed in Devens, MA and reports to the Associate Director, QC Systems and Support.Shifts Available:TBDResponsibilities:<ul><li>Serve as the site representative for QC material management program and manage the lifecycle activities of QC laboratory materials.</li><li>Support onboarding of new materials through document creation and change control.</li><li>Collaborate with QC network functions and site functions such as QC lab, supply chain and other departments for the management of QC materials.</li><li>Implement and maintain the QC material inventory management system (e.g., Kanban).</li><li>Train others on material management process and procedures as applicable.</li><li>Perform document revision, project, CAPA, and related tasks and/or continuous improvement efforts.</li><li>Create, revise, and review technical documents, such as SOPs and working instructions for sample management.</li><li>Implement 5S and FIFO principles as appropriate.</li><li>Apply critical thinking skills when working on new procedures or process improvements. </li><li>Communicate effectively with management regarding task completion, roadblocks, and needs.</li><li>Perform other tasks as required to support the QC laboratories.</li></ul>Knowledge and Skills:<ul><li>Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.</li><li>High problem-solving ability/mentality, technically adept and logical.</li><li>Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs.</li><li>Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.</li><li>Excellent organizational and critical thinking skills.</li></ul>Basic Requirements:<ul><li>Bachelor’s degree, preferably in Chemistry, Microbiology, or related science. Advanced degree preferred.</li><li>4+ years of relevant work experience, preferably in a regulated environment.&nbsp; An equivalent combination of education and experience may substitute.</li><li>Experience with material management and supply chain processes preferred.</li><li>Advanced knowledge of computerized systems and enterprise applications such as SAP and LIMS preferred.</li><li>Experience in writing and revising GMP procedures and working instructions.</li></ul>Working Conditions:<ul><li>The incumbent will be working around biohazardous materials and may be exposed to fluctuating and/or extreme temperatures on occasion.</li></ul>This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.BMSCART#LI-ONSITEGPS_2025If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Senior Specialist, QC Materials Management, Cell Therapy

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. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.The Senior Manager, Project Management will manage and/or support the aspects of initiating, planning, and executing complex, multi-disciplinary projects throughout Devens Biologics. With a breadth of hands-on project management experience in the Pharma/Biotech regulated environments, the Project Manager is expected to manage this critical initiative in support of specific site goals &amp; objectives. The Project Manager will be responsible for using Devens PMO best practices, tools &amp; templates and will be proficient in PMI program management standards, processes, procedures, and guidelines. The successful candidate must have a proven record of extensive professional experience and the drive to steer internal partners to efficient delivery of the program and projects on time &amp; within budget.&nbsp;This role will report to the Associate Director, Project Management Office (PMO) and Business Operations.Shifts Available:Monday – Friday, Standard Working HoursResponsibilities:<ul><li>Understand the business strategy and business process areas and ensure that these are best aligned. </li><li>Identify appropriate technical solutions for business needs in partnership with the process owners and agreed suppliers, aligned to the Site Business Strategy.</li><li>Partners with Devens Biologics Operations Leadership Team members and project sponsor(s) to ensure successful delivery of projects. Schedules governance / steering committee meetings for program team(s), prepares meeting materials with/for lead as requested, facilitates team meetings as needed, and documents actions &amp; decisions during project team meetings. </li><li>Apply project management expertise across the portfolio for project workstreams, managing multiple projects in parallel. </li><li>Define project scope / goals / deliverables / budget / timeline. </li><li>Develops Work Breakdown Structures (WBS), project plans and Agile Sprint planning with Project Sponsor, Workstream Leads &amp; team members.</li><li>Manages WBS in a Project Portfolio Management system (OnePlan) and/or MS-Project. Sequences WBS activities, facilities discussion with project team to estimate activity resources and durations. </li><li>Facilitates resource planning for program teams throughout the lifecycle of the initiative. </li><li>Develop critical path analyses to understand risks and opportunities within project timelines.</li><li>Monitor project performance and progress, specifically to assure successful completion of short- and long-term goals.</li><li>Identify potential risks in the program and conduct qualitative and quantitative risk analysis and develop &amp; implement risk mitigation plans and strategies.</li><li>Maintain program budgets and meet budgetary objectives by adjusting project constraints based on financial analysis.</li><li>Create and communicate project plans and manage dependencies, milestones, and deliverables.</li><li>Manages project schedules, including reconciling completed/not completed activities and proactively communicates upcoming activities to Steering Committee &amp; Workstream Leads. </li><li>Use change management methods to mitigate barriers to improvement efforts.</li><li>Aligns with Associate Director of PMO to take action(s) to drive performance of cross-functional teams. Appropriately escalates concerns to Associate Director or recommend escalation to Site Leadership Team. </li><li>Identify, handle, and resolve project-related issues and risks by developing specific action / risk mitigation /contingency plans and escalating early to Digital Transformation Program Leader when necessary.</li><li>Prepare and present the business cases and communicate status for the assigned projects to the Leadership Team and/or Steering Committee(s). Clearly and concisely frames discussion topics to senior leaders to drive decisions.</li><li>Monitor execution and quality to customer / stakeholder / sponsor standards. </li><li>Independently leads large cross-functional project(s).</li><li>Evaluate and assess the project outcome. </li><li>Serve as the primary point of contact for all project-related communications.</li></ul>Knowledge and Skills:<ul><li>Experience in leading Cross-Functional Projects and managing SME &amp; technical professionals.</li><li>Competence in Project Management methodologies such as Waterfall, Agile, Hybrid and Software Development Life Cycle (SDLC).</li><li>Solid analytical skills, problem solving and financial acumen.</li><li>Exceptional communication skills including ability to take an independent stance when interfacing with cross-functional stakeholders.</li><li>Good facilitation, change management and interpersonal skills required. Expertise in conflict resolution.</li><li>Demonstrated focus on being able to translate data and metrics into predictable, value-add business insight.</li><li>Ability to translate business requirements into viable solutions.</li><li>Knowledge of performance measurement tools and metrics.</li><li>Comfortable with uncertainty and meeting tight deadlines in the matrix environment.</li><li>Expertise in conflict resolution</li><li>Demonstrate a high degree of independence, requiring minimal supervision from senior management.</li><li>Highly motivated, highly organized, passionate self-starter: detail-oriented and operationally focused.</li><li>Ability to understand project details but keep the overall “big picture” view of projects, priorities, and strategies.</li><li>Successful experience working with cross-functional teams from Manufacturing, Quality, Site Engineering, MS&amp;T, Digital Plant (IT), Finance, Operational Excellence, Biologics Development and Cell Therapy.</li></ul>Basic Requirements:<ul><li>Bachelor’s degree of Science/Engineering/Business required; Advanced degree is a plus.</li><li>A minimum of 8 years program / project management in GxP Biopharmaceutical environment with strong experience with production and/or manufacturing operations, documented by a solid history of functional accomplishments and a proven track record.</li><li>Understanding of GMP and FDA regulatory requirements correlating to biologics.</li><li>Project Management Professional (PMP) certification is required.</li><li>Agile / Scrum Master certification and Change Management Certification is a plus.</li><li>Knowledge and previous work experience in Lean and Continuous Improvement.</li><li>Excellent computer skills with proficiency in Microsoft applications- SharePoint, Project, PowerPoint, Access, Excel, Word, OneNote, Publisher.</li></ul>#LI-ONSITEGPS_2025If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Sr. Manager, Project Management in Devens, MA

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. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.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.Bristol Myers Squibb is seeking a Associate, QC Microbiology to join our QC Microbiology team at the Cell Therapy Facility (CTF) in Devens, MA.&nbsp; The QC Associate is responsible for supporting Quality Control microbiological in-process, release, and stability testing of clinical and commercial cell therapy drug product.&nbsp; Additionally, the QC Associate will support clean utilities systems testing, environmental monitoring within the manufacturing environment, and may assist with investigations and continuous improvement efforts.&nbsp; The QC Associate role is stationed in Devens, MA and reports to the Manager, QC Microbiology for the Devens CTF.Shifts Available:Wednesday - Saturday, 6am – 4pm (position requires shift coverage consisting of weekdays, weekends, holidays and during adverse weather conditions), onsiteResponsibilities:<ul><li>Perform microbiological testing and data review of in-process, batch release, and stability samples of cell therapy drug product in accordance with applicable procedures and cGMP requirements.</li><li>Perform environmental and clean utilities monitoring within the manufacturing environment.</li><li>Ensure timely completion of testing and tasks as assigned.</li><li>May train on additional test methods and provide support to a broader spectrum of testing responsibilities.</li><li>Support investigations through data gathering or interview process.</li><li>Apply scientific principles to testing and the proper use of laboratory equipment.</li><li>Communicate effectively with management regarding task completion, roadblocks, and needs.</li><li>May participate in projects and continuous improvement efforts.</li><li>Perform other tasks as assigned.</li><li>Support for QC and manufacturing operations</li></ul>Knowledge and Skills:<ul><li>Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.</li><li>Prior experience in microbiology techniques (endotoxin, sterility, environmental monitoring, process gas &amp; water testing, aseptic technique) is preferred.</li><li>Knowledge of regulatory standards as they apply to GMP laboratories is preferred.&nbsp;</li><li>Attention to detail and demonstrated organizational skills.</li><li>Knowledge of basic electronic systems (email, MS Office, etc.) required.</li><li>Experience with LIMS and ELN computer applications preferred.</li><li>Ability to work in a high-paced team environment, meet deadlines, and prioritize work.</li><li>Ability to communicate effectively with peers and department management.</li></ul>Basic Requirements:<ul><li>Bachelor’s degree required, preferably in the life sciences.</li><li>0-2+ years of relevant microbiological testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.</li></ul>BMSCART#LI-ONSITEGPS_2025If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Associate, QC Microbiology in Devens, MA

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. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.BMS is seeking a Manager, Cell Therapy Manufacturing for a new manufacturing facility in Devens, MA. The Manager will support the start-up and commercial licensure of the Cell Therapy facility.&nbsp; This manager will be responsible for shifts that cover 24/7 cell therapy operations and will oversee manufacturing associates.Shifts Available:6pm – 6am, rotating schedule including holidays and weekends, onsiteResponsibilities:<ul><li>Manage the creation, implementation and compliance for all documentation, procedures and policies</li><li>Operate within the requirements of a validated manufacturing systems, plan, assign and oversee daily operational activities associated with assigned areas of responsibility.</li><li>Maintain operating and storage areas that are compliant, efficient, effective and safe.</li><li>Identify strategic and operational issues to prevent deviations and maintain a compliant environment. Lead and manage the development of corrective and preventative actions, deviation responses and investigations.</li><li>Manage implementation and maintenance of appropriate training curricula </li><li>Create an environment of teamwork, open communication, and a sense of urgency. Foster a culture of safety and compliance that embraces safety in the work environment and the safety of the patients by compliance with company procedures and policies, and cGMP requirements.</li><li>Efficiently coordinate, communicate, and provide Operations project information and activities status to Planning, Manufacturing, Quality Assurance / Operations, Global Supply and other associated functions in a timely manner in accordance to schedules and defined implementation timelines</li><li>Oversee operators on daily basis as they:<ul><li>Perform unit operations and support operations described in standard operating procedures and batch records in a safe and GMP compliant manner.</li><li>Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.</li><li>Maintain training assignments to ensure the necessary technical skills and knowledge.</li><li>Assist in the setup of manufacturing areas and equipment/fixtures and perform facility and equipment commissioning, qualification and validation activities.</li><li>Writing manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements</li></ul></li><li>Hire, mentor and develop exceptional people: Conduct performance reviews and identify opportunities for career growth for manufacturing associates.</li><li>This position will require shift work, including holidays and weekends.</li><li>This position will require you to work in a clean room environment, with exposure to human blood components and in close proximity to strong magnets.</li></ul>Knowledge and Skills:<ul><li>Experience in the following is highly preferred:<ul><li>Cell therapy manufacturing</li><li>Aseptic processing in ISO 5 biosafety cabinets and universal precautions for handling human derived materials in BSL-2 containment areas.</li><li>Cell expansion using incubators and single use bioreactors, Cell washing processes, Cell separation techniques and cryopreservation processes and equipment.</li></ul></li></ul>Basic Requirements:<ul><li>Bachelors in relevant science or engineering discipline, or equivalent in work experience.</li><li>5+ years of experience in cGMP biologics cell culture manufacturing</li></ul>BMSCART#LI-ONSITEGPS_2025If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Manager, Cell Therapy Manufacturing in Devens, MA (Night Shift)

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. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Reporting to the Director of OpEx, PMO &amp; L&amp;D the Senior Manager, OpEx will be responsible for developing, implementing, and managing operational strategies that identify cost savings opportunities, provide increased process efficiency, improve data availability for decision making and drive continuous improvement within the Devens Biologics Manufacturing. This will be accomplished by promoting and using Lean Six Sigma and Continuous Improvement methodologies to achieve department goals &amp; objectives.Shifts Available:Monday - Friday, Standard Working Hours - Hybrid (5 out of 10 days onsite, minimum two days per week)Responsibilities:<ul><li>Provide Operational Excellence (OpEx) support to activities in the Biologics Manufacturing department that will increase process efficiency, reduce operating costs, and improve general cycle times. </li><li>Embed OpEx Foundational skills in “The Way We Work” within the Biologics Manufacturing department. Ensure OpEx foundational skills (e.g., 5S, Gemba Walks, Visual Management, Process Maps, Standard Work, and Kaizens) are being used by Biologics Manufacturing resources. </li><li>Drive Tier meetings and visual factory for Biologics Manufacturing teams, aligned with Site &amp; Department strategy. </li><li>Collaborate with Biologics Manufacturing, Leadership Team and department functions to develop required pertinent metrics to drive performance. </li><li>Collaborate with Biologics Manufacturing Leadership Teams to drive CI project portfolio ensuring cost/benefit analysis to assess the impact or viability of alternate processes or action. </li><li>Collaborate with OpEx practitioners at the Deven Biologics Site to participate as needed in site Kaizen events and other OpEx initiatives in the Biologics Operating Unit. </li><li>Act as primary OpEx point of contact for Biologics Manufacturing by effectively partnering with Manufacturing Team members to develop routine, integrated messages on the OpEx programs. </li><li>Introduce and maintain continuous improvement program offerings and/or OpEx training to all levels of Biologics Manufacturing personnel.&nbsp; </li><li>Communicate via multiple media including Devens newsletter, Leadership Team meetings, Town Halls, etc. </li><li>Lead and/or support key complex projects through effective project management and leadership. </li><li>Lead participants of Kaizen workshops and in day-to-day continuous improvement activities &amp; applications. </li><li>Provide specific tools and lean technique training as required by the business. </li><li>Keep up to date on best practices and improvement opportunities in OpEx by networking within the Devens site, campus, GPS Biologics Operating Unit and Global GPS OpEx team.</li></ul>Knowledge and Skills:<ul><li>Excellence in business change management processes and project management skills is needed.</li><li>Strong communication/presentation skills with ability to tailor the message to the key stakeholders for effective impact and influence.</li><li>Complete varied and complex assignments with little direction.</li><li>Ability to integrate work with that of other functions to align with strategic objectives.&nbsp;</li><li>Interpersonal/facilitation skills necessary to interface with and influence all levels of the organization.</li><li>Comfortable managing in a matrix organization.</li><li>Ability to be flexible and adapt quickly to changing needs of the organization.</li><li>Ability to organize multiple work assignments and establish priorities.</li><li>Lead and/or support key complex projects through effective project management and leadership.</li><li>Achieve high customer satisfaction through effective communication of both technical and nontechnical topics with all levels of the organization both verbally and written.</li></ul>Basic Requirements:<ul><li>Bachelor’s degree in engineering is required. A Master’s degree is desired.</li><li>Lean Six Sigma Black Belt or Green Belt certification is required.&nbsp; PMP Certification a plus.</li><li>A minimum of 6-8 years GxP Biopharmaceutical experience with strong experience with production and/or manufacturing operations is preferred, documented by a solid history of functional accomplishments and a proven track record.</li><li>Demonstrates a strong knowledge of cGMP compliance and regulatory agency requirements and procedures.</li><li>Successful experience working with cross-functional teams from manufacturing, quality, site engineering, MS&amp;T, Digital Plant (IT), finance, PMO and Biologics Development.&nbsp;</li><li>Excellent computer skills with proficiency in Microsoft applications- SharePoint, Project, PowerPoint, Access, Excel, Word, Publisher, Power Automate, Visio, and Minitab/JMP.</li><li>Possesses a deep understanding of the Six Sigma and Lean philosophies and can coach others how to apply Lean Six Sigma concepts and foundational tools (e.g., Process Mapping, Visual management, 5S, Gemba, etc.).</li></ul>#LI-HYBRIDGPS_2025If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Sr. Manager, Operational Excellence in Devens, MA

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. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.<h4>Position: MLOps Engineer, Manager - Analytics Operations</h4><h4>Location: Multiple locations including Devens, MA, New Brunswick, NJ or Seattle, WA</h4>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.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Position SummaryThe GPS BI&amp;T Analytics Operations team (Global Product Development and Supply Business Insights and Technology) is building best-in-class DevOps and MLOps infrastructure for deploying innovative AI and ML solutions that drive business value at BMS.The MLOps Engineer, Manager – Analytics Operations will work directly with the Associate Director, Analytics Operations to deploy and manage ML models in production environments. This role will serve as the bridge between machine learning development and operations and work closely with small, cross-functional project-driven teams that include developers, data scientists and business stakeholders to deliver high impact business value. The successful candidate will build robust pipelines and infrastructure that enable efficient development, deployment and monitoring of machine learning solutions.The successful candidate is a creative thinker with a scientific background in computer science, mathematics, engineering or other STEM field and has expertise in one or more of the following areas: backend development with a focus on cloud or ML model deployment, deep learning frameworks, data science, machine learning and data engineering. Previous DevOps/MLOps experience is desired but not a requirement. Additionally, a successful candidate is an excellent communicator who can effectively explain complex technical information to a wide variety of stakeholders. &nbsp;Key ResponsibilitiesThe MLOps Engineer, Manager – Analytics Operations will partner with business-facing stakeholders to establish core capabilities within the team, namely:<ul><li>Design, implement, and maintain CI/CD pipelines for machine learning models.</li><li>Containerize ML models using Docker/Kubernetes and deploy them on cloud platforms (AWS (preferred), Azure or GoogleCloud).</li><li>Set up and maintain monitoring systems to track model performance, response time, error rates and resource utilization (CloudWatch, Grafana, ELK stack).</li><li>Establish alerting and notification systems to quickly detect anomalies or deviations from expected behavior.</li><li>Drive business value – By implementing the highest impact use cases, actively drive business insights and the adoption of advanced analytics. Establish the team as a source of innovative AND reliable enterprise tools.</li></ul>Qualifications &amp; Experience<ul><li>BA/BS in a scientific or quantitative major required; advanced degree (Master or PhD) preferred.</li><li>4+ years of hands-on experience in backend development, cloud or ML engineering. Previous DevOps or MLOps experience a plus but not required. The ideal candidate will have both experience deploying ML models at scale but also have acquired a set of best practices along the way. Relevant experience in high tech or the biopharmaceutical industry preferred but not required.</li><li>Expert coder in languages such as: Python, Java, C or C ++, Go, Rust, Julia. (Required).</li><li>Version control and working with multiple team members in Git required.</li><li>Proficiency in cloud platforms (AWS (preferred), Azure, Google Cloud), containerization technologies (Kubernetes, Docker) and MLOps tools (MLflow, MLOps platform) is desired.</li><li>Knowledge of deep learning frameworks (PyTorch, Tensorflow) is desired.</li><li>Knowledge of CI/CD tools and practices (Jenkins, GitLab CI, CircleCI) is desired.</li><li>Experience with data engineering using SQL, Spark, ETL/ELT and data pipelines a plus.</li><li>Strong project management skills with demonstrated ability to lead multiple projects and balance shifting priorities.</li><li>Excellent interpersonal, collaborative, team-building, written and verbal communication skills to ensure effective collaborations within cross-functional teams.</li></ul>Why You Should ApplyAround the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

MLOps Engineer, Manager - Analytics Operations

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. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.<h4>Position: Cloud Developer AI/ML, Sr. Manager - Analytics Operations</h4><h4>Location: Multiple locations including Devens, MA, New Brunswick, NJ or Seattle, WA</h4>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.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Position SummaryThe GPS BI&amp;T Analytics Operations team (Global Product Development and Supply Business Insights and Technology) is building best-in-class DevOps and MLOps infrastructure for deploying innovative AI and ML solutions that drive business value at BMS.The Cloud Developer AI/ML, Sr. Manager – Analytics Operations will work directly with the Associate Director, Analytics Operations to engineer solutions that will efficiently operationalize AI models, agentic frameworks and other advanced analytics tools using AWS and other cloud services. This role will work closely with small, cross-functional project-driven teams that will include data scientists and business stakeholders to deliver high impact business value. The successful candidate will also have the opportunity to develop custom services and UIs for building the team’s full-stack development capabilities. The candidate will also have exciting opportunities to build tools deploying the most cutting-edge technologies such as GenAI, LLMs, etc. &nbsp;The successful candidate is a creative thinker with a scientific background in computer science, mathematics, engineering or other STEM field and has expertise in one or more of the following areas: distributed computing with GPUs/TPUs, AI-related cloud services, deep learning frameworks, data science, machine learning and data engineering. Previous DevOps experience is desired but not a requirement. Additionally, a successful candidate is an excellent communicator who can effectively explain complex technical information to a wide variety of stakeholders. &nbsp;Key ResponsibilitiesThe Cloud Developer AI/ML, Sr. Manager – Analytics Operations will partner with business-facing stakeholders to establish core capabilities within the team, namely:<ul><li>Building DevOps infrastructure from the ground-up - Work with a team of developers to build automated and sustainable end-to-end solutions for the most advanced analytics tools.</li><li>Define best practices and tool adoption – Establish a framework of Ops tools and best coding practices for the entire enterprise based on innovative and business value-driven use cases.</li><li>Provide strong technical leadership – Coach junior team members on software development concepts and lead code review to ensure adoption of best practices on the team.</li><li>Drive business value – By identifying and implementing the highest impact use cases, actively drive business insights and the adoption of advanced analytics. Establish the team as a source of innovative AND reliable enterprise tools.</li></ul>Qualifications &amp; Experience<ul><li>BA/BS in a scientific or quantitative major required; advanced degree (Master or PhD) preferred.</li><li>6+ years of hands-on experience in developing cloud infrastructure and/or writing backend services. Frontend experience and previous DevOps or MLOps experience a plus but not required. The ideal candidate will have a strong ability to architect scalable, effective AI/ML solutions that drive decision-making. Relevant experience in high tech or the biopharmaceutical industry preferred but not required.</li><li>Expert coder in languages such as: Python, Java, JavaScript, C or C ++, Go, Rust, Julia. (Required).</li><li>Version control and working with multiple team members in Git required.</li><li>Experience deploying AI models such as LLMs and neural networks etc. to production desired.</li><li>Experience automating software delivery and testing by writing CI/CD pipelines desired.</li><li>Proficiency in cloud platforms (AWS (preferred), Azure, Google Cloud), containerization technologies (Kubernetes, Docker) and MLOps tools (MLflow, Kubeflow, MLOps platform) is desired.</li><li>Knowledge of deep learning frameworks (PyTorch, Tensorflow) a plus.</li><li>Experience with data engineering using SQL, Spark, ETL/ELT and data pipelines a plus.</li><li>Strong project management skills with demonstrated ability to lead multiple projects and balance shifting priorities.</li><li>Excellent interpersonal, collaborative, team-building, written and verbal communication skills to ensure effective collaborations within cross-functional teams.</li></ul>Why You Should ApplyAround the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

47 Jobs in Charlton, MA 01507, USA