Careers @BMS

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<style>\n    .footer-wrapper{padding: 74px 20px 102px 20px;background-color: #f6f4f4;font-family: system-ui, -apple-system, BlinkMacSystemFont, 'Segoe UI', Roboto, Oxygen, Ubuntu, Cantarell, 'Open Sans', 'Helvetica Neue', sans-serif;font-size: 18px;}\n    .footer-wrapper ul{list-style: none;padding: 0;margin: 0;}\n    .footer-wrapper ul li{margin: 8px 0;}\n    .footer-wrapper a {\n   \n    font-weight: 400;\n    line-height: 24px;\n    color: #595454;\n    text-decoration: none;\n  }\n  .footer-wrapper h3{font-size: 18px;\n    font-weight: 500;line-height: 24px;color: #595454;margin-top: 8px;margin-bottom: 10px;margin-right: 200px;}\n    .column-2{display: flex;flex-wrap: wrap;text-align:left;}\n    .column-2>div{flex: 0 0 50%;max-width: 50%;}\n    .column-2>div.right-side{margin-left: auto;flex: 0 0 25%;max-width: 25%;}\n    .column-2>div.right-side .social-media{display: flex;gap: 20px;font-size: 28px;}\n  .copyright{margin-top: 40px;display: block;}\n \n  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href=\"https://www.bms.com/privacy-policy.html#job\" rel=\"noopener\" target=\"_blank\">General Privacy Notice </a></li>\n <li><a  onclick=\"OneTrust.ToggleInfoDisplay()\">Your Privacy Choices</a><img src='https://static.vscdn.net/images/careers/demo/bms-staging-sandbox/1717172242::pcs-footer-privacy-choices-image-053124'></li>\n           <li><a href=\"https://careers.bms.com/faq/\">Contact Us/FAQs </a></li>\n          </ul>\n          <a style=\"color: #be2bbb;\" href=\"https://www.bms.com/\" rel=\"noopener\" target=\"_blank\" class=\"copyright\">\u00a9 2024 Bristol-Myers Squibb Company</a>\n        </div>\n        <div class=\"right-side\">\n          <h3>Follow Us</h3>\n          <ul class=\"social-media\">\n            <li><a href=\"https://www.facebook.com/BristolMyersSquibb\"><i class=\"fab fa-facebook-square\"></i></a></li>\n            <li><a href=\"https://www.instagram.com/bristolmyerssquibb/\"><i class=\"fab fa-instagram\"></i></a></li>\n            <li style=\"display: 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13.6203 3.04902 13.6203 6.81017C13.6203 8.42068 13.0613 9.90062 12.1267 11.0665L16.8745 15.8143L15.8138 16.875L11.066 12.1271Z\"\n              fill=\"#BE2BBB\" />\n          </svg></a>\n      </div>\n\n    </div>\n  </div>\n  <!-- Header first level end -->\n  <!-- Header second  level -->\n  <div class=\"header-main-menu hidden\">\n    <div class=\"header-main-menu-item\">\n      <ul>\n        <li><a href=\"https://careers.bms.com\">Careers Home</a></li>\n        <li class=\"child-sub-menu\"><a class=\"child-sub-menu-link\" href=\"https://careers.bms.com/life-at-bms/\">Life\n            at BMS <span class=\"mega-indicator\" data-has-click-event=\"true\"><svg xmlns=\"http://www.w3.org/2000/svg\"\n                height=\"1em\" viewBox=\"0 0 448 512\">\n                <path\n                  d=\"M201.4 342.6c12.5 12.5 32.8 12.5 45.3 0l160-160c12.5-12.5 12.5-32.8 0-45.3s-32.8-12.5-45.3 0L224 274.7 86.6 137.4c-12.5-12.5-32.8-12.5-45.3 0s-12.5 32.8 0 45.3l160 160z\" />\n              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0.00139961 8.75596 0.0176807 8.82956 0.0479608C8.90317 0.0782419 8.96941 0.1219 9.02434 0.176332L13.8245 4.60849C13.9369 4.71237 14 4.85318 14 5C14 5.14682 13.9369 5.28763 13.8245 5.39151L9.02434 9.82367C8.96941 9.8781 8.90317 9.92176 8.82956 9.95204C8.75596 9.98232 8.67651 9.9986 8.59594 9.99991C8.51538 10.0012 8.43535 9.98754 8.36064 9.95968C8.28592 9.93181 8.21805 9.89034 8.16108 9.83773C8.1041 9.78512 8.05918 9.72246 8.02901 9.65347C7.99883 9.58449 7.98401 9.51059 7.98543 9.43621C7.98685 9.36182 8.00448 9.28846 8.03728 9.2205C8.07007 9.15254 8.11736 9.09137 8.17631 9.04065L11.9525 5.55402L0.600022 5.55402C0.440887 5.55402 0.288268 5.49565 0.175742 5.39175C0.0632162 5.28785 -2.12134e-07 5.14694 -2.18557e-07 5Z\"\n                            fill=\"#BE2BBB\" />\n                        </svg></span></a></h5>\n                </div>\n                <div class=\"mega-sub-menu-row\">\n                  <div class=\"mega-sub-menu-column\">\n                    <div><a href=\"https://careers.bms.com/inclusion-diversity\">Inclusion & Diversity</a></div>\n                    <div><a href=\"https://careers.bms.com/developing-our-people\">Developing Our People</a></div>\n                    <div><a href=\"https://careers.bms.com/benefits\">Our Benefits</a></div>\n\n                  </div>\n                  <div class=\"mega-sub-menu-column\">\n                    <h5>QUICK LINKS</h5>\n                    <div><a target=\"_blank\"\n                        href=\"https://www.bms.com/about-us/global-diversity-and-inclusion/diversity-and-inclusion-report.html\">Global\n                        Inclusion & Diversity Report</a></div>\n                    <div><a target=\"_blank\" href=\"https://www.bms.com/about-us/our-company/global-patient-week.html\">Global Patient\n                        Week</a></div>\n                    <div><a target=\"_blank\" href=\"https://www.bms.com/life-and-science.html\">Our Stories</a></div>\n                    <div><a target=\"_blank\" href=\"https://www.bms.com/about-us/sustainability.html\">Sustainability Commitments</a></div>\n                  </div>\n                </div>\n              </div>\n            </li>\n\n          </ul>\n        </li>\n        <li class=\"child-sub-menu\"><a class=\"child-sub-menu-link\"\n            href=\"https://careers.bms.com/career-areas\">Career Areas <span class=\"mega-indicator\"\n              data-has-click-event=\"true\"><svg xmlns=\"http://www.w3.org/2000/svg\" height=\"1em\" viewBox=\"0 0 448 512\">\n                <path\n                  d=\"M201.4 342.6c12.5 12.5 32.8 12.5 45.3 0l160-160c12.5-12.5 12.5-32.8 0-45.3s-32.8-12.5-45.3 0L224 274.7 86.6 137.4c-12.5-12.5-32.8-12.5-45.3 0s-12.5 32.8 0 45.3l160 160z\" />\n              </svg></span></a>\n          <ul class=\"dropdown\">\n            <li>\n              <div class=\"mega-sub-menu\">\n                <div class=\"mega-sub-menu-title\">\n                  <h5><a href=\"https://careers.bms.com/career-areas\">Career Areas <span class=\"icon-right\"><svg\n                          xmlns=\"http://www.w3.org/2000/svg\" width=\"14\" height=\"10\" viewBox=\"0 0 14 10\" fill=\"none\">\n                          <path fill-rule=\"evenodd\" clip-rule=\"evenodd\"\n                            d=\"M-2.18557e-07 5C-2.2498e-07 4.85307 0.0632162 4.71215 0.175742 4.60825C0.288268 4.50435 0.440886 4.44598 0.600022 4.44598L11.9525 4.44598L8.17631 0.959347C8.11736 0.908627 8.07007 0.847463 8.03728 0.779504C8.00448 0.711545 7.98685 0.638181 7.98543 0.563793C7.98401 0.489404 7.99883 0.415515 8.029 0.34653C8.05918 0.277545 8.1041 0.214878 8.16108 0.162269C8.21805 0.10966 8.28592 0.0681864 8.36064 0.0403219C8.43535 0.0124575 8.51538 -0.00122584 8.59594 8.64086e-05C8.67651 0.00139961 8.75596 0.0176807 8.82956 0.0479608C8.90317 0.0782419 8.96941 0.1219 9.02434 0.176332L13.8245 4.60849C13.9369 4.71237 14 4.85318 14 5C14 5.14682 13.9369 5.28763 13.8245 5.39151L9.02434 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target=\"_blank\" href=\"https://www.bms.com/patient-and-caregivers/our-medicines.html\">Our Medicines</a></div>\n                    <div><a target=\"_blank\" href=\"https://bms.talentnet.community\">Contract Positions</a></div>\n                  </div>\n                </div>\n              </div>\n            </li>\n\n          </ul>\n        </li>\n        <li class=\"child-sub-menu\"><a class=\"child-sub-menu-link\"\n            href=\"https://careers.bms.com/student-opportunities\">Student Opportunities <span class=\"mega-indicator\"\n              data-has-click-event=\"true\"><svg xmlns=\"http://www.w3.org/2000/svg\" height=\"1em\" viewBox=\"0 0 448 512\">\n                <path\n                  d=\"M201.4 342.6c12.5 12.5 32.8 12.5 45.3 0l160-160c12.5-12.5 12.5-32.8 0-45.3s-32.8-12.5-45.3 0L224 274.7 86.6 137.4c-12.5-12.5-32.8-12.5-45.3 0s-12.5 32.8 0 45.3l160 160z\" />\n              </svg></span></a>\n          <ul class=\"dropdown\">\n            <li>\n              <div 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href=\"https://careers.bms.com/internships-co-ops\">Internships & Co-ops</a></div>\n                    <div><a href=\"https://careers.bms.com/leadership-development-programs\">Leadership Development\n                        Programs</a></div>\n                    <div><a href=\"https://careers.bms.com/advanced-degree-programs\">Advanced Degree Programs</a>\n                    </div>\n\n                  </div>\n                  <div class=\"mega-sub-menu-column\">\n                    <h5>QUICK LINKS</h5>\n                    <div><a target=\"_blank\" href=\"https://app.joinhandshake.com/employers/bristol-myers-squibb-16669\">BMS on\n                        Handshake</a></div>\n                    <div><a target=\"_blank\" href=\"https://www.wayup.com/organizations/bristol-myers-squibb-9aegbw\">BMS on WayUp</a>\n                    </div>\n                  </div>\n                </div>\n              </div>\n            </li>\n\n          </ul>\n        </li>\n        <li><a href=\"https://careers.bms.comm/events/\">Events</a></li>\n        <li><a href=\"https://careers.bms.com/how-we-recruit/\">How We Recruit</a></li>\n        <li><a href=\"https://careers.bms.com/blog/\">Career Stories</a></li>\n        <li><a href=\"https://jobs.bms.com/careers\">Search Jobs</a></li>\n      </ul>\n    </div>\n    <div class=\"header-moblie-box\">\n      <div class=\"search-box\">\n        <a href=\"https://careers.bms.com/search/\"> <span><svg xmlns=\"http://www.w3.org/2000/svg\" width=\"24\" height=\"24\" viewBox=\"0 0 24 24\"\n              fill=\"none\">\n              <path fill-rule=\"evenodd\" clip-rule=\"evenodd\"\n                d=\"M17.7933 9.64665C17.7933 14.1459 14.1459 17.7933 9.64665 17.7933C5.14738 17.7933 1.5 14.1459 1.5 9.64665C1.5 5.14738 5.14738 1.5 9.64665 1.5C14.1459 1.5 17.7933 5.14738 17.7933 9.64665ZM15.9166 16.978C14.2304 18.4215 12.0404 19.2933 9.64665 19.2933C4.31895 19.2933 0 14.9743 0 9.64665C0 4.31895 4.31895 0 9.64665 0C14.9743 0 19.2933 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target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=ht\">Haitian</a>\n                  <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=he\">\u05e2\u05d1\u05e8\u05d9\u05ea</a>\n                  <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=pt-BR\">Brazilian Portugu\u00eas</a>\n                  <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=da\">Dansk</a>\n                  <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=fi\">Suomi</a>\n                  <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=sv\">Svenska</a>\n                  <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=fr-CA\">Fran\u00e7ais (Canada)</a>\n                  <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=pt-PT\">Portugu\u00eas (Portugal)</a>\n                </div>\n             </div>\n        </div>\n\n      </div>\n    </div>\n  </div>\n</div>\n  <!-- Header second level end -->"}, "hideReferralJobCart": true, "enableTalentNetwork": 1, "homePageHeroBanner": {"opacity": 1, "image": "https://static.vscdn.net/images/careers/demo/bms/1719339615::PCS-Header-GPS.jpg", "useImage": 1, "background": "#ffffff"}, "links": {"rss": [{"url": "https://careers.bms.com/feed/"}]}, "companyName": "Bristol Myers Squibb", "navBar": {"color": "#ffffff", "title": "BMS", "opacity": 0}, "perks": [{"description": "Global platform for health and wellbeing", "title": "Wellbeing", "image": "https://static.vscdn.net/images/careers/demo/bms-sandbox/1692721708::icn_apple_ppl.png"}, {"description": "Global platform to reward your achievements", "title": "Recognition", "image": "https://static.vscdn.net/images/careers/demo/bms-sandbox/1692721668::icn_experiment_and_experience_ppl.png"}, {"description": "Generous time off to rest and recharge", "title": "Time Off", "image": "https://static.vscdn.net/images/careers/demo/bms-sandbox/1692721618::icn_yoga_pose_2_ppl.png"}, {"description": "Best-in-class benefits", "title": 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Lead and collaborate with cross-functional teams to architect, design, build, manage, and operate solutions delivering business value. Lead and collaborate with cross-functional teams to gather, understand, and share requirements as necessary to architect, design, and implement solutions. Develop and maintain solution architecture documentation, including diagrams, specifications, and other technical documentation. Provide technical guidance and support to development teams during the implementation of warehouse management, transportation management, and/or logistic solutions. Ensure that solutions are scalable, reliable, and maintainable while adhering to applicable policies and procedures. Stay current with emerging technologies, industry trends, and best practices in the warehouse management, transportation management, and/or logistic solution space. Recommend complementary and/or new solutions as appropriate. Required: 10+ years of experience in an information technology related field delivering and supporting warehouse management, transportation management, and/or logistics, with at least 5 years focused on solution architecture and implementation. Strong understanding of warehouse management, transportation management, and/or logistics processes. Demonstrated success in designing, delivering, and supporting integrated warehouse management, transportation management, and/or logistics solutions using disparate technologies. Demonstrated success designing, delivering, and supporting experience in third-party logistics integration. Exceptional analytical and problem-solving skills, with the ability to identify and resolve complex technical issues. Excellent project management and organizational skills. Excellent communication, leadership, and interpersonal skills. Experience working internationally with a globally dispersed team including management of offshore technical development team(s). Demonstrated subject matter expertise in SAP S/4 and/or SAP eWM. Prior experience working in a global life sciences supply chain planning environment.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "hybrid", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137465003976", "isPrivate": false, "custom_data": {"location": "New Brunswick - NJ - US", "RequisitionID": "R1587401", "canonical_title": "Solutions Director", "straight_line_distance": null}}, {"id": 137463608578, "name": "Manager, QA Shopfloor - Shift", "location": "Devens - MA - US", "locations": ["Devens - MA - US"], "hot": 1, "department": "Cell Therapy", "business_unit": "Global Product Development & Supply", "t_update": 1729541078, "t_create": 1724112000, "ats_job_id": "R1584730", "display_job_id": "R1584730", "type": "ATS", "id_locale": "R1584730-zh-CN", "job_description": "Functional responsibilities include ensuring manufacturing compliance with applicable procedures and batch records, providing real time review of manufacturing batch record documentation and logbooks, and working with operations to resolve manufacturing issues. The Field QA Manager role is stationed in Devens, MA and reports to the Senior Manager, Field Quality Assurance for the Devens CTF. This position works on a rotating night shift from 6pm - 6am Oversee performance of QA shop floor activities. Supervise Field Quality Assurance employees. Ensure manufacturing compliance with applicable procedures and batch records. Perform real time review of manufacturing batch records. Review manufacturing shop floor documentation. Must have strong authorship and ability to critically review investigations, interpret results and generate technical conclusions consistent with Quality risk management principles. Must be skilled in planning and organizing, decision-making, and building relationships. Knowledge of quality processes, including material disposition, change control, product complaints, deviations, investigations, and CAPA management. Previous Supervisory/Managerial Experience is preferred. Must be action-oriented and skilled in decision-making, building relationships, problem solving, conflict management, planning and organizing, resource allocation, coaching others, and analytical thinking. Understands continuous improvement and improves efficiency and productivity within the group or project. Builds relationships internally within and with cross functional teams. Must have sound knowledge and experience in FDA regulated cGMP warehousing, Quality, and compliance environments. Prefer to also have knowledge of GMP Manufacturing operations and processes. Directs quality initiatives that accomplish continuous improvement and enhance site quality system efficiencies. Routinely recognizes and resolves Quality issues; Informs management of proposed solutions. Seeks management guidance on complex issues. Able to recognize conflict and notify management with proposed recommendations for resolution. Must possess an independent mindset. Work is self-directed. Requires little direction to complete more complex tasks; completes routine tasks with little or no supervision. Able to provide directions to others within the team. Confident in making decisions for non-routine issues. Develops and revises procedures. Intermediate to advanced ability to interpret results and situations and articulate recommendations for resolution. Able to prepare written communications and communicate problems to management with clarity and accuracy. Able to effectively multi-task. Knowledge of US and global cGMP requirements. Supervisory experience highly preferred. High School Degree required. Relevant college or university degree preferred. Minimum 6+ years relevant work experience, with at least 3 years in a Quality Assurance role. Equivalent combination of education and experience acceptable.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137463608578", "isPrivate": false, "custom_data": {"location": "Devens - MA - US", "RequisitionID": "R1584730", "canonical_title": "Shift Manager", "straight_line_distance": null}}, {"id": 137465147108, "name": "Senior Specialist, Lot Disposition Scheduling and Review", "location": "Summit West - NJ - US", "locations": ["Summit West - NJ - US"], "hot": 0, "department": "Cell Therapy", "business_unit": "Global Product Development & Supply", "t_update": 1732193420, "t_create": 1732147200, "ats_job_id": "R1587616", "display_job_id": "R1587616", "type": "ATS", "id_locale": "R1587616-zh-CN", "job_description": "Manage multiple, low to medium complexity process improvement and/or technical projects. Effectively manage team meetings, including the scheduling of meetings, the preparation of agendas, the development of meeting minutes, and the follow up on action items. Serve as a member of sub-teams, tracking timelines elements to ensure that functional deliverables are completed on time and according to relevant quality standards. Develop critical path analyses with the team to understand risks and opportunities within project timelines and help develop contingency plans. Responsible for the preparation of routine status reports and communicate project progress to stakeholders. Lead operational projects including weekly huddles, operations planning and management and monitoring tools. Ensure that team recommendations related to project direction and timelines which need endorsement by governance teams are planned for review at appropriate milestones. Manage a team or supporting functions including scheduling and technical writing. Promote a culture of collaboration, cooperation, execution excellence, effective communication, and cross-functional problem-solving to enable a high-performing team. Develop and implement KPI and reporting capabilities. Collaborate with IT Business Partners in support of modeling, scheduling simulation implementations and automated scheduling tools. Perform review and ensure data completion prior to lot release. Serve as the point of contact between QA Disposition and scheduling, QC, QA, and MO operations. Meticulous attention to detail to ensure right first time and compliant release and certificate issuance. Current on industry standards as it applies to cGMPs, global regulatory guideline requirements, and departmental requirements. Executes Disposition activities in alignment with all pertinent SOPs. Ensures pertinent SOPs are available and present when executing disposition tasks. Ensures product quality and compliance by enforcing quality assurance policies and procedures; ensures the required processes, procedures, and resources are adhered to while performing responsibilities. Knowledge of US and global cGMP requirements. Advanced knowledge and experience with cGMP manufacturing, quality, and compliance to make appropriate decisions as needed. Obtains all required accesses needed to perform tasks with minimal delay. Action-oriented and customer-focused, skilled in decision-making, building relationships, problem solving, conflict management, and critical thinking. Work is self-directed and requires little to no direction to complete tasks by following work practices, lists, forms, and/or procedures. Skilled in organizing daily tasks, decision-making, and building relationships. Able to adapt as required to support departmental and site wide initiatives. Capable of independently troubleshooting complex situations utilizing all available sources of guidance. Excellent verbal and written skills to prepare clear and concise communications including communication to senior management. Supports and/ or leads continuous improvement initiatives to drive efficiency and productivity within the group and/or site. Responsive in forms of communications. Ability to work independently. Ability to matrix manage cross functional teams. Must be competent in Project Management tools and methodologies. Excellent organizational and time management skills. Experience with regulated GMP environment for manufacturing (Biologics or Cell Therapy experience is a plus). Strong analytical, problem-solving, and critical thinking skills. High attention to detail skills. High organization skills with ability to multi-task several objectives in parallel. People and project management skills. Advanced proficiency in MS Office applications. Proficient written and verbal communication skills. Ability to develop and provide training on various functions. Bachelor's degree required. An equivalent combination of education, experience and training may be considered. 5+ years relevant work experience required, within a regulated pharmaceutical manufacturing environment. PMP certification desirable. Experience in biopharmaceutical clinical, supply chain, manufacturing, and commercialization.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137465147108", "isPrivate": false, "custom_data": {"location": "Summit West - NJ - US", "RequisitionID": "R1587616", "canonical_title": "Senior Specialist", "straight_line_distance": null}}, {"id": 137465147867, "name": "NP-PA Clinical Specialist- San Francisco", "location": "San Francisco - CA - US", "locations": ["San Francisco - CA - US", "Oakland - CA - US"], "hot": 0, "department": "Not Applicable", "business_unit": "Commercialization", "t_update": 1732207461, "t_create": 1732147200, "ats_job_id": "R1587658", "display_job_id": "R1587658", "type": "ATS", "id_locale": "R1587658-zh-CN", "job_description": "Works with their team of peers and other matrix counterparts to deliver on goal expectations, provide strong Dermatology presence and education, ensure flawless execution, and build a winning culture Demand generation of the national target base of Dermatology NPs and PAs Face to face calls on target list of NPPA Influencers within specific market (unbranded and branded) Conduct in office and out of office appts as needed to best meet the needs of the Dermatology APP community Responsible for organizing and staffing National/Regional congresses as well as local/regional societies and other misc. opportunities Responsibility at congresses to support needs of all APP's in attendance Garners insights and meets the needs of the APP Dermatology community Work with a dynamic matrix team to help address customer needs and ensure we deliver on our objective of demonstrating value to our customers Collaborate with other field associates to ensure a one team approach in the Dermatology offices Adhere and showcase BMS core values and principles, practice and implement the strongest of integrity principles Input on opportunities with a solution focused mindset of driving innovation Meet or exceed sales goals, maximize promotional budgets, and execute the national sales and brand strategy in accordance with BMS polices Interpret and integrate data to develop communication strategies to drive performance and execution within the role Develop, review, and modify territory-level business plans ensuring alignment with national plans Develop, maintain and grow customer touchpoints Innovate and identify new ways to build brand equity to exceed our short and long-term goals, ensuring all legal and compliance regulations are adhered to Serve as a role model for Compliance and hold each member of the team accountable for Compliance by ensuring all practices within the team are compliant with the BMS Compliance Code of Conduct, PhRMA Code, OIG Guidelines, PDMA Policies and Procedures and all other applicable laws, regulations, policies & procedures. Minimum of 2 years of in practice NP/PA experience in the injectable or biologic arena. Immunology experience (emphasis on Dermatology, Rheumatology or Gastroenterology) Bachelor's Degree or equivalent Past or current Physician Assistant (PA)/Nurse Practitioner (NP) certification required. *Does not need to keep certification active to remain in role. Ability to travel up to 50% of the time including some weekend conferences Knowledge of pharmaceutical marketplace and the governing rules and laws. Possess a strong understanding of Commercial payers, Medicare plans and state Medicaid in geography. Background of guiding and influencing others Industry experience Working knowledge of the psoriasis market, geographic conditions, customer base Understanding of environmental and industry trends, and impact on business", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137465147867", "isPrivate": false, "custom_data": {"location": "San Francisco - CA - US", "RequisitionID": "R1587658", "canonical_title": "Clinical Specialist", "straight_line_distance": null}}, {"id": 137465148538, "name": "Senior Manager, Project Management, Global Drug Development IT", "location": "Princeton LVL - NJ", "locations": ["Princeton LVL - NJ"], "hot": 0, "department": "Not Applicable", "business_unit": "Information Technology", "t_update": 1732216499, "t_create": 1732147200, "ats_job_id": "R1587662", "display_job_id": "R1587662", "type": "ATS", "id_locale": "R1587662-zh-CN", "job_description": "Ability to understand the needs of the business and commitment to deliver the best stakeholder experience Experience working with Clinical Trial Execution related applications Experience working in CDE related technology solution management and implementation (e.g. Electronics Data Capture (EDC), Clinical Data Management & Reporting, Clinical Metadata Management, Clinical Biostatistics & Analytics etc.) Must have knowledge of the Software Development Lifecycle (SDLC) in Pharma industry along with working knowledge of the PMI Project Management Body of Knowledge (PMBOK). Requires advanced knowledge applicable to a wide range of work in own function and thorough knowledge of other functions, typically gained through a university degree and/or 6 plus years of relevant experience. Demonstrated experience leading initiatives related to continuous improvement or implementation of new technologies. Demonstrated ability to build and leverage relationships through diplomacy with a broader focus within the Function.\u200b Demonstrated ability to articulate and present complex information clearly and concisely across all levels. Skilled in stakeholder management and collaborative decision making and has ability to bring a variety of strong views and perspective to achieve objectives. \u200b Experienced in process improvement. Has lead analysis of current states, deliver strong recommendations in understanding complexity in the environment, and the ability to execute to bring complex solutions to completion.\u200b Ability to recognize the potential impact on internal/external challenges on the future state success. Conveys and takes immediate action to correct any variation in quality, ensures accuracy and completeness of others' work outputs.\u200b Demonstrated analytical thought using various data sources and internal/external environment. Understands the broader implications of actions and perspective. Synthesizes results and links patterns and trends. Considers lessons learned and best practices in conveying to the team's understanding and knowledge.\u200b Experience with software development methodologies and requirements-gathering techniques such as Agile (Scrum, SAFe, etc.) and Waterfall is preferred. Experienced in development of project structures, defining team roles and responsibilities, working with and leveraging various different staffing/sourcing models including the oversight of system integrators. Competence in business case development, definition of business outcomes and measuring outcome realization. Execute on assigned projects supporting the Digital Capability (DC) objectives of GDD IT, delivering value faster, in an incremental fashion. Ensure project deliverables, schedules, and financials adhere to established standards and are managed in alignment with BMS Project Management best practices across their assigned projects. Advise and consistently apply Project Management best practices (including Agile, SDLC and PMF) and tools. Collaborate with product managers and technical leads & Portfolio Managers on business case development for investments, translating experience & insights into improved estimates and outcomes.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137465148538", "isPrivate": false, "custom_data": {"location": "Princeton LVL - NJ", "RequisitionID": "R1587662", "canonical_title": "Senior Manager Project Management", "straight_line_distance": null}}, {"id": 137465142501, "name": "Summer 2025 - Global Regulatory CMC- Cell Therapy Internship", "location": "Summit West - NJ - US", "locations": ["Summit West - NJ - US"], "hot": 0, "department": "Intern", "business_unit": "Unknown", "t_update": 1732119610, "t_create": 1732060800, "ats_job_id": "R1587607", "display_job_id": "R1587607", "type": "ATS", "id_locale": "R1587607-zh-CN", "job_description": "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. 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. Position Summary The intern will be based in Summit, NJ and will assist the Regulatory-CMC Cell Therapy team with projects to support department goals and objectives. Key Responsibilities Support Regulatory CMC Cell Therapy group in the preparation of CMC Regulatory Strategy and submissions and interactions with Global Health Authorities. Attend and participate in various Reg CMC and matrix team meetings as needed and applicable Manage and prioritize multiple complex projects Qualifications & Experience Graduate student in a Life Sciences Program such as Chemical and Biochemical Engineering, Biomedical Engineering, Molecular Biology, Biochemistry Knowledge of protein synthesis, purification, characterization (SDS-PAGE, Western Blots, Elisa, etc.) Knowledge of cell culture, cell-based assays, flow cytometry is strongly desired Attention to detail, excellent organization skills, good verbal and written communication skills are required. Ability to work independently on routine assignments with daily check-ins and to work cooperatively with senior staff providing key assistance on complex assignment Computer experience must include familiarity with Word, Excel and PowerPoint 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 \u201cTransforming patients' lives through science\u2122 \u201d, 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 an inclusive culture, promoting diversity 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 Protocol BMS has a diverse 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 adastaffingsupport@bms.com. 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: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137465142501", "isPrivate": false, "custom_data": {"location": "Summit West - NJ - US", "RequisitionID": "R1587607", "canonical_title": "Internship", "straight_line_distance": null}}, {"id": 137465143934, "name": "Senior Manager, WW Neuropsychiatry Medical Communications", "location": "Princeton - NJ - US", "locations": ["Princeton - NJ - US", "Madison - Giralda - NJ - US"], "hot": 0, "department": "Not Applicable", "business_unit": "Commercialization", "t_update": 1732135060, "t_create": 1732060800, "ats_job_id": "R1587584", "display_job_id": "R1587584", "type": "ATS", "id_locale": "R1587584-zh-CN", "job_description": "The Senior Manager of Medical Communications 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, Worldwide (WW) Medical and medical market-level strategy Serves as the Medical Communications point of contact between WW/ and other matrix partners Additional content related activities that are required to support the medical communications team, as needed. High performing, externally focused which emphasizes teamwork, cooperation, personal accountability, and a commitment to quality; models BMS behaviors and reinforces such behaviors at all levels in the organization Serve as mentor to other leads. Ensure preparation for audit and inspection readiness Ensuring diversity and inclusion in decision making, organization and talent development The Senior Manager of Medical Communications 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, Worldwide (WW) Medical and medical market-level strategy Serves as the Medical Communications point of contact between WW/ and other matrix partners Provides medical communications management oversight Enhances bi-directional communication by understanding and sharing the WW medical communications plans to Medical and raises needs to WW Medical/Medical Communications teams, ensuring country/global level of awareness & connectivity including vendor oversight. Understand the communication needs and own the pull-through and execution of the Scientific Narrative, development & execution of functionally integrated publication plan, content plan, and application to the Scientific Communication Platform (SCP). Must have strong business acumen, ability to interface with market matrix partners & manage Medical Communications budget Ensures collection of insights to deliver high quality medical communication that enables the most impactful dialogue and interactions with customers. Establishes clear metrics aligned & regularly communicates metrics with key medical stakeholders Additional content related activities that are required to support the medical communications team, as needed. High performing, externally focused which emphasizes teamwork, cooperation, personal accountability, and a commitment to quality; models BMS behaviors and reinforces such behaviors at all levels in the organization Serve as mentor to other leads. Ensure preparation for audit and inspection readiness Ensuring diversity and inclusion in decision making, organization and talent development Advance scientific degree, PharmD, PhD or MD preferred 5+ years of Pharmaceutical/Healthcare industry experience with a focus on medical communications; experience in both local country & global preferred Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate and collaborate Experience working cross-functional, with cross-cultural project teams, and collaborating across matrix, markets and global geographies Proven ability to work in an ambiguous environment & demonstrated success driving optimal business results in a large complex corporate environment with multiple priorities and tight timelines Ability to manage timelines and quality of work using strong leadership, organizational, communication, facilitation and interpersonal skills Outstanding interpersonal, written, and verbal communication skills with exceptional time management skills Experience leading medical communications across all phases of drug development and commercialization Ability to analyze and interpret trial data Ability to influence and negotiate appropriate solutions; ability to establish strong stakeholder relationships Ability to flexibly schedule and participate in teleconferences and virtual meetings across different time zones Pharmaceutical/Healthcare Industry External compliance, transparency and conflict-of-interest regulated work environments In-depth knowledge of Good Publication Practices and guidance (GPP, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication Certified Medical Publication Professional (CMPP), and ISMPP active member highly desired Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements Working knowledge of Microsoft suite of applications, and familiar with publication management tool (DataVision/iEnvision). LI-Hybrid Position: Senior Manager, WW Medical Neuropsychiatry Medical Communications Advance scientific degree, PharmD, PhD or MD preferred 5+ years of Pharmaceutical/Healthcare industry experience with a focus on medical communications; experience in both local country & global preferred Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate and collaborate Experience working cross-functional, with cross-cultural project teams, and collaborating across matrix, markets and global geographies Proven ability to work in an ambiguous environment & demonstrated success driving optimal business results in a large complex corporate environment with multiple priorities and tight timelines Ability to manage timelines and quality of work using strong leadership, organizational, communication, facilitation and interpersonal skills Outstanding interpersonal, written, and verbal communication skills with exceptional time management skills Experience leading medical communications across all phases of drug development and commercialization Ability to analyze and interpret trial data Ability to influence and negotiate appropriate solutions; ability to establish strong stakeholder relationships Ability to flexibly schedule and participate in teleconferences and virtual meetings across different time zones Ability to travel (domestically and internationally) Pharmaceutical/Healthcare Industry External compliance, transparency and conflict-of-interest regulated work environments In-depth knowledge of Good Publication Practices and guidance (GPP, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication Certified Medical Publication Professional (CMPP), and ISMPP active member highly desired Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements Working knowledge of Microsoft suite of applications, and familiar with publication management tool (DataVision/iEnvision).", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137465143934", "isPrivate": false, "custom_data": {"location": "Princeton - NJ - US", "RequisitionID": "R1587584", "canonical_title": "Senior Manager Communications", "straight_line_distance": null}}, {"id": 137465144214, "name": "Director, Cell Therapy Supply Chain Strategy & Business Operations", "location": "Summit West - NJ - US", "locations": ["Summit West - NJ - US", "Seattle - WA - US", "Devens - MA - US"], "hot": 0, "department": "Cell Therapy", "business_unit": "Global Product Development & Supply", "t_update": 1732139735, "t_create": 1732060800, "ats_job_id": "R1587614", "display_job_id": "R1587614", "type": "ATS", "id_locale": "R1587614-zh-CN", "job_description": "Strategy & Business planning: leads cascade of yearly business calendar processes for Cell Therapy SC pillars Strategic planning process: coordinate the strategy cascade, ensure resources and priorities are aligned Goals & Objective and KPI definition and target setting Portfolio business planning: monitors and sustains the book of work and roadmap of Project and initiatives Financial budget and projections cycles Leads and supports the Cell Therapy SC pillars governance Ensure adequate KPI dashboards and performance reviews, highlighting trends and risks, define recommendations for improvement and tracking progress as required Monitors progress on Goals & Objectives Prepare and facilitate Cell Therapy SC and LT meetings Leads and coordinates consistent and adequate Cell Therapy SC change and culture initiatives for the pillars in collaboration with the functions' leadership teams Coordinate content coordination and deployment for all communication channels (newsletter, townhall, engagement sessions ), define and provide input to the Cell Therapy SC-wide communication Leads and/or coordinates culture, learning and change initiatives Promotes high standards for organizational efficiency, transparency throughout the organization in strong collaboration within the team, the leadership, and the stakeholders Identifies continuous improvement opportunities, initiates, and leads improvement initiatives, establishes, and maintains best practices and fit for purpose approaches Ensures fit-for-purpose adoption and connectivity with GPS S&BE and the Cell Therapy and GSC functions Participates in the Cell Therapy SC Strategy & Business Operations Community of Practice Strategy & Business planning: leads cascade of yearly business calendar processes for Cell Therapy SC pillars Strategic planning process: coordinate the strategy cascade, ensure resources and priorities are aligned Goals & Objective and KPI definition and target setting Portfolio business planning: monitors and sustains the book of work and roadmap of Project and initiatives Financial budget and projections cycles Ensure adequate KPI dashboards and performance reviews, highlighting trends and risks, define recommendations for improvement and tracking progress as required Prepare and facilitate Cell Therapy SC and LT meetings Coordinate content coordination and deployment for all communication channels (newsletter, townhall, engagement sessions ), define and provide input to the Cell Therapy SC-wide communication Ensures fit-for-purpose adoption and connectivity with GPS S&BE and the Cell Therapy and GSC functions Participates in the Cell Therapy SC Strategy & Business Operations Community of Practice Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick Is an ambassador for Cell Therapy Global Supply Chain and the function they represent Enables rapid decision-making by removing barriers, setting clear priorities, and streamlining processes; provides the relevant information, resources and tools that enable others to own decisions and take action. Creates a safe space for speaking truth and idea generation; encourages constructive disagreement and creative debate; celebrates both go and no-go decisions; values individuals that flag risks or present efficiencies even if they result in a change of course. Acts as a coach to the shared resources Creates strong partnerships with the stakeholders Collaboration and support: Has a deep understanding of many facets of the Cell Therapy SC pillars, including the operations, operating model, mission, needs, systems and tools, and stakeholder ecosystem involved in Cell Therapy SC pillars Able to leverage expertise/understanding of Cell Therapy GSC functions to work autonomously / using best practices to effectively and flexibly support Cell Therapy in a multitude of critical areas Remains up to date on digital solutions, such as emerging systems or tools, that can be adopted to continuously improve existing processes May act as a back-up for his peers Bachelor's degree required in engineering, supply chain or business with a Masters or MBA preferred. Minimum of 7 years of experience in operations, supply chain, preferably in the biopharma industry Excellent verbal, written and interpersonal communication skills at all levels of the organization; excellent presentation skills, both material creation and delivery Demonstrated learning agility; ability to adapt in an agile way as required Ability to set and deliver results in dynamic, rapidly evolving environments; ability to think critically about issues and understand context and likely challenges; ability to balance strategic awareness & direction setting with consistent tactical results Ability to closely monitor execution of plans, measure of results and correct deviations, as appropriate Strong problem solving, negotiating and decision-making skills; ability to implement decisions quickly Good clarity of judgement and effective at implementation of solutions. Decisively confronts and resolves issues. Shows courage. Works constructively under pressure. Good planning, analytical, time management and organizational skills Self-motivated and comfortable working alone or as part of a larger team Capability to build effective partnership and relationship in a matrix organization Creates a climate that fosters personal investment and excellence, nurtures commitment to common goals Financial management exposure, awareness, and strong acumen Ability to work in a fast-paced environment, organized and able to prioritize execution activities to meet multiple deadlines Demonstrated experience in developing, aligning, socializing, monitoring, adapting, and delivering strategies in dynamic, rapidly changing environments Demonstrated Operational Excellence and Continuous Improvement skill set and delivery Experience working with numerous systems and tools to enable digital success; up-to-date on emerging technology and able to quickly adapt to new digital ways of working / systems The starting compensation for this job based in the Washington area is a range from $194,000 - $242,000, plus incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Career Site. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick Is an ambassador for Cell Therapy Global Supply Chain and the function they represent Enables rapid decision-making by removing barriers, setting clear priorities, and streamlining processes; provides the relevant information, resources and tools that enable others to own decisions and take action. Creates a safe space for speaking truth and idea generation; encourages constructive disagreement and creative debate; celebrates both go and no-go decisions; values individuals that flag risks or present efficiencies even if they result in a change of course. Acts as a coach to the shared resources Creates strong partnerships with the stakeholders Bachelor's degree required in engineering, supply chain or business with a Masters or MBA preferred. Minimum of 7 years of experience in operations, supply chain, preferably in the biopharma industry Excellent verbal, written and interpersonal communication skills at all levels of the organization; excellent presentation skills, both material creation and delivery Demonstrated learning agility; ability to adapt in an agile way as required Ability to set and deliver results in dynamic, rapidly evolving environments; ability to think critically about issues and understand context and likely challenges; ability to balance strategic awareness & direction setting with consistent tactical results Ability to closely monitor execution of plans, measure of results and correct deviations, as appropriate Strong problem solving, negotiating and decision-making skills; ability to implement decisions quickly Good clarity of judgement and effective at implementation of solutions. Decisively confronts and resolves issues. Shows courage. Works constructively under pressure. Good planning, analytical, time management and organizational skills Self-motivated and comfortable working alone or as part of a larger team Capability to build effective partnership and relationship in a matrix organization Creates a climate that fosters personal investment and excellence, nurtures commitment to common goals Financial management exposure, awareness, and strong acumen Ability to work in a fast-paced environment, organized and able to prioritize execution activities to meet multiple deadlines Demonstrated experience in developing, aligning, socializing, monitoring, adapting, and delivering strategies in dynamic, rapidly changing environments Experience working on and leading global teams Demonstrated Operational Excellence and Continuous Improvement skill set and delivery Experience working with numerous systems and tools to enable digital success; up-to-date on emerging technology and able to quickly adapt to new digital ways of working / systems", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137465144214", "isPrivate": false, "custom_data": {"location": "Summit West - NJ - US", "RequisitionID": "R1587614", "canonical_title": "Director Supply Chain Operations", "straight_line_distance": null}}, {"id": 137465143479, "name": "Release Manager, QA Disposition", "location": "Summit West - NJ - US", "locations": ["Summit West - NJ - US"], "hot": 0, "department": "Cell Therapy", "business_unit": "Global Product Development & Supply", "t_update": 1732126698, "t_create": 1732060800, "ats_job_id": "R1587565", "display_job_id": "R1587565", "type": "ATS", "id_locale": "R1587565-zh-CN", "job_description": "Meticulous attention to detail to ensure right first time and compliant release and certificate issuance. Current on industry standards as it applies to cGMPs, global regulatory guideline requirements, and departmental requirements. Executes Disposition activities in alignment with all pertinent SOPs. Ensures pertinent SOPs are available and present when executing disposition tasks. Ensures product quality and compliance by enforcing quality assurance policies and procedures; ensures the required processes, procedures, and resources are adhered to while performing responsibilities. Knowledge of US and global cGMP requirements. Advanced knowledge and experience with cGMP manufacturing, quality, and compliance to make appropriate decisions as needed. Obtains all required accesses needed to perform tasks with minimal delay. Action-oriented and customer-focused, skilled in decision-making, building relationships, problem solving, conflict management, and critical thinking. Work is self-directed and requires little to no direction to complete tasks by following work practices, lists, forms, and/or procedures. Skilled in organizing daily tasks, decision-making, and building relationships. Able to adapt as required to support departmental and site wide initiatives. Capable of independently troubleshooting complex situations utilizing all available sources of guidance. Excellent verbal and written skills to prepare clear and concise communications including communication to senior management. Supports and/ or leads continuous improvement initiatives to drive efficiency and productivity within the group and/or site. Responsive in forms of communications. Relays disposition status in a timely manner in all required platforms. Leads projects as required by senior management. Compiles metrics for presentation to senior management as required. Writes, reviews and updates SOPs as required. Recognized as Subject Matter Expert within the group. Additional tasks as instructed by management. Work is performed in a typical office environment, with standard office equipment available and used. Work is generally performed seated but may require standing and walking for up to 10% of the time. Detail oriented with strong knowledge of cGMP regulations, regulatory guidelines applicable to biologics and cell therapy. Must be able to interpret problems and effectively communicate with clarity, brevity, and accuracy to peers and leadership. Must be skilled in planning, organizing, conflict management, and innovation management. Contributes to departmental performance and quality initiatives; able to conceptualize impact of quality initiatives in terms of cross-functional teams; emerging as a leader contributing to BMS culture and values. Requires minimal direction to completes tasks, able to obtain resources and information from established internal sources; consults with senior management for complex decisions outside established processes. Routinely recognizes and independently resolves complex quality issues; informs senior management of proposed solutions. Drives solution implementation. Able to interpret complex results and situations with degree of independence and articulate recommendations for solutions. Effectively communicates internally within the function and with internal and external cross-functional teams. Represents department in internal and external cross-functional teams. Manages conflict and issues with internal and external customers. Mentors junior Disposition team members Bachelor's degree required. Equivalent combination of education and experience acceptable. 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