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": 1733259828, "t_create": 1724112000, "ats_job_id": "R1584730", "display_job_id": "R1584730", "type": "ATS", "id_locale": "R1584730-ms", "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": 137465272499, "name": "Senior Scientist / Principal Scientist, Drug Product Development", "location": "New Brunswick - NJ - US", "locations": ["New Brunswick - NJ - US", "Summit West - NJ - US"], "hot": 0, "department": "Not Applicable", "business_unit": "Global Product Development & Supply", "t_update": 1733669283, "t_create": 1733443200, "ats_job_id": "R1588047", "display_job_id": "R1588047", "type": "ATS", "id_locale": "R1588047-ms", "job_description": "The Senior Scientist or Principal Scientist will collaborate across BMS sites with Drug Product, Analytical, API, Quality, and Regulatory functions to execute drug product formulation/process development, formulation strategies, control strategies, and support of drug application submissions and approval. Key member of a dynamic scientifically driven team, dedicated to the design, development, and characterization of robust small molecule drug product formulations. Develop oral formulations for clinical studies and commercialization. Lead drug product formulation and process development including evaluating the need and potential for enhancing oral bioavailability, stability, and processability of drug candidates through appropriate formulation strategies. Support preparation of CMC regulatory documents. Support departmental initiatives for assigned projects and methodologies. Maintain safety, regulatory, and compliance standards as they relate to the development of pharmaceuticals. Prepare technical reports, batch records, SOPs, publications, and oral presentations as required. Collaborate with cross-functional team members to develop and optimize formulations and enable technology transfer to CMOs and other sites for manufacturing and scale up activities. Develop, coach and mentor others as appropriate for the position. Senior Scientist: Completed BS in Pharmaceutical Science, Chemical Engineering, or related discipline with 7-9 years of pharmaceutical development experience; MS with 4-6 years of experience; or Ph.D. with 2-4 years of experience. Experienced in formulation development, pharmaceutical processing related to drug product development and hands on experience. Fundamental understanding of drug substance, excipients, pharmaceutical unit operations (blending, milling, sieving, granulation, tableting, encapsulation, coating, spray drying), intermediate and critical quality attributes, statistics, risk assessment approaches, and cGMP principles. Experienced in building the CMC dossier for regulatory submissions within the development section as an author/reviewer. Basic knowledge of regulatory requirements. Demonstrated problem-solving and troubleshooting skills. Strong capabilities in experimental design and execution. Ability to work independently. Ability to provide leadership, guidance, and training to others within the department. Strong verbal and written communication skills. Strong interpersonal skills and the ability and interest to serve as a team member/leader in an environment where individual initiative, collaboration, and accountability are valued.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137465272499", "isPrivate": false, "custom_data": {"location": "New Brunswick - NJ - US", "RequisitionID": "R1588047", "canonical_title": "Senior Principal Scientist", "straight_line_distance": null}}, {"id": 137465272508, "name": "Senior Principal Scientist, Drug Product Development", "location": "New Brunswick - NJ - US", "locations": ["New Brunswick - NJ - US", "Summit West - NJ - US"], "hot": 0, "department": "Not Applicable", "business_unit": "Global Product Development & Supply", "t_update": 1733670820, "t_create": 1733443200, "ats_job_id": "R1588034", "display_job_id": "R1588034", "type": "ATS", "id_locale": "R1588034-ms", "job_description": "The Senior Principal Scientist will collaborate across BMS sites with Drug Product, Analytical, API, Quality, and Regulatory functions to execute drug product formulation/process development, formulation strategies, control strategies, and support of drug application submissions and approval. Key member of a dynamic scientifically driven team, dedicated to the design, development, and characterization of robust small molecule drug product formulations. Develops oral formulations for clinical studies and commercialization. Leads drug product formulation and process development including evaluating the need and potential for enhancing oral bioavailability, stability, and processability of drug candidates through appropriate formulation strategies. Represents the organization as prime technical contact requiring cross-functional coordination inside and outside the department or company. Acts as a technical point of contact, or SME within own group as well as other departments; trains others. Leads / supports preparation of CMC regulatory documents. Leads initiatives related to continuous improvement or development of new approaches/technologies within or across departments/functions. Maintains safety, regulatory, and compliance standards as they relate to the development of pharmaceuticals. Prepares / reviews technical reports, batch records, SOPs, publications, and oral presentations as required. Required: Completed BS in Pharmaceutical Science, Chemical Engineering, or related discipline with 12-15 years of pharmaceutical development experience; MS with 9-12 years of experience; or Ph.D. with 6-8 years of experience. Experienced in oral formulation development on multiple projects and for different clinical phases, with hands on experience. Advanced understanding of drug substance, excipients, pharmaceutical unit operations (blending, milling, sieving, granulation, tableting, encapsulation, coating, spray drying), intermediate and critical quality attributes, statistics, risk assessment approaches, and cGMP principles. Experienced in building the CMC dossier for regulatory submissions within the development section as an author/reviewer. Strong knowledge of regulatory requirements. Demonstrated problem-solving and troubleshooting skills. Strong capabilities in experimental design and execution. Ability to multitask and work independently. Ability to provide leadership, guidance, and training to others within the department. Strong verbal and written communication skills. Strong interpersonal skills and the ability and interest to serve as a team member/leader in an environment where individual initiative, collaboration, and accountability are valued. Organizational and interdepartmental responsibilities with regards to leading workgroups, cross-functional teams, strategy development/ implementation/execution, and cultural initiatives. Experience in oral formulation commercialization.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137465272508", "isPrivate": false, "custom_data": {"location": "New Brunswick - NJ - US", "RequisitionID": "R1588034", "canonical_title": "Senior Principal Scientist", "straight_line_distance": null}}, {"id": 137465264563, "name": "Senior Manager, GPS BIT Data and Analytics Delivery, Product Development Data Enablement", "location": "New Brunswick - NJ - US", "locations": ["New Brunswick - NJ - US"], "hot": 0, "department": "Not Applicable", "business_unit": "Information Technology", "t_update": 1733502048, "t_create": 1733443200, "ats_job_id": "R1588036", "display_job_id": "R1588036", "type": "ATS", "id_locale": "R1588036-ms", "job_description": "Manage projects related to Data and Analytics and Data Products development. Solution architect to design and model new data enablement projects to enable analysts and scientists' team to take out some insights from data. Based on design and model lead the projects and perform end to end delivery Lead requirement gathering discussions with business to understand the business challenges and provide solution. Technical point of contact for AWS services and helps/support technical team to resolve technical issues. Collaborate to innovate new solutions in Data Integration and enablement space Review code built by technical team, provide code review feedback, fix issues in the code. Provide technical support to end users to resolve issues specific to AWS services ie Athena, and other AWS services. Evaluate emerging technologies in data and analytics area, perform technical pilots if necessary and share read out with leadership team. Keep track on project financials to ensure project is delivered within budget and timeline. Gather Data Products requirement based on requirement come up with design models for Data products. Build and deploy Data Products in higher environments in AWS marketplace. Own and maintain git repository for code base. Lead implementation of GxP (validated) projects. Technical SME to operate and develop data and analytics focused capabilities in support of the Product Development Data Enablement BIT Organization Build Data Products using AWS Services ie Glue Studio, Anthea, AWS Marketplace and own these data products. Build awareness of the technology platform strategy and lead releases and make technical recommendations across the data ecosystem. Ability to setup data ingestion pipelines in GPS datalakes using AWS services ie glue studio, S3, Lambda Hands on experience in Python, AWS Redshift/S3/ RDS/Athena, Native AWS Services, Database design and familiarity with Domino/data lake principles Hands on experience to build dashboards using Tableau/Spotfire Establish and maintain relationships with key stakeholders to understand requirements for enhancements or prototypes. Provide effort and cost estimations when required to scale prototypes. Come up with automation, innovation ideas and implement them in dataakes Experience working in Offshore/Onshore model. Prior experience in global life sciences especially in the GPS functional area will be a plus Priori experience in Cloud technologies - preferably AWS and related capabilities such as storage, compute, catalogue, data virtualization will be a huge plus Prior experience working in jira Experience working internationally with a globally dispersed team including diverse stakeholders ie offshore technical development team(s) Strong communication and presentation skills Bachelor's degree in computer science, Information Systems, Computer Engineering or equivalent is preferred. Project Management (PMP) and / OR ITIL Service Management certification is a plus", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137465264563", "isPrivate": false, "custom_data": {"location": "New Brunswick - NJ - US", "RequisitionID": "R1588036", "canonical_title": "Senior Manager Product Development", "straight_line_distance": null}}, {"id": 137465266190, "name": "Manager, QA Engineering", "location": "Warren - NJ", "locations": ["Warren - NJ"], "hot": 0, "department": "Cell Therapy", "business_unit": "Global Product Development & Supply", "t_update": 1733514756, "t_create": 1733443200, "ats_job_id": "R1588043", "display_job_id": "R1588043", "type": "ATS", "id_locale": "R1588043-ms", "job_description": "70% of the workload: Responsible for the approval of all facility and utility related plans and qualification documents with a focus on compliance with regulatory and BMS policy. 30% of the workload: Functional responsibilities include providing QA oversight of the site aseptic program including contamination control strategy, gowning, environmental monitoring, aseptic process validations / media simulations, quality culture, cleaning and disinfectants with applicable procedures. Ensuring accurate and timely maintenance of validation and qualification documents for all facility activities and design; investigations and evaluation of change control and supports Quality Risk Management program activities at the site. Assures appropriateness of validation plans, qualification protocols, associated reports and procedures. Support ECQ and Facilities related investigations in ensuring appropriate and thorough impact assessment, root cause analysis and corrective/preventive actions are documented and implemented. Ensures compliance with the site validation master plan, assist with facility start-up operations and product transfers supporting the Qualification and Validation teams. Work with Engineering/Facilities/ECQ management to ensure functional activities comply with global regulatory requirements. Provide Quality guidance on the environmental monitoring program including EM risk assessments, EM Performance Qualifications, Re-qualifications, etc. Provide input to the gowning, aseptic training, aseptic techniques and behaviors, aseptic process validations / media simulations, aseptic risk assessment. Sponsor and support the change initiatives and the implementation of process improvement initiatives. Ensure site is compliant with global and regulatory data governance and data integrity requirements. Support any other goals and objectives of the site Quality Assurance organization, as needed. 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. B.S. degree required. Minimum of six years of experience in the pharmaceutical or related industry. Equivalent combination of education and experience acceptable. Must have knowledge and experience with cGMP, manufacturing, Quality and compliance, aseptic techniques and behaviors. Strong understanding of critical building & utility systems including life-safety, lighting, mechanical, electrical, plumbing, clean rooms, compressed gases, security, and site access. Strong knowledge of facility management systems, building automation, and computerized maintenance management systems (CMMS). General understanding of critical utility systems such as compressed gas, vacuum, and HVAC Knowledge of FDA & GMP regulations, IBC/IFC building codes, OSHA, NFP, FM, LPDS and UL. Experience in design of user requirement specifications, IQ/OQ/PQ protocols, user acceptance testing and other facility qualification documentation. Must be fluent in standard Microsoft Office software; experience in asset management software (e.g. Blue Mountain RAM) and quality systems software (e.g. Veeva). Must be able to recognize and group technical / scientific attributes and drive science-based decisions in most technical areas. Must manage development of technical or scientific initiatives and activities by interdisciplinary teams. Intermediate knowledge of quality systems including CAPA, change control, and document management systems. Requires minimal direction to complete tasks, authority to make daily decisions that impact their team. Negotiates solutions cross-functionally. Drives continuous improvement and improves efficiency and productivity within the group or project. Consults management for advice on complex issues. Able to prepare written communications and communicate problems to management with clarity and accuracy. Drive strong collaboration within the site and across the network. 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