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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: flex; align-items:center\"><a href=\"https://x.com/BMSNEWS\"><svg xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\" viewBox=\"0,0,256,256\" width=\"30px\" height=\"30px\"><g fill=\"#595454\" 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href=\"https://jobs.bms.com/careers?hl=th\">\u0e20\u0e32\u0e29\u0e32\u0e44\u0e17\u0e22</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=nl\">Nederlands</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=pl\">Polski</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=uk\">Y\u043a\u0440\u0430\u0457\u043d\u0441\u044c\u043a\u0430</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=hr\">Hrvatski</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=el\">\u0395\u03bb\u03bb\u03b7\u03bd\u03b9\u03ba\u03ac</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=hu\">Magyar</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=cs\">\u010de\u0161tina</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=tr\">T\u00fcrk\u00e7e</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=ru\">P\u0443\u0441\u0441\u043a\u0438\u0439</a>\n <a 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 <a href=\"https://careers.bms.com/search\" class=\"search-logo\"><svg xmlns=\"http://www.w3.org/2000/svg\"\n width=\"16\" height=\"16\" viewBox=\"0 0 17 17\" fill=\"none\">\n <path fill-rule=\"evenodd\" clip-rule=\"evenodd\"\n d=\"M12.1203 6.81017C12.1203 9.7429 9.7429 12.1203 6.81017 12.1203C3.87745 12.1203 1.5 9.7429 1.5 6.81017C1.5 3.87745 3.87745 1.5 6.81017 1.5C9.7429 1.5 12.1203 3.87745 12.1203 6.81017ZM11.066 12.1271C9.90016 13.0615 8.42043 13.6203 6.81017 13.6203C3.04902 13.6203 0 10.5713 0 6.81017C0 3.04902 3.04902 0 6.81017 0C10.5713 0 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 </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/life-at-bms\">Life at BMS <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 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 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/research-development\">Research & Development</a></div>\n <div><a href=\"https://careers.bms.com/global-product-development-supply\">Global Product\n Development & Supply</a></div>\n <div><a href=\"https://careers.bms.com/commercial-access\">Commercial & Access</a></div>\n <div><a href=\"https://careers.bms.com/corporate\">Corporate </a></div>\n <div><a href=\"https://careers.bms.com/military-veterans\">Military and Veterans</a></div>\n\n </div>\n <div class=\"mega-sub-menu-column\">\n <h5>QUICK LINKS</h5>\n <div><a href=\"https://careers.bms.com/advanced-degree-programs\">Advanced Degree Programs</a>\n </div>\n <div><a target=\"_blank\" href=\"https://www.bms.com/researchers-and-partners/areas-of-focus.html\">Areas of Focus</a>\n </div>\n <div><a target=\"_blank\" href=\"https://www.bms.com/researchers-and-partners/in-the-pipeline.html\">In the Pipeline</a>\n </div>\n <div><a 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 class=\"mega-sub-menu\">\n <div class=\"mega-sub-menu-title\">\n <h5><a href=\"https://careers.bms.com/student-opportunities\">Student Opportunities <span\n class=\"icon-right\"><svg xmlns=\"http://www.w3.org/2000/svg\" width=\"14\" height=\"10\"\n 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 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/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 4.31895 19.2933 9.64665C19.2933 12.0407 18.4212 14.2311 16.9774 15.9174L23.6819 22.6219L22.6212 23.6826L15.9166 16.978Z\"\n fill=\"white\" />\n </svg></span> Search this site </a>\n </div>\n <div class=\"header-moblie-box-wrapper\">\n <div class=\"talent-wrap-box\">\n <a href=\"https://jobs.bms.com/careers/join\" target=\"_blank\">Join Talent Community</a>\n </div>\n <div class=\"login-wrap-box\">\n <a href=\"https://bristolmyerssquibb.wd5.myworkdayjobs.com/en-US/BMS/login\" target=\"_blank\" class=\"candidate-link\">Candidate Login <span><svg xmlns=\"http://www.w3.org/2000/svg\" width=\"2\"\n height=\"11\" viewBox=\"0 0 2 11\" fill=\"none\">\n <path\n d=\"M0.56825 10.3355C0.38625 10.3355 0.28825 10.2375 0.28825 10.0415V0.395541C0.28825 0.199541 0.38625 0.101542 0.56825 0.101542H1.12825C1.31025 0.101542 1.40825 0.199541 1.40825 0.395541V10.0415C1.40825 10.2375 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href=\"https://jobs.bms.com/careers?hl=de\">Deutsch</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=ja\">\u65e5\u672c\u8a9e</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=ms\">Bahasa melayu</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=zh-CN\">\u4e2d\u6587 (\u7b80\u4f53)</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=zh-TW\">\u4e2d\u6587 (\u7e41\u9ad4)</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=ko\">\ud55c\uad6d\uc5b4</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=th\">\u0e20\u0e32\u0e29\u0e32\u0e44\u0e17\u0e22</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=nl\">Nederlands</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=pl\">Polski</a>\n <a target=\"_blank\" href=\"https://jobs.bms.com/careers?hl=uk\">Y\u043a\u0440\u0430\u0457\u043d\u0441\u044c\u043a\u0430</a>\n <a target=\"_blank\" 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Supported methods will include all aspects of aseptic drug product processing, including small molecules, biologics and cell therapy. Functions as subject matter expert for microbiological assays and aseptic manufacturing supporting the BMS organization. Provide specific strategic microbiology support to alternative methods in support of company ESG goals. Participation in site assessments/vendor selection for CMOs/vendor with Procurement, MS&T, Quality, and other business functions. May act as SME on Quality audit team for External manufacturing sites. Involved in troubleshooting issues and ensures that testing performed by external contract laboratories is technically sound and in compliance with BMS corporate, regulatory, quality and compliance expectations and requirements. Ensures inspection readiness of the Microbiology Operations laboratory in New Brunswick and globally for QC microbiology laboratories in the network. Supports the investigation and implementation of new technologies and methods for microbiological assays. Support complex investigations involving microbiological assays or issues, including generation of CAPAs and change controls. Provides support for the preparation, review and approval of microbiological methods and validation sections of regulatory filings, as well as responses to regulatory agency questions regarding sterile drug products produced by aseptic processing. Provides dedicated support and access to expertise for customers within the Manufacturing Science & Technology Parenteral manufacturing department, by regular communication with department members. Participate in internal and external industry forums to understand evolving regulatory expectations and industry best practices. Travel to other sites or educational conferences will be required (20%). Work is performed in a cGMP compliant laboratory following techniques which require one to maintain a high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous materials. Work may be required on weekdays, weekends, holidays, and during adverse weather conditions. Supported methods will include all aspects of aseptic drug product processing, including small molecules, biologics and cell therapy. Functions as subject matter expert for microbiological assays and aseptic manufacturing supporting the BMS organization. Provide specific strategic microbiology support to alternative methods in support of company ESG goals. Participation in site assessments/vendor selection for CMOs/vendor with Procurement, MS&T, Quality, and other business functions. May act as SME on Quality audit team for External manufacturing sites. Involved in troubleshooting issues and ensures that testing performed by external contract laboratories is technically sound and in compliance with BMS corporate, regulatory, quality and compliance expectations and requirements. Ensures inspection readiness of the Microbiology Operations laboratory in New Brunswick and globally for QC microbiology laboratories in the network. Supports the investigation and implementation of new technologies and methods for microbiological assays. Support complex investigations involving microbiological assays or issues, including generation of CAPAs and change controls. Provides support for the preparation, review and approval of microbiological methods and validation sections of regulatory filings, as well as responses to regulatory agency questions regarding sterile drug products produced by aseptic processing. Provides dedicated support and access to expertise for customers within the Manufacturing Science & Technology Parenteral manufacturing department, by regular communication with department members. Participate in internal and external industry forums to understand evolving regulatory expectations and industry best practices. Travel to other sites or educational conferences will be required (20%). Work is performed in a cGMP compliant laboratory following techniques which require one to maintain a high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous materials. Work may be required on weekdays, weekends, holidays, and during adverse weather conditions. Ph.D. with 8-12 years of experience or MS with 12-15 years of experience or BS with 15+ years experience with degree in Microbiology, Molecular Biology, Virology, or Biology/Biological Sciences. Advanced knowledge of regulations for pharmaceutical and biopharmaceutical drugs, including specific review or preparation of INDs, BLAs, NDAs, ANDAs or supplements. Motivated, adaptable, and results oriented professional Capable of mentoring junior staff Experience in the inspection process for US and international Heath Authorities. Experience in aseptic manufacturing plant(s) with regulatory interaction regarding sterilization practices and aseptic technique. Ability to build strong, trusting relationships, and work across divisions, diverse business backgrounds and cultures. Excellent communication and interpersonal skills with the ability to interface with a broad range of internal and external stakeholders at all levels of the organization. Involved in pharmaceutical industry professional groups and forums Experience interacting with senior leaders and being an influencer/negotiator Direct experience in Board of Health audits for biologic or pharmaceutical production Direct experience with writing CMC Drug Product sections of regulatory filings Experience in a network role across multiple sites in a pharmaceutical company Ph.D. with 8-12 years of experience or MS with 12-15 years of experience or BS with 15+ years experience with degree in Microbiology, Molecular Biology, Virology, or Biology/Biological Sciences. Advanced experience in pharmaceutical microbiology Advanced knowledge of regulations for pharmaceutical and biopharmaceutical drugs, including specific review or preparation of INDs, BLAs, NDAs, ANDAs or supplements. Motivated, adaptable, and results oriented professional Capable of mentoring junior staff Experience in the inspection process for US and international Heath Authorities. Experience in aseptic manufacturing plant(s) with regulatory interaction regarding sterilization practices and aseptic technique. Ability to build strong, trusting relationships, and work across divisions, diverse business backgrounds and cultures. Excellent communication and interpersonal skills with the ability to interface with a broad range of internal and external stakeholders at all levels of the organization. Involved in pharmaceutical industry professional groups and forums Experience with working in a matrix environment. Experience interacting with senior leaders and being an influencer/negotiator Direct experience in Board of Health audits for biologic or pharmaceutical production Direct experience with writing CMC Drug Product sections of regulatory filings Experience in a network role across multiple sites in a pharmaceutical company", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137463120945", "isPrivate": false, "custom_data": {"location": "New Brunswick - NJ - US", "RequisitionID": "R1583966", "canonical_title": "Scientific Director", "straight_line_distance": null}}, {"id": 137463118947, "name": "Senior Specialist IT, Cell Therapy Manufacturing Systems", "location": "Summit West - NJ - US", "locations": ["Summit West - NJ - US"], "hot": 0, "department": "Cell Therapy", "business_unit": "Information Technology", "t_update": 1722006132, "t_create": 1721952000, "ats_job_id": "R1583960", "display_job_id": "R1583960", "type": "ATS", "id_locale": "R1583960-fi", "job_description": "Sr.Specialist IT, Cell Therapy Manufacturing Systems supports the successful operation of manufacturing and business functions at multi\u2010use sites through interaction with internal team members, peer, and higher-level customers as well as external service providers. The individual is responsible for development of and adherence to system governance procedures. The individual supports multiple IT projects/systems and ongoing work activities of moderate to high complexity. The individual will answer questions and resolve IT issues for manufacturing and manufacturing support staff. This is primarily an onsite position Reporting into the IT organization the candidate will be primarily responsible for driving solutions to manufacturing system related problems including building, testing, documenting, and implementing design changes. The candidate should have at least 3 years of experience in pharma/biotech projects with specific expertise in Supply Chain, Manufacturing, and IT disciplines. The candidate must have knowledge of shop floor activities, Good Manufacturing Practices (GMPs), and process automation in addition to prior experience in Manufacturing Execution System (MES) use and support. Collaborate with business stakeholders and implementation partner(s) to configure, build, and deploy the RTMS and MES systems. Collaborate with business process leads to design master data, recipes, etc., and define best practices. Provide support for operationalizing the manufacturing and peripheral systems. Accountable for uninterrupted 24/7 operation of manufacturing systems for CAR T manufacturing. Support daily operation and future enhancements of MES and other Manufacturing systems as an IT system owner and technical expert. Support integration initiatives between site Manufacturing systems and above-site, enterprise systems, e.g. LIMS, ERP, RTMS, etc. Ability to effectively communicate with both technical and non-technical team members. Teamwork and collaboration Client focus Verbal and written communication Knowledge of cGXP, GAMP, SDLC regulations, including 21CFR part 11, and good documentation practices. Knowledge of pharmaceutical, manufacturing and laboratory systems and equipment that support Biologics and clinical manufacturing. Strong technical and problem-solving skills, strong verbal and written communication skills, and the ability to work independently. Demonstrated success working in a high-performing, business results-driven environment. Understanding of computer system validation. Ability to write IQ/OQ scripts. Clear understanding of the change management process. Ability to write change controls. Work as part of a cross-functional technical team to ensure a successful implementation of systems and technology Work with business units, application developers, security, and infrastructure engineering to troubleshoot, design and build application integrations that support critical manufacturing processes. Bachelor's Degree in Chemical, Mechanical, Biomedical, Electrical or Computer engineering or MIS discipline is required. Must have 4+ years of hands-on experience in a Pharma/Biotech manufacturing and supply chain environment. Must have experience with Manufacturing Execution System Design and Support, preferably RTMS, Emerson Syncade, Informetric InfoBatch, OSIsoft PI Historian and/or Emerson DeltaV, in a Pharma/Bio-tech manufacturing environment. Experience in scheduling applications. Sound understanding of model development & creation. Experience in integrating manufacturing systems (ERP, MES, LIMS, RTMS) Understanding of supply chain, manufacturing domains, and supporting technology including manufacturing and supply chain ERP systems (e.g. Oracle, SAP). Working knowledge of regulatory requirements and how they relate to existing and new business systems and practices, primarily cGxP. Must have prior experience working on a project team to implement, customize, or enhance Manufacturing system. Author, review, and approve technical documentation, protocols, and reports. This includes but is not limited to IQ/IQ/PQ protocols, change controls, and SOP Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE). Recipe Authoring a plus Experience with Microsoft SQL Server, reporting services, database design and data architecture. Query creation in multiple database environments Experienced with Test Strategy, Test Management and Defect Tracking Tools like HP ALM.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137463118947", "isPrivate": false, "custom_data": {"location": "Summit West - NJ - US", "RequisitionID": "R1583960", "canonical_title": "Senior Systems Specialist", "straight_line_distance": null}}, {"id": 137463118954, "name": "Senior Specialist IT, Cell Therapy Manufacturing Systems", "location": "Summit West - NJ - US", "locations": ["Summit West - NJ - US"], "hot": 0, "department": "Cell Therapy", "business_unit": "Information Technology", "t_update": 1722005912, "t_create": 1721952000, "ats_job_id": "R1583959", "display_job_id": "R1583959", "type": "ATS", "id_locale": "R1583959-fi", "job_description": "Sr.Specialist IT, Cell Therapy Manufacturing Systems supports the successful operation of manufacturing and business functions at multi\u2010use sites through interaction with internal team members, peer, and higher-level customers as well as external service providers. The individual is responsible for development of and adherence to system governance procedures. The individual supports multiple IT projects/systems and ongoing work activities of moderate to high complexity. The individual will answer questions and resolve IT issues for manufacturing and manufacturing support staff. This is primarily an onsite position Reporting into the IT organization the candidate will be primarily responsible for driving solutions to manufacturing system related problems including building, testing, documenting, and implementing design changes. The candidate should have at least 3 years of experience in pharma/biotech projects with specific expertise in Supply Chain, Manufacturing, and IT disciplines. The candidate must have knowledge of shop floor activities, Good Manufacturing Practices (GMPs), and process automation in addition to prior experience in Manufacturing Execution System (MES) use and support. Collaborate with business stakeholders and implementation partner(s) to configure, build, and deploy the RTMS and MES systems. Collaborate with business process leads to design master data, recipes, etc., and define best practices. Provide support for operationalizing the manufacturing and peripheral systems. Accountable for uninterrupted 24/7 operation of manufacturing systems for CAR T manufacturing. Support daily operation and future enhancements of MES and other Manufacturing systems as an IT system owner and technical expert. Support integration initiatives between site Manufacturing systems and above-site, enterprise systems, e.g. LIMS, ERP, RTMS, etc. Ability to effectively communicate with both technical and non-technical team members. Teamwork and collaboration Client focus Verbal and written communication Knowledge of cGXP, GAMP, SDLC regulations, including 21CFR part 11, and good documentation practices. Knowledge of pharmaceutical, manufacturing and laboratory systems and equipment that support Biologics and clinical manufacturing. Strong technical and problem-solving skills, strong verbal and written communication skills, and the ability to work independently. Demonstrated success working in a high-performing, business results-driven environment. Understanding of computer system validation. Ability to write IQ/OQ scripts. Clear understanding of the change management process. Ability to write change controls. Work as part of a cross-functional technical team to ensure a successful implementation of systems and technology Work with business units, application developers, security, and infrastructure engineering to troubleshoot, design and build application integrations that support critical manufacturing processes. Bachelor's Degree in Chemical, Mechanical, Biomedical, Electrical or Computer engineering or MIS discipline is required. Must have 4+ years of hands-on experience in a Pharma/Biotech manufacturing and supply chain environment. Must have experience with Manufacturing Execution System Design and Support, preferably RTMS, Emerson Syncade, Informetric InfoBatch, OSIsoft PI Historian and/or Emerson DeltaV, in a Pharma/Bio-tech manufacturing environment. Experience in scheduling applications. Sound understanding of model development & creation. Experience in integrating manufacturing systems (ERP, MES, LIMS, RTMS) Understanding of supply chain, manufacturing domains, and supporting technology including manufacturing and supply chain ERP systems (e.g. Oracle, SAP). Working knowledge of regulatory requirements and how they relate to existing and new business systems and practices, primarily cGxP. Must have prior experience working on a project team to implement, customize, or enhance Manufacturing system. Author, review, and approve technical documentation, protocols, and reports. This includes but is not limited to IQ/IQ/PQ protocols, change controls, and SOP Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE). Recipe Authoring a plus Experience with Microsoft SQL Server, reporting services, database design and data architecture. Query creation in multiple database environments Experienced with Test Strategy, Test Management and Defect Tracking Tools like HP ALM.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137463118954", "isPrivate": false, "custom_data": {"location": "Summit West - NJ - US", "RequisitionID": "R1583959", "canonical_title": "Senior Systems Specialist", "straight_line_distance": null}}, {"id": 137463120280, "name": "Associate Director, Biostatistics", "location": "Remote - United States - US", "locations": ["Remote - United States - US"], "hot": 0, "department": "Hematology", "business_unit": "Global Drug Development", "t_update": 1722008974, "t_create": 1721952000, "ats_job_id": "R1583963", "display_job_id": "R1583963", "type": "ATS", "id_locale": "R1583963-fi", "job_description": "Core member of an EDT and key sub-teams. Contributes to all aspects of the development strategy. Independently leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning, study results presentation and interpretation, clinical study report authoring, regulatory submissions and publications. Participates in development strategy, protocols and analysis plans reviews. Participates in continuous improvement initiatives. Invests in knowledge outside of traditional statistical expertise in the clinical, regulatory and commercial environments that impact the development teams. Engages as a matrix team member on protocol teams as a scientific partner in the drug development process. Ability to present summary data and analyses to key stakeholders in a clear, concise, complete and transparent manner. Possesses technical knowledge of statistical methodology and ability to appropriately apply it in trial design and data analysis for clear, concise, high-quality results. Takes accountability for ensuring quality in all planning, design and execution of assignments associated with the assigned protocol or project. PhD degree in Statistics or Biostatistics or Master's degree with 7+ years' of relevant Pharmaceutical/R&D or other related experience, including supporting regulatory filings. Demonstrated knowledge of statistical / clinical trials methodology as it relates to clinical development. Relevant prior data analysis planning, execution and delivery experience. Excellent verbal and written communications skills. Ability to be flexible and adapt quickly to the changing needs of the organization. Strong interpersonal skills evidenced in interactions with individuals at all levels of the organization, and demonstrated ability to develop relationships within the organization and leverage the formal and informal organizational structure to assist in goal achievement, including the resolution of conflicts or their appropriate escalation", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "remote_local", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137463120280", "isPrivate": false, "custom_data": {"location": "Remote - United States - US", "RequisitionID": "R1583963", "canonical_title": "Associate Director", "straight_line_distance": null}}, {"id": 137463110090, "name": "Scientist - Cellular pharmacology\u2013 Lead Discovery & Optimization", "location": "San Diego - CA - US", "locations": ["San Diego - CA - US"], "hot": 0, "department": "Not Applicable", "business_unit": "Research and Early Development", "t_update": 1721944079, "t_create": 1721865600, "ats_job_id": "R1583884", "display_job_id": "R1583884", "type": "ATS", "id_locale": "R1583884-fi", "job_description": "Be responsible for technology innovation for high-throughput screening platforms as well as expand targeted protein degradation and proximity based assay platforms for E3 ligases. Develop innovative cellular and/or biochemical assays to discover and validate on target protein degradation and neosubstrate specificity. Bring strategic insight into program support ensuring robust and innovative solutions and approaches towards the development of cell based assays for screening, hit triage, SAR, and MOA. Possess strong collaborative and written/verbal communication skills and a positive attitude to interact with multiple stakeholders across different departments and research sites. Highly motivated self-starter who can work independently and be multi-tasking in a fast-paced team. Contribute to the writing of investigator brochures, IND applications, and other regulatory documents when appropriate. Demonstrate strong analytical and critical thinking skills with the ability to interpret complex data. Bachelor's Degree 5+ years of academic / industry experience or Master's Degree 3+ years of academic / industry experience or PhD in Cell Biology, Molecular Biology, or Biochemistry, or MS with 3+ or BS with 5+ years experiences in academia or biopharmaceutical industry Experience in ubiquitin proteasome system (UPS) and E3 ubiquitin ligases is highly essential. Superior assay design and high-throughput screening skills in cell-based assay formats as well as experience in the application of modern technology are preferred. Relevant skills include proficiency in cell-based/biochemical assay development such as AlphaLISA, ELISA, HTRF, MSD, immunoblot, high content image, FACS and qPCR. Ability to create and maintain an effective scientific network through teamwork, excellent problem solving skills and open collaborative style are of critical importance to the success of this role.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137463110090", "isPrivate": false, "custom_data": {"location": "San Diego - CA - US", "RequisitionID": "R1583884", "canonical_title": "Lead Scientist", "straight_line_distance": null}}, {"id": 137463110242, "name": "Material Handler", "location": "Bothell - WA - US", "locations": ["Bothell - WA - US"], "hot": 0, "department": "Cell Therapy", "business_unit": "Global Product Development & Supply", "t_update": 1721946921, "t_create": 1721865600, "ats_job_id": "R1583805", "display_job_id": "R1583805", "type": "ATS", "id_locale": "R1583805-fi", "job_description": "Coordinates internal and external customer requests across multiple unit operations during their shift to include personnel, material, and logistical needs. Working with production planning, the Sr. Manufacturing Associate, and other shift leads to establish daily unit operations schedule that includes people, product, and material flow across multiple shifts. Completing and reviewing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Assisting in the training of staff who are less experienced to ensure they have the necessary technical skills and knowledge. Initiation of company discrepancies/deviations for non-conforming materials and operational anomalies. Assisting in setting up warehouse operations equipment/fixtures. Reviewing Warehouse Operations procedures and providing input in ensuring documents are technically sound, promote effective and efficient operations, and comply with cGMP requirements. Performing tasks in a manner that are consistent with departmental and corporate safety policies, quality systems and GMP requirements. Coordination of tasks with staff working within Warehouse Operations. Additional duties, tasks and responsibilities as assigned by management. The incumbent will be required to work in a warehouse environment requiring ergonomic considerations. The incumbent will be required to work in manufacturing and lab spaces for moderate periods of time for inventory replenishment and delivery. Occasional excursions to labs or production areas requiring some level of gowning. Exposure to typical manufacturing, laboratory, mechanical and warehouse environments. Exposure to outdoor elements as required for material receiving, material shipment, operation of material handling equipment, etc. Majority of working hours standing and lifting of \u2264 50 lbs. Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing. Experience in: Distribution, receiving, temperature storage, issuance, and inventory control practices including cycle counting, and rejected/expired material disposition. Understanding controlled temperature, humidity, and pest control monitoring for cGMP environments. Transportation lanes and cold chain logistical movement of time critical and temperature sensitive biologics. Freight forwarder and courier direct shipments and associated documentation requirements. Use of material handling equipment - both gas powered, electric and manual. Operation of company owned vehicles for transport. Bachelor's degree in relevant science discipline or equivalent work experience. 0-3 years of experience in a cGMP warehouse environment and understanding of Supply Chain Management and APICS best practices for warehouse operations. Experience in the implementation and use of ERP/MRP software systems preferred. DOT/IATA/HazMat experience and certifications preferred.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137463110242", "isPrivate": false, "custom_data": {"location": "Bothell - WA - US", "RequisitionID": "R1583805", "canonical_title": "Material Handler", "straight_line_distance": null}}, {"id": 137463108424, "name": "Occupational Health Nurse Practitioner", "location": "Devens - MA - US", "locations": ["Devens - MA - US"], "hot": 0, "department": "Not Applicable", "business_unit": "Human Resources", "t_update": 1721924963, "t_create": 1721865600, "ats_job_id": "R1583933", "display_job_id": "R1583933", "type": "ATS", "id_locale": "R1583933-fi", "job_description": "Clinical care of workplace injury and illness including, diagnosis and treatment where appropriate; including prescriptions when indicated and emergency response. Collaborate with the team and provide clinical services. This includes medical surveillance exams, international travel health consultations, immunizations, and screening tests. Case management of work-related injury/illness and episodic personal health matters. Collaborate with appropriate stakeholders on management of return-to-work restrictions and accommodation, employment issues and policy making. Collaborate with Senior Manager to provide risk assessments for safety sensitive positions as required by medical surveillance programs. Work with BMS disability and worker's compensation insurance providers to case manage all occupational and non-occupational injuries and illnesses and short- and long-term disability claims. Investigate, monitor, and analyze illness and injury episodes and trends; develop strategies to promote and protect employee health and safety and prevent injury, including ergonomic programs. Participate in the development of BMS health and wellbeing programs in collaboration with other Occupational Health and Wellbeing team members, as well as Fitness Center program manager. Develop and implement performance objectives that are aligned with the company corporate and occupational health goals and objectives. Master's prepared licensed Nurse Practitioner in Massachusetts Current certification by a nationally recognized credentialing agency Current DEA/MCSR, CPR/BLS certification At least 3-5 years of experience in occupational health setting preferred Excellent interpersonal, verbal, and written communication skills Computer skill proficiency, including experience using electronic medical record programs FMCSA DOT examiner, case management, Spirometry, Audiometry certified recommended. 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Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. Prepares and successfully implements comprehensive territory and account plans. Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. Fair & Balanced Scientific Dialogue Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy. Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. Maintains a high level of working expertise on emerging data for approved indications. Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries. Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs. Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. Complies with all laws, regulations, and policies that govern the conduct of BMS. Portfolio Promotion Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner. Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas. Prepares and successfully implements comprehensive territory and account plans. Proactively uses available tools such as CE^3 (once implemented) to derive insights and to dynamically inform call plans. Provides feedback on experience using these tools to leadership to enable continuous improvement. Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs. Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers. Complies with all laws, regulations, and policies that govern the conduct of BMS. Advanced scientific degree and/or preferred 5+ years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude. Strong selling and promotional skills proven through a track record of performance. Customer/Commercial Mindset Demonstrated ability to drive business results. Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. Understands the patient journey and can customize engagement and deliver tailored messages. Demonstrated resourcefulness and ability to connect with customers. Patient Centricity Has a patient-focused mindset. Scientific Agility Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients. Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data. Analytical Capability Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Data-driven insights help TAS strategize and target their efforts effectively. Ability to segment HCPs based on their preferences and other relevant factors. This helps them tailor their communication and product presentations to suit individual HCP needs. Understanding how to interpret and analyze data related to BMS products, customer preferences, clinical data. Ability to use CE^3 to generate insights and do dynamic call planning. Technological Agility Understanding, adapting, and effectively using technology in various aspects of healthcare business and interacting with HCPs. Utilizing various digital communication channels such as emails, instant messaging apps, and video conferencing to stay in touch with healthcare professionals, colleagues, and clients. This enables TAS to respond promptly to inquiries, share updates, and maintain effective communication. Competency using CE^3 and other software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track interactions, and plan future engagements with healthcare professionals. Ability to use the Medical on Call technology effectively. Keeping up to date with technological advancements and changes. Advanced scientific degree and/or preferred 5+ years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. Demonstrated experience building and maintaining strong credibility with key customers, office staff, and others in the customer influence network via a customer-centric mindset and desire to create positive and differentiated Customer Experience (Cx). Experience in Dermatology is preferred. Demonstrated strong capability in account management skill sets, superior selling competencies, and proven sales performance track record of meeting or exceeding goals. Demonstrated ability to work effectively cross-functionally with a positive team mindset and can-do attitude. Strong selling and promotional skills proven through a track record of performance. Customer/Commercial Mindset Demonstrated ability to drive business results. Experience identifying, engaging, and cultivating credibility with customers across the patient care journey. Demonstrated account management skills and problem-solving mentality. Understands the patient journey and can customize engagement and deliver tailored messages. Demonstrated resourcefulness and ability to connect with customers. Ability to analyze data, such as prescribing patterns, market trends, and HCP preferences. Ability to segment HCPs based on their preferences and other relevant factors. Ability to use CE^3 to generate insights and do dynamic call planning. Ability to use the Medical on Call technology effectively.", "stars": 0.0, "medallionProgram": null, "location_flexibility": null, "work_location_option": "onsite", "canonicalPositionUrl": "https://jobs.bms.com/careers/job/137463109386", "isPrivate": false, "custom_data": {"location": "Dover - DE - US", "RequisitionID": "R1583940", "canonical_title": "Senior Specialist", "straight_line_distance": null}}, {"id": 137463108850, "name": "Radiopharmaceutical Production Operator II", "location": "Indianapolis - IN - US", "locations": ["Indianapolis - IN - US"], "hot": 0, "department": "Manufacturing Ops", "business_unit": "Unknown", "t_update": 1721930707, "t_create": 1721865600, "ats_job_id": "R1583938", "display_job_id": "R1583938", "type": "ATS", "id_locale": "R1583938-fi", "job_description": "Execute production of RayzeBio drug products (including raw material preparation, line clearance and cleaning, equipment/instrument setup, etc.) while ensuring compliance with cGMP, aseptic practice, and management expectations. 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Strong knowledge of cGMP and aseptic practice. Knowledge of injectable and/or radiopharmaceutical drug product manufacturing. Excellent professional ethics, integrity, and ability to maintain confidential information. Well organized and detail oriented. Strong interpersonal communication skills. 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Supports the efforts to align the Medical Plan with TA portfolio objectives/strategies Support transparency of the Medical Data Generation/ Investigator Sponsored Research book of work, including decision-making and support operational improvements in that space by partnering with the Medical Data Generation leads. Support the activities of multi-disciplinary groups to meet the strategic objectives and implementation milestones outlined in the Medical plan(s) Maintain Medical plans, manage dependencies across functions, and provide transparency to medical leads and senior leaders. Facilitate comprehensive project plans and progress reports for team leads, senior management and other stakeholders, as needed. Track & measure performance and identify risk areas or barriers impeding successful execution. Work with teams, Medical leadership, and/or senior management to resolve Partner with Medical Team Lead/core team to facilitate medical matrix team meetings, ensure the agenda is focused on key deliverables, risk management, issue identification and resolution. Ensure that key actions and agreements are understood and the team is held accountable for their commitments Partner with Finance and Medical leads to facilitate the budget process including trade-off discussions and on an ongoing basis ensure the brand budgets (including facilitation of annual budget, monthly projections, accruals, variance analysis and budget planning for the coming year) are on track. Identify, develop and implement new processes to facilitate continued evolution of the Operations function and improve efficiency of the Medical organization. Build relationships with key stakeholders, including Development Teams, Health Economics and Outcomes Research, Commercial and Medical team members, to influence strategic alignment on key Medical objectives. Ensure Medical Team members are fully represented in the decision-making process and knowledge exchange is taking place. Ensure key communication points are captured and disseminated. A Bachelor's degree with 5+ years of experience in pharmaceutical research, development, or commercialization. (science background strongly recommended). An advanced degree (e.g., MS, MBA) is a plus. This position requires a solid understanding of drug development and commercialization. Project management foundation and relevant experience on matrix management, budget management, metrics and leadership communication Strong written and oral communication skills and demonstrated ability to interact directly and productively with team members and management and to manage and prioritize multiple competing priorities is also required. Ability to lead and engage in complex scientific discussions to develop /summarize clear follow-up/action plans and execute. Strong experience with building relationships, leading strategic initiatives and programs, and collaborating across divisions with people of diverse business backgrounds and cultures. Highly organized and motivated individual with the ability to work independently/effectively with cross functional matrixed teams Comfort with ambiguity, driving change and innovation across a matrix. 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