Nuclear Licensing Manager JobotNuclear Licensing ManagerJanesville, WI$160,000–$200,000 / yearInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. As a Licensing Manager on our team, we are looking for the following experience: Bachelor’s in engineering, science, or related field (or equivalent: Senior Reactor Operator license or Naval Nuclear Propulsion Program experience).
Regulatory Affairs Leader - ARC GE Healthcare Technologies Inc.Regulatory Affairs Leader - ARCMadison, WIResponsibilities: Provides regulatory leadership and strategic direction for ARC regulatory programs, including global RA support for registration planning, submissions, notified body and quality system audits, and program implementation across a cross-functional team with communication to leadership. Develops regulatory strategies to help optimize regulatory submission pathways, taking into consideration regulatory requirements (including product testing, clinical data, etc), product claims and country regulatory dependencies to ensure optimized sequencing for submissions.
Associate Manager, Regulatory Affairs International Flavors & FragrancesAssociate Manager, Regulatory AffairsMadison, WIServe as the North American regulatory subject matter expert for Food Biosciences products, including food enzymes and cultures, and proactively assess regulatory developments and business impact. Our Health & Biosciences team channels a passion for nature and bioscience into sustainable, life-enhancing technologies that power innovative solutions across healthcare, food, consumer, and industrial markets.
Manager, Regulatory Affairs International Flavors & Fragrances IncManager, Regulatory AffairsMadison, WIServe as the North American regulatory subject matter expert for Food Biosciences products, including food enzymes and cultures, and proactively assess regulatory developments and business impact. Our Health & Biosciences team channels a passion for nature and bioscience into sustainable, life-enhancing technologies that power innovative solutions across healthcare, food, consumer, and industrial markets.
Regulatory Affairs Leader - ARC GE HealthCare Technologies IncRegulatory Affairs Leader - ARCMadison, WIResponsibilities: Provides regulatory leadership and strategic direction for ARC regulatory programs, including global RA support for registration planning, submissions, notified body and quality system audits, and program implementation across a cross-functional team with communication to leadership. Develops regulatory strategies to help optimize regulatory submission pathways, taking into consideration regulatory requirements (including product testing, clinical data, etc), product claims and country regulatory dependencies to ensure optimized sequencing for submissions.
Senior Manager, CMC Regulatory Affairs Arrowhead PharmaceuticalsSenior Manager, CMC Regulatory AffairsMadison, WI$140,000–$170,000 / yearArrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes.
Senior Manager, CMC Regulatory Affairs Arrowhead Pharmaceuticals IncSenior Manager, CMC Regulatory AffairsVerona, WI$140,000–$170,000 / yearArrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes.
Senior Director, Managed Access Programs, Medical Evidence Generation (Worldwide Medical Affairs) Bristol Myers SquibbSenior Director, Managed Access Programs, Medical Evidence Generation (Worldwide Medical Affairs)Madison, WI$229,380–$277,956 / yearThe MAPs Lead will provide strategic input, oversight, and coordination to ensure a streamlined and efficient approach to managed access and ensure equity, sustainability, scalability, and appropriate data capture across their respective disease areas. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Leader Medical Affairs Canon USA & AffiliatesLeader Medical AffairsMadison, WIRemote10 years’ experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team.
Senior Director, Worldwide Cell Therapy Autoimmune Medical Affairs, Neurology/Lcm Bristol Myers SquibbSenior Director, Worldwide Cell Therapy Autoimmune Medical Affairs, Neurology/LcmMadison, WI$229,380–$277,956 / yearSupport indication and ecosystem readiness by identifying specialty-specific barriers to future adoption, referral pathways, multidisciplinary care needs, patient identification considerations, institutional capability gaps, and opportunities to improve clinical practice excellence. Partner closely with Clinical Development, Translational Medicine, Regulatory, Commercial, HEOR, Market Access, Field Medical, regional medical teams, and other cross-functional stakeholders to support evidence generation, lifecycle planning, governance milestones, and indication readiness.
Clinical Affairs Specimen Operations Specialist AbbottClinical Affairs Specimen Operations SpecialistMadison, Wisconsin$61,300–$122,700 / yearThe CASO Specialist supports the clinical study portfolio for Abbott Cancer Diagnostics commercial and pipeline products, collaborating with Product Core Teams and their respective working groups to successfully meet the development, evidence generation and overall strategic needs of each Abbott Cancer Diagnostics product. Bachelor’s degree in the health or life sciences, or a field as outlined in the essential duties, or Associate’s degree in the health or life sciences and 2 years of experience in a field as outlined in the essential duties in lieu of Bachelor’s degree, or High School Degree/General Education Diploma and 4 years of experience in a field as outlined in the essential duties in lieu of Bachelor’s degree.
Clinical Affairs Specimen Operations Specialist Abbott LaboratoriesClinical Affairs Specimen Operations SpecialistMadison, WI$61,300–$122,700 / yearThe CASO Specialist supports the clinical study portfolio for Abbott Cancer Diagnostics commercial and pipeline products, collaborating with Product Core Teams and their respective working groups to successfully meet the development, evidence generation and overall strategic needs of each Abbott Cancer Diagnostics product. Bachelor's degree in the health or life sciences, or a field as outlined in the essential duties, or Associate's degree in the health or life sciences and 2 years of experience in a field as outlined in the essential duties in lieu of Bachelor's degree, or High School Degree/General Education Diploma and 4 years of experience in a field as outlined in the essential duties in lieu of Bachelor's degree.
NewAssociate Clinical Affairs Specimen Operations Specialist Abbott LaboratoriesAssociate Clinical Affairs Specimen Operations SpecialistMadison, WI$50,700–$101,300 / yearThe Associate Clinical Affairs Specimen Operations Specialist works with product core teams, working groups, clinical study managers, cross-functional support teams, and key stakeholders to ensure that product and clinical goals are met through excellent coordination and communications. This role is responsible for operational and sample management processes; including, but not limited to, all technical, system, and data management components that support the execution of clinical and regulatory affairs work.
Medical Affairs Director, Rare Disease AbbottMedical Affairs Director, Rare DiseaseMadison, Wisconsin$149,300–$298,700 / yearAct as the strategic Medical Affairs leader and primary partner to Commercial and cross-functional leadership, leveraging insights from KOL engagement, scientific conferences, publications, and emerging clinical trends to influence portfolio strategy, evidence priorities, and compliant scientific communication. Experiencedevelopingand leadingKOL engagement strategies,advisory boards, and scientificexternal engagementactivities; demonstrated ability to representthe organizationwith credibilityat scientific conferences and professional meetings.
Medical Affairs Director, Rare Disease Abbott LaboratoriesMedical Affairs Director, Rare DiseaseMadison, WI$149,300–$298,700 / yearAct as the strategic Medical Affairs leader and primary partner to Commercial and cross-functional leadership, leveraging insights from KOL engagement, scientific conferences, publications, and emerging clinical trends to influence portfolio strategy, evidence priorities, and compliant scientific communication. The Medical Affairs Director, Rare Disease owns and leads the Medical Affairs strategy for the rare disease genetics portfolio within the Cancer Diagnostics division, including scientific content development, evidence generation, external scientific engagement, and KOL partnerships.
NewAssociate Clinical Affairs Specimen Operations Specialist AbbottAssociate Clinical Affairs Specimen Operations SpecialistMadison, WisconsinThe Associate Clinical Affairs Specimen Operations Specialist works with product core teams, working groups, clinical study managers, cross-functional support teams, and key stakeholders to ensure that product and clinical goals are met through excellent coordination and communications. This role is responsible for operational and sample management processes; including, but not limited to, all technical, system, and data management components that support the execution of clinical and regulatory affairs work.
Regulatory Compliance Manager Richelieu FoodsRegulatory Compliance ManagerBeaver Dam, WI$95,000–$120,000 / yearThis role has one direct report, the Regulatory and Sustainability Specialist, and is accountable for setting priorities, providing day-to-day direction, developing backup capability, reviewing work output, and ensuring timely execution of regulatory, customer documentation, and sustainability deliverables. Reporting to the Vice President of Quality Assurance, Food Safety and Regulatory, this role ensures that new and existing products, formulas, labels/ artwork, customer documentation, and related records comply with applicable FDA, USDA, FSIS, customer, company, and emerging regulatory requirements.
Quality & Regulatory Intern Mueller Sports Medicine IncQuality & Regulatory InternPrairie Du Sac, WIWorking with the department leadership to oversee all regulatory and compliance related efforts including internal support to all departments in review and response to inquiry from government agencies, customer, or vendors. Requires good hand-eye coordination, arm, hand and finger dexterity, including ability to grasp, and visual acuity to use a keyboard, operate office equipment and read.
Quality Manager Placon CorporationQuality ManagerMadison, WIFull timeOwn all customer quality complaints end‑to‑end, including customer/sales communication, root cause analysis with Engineering, Production, Tooling, and Marketing, and implementation of corrective/preventive actions (CAPAs).Manage the site CAPA program, ensuring timely resolution, documentation, effectiveness verification, and continuous improvement. We're looking for a hands‑on leader who excels in regulated, fast‑moving environments and is passionate about building strong quality systems, guiding teams, and ensuring outstanding customer outcomes.
Director, Quality Assurance & Compliance PromegaDirector, Quality Assurance & ComplianceMadison, WisconsinExperience leading or overseeing a Quality Management System, including management review processes, governance, and executive reporting (e.g., experience in roles similar to a Management Representative or QMS lead in regulated GxP or ISO environments). Computer and Document Work: Ability to use Microsoft Office applications and electronic quality management systems (eQMS platforms such as MasterControl, Veeva, or equivalent).