Regulatory Affairs Specialist, EHS, North America Henry Schein IncRegulatory Affairs Specialist, EHS, North AmericaWI$56,604–$88,443 / yearDevelop and deliver employee environmental, health, and safety (EHS) awareness and training programs to ensure compliance with applicable federal, state, and international regulations, including OSHA, OSHA State Plans (e.g., Cal/OSHA), DOT, IATA, IMO, and EPA requirements. Proficient in Microsoft Office applications, including PowerPoint, and experienced with project management methodologies and tools commonly used in the medical device or pharmaceutical industries.
Sr. Regulatory Affairs Specialist - Food & Beverage Novozymes ASSr. Regulatory Affairs Specialist - Food & BeverageWest Allis, WI$115,000–$120,000 / yearWe collaborate openly, share knowledge, and are continuously strengthening digital ways of working to improve the speed, transparency, and consistency of regulatory deliverables. In this role, you will play a critical part in enabling safe, compliant growth across the Food & Beverages sector by transforming complex regulatory requirements into clear, actionable guidance.
Sr. Regulatory Affairs Specialist - Food & Beverage Novozymes North AmericaSr. Regulatory Affairs Specialist - Food & BeverageWest Allis, WisconsinWe collaborate openly, share knowledge, and are continuously strengthening digital ways of working to improve the speed, transparency, and consistency of regulatory deliverables. In this role, you will play a critical part in enabling safe, compliant growth across the Food & Beverages sector by transforming complex regulatory requirements into clear, actionable guidance.
Regulatory Affairs Engineer/Specialist American Orthodontics CorpRegulatory Affairs Engineer/SpecialistSheboygan, WIDetermine the types of regulatory submissions or documentation required for projects with product design changes, manufacturing changes, or labeling changes. Bachelor's degree in Biomedical Engineering, Biology, Chemistry, Technical Communication, or similar field from an accredited college or university desired.
Regulatory Affairs Engineer/Specialist American OrthodonticsRegulatory Affairs Engineer/SpecialistSheboygan, WIDetermine the types of regulatory submissions or documentation required for projects with product design changes, manufacturing changes, or labeling changes. Bachelor's degree in Biomedical Engineering, Biology, Chemistry, Technical Communication, or similar field from an accredited college or university desired.
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.
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 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 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.
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.
NewResearch Regulatory Specialist - Pediatrics Medical College of WisconsinResearch Regulatory Specialist - PediatricsMilwaukee, WisconsinFacilitate study start-up activities, including submissions to committees such as the Scientific Review Committee, Data Safety Monitoring Board, Institutional Biosafety Committee, or Radiation Safety Committee. Employees, students, applicants or other members of the MCW community (including but not limited to vendors, visitors, and guests) may not be subjected to harassment that is prohibited by law or treated adversely or retaliated against based upon a protected characteristic.
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.
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.
Director, Government Affairs Regal Rexnord CorpDirector, Government AffairsMilwaukee, WI$150,000–$200,000 / yearThe Company's end markets benefit from meaningful secular demand tailwinds, and include factory automation, food & beverage, aerospace and defense, medical, data center, warehouse, alternative energy, residential and commercial buildings, general industrial, construction, metals and mining, and agriculture. The Company's end markets benefit from meaningful secular demand tailwinds, and include factory automation, food & beverage, aerospace, medical, data center, warehouse, alternative energy, residential and commercial buildings, general industrial, construction, metals and mining, and agriculture.
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.
Automation Equipment Training Specialist AbbottAutomation Equipment Training SpecialistMadison, Wisconsin$61,300–$122,700 / yearBachelor’s Degree in Engineering (e.g., mechanical, electrical, industrial), Training and Development, or field related to the essential duties of the job; Associates Degree and 2 years of relevant experience as outlined in the essential duties in lieu of Bachelor’s Degree; or High School Diploma and 4 years of relevant experience as outlined in the essential duties in lieu of Bachelor’s Degree. Build strong customer relationships and deliver customer-centric solutions such as customized classroom instruction, in-lab coaching, hands-on/on-the-job instruction, virtual training, and other modalities, as needed.
Senior HR Service Delivery Specialist - HR Compliance Specialist Wolters KluwerSenior HR Service Delivery Specialist - HR Compliance SpecialistMadison, WI$71,300–$124,500 / yearWhile the position does not have direct people management responsibilities, it requires strong project leadership, influence, stakeholder management, and accountability for delivering compliance-focused outcomes across the enterprise. This role helps mitigate organizational risk, strengthens operational controls, and promotes consistent application of employment-related policies and practices across a multi-state organization.
Contract Specialist U.S. Department of Veterans AffairsContract SpecialistMilwaukee, WIRemote$89,508–$116,362 / yearApplying knowledge of contract types-such as firm-fixed price, firm-fixed price with economic price adjustments, and cost-reimbursement-and acquisition methods including simplified acquisitions, sealed bidding, negotiations, cost sharing, multiple awards, commercial items, and special provisions. Assists the Acquisition Team Supervisors in coordinating contracting activities, performs contract reviews and provides guidance regarding complex contracts administered by other contract specialists, identifies special training needs, and conducts mentoring and contract training.