Maintenance Manager (Food Manufacturing) CONAGRAMaintenance Manager (Food Manufacturing)Menomonie, WI$82,000–$120,000Reporting to the Plant Manager at our Menomonie, Wisconsin plant, you will lead the maintenance function to ensure reliable, efficient manufacturing operations while minimizing downtime and sustaining peak plant performance. When visiting these sites, the physical requirements below may apply: You may be required to walk around the facility, climb stairs/ladders, kneel, or perform repetitive tasks that require hand-eye coordination.
Sr Regulatory Affairs Engineer Harley-Davidson IncSr Regulatory Affairs EngineerWauwatosa, WI$83,500–$129,300 / yearThis role will also be a critical input into the product development process by helping define project requirements and supporting the smooth delivery of the product plan by determining certification test needs and working to enable undisrupted shipment, sale & registration of product. The Sr Regulatory Affairs Engineer is responsible for developing and executing processes and activities required to certify motorcycles, systems and components in all markets in which Harley-Davidson does business.
NewRegulatory 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.
Manager, Product Stewardship & Regulatory Affairs Johnson Controls International PlcManager, Product Stewardship & Regulatory AffairsWI$100,000–$167,000 / yearThe role acts as both a market‑access protector and a digital product owner for PSRA, partnering with engineering, R&D, manufacturing, supply chain, quality, legal, IT, data science, and commercial teams to embed regulatory requirements and compliance intelligence throughout the product lifecycle and enterprise workflows. Design and deploy AI‑enabled capabilities such as: Automated global regulatory horizon scanning Intelligent SDS and material risk screening Predictive compliance risk assessment by product and market AI‑assisted customer documentation and inquiry management Ensure regulatory data governance, traceability, transparency, and audit readiness across systems.
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.
Manager, Product Stewardship & Regulatory Affairs Johnson ControlsManager, Product Stewardship & Regulatory AffairsWisconsin$100,000–$140,000 / yearThe role acts as both a market‑access protector and a digital product owner for PSRA, partnering with engineering, R&D, manufacturing, supply chain, quality, legal, IT, data science, and commercial teams to embed regulatory requirements and compliance intelligence throughout the product lifecycle and enterprise workflows. This position is accountable for ensuring worldwide compliance of fire suppression hardware and chemical agents with complex chemical control laws and product safety regimes, while simultaneously owning the design, deployment, and evolution of business systems and AI‑enabled capabilities that operationalize regulatory intelligence at scale.
Director, Regulatory Affairs & Quality Assurance Imbed Biosciences, IncDirector, Regulatory Affairs & Quality AssuranceMiddleton, WIThis role is critical in advancing products through U.S. FDA pathways while expanding international market access, including achieving and maintaining CE Mark certification under EU MDR. The Director of Regulatory Affairs & Quality Assurance will lead global regulatory strategy and quality systems for Imbed Biosciences ’s portfolio of advanced wound care products.
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.
Clinical Affairs Specimen Operations Manager Exact Sciences CorpClinical Affairs Specimen Operations ManagerMadison, WI$76,000–$125,000 / yearThe CASO Manager supports the clinical study portfolio for Exact Sciences 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 Exact Sciences 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.
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.
Director, Legal Affairs The Wisconsin Credit Union LeagueDirector, Legal AffairsMadison, WIFull timeYour role will also involve consulting with regulators, credit union representatives, league staff, and legal counsel to address or resolve compliance and operational issues. To be successful as the Director of Legal Affairs at The Wisconsin Credit Union League, candidates should possess a robust set of skills that align with our core values.
Assistant to the Vice President of Student Affairs Lakeshore Technical CollegeAssistant to the Vice President of Student AffairsWIProvide operational support by answering questions, resolving issues, assisting with Welcome Center coverage, and delivering excellent customer service. Prepare, maintain, and analyze operational reports and data to support Student Affairs decision-making, identify trends, monitor outcomes, and inform continuous improvement efforts.
NewAssistant to the Vice President of Student Affairs Lakeshore CollegeAssistant to the Vice President of Student AffairsCleveland, Wisconsin$24.61–$28.95 / hourFull timeProvide operational support by answering questions, resolving issues, assisting with Welcome Center coverage, and delivering excellent customer service. Prepare, maintain, and analyze operational reports and data to support Student Affairs decision-making, identify trends, monitor outcomes, and inform continuous improvement efforts.
Senior Associate, North America Registration & Regulatory Compliance - Food Contact S.C. Johnson & Son IncSenior Associate, North America Registration & Regulatory Compliance - Food ContactRacine, WIAs the Senior Associate, North America Registration & Regulatory Compliance, you'll serve as a trusted regulatory advisor, partnering closely with Research, Development & Engineering (RD&E), Marketing, and cross-functional business teams to provide expert guidance throughout the product development lifecycle. This highly collaborative headquarters-based role offers the opportunity to influence product development, solve complex regulatory challenges, and build strong partnerships across the organization as you help bring trusted Home Storage products to consumers throughout North America.
Regulatory Compliance Manager Sartori Cheese BrandRegulatory Compliance ManagerPlymouth, WisconsinThe Regulatory Compliance Manager leads and develops a team of regulatory professionals and partners cross-functionally to support compliant product development, certifications, and operational changes. This role provides regulatory leadership for product compliance, labeling, facility registration, certifications, and export requirements while serving as the primary liaison with regulatory agencies and certification bodies.
NewRegulatory Specialist Actalent IncRegulatory SpecialistWaukesha, WI$45,760–$52,000 / yearAs a Regulatory Specialist, you will be responsible for verifying and approving new raw material suppliers, maintaining supplier documentation to meet regulatory and quality system requirements, and performing product analysis to ensure compliance with customer specifications. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
NewQuality & Regulatory Leadership Program GE HealthCare Technologies IncQuality & Regulatory Leadership ProgramWIResponsibilities: QRLPs will have a wide range of assignment selections such as: Quality Assurance, Regulatory Affairs, Product Surveillance, Complaint Handling, Production & Process Controls, Corrective & Preventative Action, Design Controls, Product Quality, QMS Compliance, and/or Global Audit. The Quality & Regulatory Leadership Program provides exposure across the GE HealthCare business and consists of three 8-month business critical assignments within the Quality & Regulatory organization.
Director of Regulatory Compliance Organic Valley Family of FarmsDirector of Regulatory ComplianceWI$150,696–$200,928 / yearo In partnership with supply quality oversee the organic fraud prevention plan, including supply chain assessments, vulnerability assessments, mitigation measures, and documentation review. The Director of Regulatory Compliance provides strategic leadership and oversite for the regulatory, compliance, and scientific functions/initiatives across CROPP/Organic Valley.
Sr. Regulatory Specialist - Food and Beverages - North America Novozymes ASSr. Regulatory Specialist - Food and Beverages - North AmericaWI$105,000–$110,000 / 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.
Regulatory Specialist A L Schutzman CompanyRegulatory SpecialistWaukesha, WisconsinAssist the Supervisor in responding to customer inquiries regarding food safety and quality related documentation; including but not limited to filling out surveys, providing existing documentation, creating technical documentation and providing information through online customer portals. Assist the Supervisor in the development of finished product specification and labeling information, as well as review of final labels; including development of nutrition facts panels, label statements, product claims and claim substantiation.
NewSenior Associate, North America Registration & Regulatory Compliance - Food Contact SC JohnsonSenior Associate, North America Registration & Regulatory Compliance - Food ContactRacine, WISenior Associate, North America Registration & Regulatory Compliance - Food Contact - SC Johnson.
Patent Litigation and Regulatory Compliance Manager Johnson Health Tech. Co., Ltd.Patent Litigation and Regulatory Compliance ManagerCottage Grove, WIPerforms patent searches on product innovations our product teams are developing, reviews status of patentable innovations on behalf of the brand companies and submits patent applications to the US Patent Office to protect the company's intellectual property. Under the direction of the Patent & Advanced Mechanics Manager, the Patent Litigation and Regulatory Compliance Manager will take a leadership role in protecting and defending the company's intellectual property, with primary responsibility for patent litigation, patent prosecution, and IP enforcement.
NewProduct Regulatory Compliance Engineer (CE, EAC & WiFi Licensing) Macpower Digital Assets Edge Private LimitedProduct Regulatory Compliance Engineer (CE, EAC & WiFi Licensing)Waukesha, WI$80,000–$115,000 / yearAs a Product Compliance Engineer , you would be responsible for providing regulatory compliance support to engineering development projects, existing product changes throughout the product life cycle and interfaces with cross-functional teams consisting of engineering, operations (industrial engineering, production, and material procurement), sourcing, quality, service, and marketing to assure ongoing product content compliance and distribution control. BASIC QUALIFICATIONS: Bachelor of Science Degree in Mechanical or Electrical Engineering or related discipline; 2+ years of relevant work experience; PREFERRED QUALIFICATIONS: Ability to perform detail-oriented work with a high degree of accuracy on multiple projects; Product Regulatory Compliance experience with specific knowledge CE, EAC, Country Specific Certifications, WiFi licensing and similar US, Canadian and Global regulations.
Sr. Regulatory Compliance Analyst Markel Group IncSr. Regulatory Compliance AnalystMilwaukee, WIThis includes race; color; sex; religion; creed; national origin or place of birth; ancestry; age; disability; affectional or sexual orientation; gender expression or identity; genetic information, sickle cell trait, or atypical hereditary cellular or blood trait; refusal to submit to genetic tests or make genetic test results available; medical condition; citizenship status; pregnancy, childbirth, or related medical conditions; marital status, civil union status, domestic partnership status, familial status, or family responsibilities; military or veteran status, including unfavorable discharge from military service; personal appearance, height, or weight; matriculation or political affiliation; expunged juvenile records; arrest and court records where prohibited by applicable law; status as a victim of domestic or sexual violence; public assistance status; order of protection status; status as a smoker or nonsmoker; membership or activity in local commissions; the use or nonuse of lawful products off employer premises during non-work hours; declining to attend meetings or participate in communications about religious or political matters; or any other classification protected by applicable law. Identify trends; evaluate alternatives to maintain compliance while meeting business goals; recommend process improvements to increase efficiency and effectiveness; provide guidance and coaching; support director and team members.
Pharmaceutical Medical Science Liaison - Dry Eye Alcon IncPharmaceutical Medical Science Liaison - Dry EyeWIThis role is part of Alcon's Research & Development function, a team that innovates boldly and delivers new products and services to help revolutionize the eye care industry, advance optimal patient outcomes and help people see brilliantly. The Pharmaceutical Medical Science Liaison - Dry Eye Medical (Science/Tech/Engineering Path) is primarily responsible for presenting scientific and clinical information on Alcon products and gathering insights to influence company strategies.
Director, Quality Assurance & Compliance Promega CorpDirector, Quality Assurance & ComplianceMadison, WIExperience 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). Travel will be required for inspections, vendor audits, and clinical site oversight activities, estimated at 1525% annually, with elevated travel during inspection preparation and submission periods.
Expert, Global Compliance AMETEK IncExpert, Global ComplianceMadison, WIJob Description: Reporting to the Director of Global Service & Quality, the Global Compliance Expert is responsible for defining, implementing, and maintaining global product regulatory compliance, certification, and trade/export compliance activities for all products, ensuring conformity with applicable international regulations throughout the full product lifecycle. AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.5 billion.
NewInvestment Compliance Consultant Northwestern MutualInvestment Compliance ConsultantMilwaukee, WIRisk Assessment & Identification: Leverages industry knowledge to determine and seek hazards that could potentially prevent the program, enterprise, or investment from achieving their objectives; designs systematic processes of identifying severity of hazards and evaluating the scale and impacts of any associated risk on the business. Project Management (NM) - Advanced, Cross Functional Partnering & Planning (NM) - Intermediate, Risk Assessment & Identification (NM) - Intermediate, Decision Making (NM) - Intermediate, Attention to Detail (NM) - Advanced, Policy & Procedure (NM) - Intermediate, Continuous Improvement (NM) - Intermediate.
Life Sciences Supply Chain and Operations - Supply Chain Planning Manager Accenture PlcLife Sciences Supply Chain and Operations - Supply Chain Planning ManagerMilwaukee, WIAs part of working with clients you will help with several aspects of life sciences integrated planning including: Integrated Planning Strategy: Design and implement IBP/S&OP frameworks tailored to life sciences environments, accounting for regulatory release cycles, CMO/CDMO network complexity, and the distinct planning dynamics of biopharma and med tech product portfolios. Accenture is a leading solutions and services company that helps the world's leading enterprises reinvent by building their digital core and unleashing the power of AI to create value at speed across the enterprise, bringing together the talent of our approximately 786,000 people, our proprietary assets and platforms, and deep ecosystem relationships.
Associate General Counsel Marquette UniversityAssociate General CounselMilwaukee, WIThe Associate General Counsel will use their advanced legal expertise to focus on certain practice areas based upon institutional needs and as work is allocated across the Office of the General Counsel (OGC), which may include, but is not limited to: labor and employment law matters; regulatory and nonprofit compliance; contract drafting and review; intercollegiate athletics; dispute and litigation management; sponsored research and intellectual property; real estate; institutional governance; and strategic legal counsel on all matters arising from university operations, including the development, interpretation, and implementation of institutional policies and procedures in alignment with the university's mission. Optimize the delivery of legal services to the university by managing outside counsel for quality and cost efficiency, improving internal OGC processes and workflows, and advancing operational and technology initiatives that strengthen service, responsiveness, and overall effectiveness in support of university strategies.
NewDirector, Supplier Quality Saputo IncDirector, Supplier QualityMilwaukee, WI$148,875–$223,315 / yearPartner with senior leaders across Procurement, Supply Chain, Operations, Research & Development, Commercialization, Regulatory Affairs, and Quality Assurance to ensure supplier quality requirements are fully integrated across the product life cycle. Drive a risk-based supplier quality management framework that proactively identifies, assesses, mitigates, and monitors supplier-related quality, food safety, regulatory, business continuity, and reputational risks.
NewVice President Internal Audit and Compliance Wisconsin Physicians Service Insurance CorpVice President Internal Audit and ComplianceMadison, WIRemote$235,000–$275,000 / yearThis Vice President drives continuous improvement, fosters a culture of integrity, and represents the Audit and Compliance functions in high visibility forums, including presentations to executive leadership and the Audit, Compliance & Risk Committee of the Board. We are open to remote work in the following approved states: Colorado, Florida, Georgia, Illinois, Indiana, Iowa, Michigan, Minnesota, Missouri, Nebraska, New Jersey, North Carolina, Ohio, South Carolina, Texas, Virginia, Wisconsin.
Licensing Engineer EnergySolutions LLCLicensing EngineerWIPrimarily responsible for license and regulatory compliance activities, such as preparing licensing documentation and submittals, supporting regulatory inspections, drafting regulatory position briefings, ensuring timely and adequate reporting to regulatory agencies. Represents Licensing and Regulatory Affairs on company teams, and effectively communicates activities/concerns to the Regulatory Affairs organization.
NewCustomer Care Representative Envista Holdings CorpCustomer Care RepresentativeMadison, WI$21.80–$26.70 / hourEnvista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. Target Market Salary Range: Actual compensation packages take into account a wide range of factors that are unique to each candidate, including but not limited to geographic location; skill sets; relevant education and certifications; depth of experience; performance; and other business and organizational needs.
Advisor- API/DS Network Contamination & Bioburden Control Strategy Eli Lilly and CoAdvisor- API/DS Network Contamination & Bioburden Control StrategyKenosha, WI$129,000–$189,200 / yearOur current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Basic Requirements: 7+ years' experience in Pharmaceutical Manufacturing with a focus on technical support of synthesis/fermentation/cell culture and purification stages of API, Drug Substance- front line manufacturing support (clinical/commercial) development of contamination control elements for manufacturing stages/systems, execution and operation of systems and continuous improvement of systems in a highly regulated environment.
Director of Environmental, Health & Safety Charter Manufacturing Company, IncDirector of Environmental, Health & SafetyMequon, WIFull timeYou will partner with leaders across the business, influence change from the shop floor to senior leadership, and help ensure our teams operate safely, responsibly, and with purpose. The Director of Environmental, Health and Safety will be expected to build constructive relationships across all levels of the business, lead through change, develop motivated and accountable teams, and help create a culture where environmental and safety performance is owned throughout the organization.
Engineering Compliance Manager Douglas Dynamics IncEngineering Compliance ManagerMilwaukee, WIWorking Environment: Predominantly office setting with occasional lab, outdoor, and manufacturing environment requiring personal protective equipment (PPE) including hearing protection, eye protection and metatarsal guards required, other safety PPE as needed. We bring these values to life through our Winning Behaviors, which shape how we serve our customers, support one another, and succeed together: Be Customer & Results Driven Consider the customer in everything you do and focus on meaningful outcomes.
NewCustomer Care Representative Envista DentistryCustomer Care RepresentativeMadison, WisconsinEnvista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.
Compliance Manager (923) ABC Supply Co IncCompliance Manager (923)Beloit, WIThe position works closely with executive leadership and departments including Legal, Human Resources, Finance, Operations, Internal Audit, and other business units to promote a culture of integrity, accountability, and regulatory compliance. Position Summary: The Compliance Manager serves as the second-in-command of the Compliance Department, supporting the Director in leading, administering, and continuously improving the organization's compliance program.
Engineering Compliance Manager Douglas DynamicsEngineering Compliance ManagerMilwaukee, WIWorking Environment: Predominantly office setting with occasional lab, outdoor, and manufacturing environment requiring personal protective equipment (PPE) including hearing protection, eye protection and metatarsal guards required, other safety PPE as needed. We bring these values to life through our Winning Behaviors, which shape how we serve our customers, support one another, and succeed together: Be Customer & Results Driven – Consider the customer in everything you do and focus on meaningful outcomes.
Manager of Product Design Compliance ITWManager of Product Design ComplianceAppleton, WisconsinActively participate in key industry associations and technical committees; pursue leadership roles (e.g., expert member, delegate, vice-chair and chair) where strategic. The Manager of Product Design Compliance ensures ITW Welding’s products meet all applicable safety, certification, and regulatory requirements.
NewManagement Assistant Veterans Affairs, Veterans Health AdministrationManagement AssistantMilwaukee, WIPosition Description/PD#: Management Assistant/PD235340 Relocation/Recruitment Incentives: Not Authorized Critical Skills Incentive (CSI):Not Authorized Permanent Change of Station (PCS):Not Authorized PCS Appraised Value Offer (AVO): Not Authorized Requirements Conditions of Employment You must be a U.S. Citizen to apply for this job To be considered for this position, you must complete all required steps in the process. The position performs a wide range of administrative, human resources, fiscal, program management, consult management, scheduling, credentialing support, and operational coordination functions that support clinical operations, regulatory compliance, accreditation readiness, and continuity of patient care within a complex healthcare environment.
University Counsel and Assistant Secretary to the Board of Trustees Lawrence UniversityUniversity Counsel and Assistant Secretary to the Board of TrusteesAppleton, WIProvides expert legal opinions, advice, and counsel on matters affecting a private liberal arts institution, including but not limited to statutory and regulatory compliance, employment law, University policies and procedures, student affairs, contracts and grants, real estate transactions, tax matters, and liability and insurance issues. Anticipates, identifies, and mitigates legal and reputational risks; provides timely and strategic counsel to University officers, often in matters of high sensitivity and significant institutional impact.
Senior Compliance Engineer Accuray IncSenior Compliance EngineerMadison, WIBut our commitment to innovation offers a truly unique opportunity: the chance to change the fight against cancer - helping to develop, introduce and support new treatment delivery systems and software that will give new hope and new health to cancer patients and cancer survivors around the world. This role partners cross-functionally with Engineering, Quality, Regulatory Affairs, and Manufacturing to proactively design for compliance, manage certification activities, and sustain approvals in a highly regulated medical device environment.
Scientist I, CMC Process Development Arrowhead PharmaceuticalsScientist I, CMC Process DevelopmentMadison, WI$85,000–$95,000 / 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.
Director, Quality Management Systems Arrowhead PharmaceuticalsDirector, Quality Management SystemsMadison, WI$180,000–$210,000 / yearManage and oversee all aspects of GxP QMS functions for clinical and commercial products, including Document Control and Training; Non-conformance Management and CAPA, Internal QMS Audits, Quality Management Review, and Change and Risk Management. Arrowhead 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.
Senior Scientist I, CMC Process Development Arrowhead PharmaceuticalsSenior Scientist I, CMC Process DevelopmentMadison, WI$115,000–$140,000 / 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.
NewPrincipal Product Manager OraclePrincipal Product ManagerMadison, WI$102,300–$209,500 / yearOracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business. With Oracle Cerner's innovative technology, we seamlessly package this valuable information into a range of services and solutions that integrate seamlessly into your favorite analytics tools, EHR applications like Millennium, and even new, groundbreaking applications developed in collaboration with our esteemed partners.
Director, Quality Management Systems Arrowhead Pharmaceuticals IncDirector, Quality Management SystemsVerona, WI$180,000–$210,000 / yearManage and oversee all aspects of GxP QMS functions for clinical and commercial products, including Document Control and Training; Non-conformance Management and CAPA, Internal QMS Audits, Quality Management Review, and Change and Risk Management. Arrowhead 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.