394 regulatory manager jobs at 203 companies in Roberts, WI
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Regulatory Change Project Manager
Cincinnati or Minneapolis
$86k-$102k/yr HybridFull Time
5+ YOEBachelor's degree or equivalent experience and typically more than five years of applicable experience. Requires regulatory, financial services, risk, compliance, analytical, facilitation, project management, and communication expertise.
Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft Access, Microsoft PowerPoint
1mo
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Quality and Regulatory Manager
Minneapolis, Minnesota, United States
$150k-$180k/yr OnsiteFull Time
7+ YOE3+ MgmtBachelor's degree or equivalent,7+ years regulatory/quality experience in medical device industry,3+ years management,expertise in FDA QSR,ISO 13485,EU MDR,global submissions,510(k)/PMA/SaMD,strong communication.
2mo
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Quality & Regulatory Manager
Vadnais Heights or Santa Rosa
$140k/yr OnsiteFull Time
15+ YOE7+ MgmtOversee and improve QMS, manage internal audits to ISO 13485 / IATF 16949, drive continuous improvement, lead quality team, 15 years manufacturing experience, 7+ years quality management, 5+ years injection molding experience, valid driver license, travel up to 20%.
2mo
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Regulatory Financial Reporting Manager
Minneapolis or New Hampshire or United States or Canada
$120k-$145k/yr RemoteFull Time
5+ YOE5+ years in bank regulatory reporting with hands-on FFIEC Call Report experience; deep FFIEC and U.S. GAAP knowledge; bachelor's in Accounting/Finance required; CPA/CFA preferred; advanced Excel and regulatory reporting systems experience.
Axiom, Wolters Kluwer, Microsoft Excel
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VP, Regulatory Specialist
San Francisco or Edina or Los Angeles or Philadelphia or Tampa or Denver or Seattle or New York City or Chicago
$105k-$193k/yr HybridFull Time
3+ YOE3+ years insurance regulatory/filing experience (P&C) with California filings, ability to prepare regulator-ready materials, strong project management and communication, bachelor\u0002s or equivalent experience.
SERFF
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Regulatory Analyst 1
Minneapolis, Minnesota, United States
$21-$23/hr OnsiteFull Time
1+ YOEBachelor's in chemistry or related field required, 1-2 years regulatory/compliance experience in the chemical industry, fluent English, proficiency with Microsoft Office/Excel, ability to manage multiple projects and handle repetitive data tasks.
Microsoft Excel, Microsoft Office Products, RMDM, WERCS, HEARS
3w
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Senior Regulatory Affairs Specialist
Mason or Minnetonka
$106k-$130k/yr OnsiteFull Time
4+ YOEPrepare and submit global regulatory filings, develop regulatory strategies, support risk management and design control, interact with regulatory agencies; 4+ years device regulatory experience and bachelor’s degree or equivalent.
Microsoft Office
2mo
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Regulatory and Localization Project Manager
Golden Valley or Melville or Aurora
$108k-$184k/yr HybridFull Time
10+ YOE10+ years working with product regulations and certifications across safety, home comfort, security, or energy efficiency; experience with agency approval processes, technical documentation and packaging, trademark/copyright considerations, Microsoft Office, and global teams.
Microsoft Office
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Senior Regulatory Affairs Specialist
Minneapolis, Minnesota, United States
OnsiteFull Time
Prepare and manage regulatory submissions, maintain licenses, provide regulatory guidance across product development, and mentor junior staff; tertiary science/engineering qualification and medical device regulatory experience required.
3mo
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Clinical & Regulatory Affairs
Brooklyn Park or Eagan or Maple Grove or Geneva or United States or Europe
HybridFull Time
Experience in clinical operations, clinical monitoring, physician support, field clinical education, global regulatory compliance, or clinical trial management within the medical device industry.
1mo
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Quality and Regulatory Manager - Back to Nature
Minneapolis, Minnesota, United States
OnsiteFull Time
5+ YOEBachelor's in food science/engineering,5+ years QA/food safety experience,certifications (GFSI Lead Auditor,FSMA PCQI,HACCP Manager,Thermal Processing),nut food safety expertise,and ability to lead audits and regulatory programs.
1mo
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Manager, Regulatory & Payer Operations Support
Minneapolis, Minnesota, United States
$96k-$144k/yr HybridFull Time
5+ YOE2+ Mgmt5+ years in healthcare reimbursement or payer operations, 2+ years leadership, DME experience, knowledge of Medicare/Medicaid/commercial payers, audit and compliance experience, strong communication and project management skills.
Microsoft Office
3mo
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VP Global Quality and Regulatory
Plymouth, Minnesota, United States
$220k-$225k/yr OnsiteFull Time
15+ YOE15+ years global regulatory/quality leadership in medical devices; engineering degree; ASQ/RAC preferred; ISO 13485/14971; FDA/CE knowledge; able to lead global teams.
eQMS, Quality Management System (QMS), Regulatory Submissions, FDA Regulations, ISO 13485, Regulatory Tools
4d
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Associate Director/Director for Regulatory Affairs
Minnesota or Minneapolis or New Hope or Michigan or Wyoming or Allegan or Denver or Hendersonville or Waunakee or Lunenburg or Navarre or Foley or Round Lake
RemoteFull Time
7+ YOE2+ MgmtAdvanced life sciences or pharmacy degree; 7–10+ years in pharmaceutical or biotechnology Regulatory Affairs; proven FDA ANDA, IND, and NDA submission leadership; generic drug strategy expertise and strong project management skills.
Food and Drug Administration (FDA)
2w
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SENIOR PROGRAM LEAD REGULATORY AFFAIRS
Plymouth, Minnesota, United States
$109k-$175k/yr HybridFull Time
6+ YOEBachelor’s degree in engineering, physical or biological science, or related field; 6+ years in medical devices, including 5+ in regulatory affairs. Expertise in FDA, global regulations, submissions, project management, and negotiations.
IDE, 510K, PMA, EU Technical Document, FDA
2w
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SENIOR PROGRAM LEAD REGULATORY AFFAIRS
Plymouth, Minnesota, United States
$109k-$175k/yr HybridFull Time
6+ YOEBachelor’s degree in engineering, physical or biological science, or related field; 6+ years in medical devices, including 5+ years in regulatory affairs. Expertise in FDA, global regulations, submissions, quality, and project management.
IDE, 510K, PMA, EU Technical Document, FDA
1mo
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Director, Utility and Regulatory Innovation
Minneapolis or California or Colorado or Connecticut or Illinois or Maine or Michigan or Minnesota or Nevada or New Mexico or New Jersey or New York or North Carolina or Oregon or South Carolina or Virginia or Washington or District of Columbia or Wisconsin
$125k-$165k/yr HybridFull Time
10+ YOE10+ Mgmt10+ years utility/regulatory experience, stakeholder facilitation, staff and budget management, fundraising and proposal development, excellent written/oral skills, proficiency with Microsoft Office, bachelor’s or master’s degree preferred.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Microsoft SharePoint
1mo
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Sr Compliance / Regulatory Analyst - Information Lifecycle Management
Minneapolis or Appleton
$82k-$110k/yr HybridFull Time
3+ YOEBachelor’s degree or substantially relevant experience, 3–10 years of related experience, and in-depth knowledge of applicable laws, regulations, regulatory requirements, and industry best practices.
Information Lifecycle Management (ILM)
2mo
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Director, Quality & Regulatory- Mergers & Acquisitions (M&A)
Colorado Springs or Nashville or Bothell or Gainesville or San Diego or Plymouth or Cambridge
$162k-$258k/yr HybridFull Time
15+ YOE15+ years in FDA-regulated medical device environments, leadership in quality/regulatory and M&A, Bachelor's required (Master's/MBA preferred), knowledge of FDA/ISO/EU MDR, QMS and KPI-driven governance.
QMS, FDA, ISO 13485, ISO 14971, EU MDR, TSLA, KPI
1mo
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Regulatory Compliance Officer Export Compliance
Greenwood or Bondurant or Brooklyn Park or Roanoke or Richmond or Sanford
OnsiteFull Time
Leads export compliance program; expert in EAR, ITAR, OFAC; conducts classifications, license management, screening, audits, and training; liaises with government agencies.
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