2,688 regulatory specialist jobs at 1,588 companies in United States
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Senior Regulatory Affairs Specialist
San Diego, California, United States
$91k-$152k/yr HybridFull Time
5+ YOE5+ years regulatory affairs experience for medical devices, proficiency with US and EU device regulations, experience supporting 510(k)/license/technical documentation submissions, strong technical writing and communication.
4w
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Sr Regulatory Affairs Specialist- Medical Devices
Schaumburg, Illinois, United States
$93k-$144k/yr OnsiteFull Time
3+ YOE3+ years regulatory/quality experience in US and Canada medical devices; authored a 510(k); Health Canada licensing experience; BS in science or related; strong writing and regulatory system skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, GUDID, UDI, US FDA electronic system
2w
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Regulatory Specialist
United States
RemoteFull Time
1+ YOEPrepare and submit regulatory documents, maintain regulatory files, ensure ICH-GCP/FDA/IRB compliance, support study start-up and audit readiness; 1–3 years clinical research/regulatory experience preferred.
CRIO, Veeva, Complion, Microsoft Office
1mo
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Regulatory Specialist
Fairfield, New Jersey, United States
$90k-$100k/yr OnsiteFull Time
Experience in regulatory affairs for cosmetics or nutrition, managing customer documentation portals, FDA compliance, KPI tracking, and cross-functional collaboration. Familiarity with regulatory databases and stakeholder communication; bachelor's in chemistry/biology preferred.
Salesforce, AODocs, PCPC, CIR, TSCA, EPA, Health Canada, EWG, VEEVA Vault
1mo
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Regulatory Specialist
Audubon, Pennsylvania, United States
OnsiteFull Time
2+ YOEPrepare and submit FDA regulatory submissions (510(k), IDE, PMA), review labeling and documentation, coordinate with cross-functional teams; 2+ years regulatory affairs experience in medical device industry; bachelor’s degree or equivalent.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Teams
2mo
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Regulatory Affairs Specialist
Logan, Utah, United States
OnsiteFull Time
2+ YOERegulatory affairs specialist with 2-5 years in medical devices, FDA/EU MDR/ISO 13485, submissions, strong communication.
FDA Regulations, 21 CFR Part 820, EU MDR, ISO 13485, MDSAP, eSTAR, EUDAMED
2mo
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Regulatory Specialist
Houston, Texas, United States
HybridFull Time
1+ YOEBachelor’s degree; at least 1 year of CRC experience; FDA/IRB/regulatory affairs experience; strong communication and MS Office; project management skills.
Microsoft Office, Excel, PowerPoint
4w
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Regulatory Specialist
Williamsburg, Virginia, United States
$66k-$117k/yr OnsiteFull Time
6+ YOEBachelor's in related field and minimum 6 years' environmental regulatory and permitting experience for energy/utility projects, valid driver's license, strong communication and project management skills.
Microsoft Office
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Regulatory Specialist
Dallas or Houston or Tulsa or Houston
HybridFull Time
3+ YOEPrepare and submit state severance tax and royalty reports; reconcile production and revenue data; support audits; 3–5 years regulatory or production accounting experience; bachelor’s degree preferred.
Microsoft Excel
2mo
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Regulatory Affairs Specialist
Huntersville, North Carolina, United States
OnsiteFull Time
3+ YOEBachelor’s degree; at least 3 years regulatory affairs experience in medical devices or pharma; strong knowledge of domestic/global regulations; RAC a plus.
Microsoft Office Suite, Regulatory software
4w
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Regulatory Specialist
Richmond, Virginia, United States
OnsiteFull Time
1+ YOEBachelor's in environmental science, 0-3 years experience, regulatory review and permitting experience preferred, strong technical writing, MS Office and Adobe Acrobat proficiency, team-oriented and detail-focused.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Adobe Acrobat
3w
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Regulatory Specialist
San Juan Capistrano, California, United States
$95k-$150k/yr OnsiteFull Time
5+ YOEPrepare and manage environmental permits, ensure regulatory compliance, coordinate agencies, produce technical reports, manage projects and staff; requires applicable environmental/engineering degree and extensive California permitting experience.
Microsoft Word, Microsoft Excel
3mo
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Regulatory Specialist
United States
$64k-$135k/yr RemoteFull Time
2+ YOEBachelor’s degree in Environmental Science, Engineering, Law, or related field; 2+ years regulatory compliance/licensing; knowledge of FPA, 18 CFR, FERC/USACE; experience with large infrastructure projects; strong communication and stakeholder management.
FERC, USACE, FPA, 18 CFR
3mo
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REGULATORY SPECIALIST
Chicago, Illinois, United States
OnsiteFull Time
5+ YOEBachelor's in Food Science, Nutrition, Biology, Engineering or related field; minimum 5 years in food manufacturing with at least 3 years in regulatory labeling; strong FDA/USDA labeling knowledge; experience with TraceGains/ESHA/SAP; cross-functional collaboration.
TraceGains, ESHA Genesis, SAP, Microsoft Office, Dragonfly (label review software), SharePoint, PLM
2w
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Sr. Regulatory Specialist
Memphis, Tennessee, United States
$70k-$83k/yr OnsiteFull Time
1+ YOEManage licensing, regulatory intelligence, controlled-substance due diligence, and provide operational regulatory support in pharmaceutical distribution/3PL environments.
Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Suspicious Order Monitoring systems
3w
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Regulatory Specialist III
Little Rock, Arkansas, United States
OnsiteFull Time
Experience with FDA regulatory submissions (IND/IDE/BLA/NDA/510(k)), strong written/verbal communication, critical thinking, and ability to prepare and maintain regulatory documents; PhD or relevant degree/experience paths described.
2mo
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Sr. Regulatory Specialist
Covington, Georgia, United States
HybridFull Time
4+ YOELead regulatory strategy, U.S. and EU submissions, STED files, cross-functional collaboration.
1mo
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Sr. Specialist, Regulatory
United States or Canada
$75k-$95k/yr HybridFull Time
3+ YOE3+ years regulatory experience in cosmetics, BS or higher in science required, working knowledge of US/Canada regulatory frameworks, strong communication and organizational skills, proficiency with Microsoft Office and web-based submission portals, willing to travel domestically.
Microsoft Excel, Microsoft Word, Adobe, Microsoft PowerPoint
1w
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REGULATORY SPECIALIST - CRI
Dallas, Texas, United States
OnsiteFull Time
1+ YOEBachelor's degree and one year each in medical or clinical, clinical research, and research regulatory affairs experience. Microsoft Office proficiency; CCRC, CCRP, and GCP certification preferred.
Microsoft Office
2mo
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Regulatory Specialist IV
Sacramento or California or United States
$102k-$125k/yr OnsiteFull Time
10+ YOE10+ years environmental/regulatory experience (8+ with advanced degree); knowledge of California permitting (CWA, CEQA, ESA, etc.), technical writing, GIS, field data, and agency coordination.
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