142 regulatory specialist jobs at 108 companies in Montclair, CA
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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
4w
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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
4w
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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/rate-filing experience (P&C), hands-on regulator interaction (California experience), ability to prepare filing materials and translate actuarial outputs, bachelor's degree or equivalent.
SERFF
3w
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Regulatory Specialist
Irvine, California, United States
$75k/yr OnsiteFull Time
2+ YOEBachelor's degree required (Master's preferred),2+ years in higher education compliance/accreditation,knowledge of accreditation standards,project management and documentation skills,Microsoft Office proficiency.
Microsoft Office Suite
2mo
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Regulatory Permitting Specialist
El Segundo or Salt Lake City
$100k-$120k/yr OnsiteFull Time
Experience preparing state/local environmental and permitting submissions, strong technical writing and communication, self-directed in fragmented regulatory environments, and willingness to travel domestically for meetings and hearings.
ArcGIS, QGIS, Google Earth
2d
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Senior Specialist Regulatory Affairs
Irvine, California, United States
$96k-$160k/yr HybridFull Time
2+ YOEBachelor's degree in engineering, life sciences, regulatory affairs, or related field and 2+ years of regulatory affairs experience. Requires regulatory submissions and compliance experience; RAC and global submissions experience preferred.
1w
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Regulatory Affairs Specialist
Burbank, California, United States
$75k-$85k/yr RemoteFull Time
2+ YOERequires 2–3 years of dietary supplement regulatory affairs experience, claims and label review experience, FDA/FTC knowledge, DSHEA and 21 CFR Part 111 familiarity, and a relevant bachelor's degree.
Claude, Notion AI, Amazon
1mo
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Regional Regulatory Specialist
Northridge, California, United States
$25-$26/hr OnsiteFull Time
0+ YOEManage regulatory documents and submissions for clinical studies; high attention to detail; 0–3+ years clinical/biological research experience; proficiency with Microsoft Office, CTMS, eRegs/eDocs; strong communication skills.
Microsoft Outlook, Microsoft Word, Microsoft Excel, CTMS, eRegs/eDocs, Office365
2mo
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REGULATORY AFFAIR SPECIALIST
Torrance, California, United States
$120k-$150k/yr OnsiteFull Time
8+ YOE8-10 years in Regulatory Affairs/Quality within medical devices; hands-on Class I; FDA 21 CFR Part 820, ISO 13485; DHF/DMR, labeling, audits; cross-functional collaboration.
1mo
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Regulatory Affairs Specialist
Torrance, California, United States
OnsiteFull Time
3+ YOE3+ years medical device experience with ≥1 year in regulatory affairs; BA/S in science/engineering or equivalent; RA certification (RAC) a plus; knowledge of global regulations, QSR820, ISO 13485, IVDR; strong communication and analytical skills.
e-MDR, MDSAP
2mo
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Senior Regulatory Affairs Specialist
Marlborough or Irvine or Arden Hills or Maple Grove
$89k-$170k/yr HybridFull Time
4+ YOEBachelor’s degree in a scientific or technical discipline, 4+ years of medical-industry regulatory affairs experience, and experience with 510(k), EU MDR, or international regulatory registrations.
Microsoft Office
3w
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Regulatory Affairs Specialist II
Duarte, California, United States
$41-$63/hr OnsiteFull Time
2+ YOEPrepare and review regulatory submissions, support investigators and manufacturing/QC/QA teams, draft SOPs and protocols; 2+ years regulatory experience with Bachelors (or 0–2 with Masters).
iRIS
1mo
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Regulatory Affairs Specialist II
Brea, California, United States
$86k-$105k/yr HybridFull Time
2+ YOEBachelor's degree, 2+ years regulatory affairs experience in medical devices (or Master's +1 year). Strong EU MDR knowledge (CER, SSCP, PSUR, PMS). Experience with international submissions and regulatory strategy.
Microsoft Office
1mo
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Regulatory Specialist II, Clinical Trials
Pasadena, California, United States
$87k-$113k/yr OnsiteFull Time
3+ YOEBachelor's degree or 3+ years clinical research experience; working knowledge of FDA/IRB regulations; preparing regulatory submissions, maintaining study documentation, and supporting quality assurance; BLS and clinical research certifications preferred.
1mo
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Regulatory Affairs Specialist, Sr.
Irvine, California, United States
$85k-$120k/yr OnsiteFull Time
5+ YOE5+ years regulatory affairs experience, experience with FDA 510(k)/PMA and international registrations, SOP and audit experience, strong analytical and communication skills.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Outlook
1mo
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Sr. Regulatory Compliance Specialist
Irvine, California, United States
$63k-$97k/yr RemoteFull Time
3+ YOE3+ years' regulatory compliance experience in food/beverage/pharmaceutical, knowledge of global food laws, label and ingredient compliance, strong communication and project leadership skills.
Microsoft Office, PIM, Decernis gComply, Decernis gComply Plus, Trustwell/Genesis
1w
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Senior Regulatory Affairs Specialist
Irvine or Marlborough or Arden Hills or Maple Grove
$89k-$170k/yr HybridFull Time
4+ YOEBachelor's degree in a scientific, technical, or related discipline and 4+ years of medical industry regulatory affairs experience, including 510(k), EU MDR, or international registrations.
Microsoft Office, 510(k), EU MDR, PMA
1mo
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State Regulatory Exam Specialist
Los Angeles, California, United States
$60k-$80k/yr OnsiteFull Time
Knowledge of multi-state auto finance regulatory requirements and consumer financial protection laws; strong verbal and written communication; detail oriented; Bachelor's degree in business required; auto finance experience preferred.
Daybreak, Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Vision, web-based application
2mo
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Senior Specialist, Regulatory Affairs
El Segundo, California, United States
$80k-$90k/yr HybridFull Time
3+ YOE3+ years regulatory experience in cosmetics/pharma/consumer goods, Bachelor's in life sciences/pharmacy/chemistry, Mandarin proficiency, Microsoft Office skills, ability to work onsite 60%+ and manage international product registrations.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1d
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Senior Regulatory Affairs Specialist - Onsite
Irvine, California, United States
$92k-$138k/yr OnsiteFull Time
4+ YOEBachelor's degree in science or engineering with 4+ years of medical device regulatory experience, or advanced degree with 2+ years. Requires FDA submissions experience; RAC and global regulatory experience preferred.
Investigational Device Exemption (IDE), Premarket Approval (PMA), 510(k), European Union Medical Device Regulation (EU MDR), ISO 13485, ISO 14971, CE Mark
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