215 regulatory manager jobs at 121 companies in Marina, CA
4d
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Regulatory Program Manager
San Jose or Sacramento
$124k-$231k/yr OnsiteFull Time
2+ YOEBachelor’s degree or equivalent relevant experience, 2+ years as a regulatory or financial analyst, Microsoft Office proficiency, and a valid California driver's license; utility regulation knowledge preferred.
Microsoft Office
3w
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Senior Regulatory Affairs Manager – Digital Solutions (on-site)
Sylmar or Santa Clara
$131k-$261k/yr OnsiteFull Time
9+ YOEBachelor's in a related field or equivalent, 9+ years regulatory experience in medical devices, QMS experience, knowledge of FDA/EU MDR/ISO13485, leading regulatory submissions and mentoring staff.
1mo
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Regulatory Lead, North America
San Jose, California, United States
$251k-$600k/yr OnsiteFull Time
JD from an ABA-accredited law school; significant regulatory experience in the US and Canada; experience engaging regulators and managing investigations; leadership experience managing teams and advising senior executives.
3w
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Senior Regulatory Affairs Specialist
Sunnyvale, California, United States
$129k-$218k/yr HybridFull Time
8+ YOERequires 8+ years of medical device regulatory affairs experience, knowledge of US, Canadian, and EU regulations, regulatory submissions, design controls, risk management, and a bachelor's degree or higher.
da Vinci, Ion, U.S. FDA 510(k), Health Canada, EU MDR, Letters to File, pre-submissions
3w
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Senior Regulatory Affairs Manager – Digital Solutions (on-site)
Sylmar or Santa Clara
$131k-$261k/yr OnsiteFull Time
9+ YOEBachelor's degree and 9 years' regulatory experience within medical devices; QMS experience; authoring global submissions (PMA, 510(k), IDE, EU MDR); FDA and Notified Body interactions; mentoring staff.
3mo
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Senior Regulatory Affairs Specialist
San Jose, California, United States
$149k-$175k/yr OnsiteFull Time
4+ YOEBachelor's in a scientific discipline, 6 years regulatory submissions experience with BS (or 4 years with MS), knowledge of FDA and international device regulations (21 CFR 820, ISO 13485, EU MDR), ability to lead regulatory strategy and prepare submissions.
2d
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Senior Principal, Technical Program Management - Regulatory Compliance
United States or San Francisco or Oakland or San Jose or Colorado or Hawaii or Illinois or Maryland or Massachusetts or Minnesota or New Jersey or New York or Vermont or Washington or Washington
RemoteFull Time
10+ YOE10+ years in regulatory compliance, risk management, or related fields; deep global regulatory framework knowledge; complex cross-functional program leadership; strategic and hands-on execution skills.
GDPR, HIPAA, SOX, Software as a Service
1w
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SubChapter Lead Regulatory Affairs - Endocrinology and Fertility
Indianapolis or Branchburg or Santa Clara or Penzberg or Carlsbad or Rotkreuz or Pleasanton or Mannheim or Tucson or Motherwell
$111k-$259k/yr OnsiteFull Time
7+ YOEBachelor's or advanced science-related degree; 7+ years in diagnostics regulatory affairs; knowledge of IVD, pharmaceutical, or medical device regulations, FDA and international submissions, leadership, coaching, and stakeholder management.
US FDA, ISO 13485, ISO 27001, Agile
2w
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Senior Program Manager, Regulatory Compliance
Sunnyvale or Boulder or New York City or San Francisco
$164k-$239k/yr OnsiteFull Time
10+ YOEBachelor's degree or equivalent practical experience, 10 years in regulatory requirements, and cross-functional collaboration experience. Preferred: large-scale initiatives, executive communication, and applied AI experience.
AI
1mo
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Director Accreditation and Regulatory Compliance
Salinas, California, United States
$84-$105/hr OnsiteFull Time
2+ YOE2+ MgmtBachelor's degree required; CA RN license preferred. Minimum 2 years clinical plus 2 years managerial hospital experience; prior accreditation/regulatory leadership with TJC, CMS, Title 22, CDPH experience preferred.
2d
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Director of Regulatory Affairs
San Jose or California
$185k-$226k/yr OnsiteFull Time
Bachelor’s degree in finance, economics, accounting, or related field; MBA or CPA or equivalent experience; expertise in rate analysis, financial forecasting, budgeting, and utility regulation; valid California driver’s license.
word processing, spreadsheet software
2mo
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Associate Director, Regulatory Affairs (Robotics & Digital Solutions) - MedTech Surgery
Santa Clara, California, United States
$157k-$271k/yr HybridFull Time
10+ YOE2+ MgmtBachelor's required (advanced degree preferred); 10+ years regulatory affairs in medical devices incl. software; 2+ years people-management; experience with FDA software/cybersecurity, US and EU MDR, and software-enabled device approvals.
2mo
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Associate Director, Regulatory Affairs (Robotics & Digital Solutions) - MedTech Surgery
Santa Clara, California, United States
$157k-$271k/yr HybridFull Time
10+ YOE2+ MgmtBachelor's required (advanced degree preferred), 10+ years regulatory affairs in medical devices (software-enabled systems), 2+ years people management, FDA and EU MDR experience, software/cybersecurity knowledge, experience with vision/robotics preferred.
2mo
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Sr. Regulatory Affairs Specialist , Medical Devices Operational Compliance Center (MD-OCC)
Sunnyvale, California, United States
$171k-$231k/yr OnsiteFull Time
7+ YOE7+ years working with engineering teams, 5+ years technical product/program management, experience with regulatory filings (FDA/21 CFR 820, ISO13485, MDD/IVD), Class II/III devices, bachelor's in scientific discipline, strong analytical and communication skills.
AI/ML, GenAI, Analytics
2mo
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Engineering Program Manager (EPM) — Ecodesign Regulatory Compliance
Cupertino, California, United States
OnsiteFull Time
Lead cross-functional ecodesign compliance programs, translate sustainability regulations into compliance plans, influence product design, and coordinate stakeholders across legal, government affairs, and engineering.
4w
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Product Manager
Santa Clara, California, United States
$135k-$155k/yr HybridFull Time
3+ YOE3+ years product management in medical devices, bachelor's degree, experience with NPI/launches, SKU lifecycle, promotional materials, Excel and CRM (Salesforce), familiarity with design controls and regulatory constraints.
Microsoft Excel, Salesforce, Microsoft Office
3mo
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Clinical Manager
Santa Clara, California, United States
$60/hr OnsiteFull Time
3+ YOE3+ MgmtRN licensed in CA; BSN required; 3 years minimum management in hospice/home health or 4 years clinical with leadership experience; strong leadership, teamwork, and regulatory knowledge.
Electronic Health Records, Regulatory Compliance Tools, Microsoft Office, Healthcare IT
3mo
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Clinical Trial Manager
Campbell, California, United States
$136k-$152k/yr HybridFull Time
5+ YOE1+ Mgmt5+ years of clinical research management, preferably in medical devices; IDE studies; FDA/GCP knowledge; strong collaboration and communication; willingness to travel 20-30%
Clinical Data Management Systems, Regulatory Compliance, GCP, FDA Regulations, IDE
1d
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Program Coordinator (Govt Regulatory)
United States or Los Angeles or San Jose or San Francisco or San Diego or Fresno or Mammoth Lakes or Long Beach
$20-$37/hr OnsiteFull Time
1+ YOEAssociate degree or equivalent education and experience required, with 1–3 years of experience. Bachelor's degree and 3–5 years of experience preferred.
3w
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Associate General Counsel, Energy & Regulatory
Santa Clara or Idaho or Ohio or Tennessee or Texas
$230k-$250k/yr HybridFull Time
7+ YOEJ.D. and bar admission,7+ years energy regulatory experience with substantive FERC and State PUC practice, generator interconnection expertise, strong project and stakeholder management, and excellent communication.
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