531 regulatory manager jobs at 291 companies in Menifee, CA
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Regulatory Program Manager III
Irvine or United States
RemoteFull Time
7+ YOE5+ MgmtBachelor's degree, project management certificate, 7+ years program/product management experience, 5+ years project leadership, strong regulatory compliance, stakeholder management, communication, leadership, and proficiency with listed IT tools; ~10% travel.
Miro, Jira, SDD, Polarion, SAP, Pro Codex, Homologation DataBase, Team Center
1mo
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Regulatory Affairs Manager
Santa Ana, California, United States
$38-$48/hr OnsitePart Time
5+ YOEBachelor's in a scientific field, 5+ years regulatory affairs experience in dietary supplements/botanicals/TCM, PCQI required, HACCP preferred, audit and FDA regulatory experience.
1mo
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Regulatory Affairs Manager I
Lake Forest, California, United States
$131k-$169k/yr OnsiteFull Time
5+ YOE3+ MgmtBachelor's degree or equivalent experience, 5 years relevant experience, 3 years leadership, experience with regulatory submissions, GxP/SOP compliance, medical device/pharma support, and fluent English.
GxP, Standard Operating Procedures (SOPs)
2w
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Manager I, Regulatory Affairs Operations
Irvine, California, United States
$98k-$137k/yr HybridFull Time
5+ YOE5+ years regulatory operations experience with Veeva RIMS administration, eCTD/submissions management, strong organization, communication, and regulatory knowledge (FDA/EMA/ICH).
Veeva Vault RIM, Veeva RIMS, eCTD, eCTD StartingPoint® Templates, eCTD Viewers, DXC (ISI) Toolbox, Microsoft Word, Microsoft Project, Microsoft Excel
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
2w
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Manager I, Regulatory Affairs Operations
Irvine, California, United States
$98k-$137k/yr HybridFull Time
5+ YOEBachelor's in science/health or equivalent, 5+ years regulatory operations experience with submissions/publishing, Veeva RIMS administration, eCTD content planning, regulatory knowledge (FDA/EMA/ICH).
Veeva Vault RIM, Veeva RIMS, eCTD, eCTD StartingPoint® Templates, eCTD Viewers, DXC (ISI) Toolbox, Microsoft Word, Microsoft Project, Microsoft Excel
2w
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Quality Assurance & Regulatory Manager
Irvine, California, United States
$100k/yr OnsiteFull Time
5+ YOE2+ MgmtBachelor's in food science or related field,5+ years QA/regulatory experience in food/supplements,2+ years leading teams,strong knowledge of FDA/FSMA/FSVP/GMP/HACCP,TraceGains experience.
TraceGains
1w
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Project Manager, Regulatory Affairs
Irvine, California, United States
$130k-$140k/yr RemoteFull Time
5+ YOEBachelor’s degree in a scientific discipline, 5–8 years of medical device regulatory affairs experience, global regulations knowledge, technical writing, project management, and Microsoft Office Suite proficiency.
Microsoft Office Suite
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Senior Regulatory Engineer
Irvine, California, United States
$135k-$169k/yr HybridFull Time
5+ YOEBachelor's in a technical field, 5+ years in automotive certification/product safety/homologation, expertise in one or more regulatory domains, familiarity with WVTA/US self-certification, proficiency with Jama/Codebeamer/Flow, ability to author DVPs and manage regulation-to-code traceability.
Jama, Codebeamer, Flow, Python, CAPL, RxSWIN
3mo
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Regulatory Affairs Coordinator
Orange or Irvine
$36-$59/hr OnsiteFull Time
3+ YOEExperience submitting IRB applications; 3-5 years RAC or assistant RAC; strong English communication; regulatory knowledge; ability to manage multiple tasks and maintain confidentiality.
OnCore, Microsoft Office, Zoom
2w
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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
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Sr. Regulatory Operations Coordinator
Irvine, California, United States
$70k-$80k/yr HybridFull Time
1.5+ YOEBA/BS in scientific/technical field,1.5+ years in regulated industry,experience with regulatory documentation,MS Office and Adobe Acrobat skills,ability to manage regulatory systems and coordinate cross-functional partners.
Microsoft Office, Adobe Acrobat, Product Lifecycle Management Systems
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Senior Manager, Regulatory Affairs US & Canada Strategy Lead, Therapeutic Neuroscience - Hybrid
Irvine or North Chicago
$125k-$237k/yr HybridFull Time
5+ YOEAdvanced degree or regulatory certification and minimum 5 years regulatory/R&D experience; experience with FDA interactions, negotiation, regulatory submissions, and US/Canada affiliate strategy.
3mo
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Regulatory Compliance Director
Carlsbad or Irvine or Milpitas or Richmond
$170k-$250k/yr HybridFull Time
8+ YOE1+ Mgmt8+ years leading regulatory compliance in consumer electronics; governance, cross-functional collaboration, international travel.
BOMs, ECR/ECO/MCO, GCF, PTCRB, Carrier Certifications
1w
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Senior Regulatory Compliance Analyst
Lake Elsinore, California, United States
$11k-$14k/mo OnsiteFull Time
3+ YOEBachelor's degree in a relevant science or engineering field, 3 years of water, wastewater, or environmental compliance experience, California Class C driver's license, and regulatory reporting and program management skills.
databases
1mo
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Principal Regulatory Affairs Specialist – Vascular (on-site)
Santa Clara or Temecula
$100k-$200k/yr OnsiteFull Time
6+ YOEBachelor's in a scientific discipline, regulatory submissions experience for medical devices, knowledge of 21 CFR 820 and ISO 13485, experience with FDA and EU MDR submissions, ability to manage programs and cross-functional teams; 6+ years preferred.
EDMS, PLM, eQMS
1w
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Public Works Regulatory Specialist (Planner III)*
San Bernardino, California, United States
$42-$59/hr FieldFull Time
2+ YOERequires 2 years of professional planning and project management experience in regulatory permitting, environmental review, or land use planning, plus a qualifying degree. California Class C driver's license required.
Geographic Information Systems (GIS), ArcGIS Pro, Microsoft Excel, Microsoft Project
1mo
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VP of Quality & Regulatory Affairs
Irvine, California, United States
$215k-$245k/yr OnsiteFull Time
10+ YOE15+ Mgmt15+ years in senior quality management (or 10+ years global quality operations), Bachelor's required (Master preferred), deep knowledge of quality systems and regulatory expectations (FDA, EU, ISO), strong leadership and change-management skills.
1mo
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Principal Regulatory Affairs Specialist – Vascular (on-site)
Santa Clara or Temecula
$100k-$200k/yr OnsiteFull Time
Bachelor's in science, experience preparing regulatory submissions for medical devices, knowledge of FDA/EU/ISO requirements, and familiarity with QMS; 6+ years preferred.
Electronic document management systems (EDMS), product lifecycle management (PLM), eQMS platforms
1mo
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Direct Materials Regulatory Filings Principal Expert
Oceanside or Mississauga
$115k-$213k/yr OnsiteFull Time
8+ YOEBS/MS/PhD in science, engineering, or management and 8+ years pharmaceutical/biopharmaceutical experience with regulatory filings and material specifications; expert knowledge of ICH, ISO, GMP, and operational excellence tools.
ICH, ISO, FMEA, Six Sigma, Lean Principles
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