6 principal analyst jobs at 6 companies in Yucaipa, CA
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Principal Survey Analyst
Riverside, California, United States
$45-$59/hr OnsiteFull Time
6+ YOEBA/BS in GIS or BS in Land Surveying plus 6+ years (or 10+ years equivalent) experience; CA PLS or ability to obtain within one year; proficiency with AutoCAD/Civil 3D, GIS, LiDAR, UAV/UAS, and survey document processing.
GPS, Robotic total stations, UAV/UAS, 3D laser scanners, LiDAR, photogrammetry, 360° cameras, AutoCAD, Civil 3D, Shapefiles, Esri File Geodatabase, GIS
3mo
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Principal Applications Functional Analyst - PLM (Irvine, CA, US, 92618)
Irvine, California, United States
$159k/yr HybridFull Time
8+ YOELead Oracle PLM (Idea to Market) implementation and management; 8+ years Oracle ERP; Fusion experience; travel up to 2%; Bachelor's in CS/IT.
Oracle Fusion, Oracle EBS, PL/SQL, VBCS, Postman, Redwood UI
1w
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Principal Risk Control Analyst
San Bernardino, California, United States
$81k-$115k/yr HybridFull Time
2+ YOERequires a bachelor's degree plus 2 years of qualifying occupational safety, environmental, or regulatory compliance experience, or 30 semester units plus 4 years. California driver's license required.
2mo
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Federal Compliance Analyst, Principal
Orange, California, United States
$112k-$154k/yr OnsiteFull Time
5+ YOEBachelor's degree or equivalent and 5+ years compliance/grants experience; knowledge of FTA requirements; strong analytical, communication, and regulatory interpretation skills.
2mo
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Principal Analyst, Power Markets Modeler
Newton or Boulder or Boston or Chicago or Glendora or Richmond or London or Auckland or Bucharest
$135k-$160k/yr HybridFull Time
Bachelor's in a quantitative field required; strong data analysis with Python or R; knowledge of North American power markets, optimization modeling, finance (NPV), and strong communication skills.
Python, R, ENELYTIX, AURORA, PLEXOS, PROMOD, SQL
1mo
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Principal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert) (62423)
Tustin, California, United States
$165k-$185k/yr HybridFull Time
7+ YOE7+ years clinical affairs experience in medical devices with EU MDR expertise, CER authorship, Class III device experience, clinical study design, and strong scientific writing and analytical skills.