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Southwest Regional Dams, Levees and Civil Works Business Class Lead
HdrLead regional dam, levee, and civil works projects and coordinate multi‑discipline teams.
United States-Arizona-Phoenix | United States-Nevada-Reno | United States-California-Walnut Creek | United States-California-Sacramento | United States-California-Los Angeles | United States-California-Pasadena | United States-Arizona-Tucson | United States-Utah-Salt Lake City | United States-Nevada-Las Vegas | United States-California | United States-California-San Diego | United States-New Mexico-Albuquerque | United States-California-Irvine | United States-California-Ventura | United States-California-Folsom
7 days ago
Hybrid
technical reviews
risk management
multidisciplinary coordination
15+ years
project management
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Perform and document ultrasonic, radiography, magnetic particle, and penetrant NDT tests.
Cudahy, CA
8 days ago
Onsite
data analysis
issue resolution
result documentation
high school
radiation safety
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Senior Test Engineer
LumicityLead QC testing of microelectronic components, ensuring aerospace/defense standards.
Los Angeles Metropolitan Area
8 days ago
Onsite
electronic testing
data analysis
compliance audits
as9100
mil-prf
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Perform quality audits, sampling, lab testing, and ensure food product compliance.
Los Angeles, CA
8 days ago
Onsite
quality audits
qc sampling
non‑conformance
quality control
respirator
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Develop and execute software verification tests for flight hardware, ensuring AS9100 compliance.
La Canada Flintridge, CA
8 days ago
Onsite
software verification
hardware verification
test development
python
c/c++
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Support GxP inspection readiness, audit records, and compliance data management.
Alameda, CA
8 days ago
Office Full-Time
inspection readiness
supplier monitoring
quality metrics
bs/b.sc
biotech
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Mid‑career environmental remediation scientist leading projects, field work, and technical reporting.
San Diego, CA
8 days ago
Field
technical plans
cost estimating
field sampling
engineering degree
cad/arcgis
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Perform IQ/OQ/PQ validation, create protocols/reports, and ensure GMP compliance for medical devices.
Santa Clara, CA
9 days ago
Office Full-Time
validation docs
pq execution
iq/oq protocols
iso 13485
six sigma
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Validate equipment and fixtures per FDA/ISO standards for medical device manufacturing.
San Jose, CA
9 days ago
Office Full-Time
validation lifecycle
iq/oq protocols
regulatory compliance
iso 13485
fda 820
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Validate equipment, fixtures, and processes for medical device/pharma compliance.
Santa Clara, CA
9 days ago
Office Full-Time
validation docs
protocol execution
project management
iso 13485
six sigma
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