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Test, package, QC raw materials/products & document release in molecular lab.
Cypress, CA
9 days ago
Onsite
documentation
testing
data analysis
pcr
elisa
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Test, package, QC raw materials/products; document, ensure regulatory compliance.
Cypress, CA
10 days ago
Onsite
documentation
product testing
quality control
pcr
elisa
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Ensures QMS compliance, drives improvements, and supports regulatory audits for medical devices.
Irvine, CA
15 days ago
Office Full-Time
policy development
quality planning
qms improvement
capa
cad
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Ensure medical devices meet regulatory requirements throughout their lifecycle.
Irvine, CA
15 days ago
Office Full-Time
regulatory submissions
gap assessment
document migration
regulatory degree
qms
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Ensures medical device regulatory compliance and manages submission processes.
Irvine, CA
15 days ago
Office Full-Time
regulatory submissions
document migration
gap assessment
rac certification
regulatory affairs
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Ensures medical device regulatory compliance throughout product lifecycle.
Irvine, CA
15 days ago
Office Full-Time
tech file
regulatory submissions
dashboard integration
fda
mdr
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Ensures medical device regulatory compliance and manages submissions throughout product lifecycle.
Irvine, CA
15 days ago
Office Full-Time
regulatory submissions
dashboard integration
document migration
regulatory
fda/eu
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Ensure medical device regulatory compliance and support submissions across global markets.
Irvine, CA
15 days ago
Office Full-Time
regulatory submissions
file support
dashboard integration
regulatory
fda
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Conversion Manager (Production)
Airtech Advanced Materials GroupOversee conversion department operations, scheduling, inventory, and team performance.
Huntington Beach, CA
20 days ago
Onsite
quality assurance
root cause
production scheduling
bachelor's
excel
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Coordinate dermatology clinical trials, managing patients, data, and regulatory compliance.
Santa Ana, CA
24 days ago
Field
data management
drug accountability
crf management
bachelor's
phlebotomy
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