Technical Documentation Jobs in Irvine
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Search Results - Technical Documentation Jobs in Irvine
NorthITE-Irvine
system patching, upgrades, and security hardening
Participate in Major Incident bridges and coordinate with vendors (Oracle, Red Hat)
Mentor L1/L2 engineers and conduct knowledge transfer sessions
Create and maintain technical documentation, SOPs...
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Yoh, A Day & Zimmermann Company-Irvine
engineering teams to develop manufacturing test strategies and procedures.
• Prepare technical documentation outlining circuit functionality and performance metrics.
Qualifications:
• Master’s degree in Electrical Engineering (or related field) with 10...
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Linwood Engineering, Inc.-Irvine
technical documentation, and construction drawings.
• Research and apply building and plumbing code requirements to ensure compliance.
• Develop coordinated design solutions and communicate effectively with the project team.
• Review drawings and perform QA...
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NorthITE-Irvine
system patching, upgrades, and security hardening
Participate in Major Incident bridges and coordinate with vendors (Oracle, Red Hat)
Mentor L1/L2 engineers and conduct knowledge transfer sessions
Create and maintain technical documentation, SOPs...
Read more
Willow Laboratories-Irvine
including advanced EMI/EMC and electrical safety requirements.
• Drive project technical timelines, manage critical vendor relationships, and oversee the creation of complete technical documentation, including detailed Bills of Materials (BOM)...
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Linwood Engineering, Inc.-Irvine
technical documentation, and construction drawings.
• Research and apply building and plumbing code requirements to ensure compliance.
• Develop coordinated design solutions and communicate effectively with the project team.
• Review drawings and perform QA...
Read more
Yoh, A Day & Zimmermann Company-Irvine
manufacturing test strategies and procedures.
• Prepare technical documentation outlining circuit functionality and performance metrics.
Qualifications:
• Master’s degree in Electrical Engineering (or related field) with 10+ years of relevant experience...
Read more
Takeda Pharmaceutical-Cambridge, 2571 mi from Irvine
for ensuring global submissions and lifecycle compliance for devices and combination products (e.g., IDE, 510(k), De Novo, PMA, CE marking under MDR, technical documentation, variations/changes, vigilance). Partners with regional leads, quality, and vendors...
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Rivian-Irvine
that improve product performance, durability, and user satisfaction.
Create and maintain essential technical documentation, including schematics, manuals, specifications, and test reports.
As a highly skilled specialist, you will contribute to the development...
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Takeda Pharmaceutical-Cambridge, 2571 mi from Irvine
for ensuring global submissions and lifecycle compliance for devices and combination products (e.g., IDE, 510(k), De Novo, PMA, CE marking under MDR, technical documentation, variations/changes, vigilance). Partners with regional leads, quality, and vendors...
Read more
Yoh, A Day & Zimmermann Company-Irvine
manufacturing test strategies and procedures.
• Prepare technical documentation outlining circuit functionality and performance metrics.
Qualifications:
• Master’s degree in Electrical Engineering (or related field) with 10+ years of relevant experience...
Read more
Takeda Pharmaceutical-Cambridge, 2571 mi from Irvine
for ensuring global submissions and lifecycle compliance for devices and combination products (e.g., IDE, 510(k), De Novo, PMA, CE marking under MDR, technical documentation, variations/changes, vigilance). Partners with regional leads, quality, and vendors...
Read more
Stanbridge University-Irvine
early with clear, actionable recommendations.
Documentation & Continuous Improvement
• Maintain clear technical documentation, including ADRs, runbooks, READMEs, and contribution guidelines.
• Identify, prioritize, and address technical debt...
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workable.com -
Irvine
5+ years of experience in engineering field.
• Excellent communication, analytical, and cross-functional collaboration skills.
• Proficiency in interpreting engineering drawings, specifications, and technical documentation.
• Experience and knowledge...
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panasonic.com -
Takeda Pharmaceutical-Cambridge, 2571 mi from Irvine
for ensuring global submissions and lifecycle compliance for devices and combination products (e.g., IDE, 510(k), De Novo, PMA, CE marking under MDR, technical documentation, variations/changes, vigilance). Partners with regional leads, quality, and vendors...
Read more
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