103 document control jobs at 86 companies in Live Oak, CA
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Document Control Specialist
Palo Alto, California, United States
OnsiteFull Time
Sciton: Medical device manufacturer focused on laser technology.
5+ YOEMinimum 5 years in document control in regulated manufacturing/engineering; familiarity with ECOs, BOMs, PLM/ERP; strong documentation and communication skills.
Foxconn Industrial InternetShanghai Stock Exchange: 601138: Global provider of smart manufacturing and cloud infrastructure solutions.
1+ YOEAssociate's or Bachelor's in CS/Info Science; 1-3 years related experience; English required, Mandarin a plus; strong document control, communication, and IT skills.
Unigen: Manufactures custom memory, storage, and AI electronic hardware solutions.
2+ YOE2-5 years in document control; PLM/ERP knowledge; BOM/PCBA understanding; MS Office; analytical/problem-solving skills; cross-functional teamwork; organized and independent.
Currier Plastics: Custom manufacturer of precision plastic components for healthcare applications.
1+ YOE1-3 years document control experience in manufacturing preferred; high school diploma; ability to read part drawings; Microsoft Office proficiency; strong attention to detail and quality management familiarity.
IQMS, Microsoft Word, Microsoft Excel, Microsoft Outlook
3+ YOEBA/BS and 3+ years in regulated medical device or biopharma document control or quality records role; experience with Propel/eQMS, SharePoint, and quality systems (21 CFR Part 820, ISO 13485).
Springtide Project Services: Technical consultancy for advanced technology facility projects.
5+ YOEHigh school diploma,5+ years document control experience in A/E/C or semiconductor/manufacturing,able to lift 25 lbs,able to stoop/kneel/crawl,5–20% travel,field safety compliance required.
Rani TherapeuticsNASDAQ: RANI: Developer of oral drug delivery technology.
5+ YOE5+ years document control manager experience in medical device industry, 10+ years in regulated industry, knowledge of 21 CFR Part 11, QSR/21 CFR Part 820, ISO 13485, experience with PLM/PDM systems, strong communication and training skills.
OkloNYSE: OKLO: Developing advanced fast fission nuclear power plants.
Bachelor's degree or equivalent experience; experience with digital document management/control platforms; strong attention to detail, organization, and communication; knowledge of document control best practices.
NokiaNYSE: NOK: Sells telecommunications infrastructure and software for global network operators.
Develop and deliver training for photonic semiconductor manufacturing, manage document lifecycle and records, administer the LMS, conduct audits and assessments, ensure ISO and regulatory compliance, and support site ramp-up.
Nova Pneuma: Developing rapid-onset inhaled medicines for acute therapeutic needs.
1+ YOE1+ years document creation/management experience; advanced Microsoft Word and Excel skills; experience creating electronic forms and document control systems preferred; regulated environment experience a plus.
Microsoft Word, Microsoft Excel, Dot Compliance eQMS, DOTcu
Document Compliance Manager- Active Clearance Required
Livermore, California, United States
$136k-$200k/yrOnsiteFull Time
Lawrence Livermore National Laboratory: Develops science and technology for United States national security.
Lead document control and records management programs, ensure compliance with federal and nuclear regulations, supervise document specialists, and manage EDMS workflows and retention schedules.
ELM-U, Windchill, Microsoft Word, Microsoft Excel, Microsoft Office Suite, Adobe Acrobat Pro
Halo Industries: Manufactures silicon carbide wafers using laser-based slicing technology.
3+ YOEBachelor's in engineering/technical writing, 3+ years document control and change management in regulated industries, experience with Arena PLM and Confluence; IATF 16949 preferred.
Senior QA Specialist, Global Document Control Management
Redwood City, California, United States
$90k-$108k/yrHybridFull Time
Revolution MedicinesNASDAQ: RVMD: Developing precision oncology therapies for RAS-addicted cancers
5+ YOEBA/BS in biological sciences, chemistry or equivalent; 5+ years Pharma/Biotech QA experience in a GxP environment; experience managing global GxP document systems; Veeva QualitySuite experience; strong communication and regulatory knowledge (ICH/GxP).
Veeva QualitySuite, QualityDocs, Training, QMS, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
Quality Operations Program Manager - Document Control
Pleasanton, California, United States
$100k-$150k/yrRemoteFull Time
Veeva SystemsNYSE: VEEV: Cloud-based software solutions for the global life sciences industry.
5+ YOEBS/BA or equivalent experience, 5+ years in regulated quality role, experience with QMS/eDMS/eQMS, knowledge of GxP and 21CFR11, strong process mapping and communication skills.
FerrotecTokyo Stock Exchange: 6890: Manufacturer of semiconductor equipment and thermal management solutions.
1+ YOE1-3 years relevant or 3 years technical experience; ability to perform mechanical inspections, read engineering drawings, use precision gaging, follow ISO quality systems and ANSI Y14.5M, and complete QC documentation.
calipers, height gage, micrometer, go/no go gauge, bore gage, sine plate, ANSI Y14.5M, ISO
LegenceNasdaq: LGN: Engineering and maintenance services for mission-critical building systems.
Perform material receiving inspections, document and track QC issues, coordinate submittals, communicate with project teams; construction or mechanical experience preferred and proficiency with Microsoft Office required.
Microsoft Outlook, Microsoft Word, Microsoft Excel
Guidance, Navigation & Control Engineer (Level 2 - 5)
Sunnyvale, California, United States
$95k-$165k/yrOnsiteFull Time
Lockheed MartinNYSE: LMT: Designs and manufactures global security and aerospace systems.
STEM Bachelor's or higher, strong control theory and math, MATLAB/Simulink and C/C++ experience, ability to document analyses and work in collaborative teams, U.S. citizenship and ability to obtain Secret clearance.
3+ YOE3+ years quality inspection in manufacturing (medical device preferred). Must interpret engineering drawings, use inspection tools, follow ISO 13485 and AQL methods, and document nonconformities.
calipers, micrometers, height gauges, vision system, microscopes, ISO 13485:2016, AQL