85 document controller jobs at 68 companies in Watsonville, CA
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Document Control Specialist
Milpitas, California, United States
$75k-$121k/yrOnsiteFull Time
Johnson & JohnsonNYSE: JNJ: Provides pharmaceutical products and medical technology healthcare solutions.
2+ YOE2–5 years document control or quality systems experience in regulated industries; knowledge of FDA QSR and ISO 13485; experience with electronic document management, change control, and Microsoft Office; Bachelor's preferred.
Agile PLM, Agile, Windchill, SAP, Microsoft Office
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.
Johnson & JohnsonNYSE: JNJ: Develops and manufactures pharmaceutical drugs and medical devices.
2+ YOE2–5 years document control or quality systems experience in regulated industry; familiarity with FDA/QSR and ISO 13485; experience with electronic document management; strong organization and communication.
Naprotek: Electronics manufacturing services for high-reliability applications.
3+ YOE3+ years document control in electronics or assembly, proficient with Manex and Microsoft Office (Word, Excel, Visio), strong data entry, documentation, communication, and organizational skills; ISO knowledge a plus.
Manex, Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft Visio
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.
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.
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
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.
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
Product Development Engineer - ECO Preparation/Submission - Document Control
Milpitas, California, United States
$95k-$162k/yrOnsiteFull Time
KLANASDAQ: KLAC: Provides process control and yield management for semiconductor manufacturing.
0+ YOEBSME or related engineer degree; proficient in MS Word/Excel; proficient in electrical/ mechanical drawing; strong communication; desired: 5 years manufacturing engineer in semiconductor; PLM/SAP; CREO/PDMLink/AutoCAD.
PLM, SAP, CREO, PDMLink, AutoCAD, Microsoft Word, Microsoft Excel
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.
Cupertino Electric: Designing and building electrical systems for data centers and infrastructure.
Experience with instrumentation and control systems for water/wastewater projects, PLC/HMI knowledge, documentation and testing skills, HS diploma required, bachelor’s in electrical preferred, US work authorization.
MS Windows, Macintosh OSX, Microsoft Office, National Instruments LabVIEW, GE Proficy, Rockwell RSLogix, Emerson Ovation, multimeter, oscilloscope
Operations Enablement Analyst, Data Center Operations
Bellevue or Livingston or New York or Sunnyvale or San Francisco or United States
$109k-$145k/yrOnsiteFull Time
CoreWeaveNASDAQ: CRWV: Cloud platform providing GPU-accelerated infrastructure for AI workloads.
3+ YOE3+ years documenting technical operations in data center or infrastructure environments; experience with SOPs, runbooks, version control, and compliance-focused documentation; strong writing and analytical skills.
Hims & Hers HealthNYSE: HIMS: Provides telehealth consultations and personalized health products online.
2+ YOE2–5+ years quality or GMP-regulated manufacturing/lab/document control experience; working knowledge of cGMP and Good Documentation Practices; bachelor’s degree preferred in chemistry/biology/biochemistry/pharmaceutical sciences; strong organization and documentation skills.