167 quality documentation jobs at 134 companies in San Francisco, CA
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System Director, Clinical Documentation Integrity
San Francisco, California, United States
OnsiteFull Time
UCSF Health: Academic medical center providing advanced patient care and research.
8+ YOEBachelor's in nursing or related field (or equivalent), 8+ years related experience, expertise in clinical documentation and coding, regulatory knowledge, and hospital management skills.
RIX Industries: A technology-focused manufacturer of gas generation, compression, and cryogenic cooling systems.
2+ YOEHigh school diploma, 2 years of quality documentation or related experience, Microsoft Office and Adobe Acrobat proficiency, technical document review skills, communication, organization, and ability to lift 50 pounds.
Microsoft Excel, Microsoft Word, Microsoft Outlook, Adobe Acrobat, PMI gun, AS9100, ISO 9001
OLIPOP: Produces and sells low-sugar prebiotic sodas for gut health.
3+ YOERequires 3–5 years of food and beverage quality, supplier quality, quality systems, or food safety experience; technical documentation review; Excel or Google Sheets proficiency; organization and strong communication.
Microsoft Excel, Google Sheets, Google Workspace, FoodLogiQ
Sila: Manufactures silicon-based anode materials to improve battery performance.
4+ YOERequires 4–6+ years of laboratory experience in research or manufacturing, analytical testing, equipment troubleshooting, quality systems, electronic documentation, and team training.
Kennesaw or Chattanooga or Birmingham or King of Prussia or Baton Rouge or Kennewick or San Luis Obispo or Emeryville or Fort Worth or Overland Park or Glendale or Palm Beach Gardens or Naperville or Overland Park
$90k-$145k/yrOnsiteFull Time
ENERCON: Multi-disciplinary engineering and environmental services for energy infrastructure.
6+ YOE6+ years quality assurance experience in regulated or engineering consulting environments; knowledge of 10 CFR Part 21/50 Appendix B, ASME/ANSI NQA-1, ISO 9001; Lead Auditor experience; ability to read engineering documents and strong communication skills.
Cutera: Designs and manufactures laser-based medical aesthetic treatment systems.
5+ YOE5+ years quality system management experience for ISO-certified technology companies; knowledge of ISO 13485, FDA/QSR, quality planning, validation, audits, and regulatory documentation.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
SanminaNASDAQ: SANM: Global provider of integrated electronics manufacturing and engineering solutions.
4+ YOEBachelor's in engineering or 8 years equivalent experience, 4+ years in quality engineering and manufacturing, GD&T, CMM, SolidWorks, Lean, Six Sigma, process validation, and technical documentation expertise.
Steri-Tek: Provides contract E-beam and X-ray sterilization services.
High school diploma or GED (or equivalent experience), experience in manufacturing/medical device preferred, strong English communication, ability to perform record reviews, audits, KPI tracking, and quality documentation.
Figure: Develops autonomous humanoid robots for commercial and residential tasks.
Review teleop data sessions, identify and document quality issues, produce assessment reports, and collaborate with AI and pilot teams. Strong attention to detail, communication, and ability to learn software required.
Endovascular Engineering: Developing mechanical thrombectomy systems for venous thromboembolism treatment.
4+ YOEMinimum 4 years quality documentation in FDA-regulated environments; ISO 13485 and FDA 21 CFR 820 preferred; knowledge of QMS, GMP, GDP; proficient with MS Office; strong communication.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Document Control Systems
BDNYSE: BDX: Manufactures medical devices, surgical instruments, and pharmacy automation systems.
5+ YOEBachelor's in engineering or science, 5+ years quality experience in medical device industry, knowledge of FDA/QMS/ISO 13485/IVDR, audit support, document/change management, project and technical writing 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.
TE ConnectivityNYSE: TEL: Manufacturer of electronic connectors and sensors for global industries.
1+ YOEHigh school diploma or equivalent; preferably 1+ year in quality inspection or manufacturing. Requires CAD and blueprint interpretation, documentation, data entry, attention to detail, and written procedure compliance.
Xona Space Systems: Operates low Earth orbit satellites for high-precision navigation services.
Requires 3+ years of quality or manufacturing inspection experience, engineering drawing and GD&T knowledge, inspection equipment proficiency, high school diploma, and strong documentation skills. Aerospace or electronics experience preferred.
Noctrix Health: Develops wearable therapeutic devices for chronic neurological disorders.
3+ YOEAssociate's or bachelor's degree and 3+ years in document control, quality systems, training administration, or quality assurance in a regulated industry. Requires eQMS, FDA, ISO 13485, records, and audit experience.
electronic Quality Management System (eQMS), Microsoft Office, Arena
Sunbelt Controls: Provides building automation and systems integration for energy-efficient facilities.
5+ YOEFive years in quality control with three years in ASME B31 piping; AWS QC-1/CWI or ICC Mechanical certification preferred; ability to read and interpret documents; able to calculate figures; problem-solving and correspondence skills; regular attendance.
AbbottNYSE: ABT: Manufactures medical devices, diagnostics, and nutritional health products.
5+ YOEBS/BA in chemistry, biology, or scientific discipline (or equivalent experience); 5+ years QA in regulated FDA medical device or ISO lab; experience with QMS, CAPA, document control, audits, and regulatory standards (ISO 17025/13485, CLIA, 21 CFR 820).
HeartFlowNASDAQ: HTFL: Provides AI-driven non-invasive cardiac diagnostic software and analysis.
5+ YOEBachelor’s degree in a technical field and 5–8 years of medical device quality engineering or product development experience; strong critical thinking, communication, documentation, and time management skills.
IEC 62304, IEC 82304, ISO 14971, ISO 13485, AAMI TIR45, ISO 81001-5-1, Software as a Medical Device (SaMD), AI/ML, Cloud Infrastructure (SaaS), Design History File (DHF), FDA, MDSAP, FDA 510k, De Novo, PMDA, EU-MDR
Technetics GroupNYSE: NPO: Designs and manufactures high-performance industrial seals and components.
3+ YOE3-5 years in quality assurance or semiconductor-related field; bachelor's degree in engineering, science, or business or equivalent experience; able to perform audits in cleanroom/production; strong analytical, communication, and documentation skills; proficient in Microsoft Office; knowledge of ISO standards and Six Sigma.