Document Control Specialist

The Document Control Specialist is responsible for managing and maintaining the integrity of documentation and record-keeping in compliance with ISO 13485:2016 standards. This role involves handling quality plans, production documentation, inspection reports, calibration activities, and supplier-related records, ensuring that all documentation is accurate, up-to-date, and readily accessible within the IQMS system.

Duties:

  • Manage and update quality plans, in-process documents, and drawings in the IQMS system.
  • Ensure accurate and timely upload of supplier-related documents to the IQMS system.
  • Review and save last-shot paperwork from production runs.
  • Verify batch production records for completeness and accuracy.
  • Perform COC (Certificate of Conformance) verification and authorization.
  • Ensure proper storage and traceability of material certificates.
  • Verify and save inspection reports for compliance with company standards.
  • Handle supplier-related documentation, ensuring timely uploads and updates in the IQMS system.
  • Maintain compliance with ISO 13485:2016 requirements and company quality standards.
  • Identify opportunities for process improvement in document control and record management systems.

When Required:

  • Participate in Material Review Board (MRB) activities, including quarantine, meeting coordination, disposition, and record-keeping.
  • Coordinate calibration activities for tools and ensure up-to-date calibration records.

Skills and Requirements:

  • High school diploma or equivalent required;
  • Ability to read part drawings and translate dimensional and cosmetic requirements from a drawing into written work instructions for machine operators.
  • One to three years of experience in document control, preferably in a manufacturing environment.
  • Experience working in an ISO 13485:2016-certified company is a plus.
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
  • Strong attention to detail and organizational skills.
  • Ability to work collaboratively across departments and with external suppliers.
  • Familiarity with quality management processes.
  • Must be able to read, write, and verbally communicate in English.
Department: Quality Assurance
Job Location: San Jose CA
Shift: First

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