ISO 13485 Documentation of Development

Only for registered members Canada

1 month ago

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Job summary

We are an orthopedic implant manufacturing company seeking an experienced ISO 13485 professional to prepare complete QMS documentation.

Responsibilities

  • Create and refine Quality Manual
  • QMS Procedures
  • Standard Operating Procedures (SOPs)
  • Work Instructions
  • Forms Formats Logs Device Master Record structure Production Inspection Packaging Sterilization documentation Basic integration with ISO Risk Management advantage
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