ISO 13485 Documentation of Development
1 month ago

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
- ,
Job description
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