- Auditing experience
- Knowledge of QMS Documentation and Implementation in ISO 9001:2015, ISO 13485:2016 etc
- Worked in ISO certified Quality Management System Company
- Preparing QMS Documentations ISO 9001, ISO 13485
- Should have Knowledge in Quality Management System
- Should plan the audits
- Handling projects in certification
- Valuable communication skills
- Added advantage
- Worked as Management Representative in any organization
- Worked with QMS Consultant or Certification Body.
- CDSCO Registration
- Knowledge of Usfda registration / 510K
- Preference worked in medical device Industry.
Qualification : -
- Bsc/Msc/ BE/ Biotechnology / Biochemistry / Microbiology/ Life sciences
- QMS Documentation, Implementation and preparation of Technical files / QMS Auditor
- Should have background in either Medical devices or Pharma Industries or QMS certified Industry.
📌 Quality Management System Documentation / QMS Auditor (Pune)
🏢 EC International Certification
📍 Pune
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