Quality Management System Documentation / QMS Auditor

• 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
• Good 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.