Job Description
QUALITY CONTROL & REGULATORY AFFAIRS
- Maintenance of Quality Manual
- Standard Operating Procedure
- Device and Plant Master Files
- Quality certification audits, documentation
- Manufacturing license for medical devices (Class A&B)
- Inspecting the final output, model, specifications and design and approving the final products.
Key Skills
Medical Devices, ISO 13485, Quality Control Management, Inspection Quality Management and Regulatory Compliance
Interested candidates can send their resumes on 7984462209