Excellent communication and from medical device industry experience Urgent
· Maintaining Quality Management System documentation as per standard/guideline requirements. (ISO,FDA,EU)
· Organizing & documenting yearly MRM and maintaining all documents as per the requirements.
· Preparation of SOPs, WIs & quality formats related documentation.
· Identifying gaps in written & followed processes and updating documents accordingly.
· Conducting Internal audits in the company and maintain the necessary documentation.
· Conducting shop floor training as per Quality - training calendar and maintaining records.
· External audit coordination and compliance.
· Ensuring timely calibration of measuring equipment’s
· COC preparation and checking
Salary : 0,00,000 - 0,00,000 P.A As per rules of Industry