Work from Office
Full Time
•5-6 years' experience in professional experience in medical device regulatory , Experience with systems for quality management, product development, and follow-up of procedures.
•Responsible for Quality compliant Investigation.
• Evaluation of compliant event and device allegation of customer and determine adverse event or report failure.
• Investigating the Complaints and prepare technical investigation summary as per the GDP.
• Investigating and Failure analysis of Recalled products and devices, Identifying the root cause and analysis of CAPA, Codes of failure.
•Be able to handle ad-hoc changes in priority/planning and independently.
•Be able to think from customer expectation perspective
•Be able to work in different teams simultaneous
Cyient
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