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4 - 8 years
6.0 - 15.0 Lacs P.A.
Vadodara
Posted:2 months ago| Platform: 
Work from Office
Full Time
1. Implement and maintain the quality system on the lines of ISO 13485 and GMP 2. Responsible for control of all levels of documents & their history in accordance with EU MDR 3. Coach and Guide the team to support company goals by : Identifying factors that are critical to quality Improving capabilities & increasing stability of process control measures Participate in the new product registration/ life-cycle management discussions to provide inputs on the procedure for analysis, mainly validations
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