Sr Executive - Quality Assurance (Medical Devices)

4 - 8 years

6 - 15 Lacs

Posted:1 month ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

1. Maintain the QMS documents 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 prospective and retrospective stability studies
  • Participate in the new product registration/ life-cycle management discussions to provide inputs on the procedure for analysis, mainly validations

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Care Group logo
Care Group

Government Administration

Nijmegen Gelderland

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