3 - 8 years
15 - 30 Lacs
Posted:1 month ago|
Platform:
Hybrid
Full Time
We are expanding our Quality and Regulatory Affairs (QARA) function to support the implementation of a Quality Management System (QMS) aligned with ISO 13485, EU MDR, and related global medical-device frameworks.
This position suits someone who enjoys structure and precision, understands how QMS frameworks work, and can translate regulatory requirements into clear internal documentation and workflows.
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