About the Role
**Job title: Systems Design Quality Engineer (Medical）**
**Your Role &** **Responsibilities:**
* Assesses medical device suppliers, products, verification, product safety risk, regulatory compliance for suitability and effectiveness for global markets
* Creates and executes comprehensive process validation strategies using statistical tools to ensure seamless transition of new products to production, meeting quality and regulatory standards, working under limited supervision.
* Handles the entire design control process, from eliciting and validating design inputs to managing verification, validation, and smooth design transfer, ensuring rigorous adherence to regulatory and quality standards.
* Keeps a check on the drafting and updating of detailed quality engineering documents, including quality plans for hardware, software, and systems, ensuring all documentation is accurate, up-to-date, and compliant with regulatory requirements.
* Ensures success of quality improve...
**Your Role &** **Responsibilities:**
* Assesses medical device suppliers, products, verification, product safety risk, regulatory compliance for suitability and effectiveness for global markets
* Creates and executes comprehensive process validation strategies using statistical tools to ensure seamless transition of new products to production, meeting quality and regulatory standards, working under limited supervision.
* Handles the entire design control process, from eliciting and validating design inputs to managing verification, validation, and smooth design transfer, ensuring rigorous adherence to regulatory and quality standards.
* Keeps a check on the drafting and updating of detailed quality engineering documents, including quality plans for hardware, software, and systems, ensuring all documentation is accurate, up-to-date, and compliant with regulatory requirements.
* Ensures success of quality improve...
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