Role Overview: ExP-5+ years • Senior Design Quality Engineer (L3) for medical devices • Ensures QMS compliance, design control, and regulatory adherence • Supports product development and design-to-manufacturing transfer Key Responsibilities:
- Support design changes and recent product development • Review and approve technical documentation, DHF, and risk files • Ensure data integrity and audit DHF records • Create risk management documentation • Analyze post-market and risk data • Participate in design verification/validation reviews Additional Details:
- The candidate will join our R&D; Division – location: Trivandrum, Puliyarakonam, working 5 days a week • Interview process: 2 rounds – L1 virtual, L2 face-to-face with our R&D; head Interested candidates pls share your updated resume to [email protected] Or Call to (phone hidden)