About this role
Technical lead MDR, PFMEA (133782) at HCLTech: Supercharging Progress | AI, Cloud and Engineering. Location: India. Role: leading mdr, conducting pfmea, developing sops Requirements: 4+ years complaint handling or post-market surveillance experience in medical devices, working knowledge of FDA MDR and EU MDR, PFMEA and ISO 13485 experience, eQMS complaint module familiarity, strong documentation and communication skills. Category: Quality Assurance Seniority: Mid Level Tools: eQMS Certifications: mdr, iso 13485, pfmea Commitment: Full Time Workplace: Onsite Languages: English