Back to jobsOwn and implement the Quality Management System for ophthalmic lens manufacturing, edging, and mounting operations
Ensure compliance with ISO 13485:2016 and CDSCO MDR 2017 requirements
Establish, maintain, and continuously improve QMS processes for Class A ophthalmic devices
Lead Management Reviews, Internal Audits, CAPA closures, and compliance monitoring
Maintain audit calendars, compliance dashboards, SOPs, Work Instructions, Quality Manuals, and quality documentation
Manage document control processes and ensure adherence to regulatory standards