Key: At 1 year of experience, the person should normally assist and execute activities under the direction of the QA Manager/MR, rather than independently approve major regulatory decisions, validation conclusions, or final product release.Job Responsibilities
Qualification/Experience
1 year of experience in the medical device industry
Basic working knowledge of ISO 13485
Basic knowledge of Medical Devices Rules, 2017 (MDR), CDSCO requirements and applicable forms
Knowledge of basic medical-device quality practices and documentation