Job description
Job Description: Job Description: 1. Responsible for Overall QA activities & to look after QMS compliance in accordance with ISO 13485/cGMP. 2. Preparation & Up-gradation of SOP, Specifications 3. Maintain the Records of BMR, BPR, Batch Inspection Documents 4. Maintaining Document & Record Control 5. Preparation & Up-gradation of Routine Validation Protocol & Reports. 6. Handling CAPA, Non- Conformance & Deviations 7. Require understanding on QA & Regulatory activities in medical device industr…