:
:
- Responsible for Overall QA activities & to look after QMS compliance in accordance with ISO 13485/cGMP.
- Preparation & Up-gradation of SOP, Specifications
- Maintain the Records of BMR, BPR, Batch Inspection Documents
- Maintaining Document & Record Control
- Preparation & Up-gradation of Routine Validation Protocol & Reports.
- Handling CAPA, Non- Conformance & Deviations
- Require understanding on QA & Regulatory activities in medical device industry
- oversee the risk management process and related activities.
QA for MDR (MEDICAL DEVICE RULES) / ISO13485
COMPULSORY
📌 QA or RA Executive for Surat
🏢 RECEX
📍 Surat