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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 (India)
🏢 RECEX
📍 India
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