1. Create and maintain company quality documentation, such as manuals, procedures, etc.
2. Continuously improve QA processes and procedures.
3. Preparation of QA reports.
4. Responsible for Compliance of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012
📌 Quality Assurance Executive (Kundli)
🏢 MACOM
📍 Kundli