Documentation executive
VapiMeril
...complete lifecycle traceability from design and development to commercialization.Key Responsibilities:1. Regulatory & Technical File PreparationPrepare and maintain Technical Files in accordance with CDSCO Medical Device Rules (MDR 2017).Compile and manage Device Master Files (DMF), Plant Master Files (PMF), and regulatory [...]
Category Manufacturing & Production
1 day ago in Internshala