Assists in obtaining and maintaining government approval for,

medical devices , and related materials. He/she advise project teams on subjects such as premarket

regulatory

requirements, import-export and labelling requirements, Materiovigilence, or CPCB, & clinical study compliance requirements.
Check, analyse and implementation of regular updates on scientific information provided by Indian regulators to maintains the strict regulatory compliance as per the latest regulations.
Preparation, Compilation & Review the technical documents as per MDR-17 & Drugs and Cosmetics Act & Rules and various guidelines published by CDSCO to obtain the Import license for the various Medical Devices.
Well aware about the applicable guidelines issued by BIS, Legal Metrology, NPPA, DOP, CPCB etc.
Well aware about Post Approval Changes and related activities.
Well aware about Materiovigilance Activities.
Basic understanding about Corporate Quality Management Sy...