About the Role
The candidate shall facilitate documentation, lead quality control management, seek approvals for certification. Industry experience with 8+ years in regulatory affairs and relevant CE/FDA certification for the medical products involving implants, rehabilitation devices, pharmaceutical products, etc. The candidate shall have experiences in filing regulatory documentation and coordinating with governmental agencies ICMR, CDSCO, etc.
The candidate shall have an experience of 8+ years with a Bachelors’ degree (arts, law, mechanical, biomedical, industrial engineering or similar) or 6+ years with a Masters’ degree with 60% or 6.0 CGPA on 10-point scale.