About the Role
The candidate shall manage the facility independently with proven excellence in medical device manufacturing and with leadership qualities to manage a large team. Shall be responsible for day-to-day operations. The candidate shall have industry experience of 10+ years in engineering, research & development, quality control and ISO, BIS documentation for the manufacturing and testing of medical products involving implants, rehabilitation devices, pharmaceutical products etc. The candidate shall have experiences in filing regulatory documentation and coordinating with governmental agencies QCI, NABL, etc. The candidate shall also assist in obtaining different ISO certifications for the establishment of the manufacturing facility and the testing /certification facilities.
The candidate shall have an experience of 10+ years with a B.Tech./ B.E. degree (mechanical, production, industrial engineering or similar) or 8+ years with a M.Tech./M.E. degree (mechanical, production, industrial engineering or similar) with 60% or 6.0 CGPA on 10-point scale.