Quality Assurance And Regulatory Affairs Manager
Jana Med Tech · Bengaluru · onsite · Posted 44d ago
₹8.4L - ₹24.0L PA8–13 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Responsibilities:
* Lead quality assurance & regulatory affairs for medical devices compliance with FDA, CDSCO, EUMDR, ISO13485 standards.
* Develop SOPs, MR/MDR documentation, ensure manufacturing excellence.
Perks and benefits
Provident fund, Health insuranceSourced from naukri
Skills
SOPMdrEU MDRFDAISO 13485CDSCO510kMedical DevicesManufacturingMRDocumentation