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About the Role

The RA Executive will support product registrations, dossier preparation, technical documentation and ongoing regulatory compliance for diagnostics products in domestic and export markets, coordinating with R&D, QA, manufacturing and commercial teams to maintain timely submissions.

Key Responsibilities
  • Prepare and review regulatory dossiers and technical files for India (CDSCO) and export markets.
  • File and track applications via the CDSCO SUGAM portal — MD-05/MD-09 (manufacturing) and MD-13/MD-14/MD-15 (import) as applicable.
  • Maintain Device Master Files (DMF), submission trackers and regulatory correspondence.
  • Coordinate responses to authority queries and submission deficiencies.
  • Review labels, IFUs and product claims for compliance; issue / coordinate Free Sale Certificates (CFS) for exports.
  • Monitor regulatory changes (CDSCO MDR 2017, ISO 13485, ISO 14971, EU IVDR, FDA) and assess business impact.
Desired Candidate Profile
  • Education: B.Pharm / M.Pharm, M.Sc / B.Sc (Life Sciences, Biotech, Microbiology) or B.Tech; RA PG diploma a plus.
  • Experience: 2–5 years of RA experience in diagnostics or medical devices.
Technical Skills & Keywords
  • CDSCO, SUGAM portal, Medical Device Rules 2017 (MDR 2017), MD-05 / MD-09 / MD-13 / MD-14 / MD-15, ISO 13485:2016, ISO 14971, technical file / DMF / DHF, IVD registration, labelling & IFU compliance, Free Sale Certificate (CFS), post-market surveillance, 21 CFR Part 11 / FDA, EU IVDR / CE awareness.
Preferred / Good to Have
  • Export-dossier and country-specific registration experience.
  • IVD-specific (vs general device) regulatory experience.
  • ISO 14971 risk-file and regulatory-intelligence tool exposure.
What We Offer
  • A rare opportunity to help build a greenfield IVD diagnostics business from the ground up.
  • Modern, ISO 13485 / CDSCO-compliant manufacturing environment with cleanroom infrastructure.
  • Direct collaboration with R&D, Regulatory and senior leadership — visible impact, fast decisions.
  • Competitive compensation, commensurate with experience (negotiable; as per industry standards).
  • Accelerated career growth in a fast-scaling, export-oriented MedTech company.

About the Company

Arni Medica

Medical Equipment Manufacturing

Arni Medica is a leading medical device manufacturer specializing in contract manufacturing, new product development, and high-quality production of nephrology and healthcare products.

Industry: Medical Equipment Manufacturing

Regulatory Affairs Executive at Arni Medica - Hyderabad