RAQA Specialist

📋 Description Regulatory affairs support for India Medical Device Rules Convert/create technical documentation and registration strategy Submit medical device dossiers and ensure marketing material compliance Coordinate with sales/marketing on regulatory strategy Support QMS activities and regulatory projects/tools Assist and support other teams and regulatory tasks as needed 🎯 Requirements Strong knowledge of India medical device regulations and related rules Experience in medical device registrations and promotional requirements Computer literacy (Word/Excel/PowerPoint/Outlook) 8-10 years in regulatory affairs for medical devices Bachelor's or Master's in medical technology, life sciences or similar English proficiency; ability to translate technical docs into regulatory docs 🎁 Benefits Note: Benefits not provided in posting