Added
3 minutes ago
Type
Full time
Salary
Salary not provided

Related skills

documentation qa qms microsoft word regulatory compliance
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📋 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
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