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Regulatory Affairs Associate I Job at Teva Pharmaceuticals

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Looking to build a career in Regulatory Affairs publishing with a global pharma leader? Teva Pharmaceuticals is hiring a Regulatory Affairs Associate I in Navi Mumbai. This role focuses on eCTD submission publishing, lifecycle management, and regulatory compliance across US, EU, and Canada markets.

This is a high-value opportunity for candidates with 1โ€“3 years of regulatory publishing experience, especially those skilled in Veeva Vault, eCTD tools, and ICH guidelines. If you’re targeting roles in Regulatory Affairs jobs in India, this position offers strong exposure to global submissions.


๐Ÿ“Œ Job Details

  • Role: Regulatory Affairs Associate I โ€“ RA Publishing
  • Location: Navi Mumbai, India
  • Experience: 1โ€“3 years
  • Qualification: B.Pharm / M.Pharm / Life Sciences
  • Department: Regulatory Submission Management

๐Ÿงฉ Key Responsibilities

  • Publish and dispatch eCTD submissions for US, EU, and Canada markets
  • Handle post-approval submissions and lifecycle management activities
  • Perform document-level publishing and QC checks as per agency guidelines
  • Troubleshoot submission issues and ensure 100% quality compliance
  • Collaborate with cross-functional teams for submission planning
  • Maintain knowledge of ICH, eCTD, NeeS, and regulatory standards
  • Work with tools like Veeva Vault, Lorenz Validator, ISI Toolbox, Adobe Acrobat

๐ŸŽ“ Qualifications & Skills

  • Education: B.Pharm / M.Pharm / MSc Life Sciences
  • Experience: 1โ€“3 years in Regulatory Affairs publishing (preferred)
  • Strong understanding of:
    • eCTD submission structure
    • ICH guidelines & global regulatory frameworks
  • Hands-on experience with:
    • Veeva Vault
    • Global Insight
    • Lorenz Validator
  • Excellent communication and documentation skills
  • Ability to work in a global, cross-cultural environment

๐Ÿ’ฐ Salary Insight (Estimated)

  • โ‚น4.5 LPA โ€“ โ‚น7 LPA (based on industry benchmarks for RA publishing roles in India)

๐ŸŒŸ Benefits

  • Global exposure in regulatory submissions (US/EU markets)
  • Flexible work environment and career development programs
  • Learning platforms and internal mobility opportunities
  • Health and wellness support programs
  • Inclusive and collaborative workplace culture

๐Ÿ“ฅ How to Apply

Application Link

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