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Regulatory Affairs Associate Job – Teva

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Teva Pharmaceuticals

B.Pharm / M.Pharm / MSc Life Sciences

Mumbai, Hybrid

2–4 years

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Looking for a Regulatory Affairs job in Mumbai? Teva Pharmaceuticals is hiring a Regulatory Affairs Associate in Navi Mumbai with a hybrid work model. This opportunity is ideal for B.Pharm, M.Pharm, or Life Sciences graduates with 2–4 years of experience in regulatory publishing and eCTD submissions.

If you’re aiming to build a career in Regulatory Affairs, eCTD publishing, and global submissions (EU/US markets), this role offers strong exposure to international regulatory frameworks and advanced publishing tools.


📌 Job Overview

  • Position: Regulatory Affairs Associate
  • Company: Teva Pharmaceuticals
  • Location: Navi Mumbai, Maharashtra
  • Work Mode: Hybrid
  • Job Type: Full-Time
  • Experience: 2–4 Years
  • Qualification: B.Pharm / M.Pharm / MSc Life Sciences

🧪 Key Responsibilities (Regulatory Affairs & eCTD Publishing)

  • Prepare, 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 regulatory guidelines
  • Troubleshoot submission issues and ensure submission-ready documents
  • Collaborate with scientific teams for planning and publishing
  • Maintain knowledge of ICH guidelines, eCTD/NeeS formats, and regulatory standards
  • Work with publishing tools such as:
    • Veeva Vault
    • Global Insight
    • ISI Toolbox
    • Lorenz Validator
    • Adobe Acrobat

🎓 Eligibility Criteria (Who Can Apply?)

Candidates must have:

  • B.Pharm / M.Pharm / MSc Life Sciences
  • 2–4 years of experience in Regulatory Affairs / Publishing
  • Hands-on experience in eCTD submissions (US/EU markets preferred)
  • Understanding of ICH guidelines and regulatory frameworks
  • Familiarity with publishing tools like Veeva Vault or Lorenz

💼 Why Join Teva Pharmaceuticals?

  • Work with a global pharmaceutical leader
  • Exposure to international regulatory submissions (US/EU/Canada)
  • Hands-on experience in eCTD publishing and lifecycle management
  • Opportunity to grow in Regulatory Affairs and Global Compliance
  • Hybrid work flexibility

💰 Salary Insight (Expected Range)

  • ₹5.5 LPA – ₹9 LPA (Estimated)
    (Based on industry standards for Regulatory Affairs roles with 2–4 years experience in India)

📩 How to Apply

Interested candidates can apply via:

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