✔ Verified by Medical Jobs India
Hiring Regulatory Affairs Specialist II
🏢 Teva Pharmaceuticals
📍 Navi Mumbai
🎓 B.Pharm / M.Pharm / MSc
📑 Regulatory Affairs
Teva Pharmaceuticals is hiring Regulatory Affairs Specialist II for global regulatory publishing and submission roles. Great opportunity for candidates interested in eCTD submissions, regulatory affairs, and pharma compliance.
👉 New to Regulatory Affairs? B.Pharm Career Guide
📋 Job Overview
- Role: Regulatory Affairs Specialist II
- Location: Navi Mumbai
- Job Type: Full-Time
- Industry: Pharma / Regulatory Affairs
- Experience: Freshers (M.Pharm/MSc) / 2+ Years (B.Pharm)
📌 Key Responsibilities
- Publish eCTD submissions (EU, US, Canada)
- Handle lifecycle management activities
- Perform document-level publishing & QC checks
- Ensure regulatory compliance
- Collaborate with global teams
- Maintain submission timelines & accuracy
📘 Learn basics: Regulatory & Data Standards Guide
🎓 Qualifications & Requirements
- B.Pharm / M.Pharm / MSc (Life Sciences)
- Knowledge of eCTD / NeeS
- Understanding of ICH guidelines
- Exposure to regulatory tools (preferred)
🎯 Crack interviews: Top Interview Questions Guide
💻 Key Skills
- eCTD publishing
- Regulatory documentation
- Veeva Vault / Adobe Acrobat
- Attention to detail
- Communication skills
🧠 Practice now: Pharma Quizzes
🚀 Career Growth
- Senior Regulatory Affairs Specialist
- Regulatory Manager
- Global Submission Lead
- Regulatory Operations Head
📊 Salary insights: Pharma Salary Guide
💰 Salary (Estimated)
- ₹6 – ₹12 LPA
🌍 Why Apply
- Global regulatory exposure
- Work on EU, US & Canada submissions
- Strong career growth in regulatory domain
- Learning & development opportunities
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile aligns with regulatory affairs submissions, compliance guidelines, dossier preparation, and global healthcare standards before proceeding.
Kindly read the full job description carefully before applying. Ensure your profile aligns with regulatory affairs submissions, compliance guidelines, dossier preparation, and global healthcare standards before proceeding.
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