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Teva Pharma Hiring Regulatory Affairs Associate I & II | Mumbai | 1–4 Years | B.Pharm, M.Pharm, Life Sciences
Teva Pharmaceuticals
Mumbai / Navi Mumbai
1–4 Years
Regulatory Affairs
B.Pharm / M.Pharm / Life Sciences
📄 Job Overview
Teva Pharmaceuticals, a global leader in generic medicines, is hiring Regulatory Affairs Associate I & Associate II for US/EU/Canada submissions, eCTD publishing, ANDA lifecycle management, and regulatory documentation across global markets.
1️⃣ Regulatory Affairs Associate I – Job Responsibilities
🔬 Key Responsibilities:- Publish and dispatch eCTD submissions for EU, US, and Canada.
- Manage post-approval submissions and ensure timely delivery.
- Perform document-level publishing & troubleshooting.
- Work with Veeva Vault, Lorenz Validator, ISI Toolbox, Adobe Acrobat.
- Collaborate with scientific teams for submission planning.
- Maintain updated knowledge on ICH, eCTD, NeeS, and global RA guidelines.
- B.Pharm / M.Pharm / Master's in Life Sciences
- 1–3 years experience (Regulatory Publishing preferred)
- Strong English communication skills
2️⃣ Regulatory Affairs Associate II – Job Responsibilities
🔬 Key Responsibilities:- Prepare, review & submit regulatory submissions to US FDA.
- Manage ANDA annual reports, supplements & lifecycle updates.
- Evaluate change controls and ensure FDA compliance.
- Maintain RA databases & trackers.
- Train Associate I team members.
- Support regulatory excellence & process improvement.
- M.Pharm (RA/QA preferred)
- 4+ years experience in Regulatory, QA, Analytical, or Pharma operations
- Excellent documentation & time management skills
⭐ Why Join Teva Pharmaceuticals?
- Work with the world's largest generic medicine manufacturer.
- Exposure to FDA, EMA & Health Canada regulatory frameworks.
- Career growth in global Regulatory Affairs.
- Inclusive and collaborative work culture.
📌 Note Before You Apply:
Read the entire job description carefully before applying. Ensure your skills match the role requirements for better shortlisting.
Read the entire job description carefully before applying. Ensure your skills match the role requirements for better shortlisting.
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