Regulatory Affairs Associate
Teva Pharmaceuticals
2 - 4 years
Mumbai
Posted: 20/03/2026
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Job Description
Qualification: B. Pharm/M. Pharm/ Master of Life Sciences
Experience: 2-4 years of relevant experience in Regulatory Publishing preferably in EU and US market
General Duties & Responsibilities:
- Publish and dispatch major and complex routine/lifecycle management eCTD submission projects for EU, US and Canada.
- Exposure in handling post approval submissions publishing and transmitting quality submissions to agency.
- Perform document level publishing activities, troubleshoot document issues and perform quality control checks for submission ready documents as per the agency guidance.
- Collaborate with scientific personnel for planning, preparation and publishing.
- Maintain working knowledge of internal and external publishing standards.
- Basic knowledge of ICH and eCTD related specification/guidelines governing regulatory submissions (eCTD, NeeS, paper)
- Must be aware of Technical systems like Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, Lorenz Validator
Interested candidates can share their CV to ankita.sonawane@teva.co.in
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