Required Regulatory Affairs Associate at Teva- Apply before 30th May 2025

Teva Pharmaceuticals

Website Teva

Position Title: Regulatory Affairs Associate I – Publishing

Location: Navi Mumbai | Experience: 1–3 Years


About Teva

Teva Pharmaceuticals is a global leader in generic medicines and a key player in specialty pharmaceuticals. With a commitment to improving health and enhancing access to quality healthcare solutions, Teva operates in over 60 countries and touches the lives of millions of patients every day.


Role Summary

As a Regulatory Affairs Associate I – Publishing, you will support global regulatory operations by publishing high-quality submissions for EU, US, and Canadian health authorities. You will ensure timely and accurate documentation and contribute directly to lifecycle management of critical medicines.


Key Responsibilities

  • Publish and dispatch eCTD submissions for EU, US, and Canada, including complex lifecycle management submissions

  • Manage post-approval publishing and ensure timely, compliant dispatch to regulatory agencies

  • Perform document-level publishing, troubleshoot issues, and conduct quality control checks

  • Collaborate with regulatory and scientific teams to plan and publish submissions

  • Maintain up-to-date knowledge of regulatory standards and publishing technologies

  • Work with tools such as Global Insight, Veeva Vault, ISI Toolbox, Lorenz Validator, Adobe Acrobat


Candidate Profile

  • Educational Qualification: B.Pharm, M.Pharm, or Master’s in Life Sciences

  • Experience: 1–3 years, preferably in regulatory publishing for the EU and US markets

  • Skills Required:

    • Strong knowledge of eCTD, NeeS, ICH guidelines

    • Familiarity with regulatory systems and technical tools

    • Excellent written and spoken English

    • Collaborative mindset and sensitivity to cultural diversity in a global work environment


Industry

Pharmaceuticals / Healthcare / Clinical Research

Functional Area

Regulatory Affairs


Job Location

Navi Mumbai, India


Application Deadline

30th May 2025


Take the next step in your regulatory career at Teva—apply now and help make quality medicines more accessible worldwide.

To apply for this job please visit careers.teva.