Regulatory Affairs Associate I – Teva Pharmaceuticals, Navi Mumbai

Published on

October 23, 2025

Regulatory Affairs Associate

Teva Pharmaceuticals

B.Pharm or M.Pharm

Navi Mumbai

1–4 years

Verified Job

Online Application

Teva Pharmaceuticals — a global leader in generic medicines and a key contributor to the WHO Essential Medicines List — is hiring a Regulatory Affairs Associate I for its Navi Mumbai site. This role is ideal for pharmacy graduates passionate about regulatory lifecycle management, EU submissions, and global market compliance.

🚀 Key Responsibilities

As a Regulatory Affairs Associate I, you will:

Manage regulatory lifecycle activities for assigned products in the EU and International markets.
Ensure regulatory modules are kept up to date as per standard procedures.
Prepare, compile, and submit variations directly to authorities or via Teva’s 3rd party client business (Medis).
Track and follow up on variation submissions, approvals, and updates.
Draft responses to regulatory authority or client deficiency queries.
Ensure all regulatory databases and trackers are maintained accurately.
Provide regular progress updates to management and stakeholders.
Participate in strategic projects within the Regulatory Affairs team.

🎓 Required Qualifications & Skills

Education: B.Pharm or M.Pharm
Experience: 1–4 years in Regulatory Affairs, specifically with EU & International markets
Technical Skills:
- Strong knowledge of RA lifecycle management
- Proficiency in MS Office and regulatory databases
- Understanding of variation filing procedures
Soft Skills:
- Excellent communication and presentation abilities
- Strong organizational and time-management skills
- Strategic mindset with flexibility to adapt to regulatory changes
- Proactive and capable of working independently and collaboratively