Regulatory Affairs Associate I – Teva Pharmaceuticals

Regulatory Affairs Associate I – Teva Pharmaceuticals | Bangalore, India

📅 Posted on: July 21, 2025

📍 Location: Bangalore, India – 560064

🏢 Company: Teva Pharmaceuticals

🔖 Job ID: 62841

📂 Category: Regulatory Affairs | Full-time

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🏢 About Teva Pharmaceuticals

At Teva, we’re united by a powerful mission — making good health more affordable and accessible for people across the globe. As the world’s leading manufacturer of generic medicines, we’re proud to impact over 200 million lives every day through our essential pharmaceutical products. With operations in nearly 60 countries, Teva is continuously innovating and expanding, and we're looking for passionate individuals to grow with us.

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🚀 Position: Regulatory Affairs Associate I

As a Regulatory Affairs Associate I, you will support the EU Generics Labeling Managers and Labeling Germany Managers in ensuring pharmaceutically and medically accurate labeling for various regulatory procedures. You will also play a key role in managing translations for EU Centralized Procedures (CPs).

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🔍 Key Responsibilities:

📌 Editorial Tasks:

Perform editorial reviews of SmPC, PIL, and packaging materials.

Adapt product texts to the latest QRD template.

Proofreading and providing information into the regulatory database (GRIDS).

Super-editor responsibilities for GRIDS.

Coordination with internal departments and service providers.

📌 Innovation & Compliance:

Monitor EU regulatory literature for updates and innovations.

Stay updated with regulatory guidelines and best practices.

📌 Translation Management:

Coordinate all translation steps for English product information into EU member state languages.

Internal quality checks and liaison between stakeholders and translation agencies.

Preparation of required submission documents.

📌 Tools & Systems:

SAP: Invoice release and cost center administration.

ARIBA: Manage purchase requisitions related to service contracts like translations.

🤝 Team Collaboration:

Participate actively in team efforts and handle additional tasks as directed by management.

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🎓 Qualifications and Experience:

Experience in Regulatory Affairs or good understanding of EU pharmaceutical law.

Education: Diploma in Pharmacy, Pharmaceutical-technical assistant, or Medical assistant.

Skills:

Proficient in MS Office

Intermediate to advanced English (spoken & written)

Basic knowledge of project management

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✅ Why Join Teva?

Work with a global leader in generics and specialty medicines.

Collaborate in a supportive and innovation-driven environment.

Contribute to the health of millions across the globe.

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📌 How to Apply:

Apply here: Application link