Regulatory Affairs Associate I – Teva Pharmaceuticals | Pharma Graduates

Regulatory Affairs Associate I – Teva Pharmaceuticals | Pharma Graduates | Bangalore Location | 1+ Year Experience

Apply for Regulatory Affairs Associate I at Teva Pharmaceuticals in Bangalore. Open to Pharma graduates with 1+ year of regulatory affairs or editorial experience.

Regulatory Affairs Associate I – Join Teva’s Global Labeling Team

Teva Pharmaceuticals, a global leader in generic and specialty medicines, is hiring a Regulatory Affairs Associate I for its Bangalore location. This opportunity is ideal for pharmaceutical and medical science graduates with basic knowledge or hands-on experience in regulatory affairs, European pharmaceutical law, or editorial roles.

As a Regulatory Affairs Associate, you will support the Labeling and Translation Management teams for EU Centralized Procedures (CPs), ensuring pharmaceutical and medically accurate product labeling across markets.

Job Location

Location: Bangalore, India
Position Type: Full-Time, Associate Level

About Teva Pharmaceuticals

Teva operates in over 60 countries and delivers high-quality generic and specialty medications to more than 200 million people every day. Our employees are united by a shared mission: to make good health more affordable and accessible. At Teva, your work contributes to a healthier world.

Key Responsibilities

Editorial & Labeling Tasks

• Review and edit product labeling materials (SmPC, PIL, packaging) based on templates
• Adapt texts using QRD templates and perform proofreading
• Maintain product information in internal systems (e.g., GRIDS)
• Act as super-editor in GRIDS for consistency and regulatory compliance

Translation Management

• Coordinate all translation steps post-translation request for EU CPs
• Liaise with internal stakeholders, local markets, and translation agencies
• Manage translation reviews, QC checks, and final document submissions

Process and Compliance Monitoring

• Track EU regulatory environment updates, guidelines, and innovations
• Support cross-departmental inquiries and collaborate with service providers

Administrative Support

• Manage service contracts, purchase requests, and invoice releases in SAP/ARIBA

Required Qualifications

Educational Background

• Diploma or Degree in Pharmaceutical Technology, Medical Assistant Training, or equivalent in Life Sciences
• Preferred: Bachelor’s in Pharmacy, Biotechnology, or Biomedical Sciences

Skill Set

• Intermediate to advanced English (spoken/written)
• Proficient in MS Office
• Basic understanding of EU pharma regulatory frameworks
• Project coordination or editorial experience preferred

Why Choose Teva?

• Join a globally recognized pharmaceutical innovator
• Get hands-on exposure to international labeling procedures and regulatory systems
• Be part of a diverse team contributing to affordable healthcare
• Enjoy learning opportunities and long-term career paths

Accepted Courses for Eligibility

Candidates from the following educational backgrounds will be considered:

• D.Pharm, B.Pharm, M.Pharm
• B.Sc / M.Sc in Life Sciences (Microbiology, Biotech, Biochem, Zoology, etc.)
• Medical/Diploma graduates in Allied Health Sciences

Apply Online

If you are passionate about global healthcare compliance and have the necessary background in Pharma or Life Sciences, this could be your next step forward.

📩 Send your resume to: Rekha.Rathod@teva.co.in
🔗 Or apply online: Click to Apply

Summary Table