Teva Pharmaceuticals
📌 Published on: 20 August 2025
Position: Regulatory Affairs Associate I
Openings: Single Opening
Eligibility: Freshers (0–1 year)
Qualification: B.Pharm
Hiring Mode: Online Application
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About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making healthcare more affordable and accessible. Operating in nearly 60 countries, Teva’s portfolio includes many products on the WHO Essential Medicines List, positively impacting over 200 million lives every day. With a diverse and inclusive culture, Teva drives innovation in pharmaceuticals while offering professionals opportunities to grow in regulatory, clinical, and technical domains.
Role: Regulatory Affairs Associate I
Location: Bengaluru
Responsibilities:
📌 Editorial Tasks
Review SmPC, PIL, and packaging materials using defined review protocols.
Adapt texts to QRD templates and ensure regulatory accuracy.
Proofread documents & update GRIDS database.
Act as a GRIDS super-editor & collaborate with internal teams.
📌 Translation Management (EU Centralized Procedures – CPs)
Plan & coordinate translations of product information into multiple EU languages.
Liaise with translation agencies & local markets for linguistic reviews.
Conduct QC checks and prepare submission documents (annotated Word, clean PDFs).
📌 Regulatory & Administrative Tasks
Monitor EU regulatory updates (guidelines, best practices).
Handle SAP cost center administration (invoices, accounting).
Manage purchase requisitions (ARIBA) for translation services.
Eligibility Criteria
Qualification: B.Pharm
Experience: 0–1 year (Freshers eligible)
Skills Required:
✔ Knowledge of regulatory guidelines & documentation
✔ Strong attention to detail & proofreading ability
✔ Good coordination & communication skills
✔ Familiarity with SAP/ARIBA systems (preferred)
Hiring Procedure
Mode of Application: Apply Online via Teva Career Page
Website Link: Apply Here
Documents Required:
Updated Resume
Educational Certificates (B.Pharm)
ID Proof