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Teva Pharmaceuticals, a global leader in generic medicines and healthcare solutions, is hiring a Regulatory Affairs Associate I in Goa, India. This is an excellent opportunity for B.Pharm/M.Pharm graduates with 2-4 years of RA experience to join one of the most respected pharmaceutical organizations in the world.
As part of Teva’s Regulatory Affairs team, you’ll play a key role in compiling, maintaining, and submitting CMC dossiers (Modules 2.3 & 3) for worldwide product registrations. This position offers global exposure, professional growth, and the chance to contribute to making medicines affordable and accessible.
Key Responsibilities
- Compile Module 3 and Module 2.3 (Quality Overall Summary) for global regulatory submissions.
- Evaluate dossiers for completeness, accuracy, and compliance with ICH and GMP guidelines.
- Assess change controls and strategize filing categories as per international regulatory standards.
- Compile variation packages and respond to regulatory authority queries.
- Liaise with cross-functional teams, suppliers, and external stakeholders to ensure smooth submissions.
- Maintain departmental databases and tracking systems.
- Stay updated with EU, US, and RoW regulatory guidelines, pharmacopoeias, and industry updates.
- Adhere to company SOPs, occupational safety, and environmental compliance standards.
Qualifications & Skills Required
- Education: B.Pharm / M.Pharm
- Experience: 2–4 years in Regulatory Affairs (Europe & International markets)
- Strong command of written and spoken English
- Proficiency in IT tools and documentation systems
- Excellent organizational, communication, and team collaboration skills
- Proactive, detail-oriented, and results-driven
Benefits of Working with Teva Pharmaceuticals
- Work with a global pharmaceutical leader trusted by millions worldwide
- Exposure to international regulatory markets
- Opportunities for career growth and cross-functional collaboration
- Diverse and inclusive workplace culture
How to Apply
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