Regulatory Affairs Associate I – Teva Pharmaceuticals
Location: Navi Mumbai, India – 400706
Category: Regulatory Affairs / Pharmaceutical Operations
Job Type: Full-Time
Experience Required: Fresher / 0–3 Years
Job ID: 64645
Company Overview
Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making healthcare more affordable and accessible worldwide. Operating in nearly 60 countries, Teva reaches over 200 million patients daily with medicines recognized on the World Health Organization’s Essential Medicines List.
Working at Teva means contributing to a diverse, collaborative, and innovative environment while supporting global health initiatives.
Position Overview
Teva Pharmaceuticals is seeking a Regulatory Affairs Associate I to join our GRO Regulatory Data Analytics team. This role provides an excellent opportunity for freshers and recent graduates to gain hands-on experience in regulatory operations, data management, and global product registration.
The Regulatory Affairs Associate I will ensure the accuracy, integrity, and compliance of regulatory product data, supporting Teva’s global regulatory operations and regulatory technology initiatives.
Key Responsibilities
Manage regulatory data in compliance with xEVPMD to maintain Article 57 compliance.
Support creation, maintenance, and quality control of product registration data in line with Teva Global Regulatory Affairs requirements.
Serve as a subject-matter expert (SME) for data management in current and future regulatory data systems.
Conduct data procurement from regulatory dossiers, requiring understanding of dossier structure, content, and registration workflows.
Perform data integrity checks and quality control to ensure accuracy and completeness of the global registration database.
Represent the GRO Regulatory Data Analytics team across Global Regulatory Affairs and build strong relationships with stakeholders.
Contribute to projects focused on regulatory data quality improvement, system integration, and regulatory technology implementations.
Qualifications
Educational Requirements:
Bachelor’s or Master’s degree in Life Sciences, Biotechnology, Pharmaceutical Sciences, or Information Technology.
Preferred: Master’s in a scientific or IT discipline.
Experience:
Fresher or 0–3 years of relevant experience.
Experience or interest in pharmaceutical regulatory affairs is preferred.
Skills & Competencies:
Strong aptitude for regulatory data management.
Understanding of regulatory dossiers and product registration processes.
Ability to perform quality control and data integrity verification.
Strong organizational and analytical skills.
Effective communication and collaboration with cross-functional teams.
Familiarity with regulatory information management systems is a plus.
Reporting
Reports To: Manager, Regulatory Data Analytics
Equal Employment Opportunity
Teva Pharmaceuticals is committed to equal opportunity and a diverse, inclusive workplace. Employment decisions are made without regard to age, race, color, religion, gender, disability, sexual orientation, gender identity, veteran status, or any other legally protected status. Reasonable accommodations are available for candidates requiring support during the recruitment process.
Why Join Teva?
Work with the world’s leading generic medicine manufacturer.
Contribute to global healthcare impact and patient accessibility.
Grow in a collaborative, innovative, and supportive environment.
Launch a career in regulatory affairs with exposure to global operations and regulatory technology initiatives.
Apply Today: Start your career as a Regulatory Affairs Associate I at Teva Pharmaceuticals and gain hands-on experience in global regulatory operations, data analytics, and pharmaceutical product registration.
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