Teva Pharmaceuticals, a global leader in generic medicines and a trusted name in affordable healthcare, is hiring a Regulatory Affairs Associate I in Navi Mumbai, India.
If you have a strong background in life sciences or information technology and a keen interest in pharmaceutical regulatory affairs, this is your chance to join a mission-driven organization impacting over 200 million lives daily.
🧭 About Teva Pharmaceuticals
Teva Pharmaceuticals is among the world’s largest manufacturers of generic medicines, known for making healthcare more accessible and affordable. With a diverse workforce across 60 countries, Teva continues to innovate and ensure that patients receive high-quality, essential medications.
💼 Job Overview
Position: Regulatory Affairs Associate I
Location: Navi Mumbai, India (400706)
Department: Global Regulatory Affairs – Regulatory Data Analytics
Job ID: 61916
Employment Type: Full-time
Experience: 1–3 years
Salary Range: ₹5,00,000 – ₹9,00,000 per annum (estimated based on industry standards)
🧩 Key Responsibilities
- Execute Regulatory Data Analytics operations in line with SOPs and Work Instructions.
- Manage and maintain Teva’s global product registration data in compliance with xEVMPD and Article 57 requirements.
- Extract and analyze data from regulatory dossiers to ensure accuracy and integrity.
- Perform Quality Control (QC) and data verification to maintain compliance within the Global Registration Database.
- Collaborate across Global Regulatory Affairs teams and support system integration for data management projects.
- Contribute to initiatives improving data quality, regulatory data reuse, and digital transformation within regulatory systems.
🎓 Qualifications & Skills
Required:
- Bachelor’s or Master’s degree in Life Sciences or Information Technology.
- 1–3 years of relevant experience, preferably in regulatory operations or regulatory affairs.
- Strong understanding of regulatory dossier structure, data workflows, and documentation systems.
- Detail-oriented with strong data management and analytical skills.
Preferred:
- Experience in pharmaceutical regulatory data systems or Regulatory Information Management (RIM).
- Prior involvement in regulatory submission processes or data analytics within pharma.
🌍 Why Join Teva?
- Be part of a global healthcare leader impacting millions of lives.
- Opportunity to work with cutting-edge regulatory technologies and digital data systems.
- Inclusive and diverse work culture with career development support.
- Competitive compensation and comprehensive benefits.
📝 How to Apply
