Apply for Teva Pharma Hiring Regulatory Affairs Associate I Navi Mumbai. 1–3 years experience in regulatory data analytics required.
Position: Regulatory Affairs Associate I
Company: Teva Pharmaceuticals
Location: Navi Mumbai, India (400706)
Qualification: Bachelor’s or Master’s Degree in Life Sciences or Information Technology
Experience: 1–3 Years
Employment Type: Full Time
Department: Global Regulatory Affairs – Regulatory Data Analytics
Job ID: 61916
Application Mode: Online Application
Salary Range: ₹5,00,000 – ₹9,00,000 per annum (estimated)
About Teva Pharmaceuticals
Teva Pharmaceuticals is one of the world’s leading pharmaceutical companies, recognized globally for its expertise in generic and specialty medicines. With operations across 60 countries, Teva’s mission is to make healthcare more accessible and affordable for all. The company is dedicated to improving patient health through quality, innovation, and commitment, serving over 200 million people daily with its trusted medicines. Teva Pharma Hiring Regulatory Affairs Associate I
By joining Teva, you become part of a global team that values integrity, collaboration, and continuous learning.
Job Overview
Teva Pharmaceuticals is hiring for the position of Regulatory Affairs Associate I at its Navi Mumbai office. This role offers an exciting opportunity to work in Regulatory Data Analytics, ensuring the accuracy, integrity, and compliance of global product registration data. Teva Pharma Hiring Regulatory Affairs Associate I
Ideal candidates will have a strong foundation in life sciences or information technology and an interest in regulatory operations within the pharmaceutical industry.
Key Responsibilities
As a Regulatory Affairs Associate I, your primary responsibilities will include: Teva Pharma Hiring Regulatory Affairs Associate I
- Executing Regulatory Data Analytics operations according to established SOPs and Work Instructions.
- Managing and maintaining Teva’s global product registration data in compliance with xEVMPD and Article 57 requirements.
- Extracting and analyzing data from regulatory dossiers to ensure accuracy and data integrity.
- Performing Quality Control (QC) and verification checks within the Global Registration Database.
- Collaborating with Global Regulatory Affairs teams to support system integration and digital data projects.
- Contributing to data quality improvement initiatives, regulatory data reuse, and digital transformation within regulatory operations.
Required Qualifications and Skills
Educational Qualification:
- Bachelor’s or Master’s degree in Life Sciences or Information Technology.
Experience:
- 1–3 years of relevant experience in regulatory affairs, regulatory operations, or data analytics within the pharmaceutical sector.
Technical & Professional Skills:
- Strong understanding of regulatory dossier structures, data workflows, and documentation systems.
- Excellent analytical, organizational, and problem-solving abilities.
- Attention to detail and commitment to maintaining data accuracy.
Preferred Skills:
- Experience with Regulatory Information Management (RIM) systems or regulatory data systems.
- Exposure to regulatory submission processes or pharmaceutical data analytics.
Why Join Teva Pharmaceuticals?
- Be part of a global healthcare leader with a strong focus on innovation and patient care.
- Work with advanced regulatory technologies and digital data management systems.
- Enjoy an inclusive and diverse workplace that supports continuous learning and growth.
- Competitive salary structure and comprehensive employee benefits.
- Teva Pharma Hiring Regulatory Affairs Associate I
How to Apply
Interested candidates can apply online through the official Teva Pharmaceuticals Career Portal by searching for Job ID: 61916 – Regulatory Affairs Associate I, Navi Mumbai. Teva Pharma Hiring Regulatory Affairs Associate I
Ensure your resume highlights your regulatory experience, data management expertise, and knowledge of pharmaceutical compliance systems. Teva Pharma Hiring Regulatory Affairs Associate I
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