Job Title: Regulatory Affairs Associate I
Location: Navi Mumbai, India
Company: Teva Pharmaceuticals
Job ID: 65468
Experience Required: 1–3 years in Regulatory Affairs, Pharmaceutical, Biotechnology, or Medical Device Industry
Qualification: Bachelor’s or Master’s in Life Sciences or Information Technology
Company Overview:
Teva Pharmaceuticals is a global leader in generic medicines and a trusted provider of products on the World Health Organization’s Essential Medicines List. Operating in nearly 60 countries, Teva is committed to making healthcare more affordable and accessible, impacting over 200 million patients daily worldwide. Our diverse, inclusive workforce is dedicated to improving global health through innovation, collaboration, and high-quality pharmaceutical solutions.
Role Summary:
The Regulatory Affairs Associate I will provide critical support for global and regional regulatory reporting, data management, and compliance functions. This role ensures accurate retrieval, analysis, and reporting of regulatory data while supporting the Global Regulatory Affairs (GRA) Compliance function. The associate will collaborate with cross-functional teams to ensure that all regulatory data meets quality and compliance standards.
Key Responsibilities:
Data Management & Reporting:
Generate global and regional metrics and reports to support regulatory and business objectives.
Work with EU Gx & Specialties teams for regular reporting; provide ad hoc reports globally as required.
Perform data entry, retrieval, and analysis from GRIDS and Teva RA systems.
Assist in preparing reports for internal and external stakeholders.
Compliance & Documentation Support:
Support GRA Compliance by managing SOPs and Work Instructions through Document Management Systems (DMS) and Learning Management Systems (LMS).
Monitor periodic reviews and ensure compliance with regulatory standards.
Liaise with R&D, portfolio, and RA teams to ensure data accuracy and regulatory compliance.
Ensure familiarity with company IT systems for efficient and accurate data retrieval.
Qualifications & Skills:
Bachelor’s or Master’s degree in Life Sciences or Information Technology (MS preferred).
1–3 years of experience in regulatory operations, regulatory affairs, or related pharmaceutical/biotech/medical device industries.
Strong experience in handling large datasets, data management, and reporting.
Proficiency in database management and data retrieval tools.
Excellent organizational, analytical, and communication skills.
Why Join Teva:
Opportunity to work with a global leader in pharmaceuticals impacting millions of patients.
Collaborate with diverse teams across multiple geographies.
Exposure to regulatory operations, compliance, and data management within a leading pharmaceutical company.
Inclusive and supportive workplace committed to equal employment opportunities and accessibility.
Equal Employment Opportunity Statement:
Teva Pharmaceuticals is committed to creating a diverse and inclusive workplace. Employment decisions are made without regard to age, race, color, religion, sex, disability, sexual orientation, gender identity, veteran status, or any other legally protected status. Reasonable accommodations are provided for candidates throughout the recruitment process as needed.
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