Regulatory Affairs Associate I – Global Regulatory Operations
Location: Navi Mumbai, India (400706)
Company: Teva Pharmaceuticals
Employment Type: Full-Time
Job ID: 65468
Experience Required: 1–3 Years
Function: Regulatory Affairs | Regulatory Operations | Compliance
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making healthcare more affordable and accessible worldwide. Operating across nearly 60 countries, Teva’s diverse workforce is united by a shared mission to improve patient outcomes and public health. Every day, over 200 million people rely on Teva medicines, including many listed on the World Health Organization’s Essential Medicines List.
Job Overview
Teva Pharmaceuticals is seeking a Regulatory Affairs Associate I to support Global Regulatory Affairs (GRA) compliance, metrics, and reporting activities. This role is based in Navi Mumbai, India, and is ideal for regulatory professionals with experience in regulatory operations, data management, and pharmaceutical compliance systems. The position plays a critical role in supporting EU and global regulatory metrics, reporting accuracy, and system-based data analysis.
Key Responsibilities
Prepare and deliver EU GxP and Specialty regulatory metrics and compliance reports
Support the Global Regulatory Affairs (GRA) Compliance function
Generate ad hoc regional and global regulatory reports as required
Perform GRIDS system data entry, retrieval, and analysis
Extract and analyze data from Teva Regulatory Affairs systems to support business decision-making
Assist in managing GRA procedures, SOPs, and Work Instructions via established Document Management Systems (DMS) and Learning Management Systems (LMS)
Monitor periodic reviews and ensure procedural compliance
Collaborate cross-functionally with R&D, Portfolio Management, Regulatory Affairs, and other business units to ensure data accuracy and regulatory compliance
Ensure efficient and accurate use of internal IT systems for regulatory data handling
Required Qualifications
Bachelor’s or Master’s degree in Life Sciences or Information Technology
Strong academic foundation in scientific or regulatory-related disciplines
Preferred Qualifications
Master’s degree in a scientific or information technology discipline
Prior experience in regulatory operations, regulatory affairs, pharmaceuticals, biotechnology, or medical devices
Experience Requirements
1 to 3 years of relevant experience in regulatory affairs or regulatory operations
Demonstrated experience in data management and handling large, complex datasets
Proven proficiency in database systems and regulatory data retrieval tools
Key Skills & Competencies
Strong analytical and reporting skills
Experience with regulatory IT systems and compliance platforms
High attention to detail and data accuracy
Ability to work cross-functionally in a global regulatory environment
Effective communication and stakeholder coordination skills
Equal Employment Opportunity
Teva Pharmaceuticals is an equal opportunity employer and is committed to fostering a diverse, inclusive, and accessible workplace. Employment decisions are made without regard to age, race, religion, gender, sexual orientation, disability, veteran status, or any other protected characteristic. Reasonable accommodations are available throughout the recruitment process and will be handled confidentially.
Why Apply via ThePharmaDaily.com
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Apply now to advance your regulatory affairs career with Teva Pharmaceuticals in Navi Mumbai.
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