Regulatory Affairs Associate I – Teva Pharmaceuticals
Location: Navi Mumbai, India
Job Type: Full-Time
Experience Required: 1–3 years in Regulatory Affairs, Pharmaceuticals, Biotechnology, or Medical Devices
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making healthcare more affordable and accessible worldwide. With a presence in nearly 60 countries and a diverse workforce, Teva produces many of the medicines on the World Health Organization’s Essential Medicines List. Every day, over 200 million people rely on our medicines, and we are constantly seeking new ways to improve patient outcomes while fostering innovation and professional growth.
Role Overview
The Regulatory Affairs Associate I will play a critical role in supporting Global Regulatory Affairs (GRA) compliance and reporting initiatives. This position focuses on data management, metrics reporting, and procedural support, ensuring regulatory operations adhere to global standards and company SOPs.
Key Responsibilities
Prepare, manage, and report EU Gx and Specialty metrics; provide ad hoc regional and global reports as required.
Enter, retrieve, and analyze data from GRIDS and other Teva regulatory systems.
Assist with managing GRA procedures and learning systems, including SOPs and Work Instructions, through established Document Management Systems (DMS) and Learning Management Systems (LMS).
Liaise with cross-functional teams (R&D, portfolio, RA, etc.) to ensure compliance of all regulatory data.
Support GRA compliance initiatives by ensuring timely and accurate processing of regulatory information.
Maintain and update data for internal reporting and regulatory tracking purposes.
Required Qualifications & Experience
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or Information Technology.
1–3 years of experience in regulatory operations, regulatory affairs, pharmaceuticals, biotechnology, or medical device industry.
Strong proficiency in data management and handling large datasets.
Experience in using databases to retrieve and analyze information accurately and efficiently.
Strong organizational and communication skills, with the ability to work collaboratively in a global team environment.
Preferred Qualifications
Master’s degree in a scientific or IT-related discipline.
Familiarity with global regulatory processes and compliance systems.
Prior experience in EU regulatory reporting and metrics management.
Why Join Teva
Be part of a global leader in pharmaceuticals and contribute to life-changing therapies.
Gain exposure to regulatory operations across multiple international markets.
Develop your expertise in regulatory compliance, data analytics, and process management.
Work in a diverse, inclusive, and collaborative environment that values innovation and professional growth.
Equal Opportunity
Teva Pharmaceuticals is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive workplace. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, sex, national origin, age, disability, or any other protected status.
Apply Now
Join Teva Pharmaceuticals and contribute to global healthcare solutions while advancing your career in regulatory affairs.
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