Regulatory Coordinator – Teva Pharmaceuticals
Location: Navi Mumbai, India
Job ID: 65672
Job Type: Full-Time
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic medicines and a trusted producer of many products listed on the World Health Organization’s Essential Medicines List. Operating across nearly 60 countries, Teva is committed to making healthcare more affordable and accessible, positively impacting the lives of millions worldwide. Every day, over 200 million people rely on Teva medicines, reflecting our dedication to health, innovation, and patient care.
Position Overview
Teva Pharmaceuticals is seeking a Regulatory Coordinator to support the Director of Regulatory Affairs and Senior Directors in International Markets. The incumbent will organize and execute essential regulatory tasks to ensure compliance with global regulations and internal standards. This role also includes administrative support for the Regulatory Affairs team in India and across international operations.
Key Responsibilities
Collaborate with Line Manager to ensure timely completion of regulatory tasks and deliverables.
Manage calendars, schedule meetings, and monitor team inboxes; assist in data collection and preparation of presentations.
Coordinate team meetings, global site visits, townhalls, and off-site events.
Provide data entry and documentation support for regulatory submissions and compliance activities.
Manage vendor relations, purchase order generation, invoice processing, archival, and reconciliation for India and international markets.
Facilitate cross-site collaboration to streamline regulatory operations and enhance efficiency.
Maintain accurate records, support process documentation, and assist with compliance reporting.
Qualifications & Experience
Education: M.Pharm or equivalent.
Experience: 2–3 years of experience in regulatory affairs or related pharmaceutical operations.
Strong understanding of pharmaceutical processes and departmental workflows.
Proficient in Microsoft Word, Excel, PowerPoint, and Outlook.
Excellent written and verbal communication skills.
Strong organizational skills, able to work under pressure and meet tight deadlines.
Ability to work independently, take initiative, and collaborate effectively within a team.
Computer literacy and familiarity with regulatory submission tools preferred.
Why Join Teva
Opportunity to work with a global leader in generic medicines and contribute to improving patient access worldwide.
Exposure to international regulatory operations and cross-functional collaboration.
Structured career growth with development opportunities in Regulatory Affairs.
Inclusive, diverse, and supportive work environment aligned with global best practices.
Equal Employment Opportunity
Teva Pharmaceuticals is committed to equal employment opportunity for all candidates, regardless of age, race, religion, sex, disability, gender identity, sexual orientation, veteran status, or any other legally protected status. We strive to create a diverse and inclusive workplace and provide reasonable accommodations for candidates during the recruitment process.
Application Note for Current Employees:
Current Teva employees should apply via the internal career portal "Employee Central" for priority consideration and access to internal opportunities.
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