Regulatory Coordinator
Location: Navi Mumbai, Maharashtra, India (400706)
Employment Type: Full-Time
Function: Regulatory Affairs | International Markets
Industry: Pharmaceuticals | Life Sciences
Job ID: 65672
Company: Teva Pharmaceuticals
Date Posted: January 22, 2026
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in innovative biopharmaceuticals and high-quality generics, serving patients across international markets. With a strong commitment to collaboration, integrity, and continuous improvement, Teva provides a dynamic environment where professionals can contribute meaningfully to global healthcare while advancing their careers.
Position Overview
The Regulatory Coordinator plays a key support role within the Regulatory Affairs function, assisting senior regulatory leadership across India and International Markets. This position focuses on regulatory coordination, administrative support, and operational execution to ensure compliance with global regulatory requirements and internal standards. The role requires strong organizational skills, attention to detail, and the ability to work effectively in a globally distributed environment.
Key Responsibilities
Provide day-to-day regulatory coordination support to the Director, Regulatory Affairs and Senior Regulatory leaders in International Markets.
Work closely with the line manager to ensure timely completion of assigned tasks and deliverables.
Manage calendars, schedule meetings, and coordinate team inboxes as required.
Support preparation of regulatory data, reports, and PowerPoint presentations for internal and global stakeholders.
Coordinate team meetings, global leadership visits, town halls, and off-site events.
Provide data entry and documentation support for regulatory compliance activities and regulatory submissions.
Manage vendor coordination, purchase order (PO) creation, invoice processing, reconciliation, and archival activities for GRA India and International Markets.
Enable effective collaboration across global regulatory sites to support operational efficiency and execution.
Experience and Qualifications
Education
Master of Pharmacy (M.Pharm) is required.
Experience
2–3 years of relevant experience in the pharmaceutical industry, preferably supporting Regulatory Affairs or related functions.
Skills and Competencies
Basic understanding of pharmaceutical company functions and regulatory processes.
Strong proficiency in Microsoft Word, Excel, PowerPoint, and Outlook.
Excellent written and verbal communication skills.
Ability to work under pressure and manage multiple tasks within tight deadlines.
Strong organizational, time management, and coordination skills.
Ability to work independently as well as collaboratively within cross-functional and global teams.
High level of computer literacy and attention to detail.
Why Join Teva
At Teva, professional growth and personal wellbeing go hand in hand. Employees benefit from structured development programs, flexible work arrangements where applicable, comprehensive benefits, and access to Teva’s global career development platform. The organization fosters an inclusive culture that values diverse perspectives and empowers employees to shape meaningful careers in global healthcare.
Equal Employment Opportunity
Teva Pharmaceuticals is committed to providing equal employment opportunities to all qualified individuals. Employment decisions are made without regard to age, race, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally protected status. Reasonable accommodations are available throughout the recruitment process upon request.
This role is well-suited for professionals seeking to build a long-term career in Regulatory Affairs coordination within a global pharmaceutical organization.
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