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Regulatory Coordinator

Teva Pharmaceuticals
Teva Pharmaceuticals
2-3 years
Not Disclosed
10 Jan. 9, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Regulatory Coordinator

Location: Navi Mumbai, Maharashtra, India
Category: Regulatory Affairs / Pharmaceuticals
Job Type: Full-Time
Job ID: 65672


About Teva Pharmaceuticals

At Teva Pharmaceuticals, our mission is to make healthcare more affordable and accessible, helping millions around the world lead healthier lives. As the world’s leading manufacturer of generic medicines and a proud producer of several products on the World Health Organization’s Essential Medicines List, Teva impacts over 200 million people daily. Join us to contribute to meaningful work and make a global difference in healthcare.


Role Overview

The Regulatory Coordinator will provide critical support to the Director of Regulatory Affairs and Senior Directors across International Markets. This role ensures compliance with local and global regulations, supports regulatory submissions, and coordinates operational activities for the Regulatory Affairs team in India and abroad.


Key Responsibilities

  • Collaborate closely with the Line Manager to ensure tasks are completed within agreed timelines.

  • Manage calendars, schedule meetings, monitor team inboxes, and assist with data collection and PowerPoint presentations.

  • Coordinate and manage team meetings, global visits, townhalls, and off-site events.

  • Provide data entry support for regulatory compliance activities and submissions.

  • Manage vendors, PO generation, invoice processing, archival, and reconciliation for the India and International Markets Regulatory teams.

  • Facilitate global collaboration across multiple sites to ensure operational efficiency and execution of regulatory tasks.

  • Support the preparation of regulatory documents and compliance tracking as needed.


Qualifications & Experience

  • M.Pharm or equivalent degree in a pharmaceutical discipline.

  • 2–3 years of experience in Regulatory Affairs or relevant pharmaceutical operations.

  • Basic understanding of processes and departmental functions within a pharmaceutical company.

  • Proficient in Microsoft Word, Excel, Outlook, and general computer literacy.

  • Strong oral and written communication skills.

  • Ability to work effectively under pressure and tight deadlines in a global organization.

  • Strong time management, organizational skills, and ability to work independently and collaboratively as part of a team.


Why Join Teva

  • Contribute to a global mission to improve healthcare accessibility and affordability.

  • Engage in a dynamic, international work environment with opportunities for professional growth.

  • Work for a company committed to diversity, equity, and inclusion, supporting employees across all levels.

  • Participate in meaningful projects that impact millions of patients worldwide.


Equal Opportunity & Accessibility

Teva Pharmaceuticals is committed to equal employment opportunity and an inclusive workplace. All candidates will be considered without regard to age, race, religion, gender, sexual orientation, disability, or other legally protected status. Reasonable accommodations are available to support candidates throughout the recruitment process.