Teva Pharmaceuticals Hiring For Regulatory Coordinator: Apply Now

Teva Pharmaceuticals has opened applications for the role of Regulatory Coordinator at its Navi Mumbai facility. This opportunity is well‑suited for M.Pharm graduates with 2–3 years of experience in regulatory affairs, compliance, or pharmaceutical operations.

As one of the world’s leading biopharmaceutical companies with a strong presence in both generics and specialty medicines, Teva offers an excellent platform for professionals seeking exposure to global regulatory processes. The role allows you to contribute to the development and maintenance of high‑quality medicines used by millions of patients worldwide.

If you are searching for a Regulatory Affairs job in Navi Mumbai, this position presents a strategic next step—especially for those looking to expand their skills in international regulatory submissions, documentation management, and compliance workflows.

Teva Pharmaceuticals Hiring For Regulatory Coordinator

Job Overview

Position: Regulatory Coordinator
Department: Regulatory affairs
Location: Navi Mumbai, Maharashtra
Experience: 2 to 3 Years
Qualification:M.Pharm
Job Type: Full-Time

Key Responsibilities

Task & Timeline Coordination:Work closely with the Line Manager to ensure that all assigned activities are completed within agreed timelines, maintaining smooth workflow across regulatory functions.
Administrative & Scheduling Support:Manage calendars, schedule meetings, and monitor team inboxes when required. Assist with data collection and prepare PowerPoint presentations based on team needs.
Team Events & Meeting Management:Coordinate and manage internal team meetings, global stakeholder visits, townhalls, and off‑site events to ensure seamless planning and execution.
Regulatory Data Support:Provide data entry support to regulatory teams to help maintain compliance and assist with regulatory submissions as needed.
Vendor & Procurement Management:Handle vendor coordination, purchase order (PO) creation and processing, as well as invoice management for GRA India and international markets. Support archival and reconciliation activities as required.
Global Collaboration:Facilitate smooth communication and collaboration across global sites to support operational efficiency and ensure aligned regulatory execution.

Required Skills & Qualifications

Educational Qualification:M.Pharm degree with 2–3 years of relevant experience in regulatory affairs, pharmaceutical operations, or compliance‑related functions.
Pharma Industry Understanding:Basic knowledge of key processes, functions, and departmental workflows within a pharmaceutical organization.
Technical Skills:Proficiency in Microsoft Word, Excel, and Outlook, along with solid computer literacy to manage documentation, tracking, and communication tasks effectively.
Communication Abilities:Strong oral and written communication skills, essential for interacting with global stakeholders, preparing reports, and coordinating cross‑functional activities.
Workload & Stress Management:Ability to work under pressure, manage tight deadlines, and operate efficiently within a global, fast‑paced environment.
Organizational Skills:Effective time management, task prioritization, and organizational capabilities to support multiple regulatory and administrative activities simultaneously.
Teamwork & Independence:Capable of working both independently using own initiative and collaboratively as part of a team, ensuring smooth project execution across departments.

Preferred Skills & Experience (Good to Have)

Candidates with the following additional skills and experience will have an advantage:

Strong Time‑Management:Ability to manage tasks efficiently, prioritize workload, and meet tight deadlines while handling multiple literature batches.
Excellent Communication Skills: Clear and professional written and verbal communication in English, essential for summarizing scientific content and interacting with global teams.
High Motivation & Work Ethic: Demonstrates enthusiasm, accountability, and a proactive approach, thriving in a fast‑paced, deadline‑driven environment.
Process Discipline: Consistent adherence to Standard Operating Procedures (SOPs), policies, and quality guidelines, ensuring accuracy and audit readiness.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

Also Check: Clarivate Hiring Freshers For Associate Pharmacovigilance Specialist