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TEva Hiring for Regulatory Affairs Associate I – UK/IE & EU Markets

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Teva Pharmaceuticals has announced an exciting opening for a Regulatory Affairs Associate I in Navi Mumbai. This role is ideal for M.Pharm professionals with 2–4 years of regulatory or pharmaceutical experience, especially those seeking to work with a global leader in generic medicine and lifecycle management of Marketing Authorisations (MAs).

If you’re looking for a strong career path in Regulatory Affairs (RA) with hands-on exposure to UK/IE submissions, variations, product information management, and compliance, this opportunity is worth considering.


Key Responsibilities

As a Regulatory Affairs Associate I, you will:

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Regulatory Documentation & Submissions

  • Support UK/IE RA teams with full administrative and regulatory documentation management.
  • Prepare and submit simple variations and label/leaflet updates.
  • Maintain product information in the Teva Document Management System.
  • Provide UK/IE-specific documentation for EU submissions (new MAAs, variations).

Process & Data Management

  • Keep regulatory systems and databases accurate and up to date.
  • Monitor team mailboxes and assist with regulatory workflow tracking.
  • Support internal documentation requests, mock-up proofreading, and artwork coordination.

Compliance & Lifecycle Activities

  • Ensure all files comply with Teva procedures.
  • Assist with cancellation processes, lifecycle updates, and cross-functional RA tasks.

Stakeholder Collaboration

Work closely with:

  • UK/IE and EU Regulatory Affairs
  • QA/QC teams
  • Supply Chain
  • Medical Affairs, PV
  • Marketing, Portfolio, Artwork Teams
  • External partners and regulatory authorities (MHRA, HPRA)

🎓 Eligibility & Qualifications

Educational Requirement

  • M.Pharm (mandatory)

Experience

  • 2–4 years in the pharmaceutical industry, preferably in Regulatory Affairs.

Skills Needed

  • Strong communication (written & verbal)
  • Ability to work under pressure with tight deadlines
  • Excellent organisational and time-management skills
  • Proficient in Microsoft Word, Excel, Outlook
  • Ability to work independently and in a team
  • Understanding of pharma workflows and RA processes

🌟 Why Join Teva Pharmaceuticals?

Working at Teva means joining:

  • The world’s leading generic medicines manufacturer
  • A global workforce across 60+ countries
  • Teams supporting products used by 200 million patients daily
  • A culture rooted in diversity, inclusion, integrity, and healthcare impact

📍 Job Location

Navi Mumbai, Maharashtra – 400706 (India)
Hybrid work model may apply as per company guidelines.


💼 How to Apply

Application Link

TEva Hiring for Regulatory Affairs Associate I - UK/IE & EU Markets
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