Join Teva Pharmaceuticals as a Regulatory Affairs Associate I

Published on

September 12, 2025

Regulatory Affairs Associate I

Teva Pharmaceuticals

B. Pharm/M. Pharm/ Master of Life Sciences.

Navi Mumbai

1 – 3 years

Verified Job

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Teva Pharmaceuticals, a global leader in generic medicines and specialty pharmaceuticals, is hiring Regulatory Affairs Associate I in Navi Mumbai (400706). If you are an M.Pharm or M.Sc. graduate with 2–3 years of Regulatory Affairs post-approval experience, this is your chance to contribute to life-changing medicines while advancing your career in regulatory compliance.

At Teva, you’ll work on EU regulatory submissions, dossier compliance, and post-approval maintenance—directly impacting patient access to affordable and essential medicines worldwide.

Key Responsibilities

As a Regulatory Affairs Associate I, you will:

Prepare, compile, review, and submit high-quality post-approval submissions in compliance with EU legislation.
Ensure marketing authorization compliance with current regulations and internal standards.
Plan and monitor submissions for allocated procedures, keeping all stakeholders informed.
Maintain regulatory documentation and databases as per in-house procedures.
Provide regulatory support to internal teams, project stakeholders, and external agencies.
Stay updated on current and upcoming EU regulatory guidelines.
Communicate effectively with European regulatory agencies and other Teva sites.

Qualifications & Skills

Degree Required: M.Pharm or M.Sc.
Experience: 2–3 years in post-approval regulatory affairs (preferably EU procedures).
Pharma Industry Background: 2–3 years.
Knowledge of European regulatory processes desirable.
Strong written and verbal communication skills.
Ability to work under pressure and manage deadlines.
Attention to detail, teamwork, and strong organizational skills.
Computer literacy and analytical mindset.