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Teva Pharmaceuticals
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Regulatory Affairs Associate III

Regulatory Affairs Associate III

Teva Pharmaceuticals

5 years

5 - 8 Lacs

bengaluru

Posted:1 week ago| Platform: GlassDoor logo

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Skills Required

labeling mrp resolve compliance updating calculations content ip monitoring pharmacovigilance collaboration packaging network support recruitment

Work Mode

On-site

Job Type

Part Time

Job Description

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Regulatory Affairs Associate III

Date: Sep 8, 2025

Location: Bangalore, India, 560064

Company: Teva Pharmaceuticals

Job Id: 62828

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

Ensure the pharmaceutical, medical, and regulatory accuracy of English product information (SmPC, Labeling, PIL) for European procedures (MRP, DCP, CP) of innovative, biosimilar and generic products.
Provide internal pharmaceutical and medical expertise to address internal and authority-related inquiries and resolve labeling issues.
Ensure regulatory compliance for all maintained innovative, biosimilar and generic EU procedures (MRP, DCP, CP) regarding labeling.

How you’ll spend your day

Labeling

Responsible for creating and updating compliant English product information for EU procedures.
Providing instructions and guidance to local RA (e.g. calculations due to new excipients warnings).
Discussion of the content of product information for innovative products (pre- and post-approval) in project teams.
Evaluate and approve change requests; coordinate submissions with EU regulatory units.
Collaborate on patent-related issues with Global IP Group.
Contribute to readability studies and ensure PIL readability and compliance with legal requirements.
Adaption to reference medicinal product (generic, hybrid, biosimilar procedures).
Preparation of Expert statements (justification) for type II variations.
Providing scope of variation to regulatory affairs.
Performing plausibility check and providing wording to be in line with QRD requirements and Standard Terms for module 3 updates.

Monitoring

Monthly monitoring and communicating safety updates from EU authority websites.
Track reference product updates and legal/guidance changes affecting product information.

Pharmacovigilance

Assess need for updates based on Company Core Safety Information (CCSI).
Implement PV triggered and non-PV triggered safety updates (e. g. PRAC/PSUSA/PSUFU, Referrals (Articles 31 + 107i), article 30 procedures, etc.) in line with SOPs; collaborate on safety-related actions with Pharmacovigilance and QA.
Participation in Product Safety Group (PSG) Meetings.
Implementation of internal signals (including determining PIL wording).

Scientific Work & Authority Communication

Respond to authority deficiency letters in collaboration with other departments.

Mockups

Coordinate creation and approval of packaging mockups, Braille, and specimens.
Address authority queries and ensure compliance with EU regulations.

Your experience and qualifications

Experience: 5 to 6 years in relevant fields, (medicinal information and EU labeling in the pharmaceutical industry) ideally in Regulatory Affairs.
Education: Completed at least 8-semester university degree in natural sciences (e.g., Pharmacy [preferred], Biology, Human Biology, Medicine, Food Chemistry)
Other: Advanced English (spoken and written), strong MS Office skills, knowledge of European Pharmaceutical Law and Regulatory Affairs.

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Apply now »

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Teva Pharmaceuticals

Pharmaceutical Manufacturing

Tel-Aviv Petach Tikva

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Regulatory Affairs Associate III