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Regulatory Affairs Associate III

Regulatory Affairs Associate III

Teva Pharmaceuticals

0 years

4 - 8 Lacs

navi mumbai

Posted:2 weeks ago| Platform: GlassDoor logo

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On-site

Job Type

Part Time

Job Description

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Regulatory Affairs Associate III

Date: Nov 21, 2025

Location: Navi Mumbai, India, 400706

Company: Teva Pharmaceuticals

Job Id: 65039

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

Responsible for driving all the activities independently pertaining to Regulatory Affairs of assigned project for Solid Oral Dosage forms.

How you’ll spend your day

Independently compile high-quality CMC (m2 & m3) dossier and review the compilation of peers for new registration, query responses to review letters from agency and post approval supplements (on need basis) for EU in CTD format as per the submission timelines.
Additional support leveraging dossiers for International Market regions.
Assist submissions team with CMC related m1 administrative documentation
Provide strategic input and regulatory intelligence to allotted R&D projects, including cross-functional initiatives
Effective supervision and coaching of peers/ junior team members
Support due diligence process pre-filing and implement action plan to address deficiencies
Assess submission documentation in consideration and compliance with the regulatory requirements and to provide inputs to cross functional teams.
Coordinate (on need basis) with external parties and cross functional teams to obtain essential scientific data and documents required for regulatory submissions
Escalate key issues to management (risk of delays to submissions, risk to approvability, complex supporting data requirements)
To deputize for Manager during his/her absence

Your experience and qualifications

Qualification: Graduation/ Post graduation in Science/ Pharma discipline

Desired Experience:

Minimum 6+ Yrs (for post-graduates)/ 8+ Yrs (for graduates) in core pre-approval regulatory activity in EU and allied markets for Solid Oral Dosage forms. Preference for additional experience in formulation/ analytical development.
Regulatory knowledge throughout new development & product lifecycle with substantial experience with various products and on different Markets.

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.

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Regulatory Affairs Associate III