Job Detail in India

Regulatory Affairs Associate I (On site) - Teva Pharmaceuticals

Date Posted: Apr 19, 2024
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Job Detail

  • Location:
    Bengaluru, Karnataka, India
  • Company:
  • Type:
    Full Time/Permanent
  • Shift:
    No
  • Career Level:
    No
  • Positions:
    No
  • Experience:
    2 Year
  • Gender:
    No Preference
  • Degree:
    No
  • Apply Before:
    May 19, 2024

Job Description

Regulatory Affairs Associate I

Date: Apr 18, 2024
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job Id: 55405
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.
How you’ll spend your day
  • Assessment of change controls for registration impact and implementation of all necessary dossier changes in; Europe and International Market
  • Responsible for compilation of the variations for the products in the product portfolio in collaboration with other stakeholders
  • Compiling variation packages
  • Experienced in managing, regulatory database and Trackwise.
Your experience and qualifications
Qualification:
Academic degree- and thinking level with a chemical/pharmaceutical background.
Experience:
  • 2-5 years of experience in CMC Regulatory Affairs; Mainly in Europe and International Market
  • Knowledge on registration procedures and pharmaceutical regulations
  • Interest and capability to work with different software, including Document Management System
  • Accurate, able to prioritize and work according to agreed timelines.
  • Working independently with a moderate level of guidance and direction.
  • Solve complex problems using existing solutions and support.
  • Identify & implement process improvements.
  • Team player
Reports To
Sr Manager – CMC Regulatory Affairs
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.

Skills Required

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Company Overview

, India

Teva Pharmaceutical Industries Ltd. is a leading global pharmaceutical company that delivers high-quality, patient-centric healthcare solutions to millions of patients every day. Teva is the world’s largest generic medicines producer, leveraging its... Read More

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