Opportuntiy to work as Regulatory Affairs Associate at Teva- Apply Before 30th November 2023

Teva Pharmaceuticals

Website Teva

About Teva

Teva Pharmaceuticals is recognized as the largest producer of generic medicines worldwide, dedicated to enhancing health and expanding the availability of high-quality healthcare solutions on a global scale. The company’s success is fundamentally attributed to its workforce, comprising individuals across more than 80 countries. Together, these employees contribute to delivering a vast array of medications to 200 million individuals daily, effectively establishing the world’s most extensive collection of medicines. Teva’s offerings encompass a distinctively varied range of products and remedies tailored to meet the needs of patients. The company’s focus is underpinned by a promising pipeline of innovations concentrated in its core therapeutic domains.

Post: Regulatory Affairs Associate I

Job Description


  • RA Lifecycle Management: Project manager (PM) role for Medis dossiers on behalf of Teva’s 3rd party client business (Medis), ensuring seamless information flow and provision of supporting documents to clients.
  • Liaison: Act as a liaison between Teva’s 3rd party client business (Medis), supply chain, Teva site RA, and other relevant functions.
  • Product Lifecycle Management: Manage specific products for the European and international markets.
  • Regulatory Modules: Ensure that regulatory modules under Product Manager responsibility are always up-to-date, following agreed-upon procedures.
  • Variations: Inform, prepare, and submit variations to authorities or Teva’s 3rd party client business (Medis).
  • Follow-Up: Monitor variation submissions, timelines, and approvals, adhering to established procedures.
  • Deficiency Responses: Compile answers to any deficiency questions from authorities or clients.
  • Communication: Ensure timely communication of variation outcomes and maintain up-to-date databases/lists according to agreed procedures.
  • Reporting: Provide regular status updates to management and participate in goal setting and follow-up with supervisors.
  • Specialized Projects: Work on other specialized projects as defined by RA managers.

Candidate Profile

Qualifications and Experience:

  • M.Pharm/M.Sc: 2-3 years of regulatory affairs experience.
  • B.Pharm/BSc: 5+ years of regulatory affairs experience.

Additional Information

  • Experience: 3+ years
  • Qualification: M.Pharm, B.Pharm, M.Sc
  • Location: Navi Mumbai
  • Industry Type: Pharma/Healthcare/Clinical Research
  • Job ID: 52304
  • End Date: 30th November 2023
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To apply for this job please visit careers.teva.