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Regulatory Affairs Associate Job – M.Pharm/M.Sc grads

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If you’re looking to build a strong career in Regulatory Affairs, Teva Pharmaceuticals โ€” one of the worldโ€™s leading generic medicine manufacturers โ€” is hiring for the role of Regulatory Affairs Associate I in Bangalore. This is a fantastic opportunity for life science and pharmacy professionals with 2โ€“3 years of regulatory or pharmaceutical experience.

As part of Tevaโ€™s International Markets Regulatory Affairs team, youโ€™ll support global submissions, regulatory documentation, and compliance activities that ensure safe and effective medicines reach patients across the world.

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โญ Key Responsibilities

As a Regulatory Affairs Associate I, you will:

  • Complete assigned regulatory tasks and projects for International Market RA under manager/senior RA guidance.
  • Maintain documentation and regulatory IT systems according to internal SOPs.
  • Update trackers, ensure on-time completion, and maintain compliance standards.
  • Communicate effectively with Teva units, international partners, and Health Authorities.
  • Assist with contract documents, EC submissions, and other regulatory deliverables.
  • Perform additional department duties as assigned by senior RA staff.
  • Complete LMS-assigned training modules within defined timelines.
  • Participate in team meetings and provide status updates.
  • Stay updated with current and upcoming regulatory legislation and guidelines.

๐ŸŽ“ Qualifications & Experience

Educational Qualifications

  • M.Pharm / M.Sc / Life Sciences
  • OR a university degree with sufficient exposure to regulatory concepts.

Required Experience

  • 2โ€“3 years in Pharmaceutical Industry.
  • Preferable: Regulatory Affairs experience.
  • Acceptable: R&D, Development, or Quality Assurance.
  • Exposure to European or International Market regulatory documentation.

Required Skills

  • Understanding of core regulatory principles and procedures.
  • Ability to use internal SOPs to solve routine problems.
  • Proficiency in Office-365 and Veeva Vault.
  • Strong compliance focus and organizational skills.
  • Basic project management knowledge.
  • Ability to escalate issues beyond personal scope.
  • Bonus: Knowledge of French or German.

๐Ÿ’ผ Benefits of Working at Teva

  • Opportunity to work with a global pharmaceutical leader.
  • Exposure to international regulatory markets.
  • Skill-building in compliance, documentation systems, and regulatory submissions.
  • Inclusive and diverse work environment.
  • Strong learning and development ecosystem.

๐Ÿ“ฉ How to Apply

Application Link

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