Regulatory Affairs Specialist

6 days ago


Bengaluru, Karnataka, India Parexel Full time

Parexel seeks a dedicated Regulatory Affairs Specialist to support the life cycle management of biologic products in regulated and emerging markets.

Key Responsibilities:

  • 8-9 years of experience in handling pre and post-approval life cycle management of biologic products in various markets (EU/US/Canada) and emerging markets.
  • Good understanding of regulatory frameworks, including regional trends, for various types of applications and procedures.
  • Experience in supporting the compilation, submission, and approval of country-specific submission files (MAA, LCM, and post-approval changes).
  • Contribution to preparation (including authoring where relevant) and delivery of simple and complex regulatory maintenance submissions from a global and/or regional perspective.
  • Supporting affiliates in updating local requirements based on guidance from regulatory agencies and input from affiliates/distributors.
  • Strong understanding of local and international regulatory guidelines.
  • Preparation and review of Marketing Authorization Applications & Variations for various types of medicinal products for filing in regulated, emerging, and EU markets.
  • Liaising closely with cross-functional members with aligned product responsibilities.
  • Execution and maintenance of submission delivery plans, submission content plans, and proactive provision of status updates to designated stakeholders.
  • Working experience in Regulatory Information Management Systems like Veeva Vault.
  • Strong communication and collaboration skills.


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