Regulatory Affairs Specialist

3 weeks ago


Bengaluru, Karnataka, India Parexel Full time

About the Role

Parexel is seeking a highly skilled Regulatory Affairs professional to join our team. As a Regulatory Affairs Consultant, you will be responsible for managing the pre- and post-approval life cycle of biologic products in various markets, including regulated (EU/US/Canada) and emerging markets.

Key Responsibilities

  1. Develop and implement regulatory strategies for biologic products, ensuring compliance with regional trends and guidelines.
  2. Prepare and submit country-specific submission files, including Marketing Authorization Applications and Variations, for filing in regulated, emerging, and EU markets.
  3. Support affiliates in updating local requirements based on guidance from regulatory agencies and input from affiliates/distributors.
  4. Collaborate with cross-functional teams to ensure alignment on product responsibilities and submission delivery plans.
  5. Execute and maintain submission delivery plans, submission content plans, and provide status updates to designated stakeholders.
  6. Utilize Regulatory Information Management Systems like Veeva Vault to streamline submission processes.

Requirements

  1. 8-9 years of experience in regulatory affairs, with a focus on biologic products.
  2. Strong understanding of regulatory frameworks, including regional trends and guidelines.
  3. Excellent communication and collaboration skills, with the ability to work independently.


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