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Junior Regulatory Affairs Advisor

pwc · Brussels

New
Junior 🇬🇧 English
Regulatory submissions Regulatory intelligence Veeva RIM

Job description

About the role

Join PwC’s Life Sciences practice as an Associate Regulatory Affairs Advisor, supporting clients in navigating the evolving regulatory landscape across EMA, FDA and national authorities.

Key responsibilities

  • Help clients interpret global regulatory requirements and develop practical solutions.
  • Support regulatory strategy, submissions and health authority interactions.
  • Assess and improve regulatory affairs processes, operating models and RIM solutions.
  • Translate regulatory and scientific information into clear, actionable insights.

Required profile

  • 1–2 years of regulatory affairs experience in pharma, biotech or life sciences.
  • Exposure to EU pharmaceutical regulation, EMA procedures and national competent authorities.
  • Bachelor’s or Master’s degree in a scientific discipline (Pharmacy, Biomedical Sciences, Chemistry, etc.).
  • Fluent English; additional European languages a plus.

Required skills

  • Regulatory submissions and lifecycle management.
  • Regulatory intelligence and health authority interaction.
  • Experience with regulatory information management platforms (e.g., Veeva RIM).

Questions fréquentes

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Published 7 hours ago

Expires 1 month from now

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Brussels