Job Description

Role Summary

Regulatory Affairs Manager – Biosimilars (Location: Madrid, on‑site)

Permanent contract

Responsibilities
  • Monitor changes in the regulatory landscape, identify their impact, and propose solutions to maintain compliance.
  • Define regulatory strategy for each product in coordination with Management and Business teams.
  • Build strong collaborative partnerships with internal and external teams to ensure organizational success and patient safety.
  • Identify and mitigate regulatory risks, adapting strategies to evolving regulations and Health Authority feedback.
  • Interpret and communicate legislative changes affecting product registration, manufacturing, or development.
  • Support the review of license and quality agreements for targeted geographies.
  • Lead engagement with Health Authorities during Scientific Advice procedures and responses to deficiency letters.
  • Prepare, review, and approve regulatory submiss...

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