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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