Head of Regulatory Affairs - Europe Cluster
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- Schiphol, Países Baixos
- Países Baixos
Resumo da vaga pela JobGrid
Head of Regulatory Affairs - Europe Cluster at Eva Pharma in Schiphol, Netherlands, is a hybrid full-time Executive role in Finance, Legal & Compliance. JobGrid presents the structured job facts separately from the employer description, keeps the original language boundary intact, and normalizes the role for comparison with similar vacancies. Candidates are routed to the original public application page through JobGrid with non-personal referral parameters; no salary is listed in the payload.
- Role facts: Head of Regulatory Affairs - Europe Cluster, Eva Pharma, Schiphol, Netherlands, hybrid, full time, Executive, Finance, Legal & Compliance.
- Source freshness: posted on 2026-06-11 and last checked on 2026-06-11.
- Original language: the job content is in English, and JobGrid preserves the source boundary rather than rewriting employer copy.
- Comparable classification: JobGrid normalizes the vacancy into a structured role record for easier comparison across similar jobs; salary context is not available because no salary
Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.
Job Summary:
We are seeking a Head of Regulatory Affairs to join our team.
Lead and oversee all Regulatory Affairs activities across the European Union, ensuring regulatory compliance, lifecycle management, and strategic regulatory support for existing and new products. Drive regulatory strategy, manage the team of Regulatory Affairs, provide regulatory intelligence, support business development initiatives, and ensure successful execution of regulatory submissions and approvals across a diverse product portfolio.
Key Responsibilities
- Develop and execute EU regulatory strategies for new and existing products to ensure compliance and business objectives are met.
- Oversee all regulatory submissions, variations, renewals, extensions, and lifecycle management activities.
- Ensure compliance with EU regulatory requirements for medicinal products, and combination products.
- Lead, coach, and develop a team of Regulatory Affairs, ensuring high-quality and timely delivery of regulatory activities.
- Monitor regulatory developments, assess business impact, and provide regulatory intelligence and recommendations.
- Partner with Business Development, R&D, Quality, and external stakeholders to evaluate regulatory feasibility and support strategic projects.
- Identify and mitigate regulatory risks, providing guidance on timelines, requirements, and market entry pathways.
- Develop and deliver regulatory training programs to strengthen compliance awareness and regulatory knowledge across the organization.