Head of Regulatory Affairs - Europe Cluster

Eva Pharma
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📍 Schiphol, Noord-Holland, NetherlandsFull time

About this role

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.

  • Degree in Pharmacy, Life Sciences, Natural Sciences, or a related field.
  • Minimum 10 years of Regulatory Affairs experience within the pharmaceutical industry.
  • Strong knowledge of EU regulatory requirements, lifecycle management, and regulatory submission processes.
  • Proven leadership experience managing and developing regulatory teams.
  • Excellent strategic thinking, stakeholder management, communication, and cross-functional.

Frequently Asked Questions

Is the salary disclosed for the Head of Regulatory Affairs - Europe Cluster position at Eva Pharma?
The salary for this Head of Regulatory Affairs - Europe Cluster role at Eva Pharma is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Head of Regulatory Affairs - Europe Cluster position at Eva Pharma located?
This Head of Regulatory Affairs - Europe Cluster role at Eva Pharma is based in Schiphol, Noord-Holland, Netherlands. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Head of Regulatory Affairs - Europe Cluster role at Eva Pharma full-time or part-time?
This is listed as a Full time position. It is posted as a Head of Regulatory Affairs - Europe Cluster role at Eva Pharma.
How do I apply for the Head of Regulatory Affairs - Europe Cluster position at Eva Pharma?
Click the "Apply Now" button on this page. You will be redirected to Eva Pharma's official application portal hosted on workable where you can submit your application directly.
When was the Head of Regulatory Affairs - Europe Cluster job at Eva Pharma posted?
This Head of Regulatory Affairs - Europe Cluster position at Eva Pharma was posted on Jun 11, 2026. Apply as soon as possible — early applications are often reviewed first.
Head of Regulatory Affairs - Europe Cluster
Eva Pharma
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