Are you based in Pamplona area and passionate about the Scientific, Regulatory Affairs & Safety sector and looking to join a dynamic and international team?

Asphalion is growing and with our new offices in Pamplona we are looking for different expertise and profiles in the Regulatory Affairs sector to join us!

Our expert team has delivered solutions to over 1,000 Pharmaceutical, Biotechnological and Medical Technology companies from more than 50 countries in over 5,000 projects, covering non-clinical and clinical development, CMC, dossier writing, regulatory procedres, vigilance, eSubmissions and data management, both for medicinal products and medical devices.

Your Role

As a member of our team, you will be involved in various projects, focusing on regulatory related documentation required during clinical development, registration, and safety stages.

Key Responsibilities

• Contribute to a range of scientific and regulatory affairs projects.
• Prepare and review documentation for clinical development and registration processes.
• Ensure compliance with relevant safety regulations and standards.

Qualifications

• Background in life sciences, engineering, or a related field.
• Experience in regulatory affairs or a similar role within the medical device sector is a plus.
• Strong communication and organisational skills.
• Ability to work collaboratively within an international team.

Why working at Asphalion?

📅 Flexible schedule

💻 Homeoffice & Hybrid Model

⚖️ Life / Work balance

🤸🏽Asphawellbeing: Asphalion´s programme focused on the physical, psychological and emotional well-being of our employees

💬 Communication

🤝 Internal activities

🌳 RSC Activities

🤗 Buddy Programme

↗️ Annual training plan and career path

⚙️ Wide variety of projects, new challenges and experiences.

✅ Equal Opportunity Employer

Our people and their well-being are our priority