
Regulatory Affairs Specialist
- Arnhem, Gelderland
- Vast
- Voltijds
Our client is a medium-sized, sustainability-driven medical device manufacturer based in the eastern region of the Netherlands. Known for its commitment to patient impact and innovation, this company operates globally with a growing footprint across multiple regulated markets. The culture is entrepreneurial and collaborative, with strong emphasis on professional development, well-being, and long-term employee engagement.Essential Requirements:Minimum of 3 years of experience in Regulatory Affairs within the medical device industryBSc or MSc in Biomedical Engineering, Chemical Engineering, or a related technical fieldProven ability to maintain and manage international product registration filesStrong command of English, both written and spokenDetail-oriented with excellent multitasking and project management skillsCommunicative and proactive mindset with a structured and energetic approachDesirable Requirements:Cross-functional experience with Quality, R&D, or Clinical departmentsKnowledge of evolving international regulatory landscapes and upcoming compliance trendsProcess improvement experience within regulatory systems or documentation workflowsAdditional Insights:
The position is full-time and located in the eastern Netherlands, with hybrid working flexibility. The organization offers robust development opportunities, 30+ vacation days and great additional benefits.