Regulatory Affairs Specialist – Medical Devices (SaMD)
UpHill HealthLisbon, Portugal
Posted January 12, 2026
Full Time
About the Company
UpHill is a healthtech company that develops best-practice clinical pathways and care orchestration software to help healthcare providers and life sciences companies across Europe streamline their processes.
Job Description
We are looking for a Regulatory Affairs Specialist to build, own and operate our regulatory and quality framework. The ideal candidate has experience in Regulatory Affairs, Quality or Compliance in a medical device company, with practical experience with EU MDR, ISO 13485, technical documentation and audits.
Requirements
- 3+ years of experience in Regulatory Affairs, Quality or Compliance in a medical device company
- Practical experience with EU MDR, ISO 13485, technical documentation and audits
- Eligibility (or a clear path) to act as PRRC (Person Responsible for Regulatory Compliance)
- Experience working with NBs (Notified Bodies)
- Comfortable working with engineers and product teams
- Fluent English
Benefits
- Competitive salary
- Flexible work options
- Comprehensive health insurance
- Top-tier equipment – new PC plus budget for peripherals
- A no-BS culture built on trust, impact, and collaboration
