Regulatory Affairs Specialist
$80,000–$100,000 year
Remote · London, England, United Kingdom or GB
Job Summary
The Regulatory Affairs Specialist will support regulatory activities to ensure compliance and maintain approvals for Teleflex Medical products in the EMEA region. Responsibilities include coordinating regulatory submissions, reviewing change orders, providing regulatory input for cross-functional projects, liaising with internal teams for technical data, and supporting regulatory inspections. Strong qualifications include a relevant degree, 3 years of medical device industry experience, and technical writing skills. The role requires self-driven initiative, good organizational skills, and excellent communication abilities.
Required Qualifications
- Degree in a relevant Science or Engineering discipline
- 3 years medical device industry experience within quality or regulatory
- Basic knowledge and understanding of EU and international medical device regulations, standards and guidance documents
Desired Qualifications
- Technical writing expertise
- Project Management skills and experience
- Pharmaceutical and/or Drug/ Device Combination device experience and Clinical expertise
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.