💼 About This Role

You'll ensure regulatory compliance across EMEA supply chain operations, coordinating product safety, documentation, and audit readiness. You'll act as a regional subject matter expert, interpreting complex frameworks and collaborating across teams. This high-impact role offers flexible working and exposure to international regulatory operations.

🎯 What You'll Do

• Ensure site-level regulatory compliance across EMEA
• Manage medical device vigilance and incident reporting
• Prepare documentation for import, export, and trade compliance
• Maintain Safety Data Sheets and labeling compliance

📋 Requirements

• Experience in regulatory affairs within medical devices, pharma, or life sciences
• Knowledge of EU Medical Device Regulation, vigilance reporting, SDS standards
• Ability to manage multiple priorities and country-specific compliance
• Eligibility to work in the United Kingdom

✨ Nice to Have

• Experience with regulatory authorities or notified bodies
• Additional European languages
• Professional certification in regulatory affairs or quality management

🎁 Benefits & Perks

• 🌍 EMEA regional portfolio exposure
• 💼 Professional training in regulatory affairs
• 🏢 Flexible working (hybrid or remote)
• 🧘 Wellbeing resources and employee benefits
• 🤝 Cross-functional collaboration

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Hiring Manager Interview· 60 min
3. 3Offer