💼 About This Role

You'll ensure regulatory compliance and audit readiness across EMEA for a multinational life sciences company. You'll manage medical device vigilance and regulatory documentation supporting import/export and trade compliance. This role offers high impact in a fast-moving, cross-functional environment.

🎯 What You'll Do

• Ensure site-level regulatory compliance and audit readiness across EMEA
• Manage medical device vigilance activities and incident reporting
• Prepare and maintain import/export regulatory documentation
• Coordinate Safety Data Sheets, hazard classifications, and labeling compliance

📋 Requirements

• Experience in regulatory affairs within medical devices, pharmaceuticals, or life sciences
• Understanding of EU Medical Device Regulation, vigilance reporting, and SDS standards
• Organizational skills to manage multiple country-specific compliance requirements
• Eligibility to work in the United Kingdom

✨ Nice to Have

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

🎁 Benefits & Perks

• 📚 Professional training and development
• 🏠 Flexible working arrangements
• 🌍 Exposure to international regulatory operations
• 💪 Wellbeing resources and standard benefits
• 🤝 Inclusive and supportive work environment

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical/Case Interview· 45 min