At a Glance
- Tasks: Lead regulatory compliance and quality assurance for medical devices in the UK and Ireland.
- Company: Join Medtronic, a leader in medical technology with a focus on patient safety.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a strong emphasis on continuous improvement and patient safety.
- Why this job: Make a real difference in healthcare by ensuring quality and compliance in innovative medical devices.
- Qualifications: Experience in regulatory affairs and quality management systems is essential.
The predicted salary is between 60000 - 80000 £ per year.
Medtronic Ltd. in the UK and Ireland seeks a Quality & Regulatory Affairs Manager to lead regulatory compliance, post-market surveillance, and ISO 13485 alignment.
You'll oversee the UKI QRA team, serve as primary contact with MHRA/HPRA, and drive regulatory strategy across UK/EU regions, ensuring local projects meet requirements.
Role emphasizes cross-functional collaboration, audits, and continuous improvement of quality systems to support patient safety and business goals.
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We think you need these skills to ace Regulatory & Quality Lead, Medical Devices (UK & IE) in Watford
Regulatory Compliance
Post-Market Surveillance
ISO 13485
Quality Systems Management
Cross-Functional Collaboration
Auditing Skills
Continuous Improvement
