At a Glance
- Tasks: Support quality systems and regulatory compliance for medical devices and combination products.
- Company: PA Consulting, a leading firm in the UK with a focus on innovation.
- Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
- Other info: Join a dynamic team and contribute to impactful projects in the medical field.
- Why this job: Make a real difference in healthcare by ensuring the safety and effectiveness of medical devices.
- Qualifications: Experience in medical device quality and regulatory standards is essential.
The predicted salary is between 49500 - 60500 £ per year.
PA Consulting, based in the UK, seeks an experienced Medical Device Quality Specialist Consultant to support quality systems, regulatory compliance, and lifecycle management of medical devices and combination products. You will work with multi-disciplinary teams across ISO 13485, 21 CFR Part 4, FDA, UK MDR and EU MDR requirements.
You’ll lead regulatory submissions, risk management (ISO 14971), supplier quality, CAPA, and post-market activities, contributing to development from early stages.
Medical Device Quality & Regulatory Consultant in Royston employer: PA Consulting
At PA Consulting, we pride ourselves on being an excellent employer that fosters a collaborative and innovative work culture. As a Data Architect, you will have the opportunity to lead transformative projects in a hybrid working environment, allowing for flexibility while engaging with clients and colleagues. We are committed to your professional growth, offering continuous learning opportunities and the chance to work on cutting-edge AI-driven data solutions that make a real impact.
