At a Glance
- Tasks: Support development and lifecycle management of medical devices while ensuring safety and compliance.
- Company: Join PA Consulting, a leader in medical device consultancy with a focus on quality.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Collaborate with cross-functional teams in a dynamic and supportive environment.
- Why this job: Make a real impact in healthcare by navigating regulatory complexities and enhancing product safety.
- Qualifications: 8+ years in medical devices and strong consultancy experience required.
The predicted salary is between 59400 - 72600 £ per year.
PA Consulting seeks an experienced Medical Device Quality Specialist Consultant to support development and lifecycle management of medical devices and combination products. You will navigate regulatory complexity, embed robust quality systems, and ensure safety and compliance from development through post-market.
Strong consultancy experience and 8+ years in medical devices are valued. The role involves:
- Cross-functional teams
- Risk management per ISO 14971
- Regulatory submissions
Senior Medical Device Quality & Regulatory Consultant in London employer: Whereby
Pleo is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals looking to make a significant impact. With a strong focus on employee growth, Pleo offers ample opportunities for career advancement and skill development, particularly in the vibrant tech hub of [location]. The company values its employees by providing a supportive environment that encourages creativity and teamwork, ensuring that every team member feels valued and empowered to drive success.
