Medical Device Quality Engineer - ISO 13485 & FDA

Medical Device Quality Engineer - ISO 13485 & FDA

Full-Time 40000 - 50000 Β£ / year (est.) No working from home possible
Omega Resource Group

At a Glance

  • Tasks: Ensure medical devices meet ISO 13485 standards and manage quality systems.
  • Company: Join a leading company in the medical device industry in Gloucestershire.
  • Benefits: Competitive salary, career development, and a supportive team environment.
  • Other info: Collaborative atmosphere with opportunities for professional growth.
  • Why this job: Make a difference in healthcare by ensuring quality and safety in medical devices.
  • Qualifications: Degree in a relevant field and experience in regulated environments required.

The predicted salary is between 40000 - 50000 Β£ per year.

Omega Resource Group is looking for a Quality Professional in Gloucestershire. This role focuses on ensuring medical devices conform to ISO 13485 and related regulations.

Responsibilities include:

  • Managing the Quality Management System
  • Leading investigations into non-conformance
  • Collaborating across teams

The ideal candidate holds a degree in a relevant field and has experience in regulated environments. Strong analytical and communication skills are essential.

Contact Nick Sollis for further details.

Medical Device Quality Engineer - ISO 13485 & FDA employer: Omega Resource Group

At Omega Resource Group, we pride ourselves on being an exceptional employer in Gloucestershire, offering a dynamic work culture that fosters collaboration and innovation. Our commitment to employee growth is evident through continuous training opportunities and a supportive environment that encourages professional development. Join us to be part of a team dedicated to making a meaningful impact in the medical device industry while enjoying the unique advantages of working in a vibrant community.

Omega Resource Group

Contact Details:

Omega Resource Group Recruitment Team

We think you need these skills to ace Medical Device Quality Engineer - ISO 13485 & FDA

ISO 13485
Quality Management System
Non-Conformance Investigation
Regulatory Compliance
Analytical Skills
Communication Skills
Collaboration