Quality Professional in England

Quality Professional in England

England Full-Time 35000 - 45000 Β£ / year (est.) No working from home possible
Omega Resource Group

At a Glance

  • Tasks: Ensure medical devices meet quality standards and regulatory requirements.
  • Company: Leading company in the medical device industry with a focus on quality.
  • Benefits: Competitive salary, day shifts, and opportunities for professional growth.
  • Other info: Collaborative environment with a strong emphasis on problem-solving.
  • Why this job: Join a vital role in healthcare innovation and make a difference.
  • Qualifications: Experience in quality assurance and knowledge of regulatory standards.

The predicted salary is between 35000 - 45000 Β£ per year.

Role: Quality Professional Want to make an application Make sure your CV is up to date, then read the following job specs carefully before applying.

  • Day Shift
  • Gloucestershire

The Quality Engineer plays a central role in ensuring that all medical devices are designed, manufactured, and released in full compliance with ISO 13485, FDA 21 CFR Part 820, and all applicable regulatory and customer requirements.

This role combines analytical problem-solving, xxuwjjq process optimisation, and cross-functional collaboration to maintain t...

Quality Professional in England employer: Omega Resource Group

At Omega, we pride ourselves on being an exceptional employer, offering a supportive work culture that values collaboration and professional growth. As an Electrical Estimator in Castleford, you will enjoy competitive salaries, a generous car allowance, and comprehensive benefits including private healthcare and life insurance, all while working closely with key clients in the water sector. Join us to be part of a dynamic team where your expertise will directly contribute to impactful projects across Yorkshire.

Omega Resource Group

Contact Details:

Omega Resource Group Recruitment Team

We think you need these skills to ace Quality Professional in England

ISO 13485
FDA 21 CFR Part 820
Regulatory Compliance
Analytical Problem-Solving
Process Optimisation
Cross-Functional Collaboration
Attention to Detail