Quality Engineer - Medical Devices, CAPA & Compliance Lead

Quality Engineer - Medical Devices, CAPA & Compliance Lead

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

At a Glance

  • Tasks: Lead quality engineering activities and ensure compliance with industry standards.
  • Company: Innovative medical devices company based in Didcot.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Collaborative environment with a focus on continuous improvement and innovation.
  • Why this job: Make a difference in healthcare by ensuring the quality of life-saving devices.
  • Qualifications: Experience in quality engineering and knowledge of ISO 13485 and 21 CFR Part 820.

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

Didcot-based medical devices company seeks a Quality Engineer to own core Quality Engineering activities, including CAPA, non-conformities, complaints, change control and audits, ensuring ISO 13485 and 21 CFR Part 820 compliance.

You will contribute to e QMS rollout, supplier quality management and manufacturing quality improvements while collaborating with Engineering and Development teams.

Familiarity with MDR/UKCA is advantageous.

#J-18808-Ljbffr

Quality Engineer - Medical Devices, CAPA & Compliance Lead employer: Energy Jobline CVL

Join a well-established property maintenance contractor in Birmingham, where you will enjoy a supportive work culture and the opportunity for career progression. With benefits such as a company van, fuel card, and ongoing training, this role not only offers stability but also the chance to develop your skills in a hands-on environment backed by an experienced office team. Experience a rewarding career with guaranteed annual leave and social events that foster a strong team spirit.

E

Contact Details:

Energy Jobline CVL Recruitment Team

We think you need these skills to ace Quality Engineer - Medical Devices, CAPA & Compliance Lead

Quality Engineering
CAPA
Non-Conformities Management
Complaints Handling
Change Control
Auditing
ISO 13485 Compliance