Senior Quality Engineer Medical Devices Manufacturing

Senior Quality Engineer Medical Devices Manufacturing

Full-Time 40000 - 55000 £ / year (est.) No working from home possible
SAVA

At a Glance

  • Tasks: Identify process gaps and implement solutions to enhance quality in medical device manufacturing.
  • Company: Join SAVA, a leader in innovative medical device production.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Hands-on role with mentoring opportunities and cross-functional collaboration.
  • Why this job: Make a real impact on quality standards in a fast-paced environment.
  • Qualifications: Experience in quality engineering and knowledge of ISO 13485.

The predicted salary is between 40000 - 55000 £ per year.

SAVA is hiring a Senior Quality Engineer to join the Manufacturing team and identify critical gaps in the process while implementing robust solutions.

The role sits at the heart of quality in production, driving CAPA and continuous improvement to scale our quality architecture.

You will work hands-on on the floor, coordinate with multiple functions, and mentor QA staff, ensuring alignment with ISO 13485 and regulatory requirements while maintaining speed and quality in a fast‑moving environment.

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Senior Quality Engineer Medical Devices Manufacturing employer: SAVA

Sava is an exceptional employer that values innovation and collaboration, providing a dynamic work environment in Greater London. Employees benefit from comprehensive professional development opportunities, a supportive culture that encourages growth, and the chance to make a meaningful impact in clinical operations. With a focus on compliance and excellence, Sava offers a unique advantage for those looking to advance their careers in the healthcare sector.

SAVA

Contact Details:

SAVA Recruitment Team

We think you need these skills to ace Senior Quality Engineer Medical Devices Manufacturing

Quality Assurance
CAPA (Corrective and Preventive Action)
Continuous Improvement
ISO 13485
Regulatory Compliance
Mentoring
Process Improvement