Quality Compliance Engineer: ISO 13485 & MDR (Flexitime)

Quality Compliance Engineer: ISO 13485 & MDR (Flexitime)

Full-Time 35000 - 45000 Β£ / year (est.) No working from home possible
Yolk Recruitment Ltd

At a Glance

  • Tasks: Enhance quality systems and ensure compliance in a regulated medical device environment.
  • Company: Leading manufacturing business in Wales with a focus on quality and compliance.
  • Benefits: Flexitime, competitive salary, and opportunities for professional growth.
  • Other info: Collaborate with senior stakeholders and support regulatory inspections.
  • Why this job: Make a real impact on quality processes in the medical device industry.
  • Qualifications: Strong auditing background and knowledge of ISO 13485 and EU MDR.

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

Yolk Recruitment Ltd is supporting a leading manufacturing business in Wales, seeking a Quality Compliance Engineer.

This role offers the chance for an experienced quality professional to enhance a robust Quality Management System in a regulated medical device environment.

You'll influence internal audit programmes, collaborate with senior stakeholders, and support regulatory inspections, ensuring compliance across quality processes.

Ideal candidates will have strong auditing backgrounds and extensive knowledge of ISO 13485, GMP, MDSAP, and EU MDR.

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Yolk Recruitment Ltd

Contact Details:

Yolk Recruitment Ltd Recruitment Team

We think you need these skills to ace Quality Compliance Engineer: ISO 13485 & MDR (Flexitime)

Quality Management System
ISO 13485
GMP
MDSAP
EU MDR
Auditing Skills
Regulatory Compliance