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Production Quality Engineer - Medical Devices

TN United Kingdom

Lichfield

On-site

GBP 35,000 - 55,000

Full time

8 days ago

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Job summary

An established industry player seeks a skilled Production Quality Engineer to ensure top-notch quality in medical devices. This role involves working closely with the production team, conducting inspections, and managing supplier quality assessments. The ideal candidate will possess strong document control skills and a solid understanding of medical technology. With a commitment to career progression and hands-on training, this opportunity offers a dynamic work environment where your expertise will make a significant impact on product quality and compliance. Join a forward-thinking company dedicated to excellence in the medical field.

Benefits

Competitive Salary
Career Progression Opportunities
Hands-on Training
Benefits Package

Qualifications

  • Experience in quality engineering for medical devices.
  • Strong knowledge of ISO 13485 and QMS.

Responsibilities

  • Conduct supplier quality assessments and manage customer returns.
  • Oversee document control, CAPA, and complaints processes.

Skills

Quality Engineering
Document Control
Inspection Skills
Supplier Quality Assessment
CAPA Management

Job description

Production Quality Engineer - Medical Devices, Lichfield

Client: Newton Colmore Consulting Ltd

Location: Lichfield, UK

Job Category: Not specified

EU work permit required: Yes

Job Reference: 8e0594e49213

Job Views: 3

Posted: 02.05.2025

Expiry Date: 16.06.2025

Job Description:

Newton Colmore is working with a medical technology company near Lichfield, assisting them in their search for a Production Quality Engineer to work closely with their production team.

The ideal candidate will be an experienced quality engineer, working on market-leading medical devices, ensuring parts from suppliers meet design specifications and quality standards. Responsibilities include supplier quality assessments, creating and following up on SCARs, maintaining Device History Records (DHR), conducting incoming inspections, managing customer returns, and overseeing document control, CAPA, and complaints processes.

We are looking for an individual with medical technology knowledge, strong document control, and inspection/testing skills.

The company offers a competitive salary, benefits, career progression opportunities, and hands-on training.

The recruitment process involves a two-stage interview to assess your skills and experience, and to provide more information about the company and role.

To apply, click 'Apply Now'. If your skills match, we will contact you to discuss further.

Newton Colmore Consulting specializes in recruitment within medical devices, scientific engineering, software, robotics, electronics, and related sectors across Europe and the US.

Keywords: Medical Devices, Quality Engineer, Quality Control, ISO 13485, QMS, Project Engineer, ISO 14971

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