Enable job alerts via email!

Production Quality Engineer - Medical Devices

Newton Colmore Consulting

Lichfield

On-site

GBP 35,000 - 55,000

Full time

30+ days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

An innovative medical technology company is seeking a skilled Production Quality Engineer to join their dynamic team. This exciting role offers the chance to work on cutting-edge medical devices while ensuring that all parts from suppliers meet stringent design specifications and quality standards. You will play a vital role in supplier quality assessments, maintain the Device History Record, and collaborate closely with the production team. With a commitment to career progression and hands-on training, this position is perfect for those passionate about quality engineering in the medical field. Join a forward-thinking organization dedicated to improving lives through technology.

Competitive salary

Benefits package

Career progression opportunities

Hands-on training

Experience in quality engineering within medical technology.
Strong skills in document control and inspection testing.

Conduct incoming inspections of parts and manage customer returns.
Ensure compliance with document control, CAPA, and complaints processes.

Medical Technology Knowledge

Document Control

Inspection Testing Skills

Quality Control

Bachelor's Degree in Engineering or related field

ISO 13485

QMS

ISO 14971

Production Quality Engineer - Medical Devices

Newton Colmore is working with a medical technology company near Lichfield, and we are assisting them with their search for a key quality hire to work closely with their production team.

The role as an experienced quality engineer will give you the opportunity to work on market leading medical devices whilst working closely with the production team to ensure that the parts delivered from the company's suppliers meet the design specifications and quality requirements. The quality engineer will help the production team in supplier quality assessments including creating and following up on SCARs and will also ensure that the Device History Record (DHR) is up to date for products manufactured. This is a key new role within the team, and you will be reporting directly to the head of the team and collaborating with the five members of the production team.

This role will also cover key responsibilities such as:

Incoming inspection of parts
Customer returns
Ensuring that document control, CAPA, and the complaints process is followed effectively

The company is looking for an experienced quality engineer with medical technology knowledge, mixed with strong document control and inspection testing skills.

In return for your hard work, the company offers a competitive salary and benefits package, as well as excellent career progression opportunities and hands-on training.

In regard to the process, there is a two-stage interview process where you will be invited to showcase your skills and experience while finding out more about the company, their mission, and what they can offer you.

To enter the recruitment process, click apply now and if you have the right skills and expertise, I will be in touch to discuss the opportunity further.

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

Get your free, confidential resume review.

or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.