Graduate / Junior Quality & Product Development Engineer — Medical Devices

Location: Manchester, UK

Employment type: Full-time, permanent

Salary: £34,000–£40,000 per annum, depending on relevant experience, with a salary review after six months.

About ISOBAR

ISOBAR designs and manufactures personalised compression therapy systems incorporating compression dose management technology for the health, sports and travel markets.

Our on-demand manufacturing process combines specialist flat-knit technology with digital systems to create technically knitted garments matched to individual customers.

We are looking for a motivated graduate or early-career engineer to help coordinate this market-entry programme while contributing to quality assurance, product testing and manufacturing improvement.

The role

You will coordinate programme activities and deliver defined work packages under the supervision of an experienced internal lead or retained adviser.

Your work will include maintaining project schedules, organising testing, preparing controlled documentation, analysing results and following up actions across manufacturing, software and external specialists.

You will receive structured training and progressively take on greater responsibility as your skills develop. Regulatory strategy, test protocols, technical conclusions and market-release decisions will be reviewed and approved by the designated experienced lead or adviser.

This is a practical development role combining detailed quality work with hands-on involvement in manufacturing and product development.

Key responsibilities

Coordinate the market-entry programme

• Maintain the programme schedule, action register and document tracker.
• Track deliverables, dependencies and deadlines, and flag delays or evidence gaps to your supervisor.
• Organise project meetings, record decisions and follow up agreed actions.
• Coordinate samples, information and documentation between internal teams, laboratories and external advisers.
• Prepare progress updates for management, identifying decisions requiring senior review.

Support quality systems and technical documentation

• Help develop and maintain quality procedures, work instructions, inspection records and product specifications.
• Prepare and organise evidence for the EU MDR technical file and FDA design and development records, including documents commonly described as the Design History File.
• Maintain traceability between ...

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