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Quality Systems Engineer

Job in Belfast, County Antrim, BT1, Northern Ireland, UK
Listing for: HIRANI
Full Time position
Listed on 2026-02-27
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering, Biomedical Engineer
Job Description & How to Apply Below

We are expanding our team and are recruiting a Quality Systems Engineer. In this role you will play a key part in our Quality Team, reporting to the Head of Quality, responsible for the maintenance of the quality system to ISO 13485 standards and associated product certification.

As a Quality Systems Engineer, you will:

Support the maintenance and continuous improvement of our ISO 13485 compliant Quality Management System with activities including document control, training management and change management.

Draft and update procedures, work instructions, and quality documentation.

Collaborate closely with Engineering (Software and Hardware) and Customer Support teams to investigate and identify root causes of quality-related issues from customer complaints, internal non-conformances and audit findings.

Assist with the implementation of CAPAs and closure of non-conformances.

Collaborate with cross-functional teams on documentation creation, risk management, and validation activities.

Support quality compliance for SaMD products, including lifecycle and version control.

Participate in internal and external audits.

Analyse quality data and contribute to process improvement initiatives.

Required experience:

2+ years of experience in a Quality role within the medical device industry

Hands-on knowledge of ISO 13485 and 21 CFR 820

Strong attention to detail and problem solving skills

Ability to work as part of a multi-disciplinary, fast-paced diverse team

Ability to work independently and prioritise tasks

Excellent communication, interpersonal, organisational and IT skills

Helpful experience:

Experience with electronic Quality Management Systems (eQMS)

Exposure to software as a medical device / IEC 62304

Technical/procedural writing experience

Familiarity with medical device regulatory requirements in the UK, EU, or US

Experience in an electronics-related medical device manufacturing environment would be advantageous

Minimum Qualifications:

A Bachelor’s or Master’s degree in a Life Science, Engineering, or a related field

Salary & Benefits:

Competitive salary and performance-based bonus scheme

Competitive benefits including pension match and private medical insurance

Work with an awesome team of smart and motivated people on cool and unique technology that can positively impact the lives of millions of people

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