Quality Assurance Specialist

Cure Talent; Greater London; Hybrid; GBP 45,000 - 60,000; Full time

Job summary

Cure Talent is partnering with a growing healthcare technology company in London for a QA Specialist on a six‑month fixed‑term contract with hybrid working. You will support the quality management system, handle document control, CAPA, change control and internal audits to enable faster, compliant delivery of software and hardware products.

The ideal candidate has experience in medical devices or medical technology, knows ISO 13485/EU MDR/FDA QSR, and can collaborate across teams to drive

Qualifications

• Experience in medical devices or medical technology quality.
• Familiar with ISO 13485, EU MDR, FDA QSR/21 CFR Part 820, EN 62304.
• Experience with QMS processes, document control, SOPs, nonconformances, CAPA, change control and internal audits.
• Experience supporting regulated software and hardware products.
• Strong organisation, attention to detail, and communication skills.

Responsibilities

• Maintain and improve the quality management system and workflows.
• Review processes to identify gaps and opportunities for improvement.
• Govern quality activities including nonconformances, CAPA, change control, internal audits and quality metrics.
• Generate, review and revise SOPs, technical documentation and quality records.
• Work cross-functionally to support compliance across software and hardware products.

Skills

Quality assurance

Medical devices

Quality systems

Documentation

Regulated software

Tools

Qualia

Job description

Position Overview

Company Overview

We are delighted to be partnered with a growing healthcare technology company focused on improving ear and hearing health. Its integrated platform supports ear and hearing assessment, diagnosis and treatment within a single appointment, complemented by a training programme that helps practitioners deliver confident, effective care. As the business continues to expand, it is seeking a QA Specialist to join its team on a six-month fixed-term contract, based in London with hybrid working.

Position Overview

The QA Specialist will support the development and continuous improvement of quality and regulatory processes across software and hardware-related products. The role will help strengthen the quality management system, improve process consistency and support faster, more effective decision-making as the organisation scales.

Working cross-functionally, the successful candidate will manage and improve quality activities including document control, SOPs, nonconformances, CAPA, change control and internal audits. They will also review existing processes, identify opportunities for improvement, maintain quality records and contribute to technical documentation. This is an opportunity to make a visible contribution within a collaborative, fast-paced healthcare technology environment.

In practice, the team is looking for someone who can provide hands-on support to help close existing quality gaps, reduce the backlog of open findings and improve delivery speed. Experience working with legacy technology, an evolving QMS setup such as Qualia or a comparable system, and a pragmatic approach to quicker decision-making would all be valuable.

About the Ideal Candidate

The ideal candidate will be a pragmatic and detail-oriented quality professional with experience in medical devices or medical technology. They will be confident supporting regulated software and hardware products, improving quality systems and collaborating across teams. Strong organisation, communication skills and a systematic approach will be important.

Role Responsibilities

• Support the maintenance and continuous improvement of the quality management system, including the optimisation of workflows and quality processes.
• Review existing processes to identify gaps, inefficiencies and practical opportunities for improvement.
• Govern quality activities including nonconformances, CAPA, change control, internal audits and quality metrics.
• Generate, review and revise SOPs, technical documentation and associated quality records.
• Work cross-functionally to support compliance across software and hardware products, embedding consistent and sustainable quality practices as the business grows.

Key Requirements / What We Look For

• Experience in quality assurance, quality operations or quality systems within medical devices or medical technology.
• Working knowledge of ISO 13485, EU MDR, FDA QSR / 21 CFR Part 820 and EN 62304.
• Experience with QMS processes, document control, SOPs, nonconformances, CAPA, change control and internal audits.
• Experience supporting regulated software and hardware products.
• Strong organisation, attention to detail, communication skills and a pragmatic approach to process improvement.