Quality Assurance Officer - Medical Devices

Quality Assurance Officer - Medical Devices

Full-Time 40500 - 49500 £ / year (est.) Home office (partial)
Radar Recruitment

At a Glance

  • Tasks: Support and improve the Quality Management System for medical devices and consumer healthcare products.
  • Company: Join a growing international healthcare business with a diverse product portfolio.
  • Benefits: Competitive salary, hybrid work model, and exposure to various quality activities.
  • Other info: Work closely with cross-functional teams and gain valuable regulatory insights.
  • Why this job: Broaden your QA experience in a dynamic, international environment.
  • Qualifications: 2 years of QA experience in a regulated environment, ideally with medical devices.

The predicted salary is between 40500 - 49500 £ per year.

We are currently working on an exciting opportunity for a Quality Assurance Officer to join a growing international healthcare business with a diverse product portfolio spanning medical devices, consumer healthcare and cosmetics products.

This is a great opportunity for a QA professional who wants genuine exposure across QMS, medical devices, complaints, CAPA, supplier quality, technical documentation and regulatory compliance. The business operates across multiple European markets, so this is a role where you’ll need to be technically strong, highly organised and comfortable keeping up with changing regulations.

What will you be doing?

  • You’ll play a key role in supporting the day-to-day operation and continuous improvement of the Quality Management System, including:
  • Supporting the maintenance and improvement of the ISO 13485 QMS
  • Updating SOPs, work instructions and quality documentation
  • Supporting internal audits and preparation for external Notified Body and regulatory audits
  • Reviewing batch records, Certificates of Analysis and imported product documentation prior to release
  • Managing and investigating non-conformances and CAPAs
  • Supporting customer and trade complaint investigations, including root-cause analysis and complaint trending
  • Supporting supplier quality activities, quarantine processes, returns and product traceability
  • Reviewing labelling, packaging copy and artwork against regulatory and technical requirements
  • Maintaining technical documentation for medical devices and consumer products
  • Monitoring regulatory developments including PPWR, CLP, REACH and GPSR
  • Working closely with Supply Chain, Marketing, Regulatory, Technical and external partners

What are we looking for?

  • Ideally, you’ll have a minimum of 2 years’ hands‑on QA experience within a regulated environment, with experience in:
  • Medical Devices / ISO 13485 environment - ideal
  • A good understanding of UK/EU Medical Device Regulations (MDR)
  • QMS processes and documentation
  • CAPA and non-conformance management
  • Complaint handling and investigation
  • Batch release / quality documentation
  • Experience within healthcare, cosmetics or other regulated consumer products would also be advantageous.

You’ll also need to be someone who is:

  • Highly detail-oriented – comfortable working with technical documentation and quality records.
  • A quick learner – able to understand and apply new regulations as they develop.
  • Analytical – capable of investigating issues, identifying root causes and following actions through.
  • A strong communicator – comfortable working across Quality, Supply Chain, Marketing, Regulatory and external stakeholders.
  • Hands‑on and adaptable – this is a broad QA role in a lean and agile environment, so you’ll need to be comfortable getting involved in both technical quality activities and the more administrative/detail‑heavy aspects of the role.

Why consider it?

This is an excellent opportunity for someone looking to broaden their experience across medical devices, consumer healthcare and wider regulated products, while working within an international organisation. You’ll gain exposure to a broad range of quality activities rather than being restricted to one narrow area of QA.

Quality Assurance Officer - Medical Devices employer: Radar Recruitment

Join a dynamic and forward-thinking international business in Hull, where your leadership as a Sales Team Manager will not only drive significant growth but also foster a culture of collaboration and innovation. With a strong emphasis on employee development, you'll have access to coaching opportunities and the autonomy to shape a high-performing sales team, all while managing key customer accounts in a supportive environment that values your contributions. This role offers a unique chance to make a meaningful impact in a company renowned for its exceptional service and commitment to excellence.

Radar Recruitment

Contact Details:

Radar Recruitment Recruitment Team

We think you need these skills to ace Quality Assurance Officer - Medical Devices

ISO 13485
UK/EU Medical Device Regulations (MDR)
Quality Management System (QMS)
CAPA management
Non-conformance management
Complaint handling and investigation
Batch release documentation