Quality Engineer- Medical Devices

Job description

We are recruiting on behalf of a global medical device leader for a talented Quality Engineer to join their team on a 12-month contract. This role is perfect for an experienced quality professional who wants to expand their skills, work on high-profile projects, and gain exposure in a regulated environment without committing to a permanent role.

What You’ll Be Doing

• Lead quality improvement initiatives to enhance processes, reduce costs, and ensure regulatory compliance.

• Support change controls, risk assessments, and process validations.

• Analyse data and spot trends using statistical tools.

• Write and review CAPAs, non-conformance reports, and supplier corrective actions.

• Conduct audits and support inspections by ISO and FDA regulators.

• Collaborate across teams to embed best practices in quality standards.

What You’ll Need

• 3+ years’ experience in a regulated environment – ideally medical devices or FDA/ISO 13485 certified manufacturing.

• Degree in Quality, Science, or Engineering.

• Strong MS Excel, Word, and PowerPoint skills.

• Experience with FMEAs, root cause analysis, and statistical analysis.

• Excellent attention to detail and problem-solving ability.