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.
Skills: Quality Manager Communication CAPA