At a Glance
- Tasks: Ensure quality and compliance in medical device development and testing.
- Company: Global medical device company with a collaborative culture.
- Benefits: Competitive salary, full-time hours, and valuable experience in a dynamic field.
- Other info: 12-month contract with opportunities for professional growth.
- Why this job: Join a team making a real difference in healthcare through innovative quality engineering.
- Qualifications: Experience in quality assurance and a passion for medical technology.
The predicted salary is between 33000 - 60000 £ per year.
We are seeking a skilled and adaptable Quality Engineer to join a global medical device company based in Witney. This is a highly collaborative, cross-functional role where you will support a range of processes from R+D to clinical groups to transport and sterilisation. We are looking for a professional who has interest in supporting Design Validation or Test Method Validation (TMV), who can make critical quality and compliance decisions during product development, validation, and testing. Acting as a Subject Matter Expert (SME), you will manage project activities to ensure our processes meet both business and customer needs flawlessly.
Role Details:
- Location: Witney, Oxfordshire
- Salary: £33,000 - £60,000 per annum
- Hours: Full-Time, 37.5 hours per week (Monday to Friday)
- Contract Length: 12 Months
Key Responsibilities:
- Validation Compliance Decisions: Make definitive Quality and Compliance decisions on products throughout development, validation, processing, and testing phases.
We think you need these skills to ace Quality Engineer - Design & Test Validation
Quality Assurance
Design Validation
Test Method Validation (TMV)
Compliance Decision Making
Project Management
Cross-Functional Collaboration
Subject Matter Expertise (SME)
