At a Glance
- Tasks: Ensure quality compliance and collaborate on exciting projects in a global medical devices company.
- Company: Join a leading global medical devices company in a dynamic environment.
- Benefits: Competitive salary, full-time hours, and hands-on experience in quality management.
- Other info: 12-month contract with excellent opportunities for professional growth.
- Why this job: Launch your career in a high-compliance field with real impact on healthcare.
- Qualifications: Recent graduate with attention to detail and a passion for quality engineering.
The predicted salary is between 33000 - 45000 £ per year.
About the Role
Are you a motivated recent graduate looking to launch your career in a high-compliance, pharmaceutical environment? We are seeking a detail-oriented Graduate Quality Engineer to join a global medical devices company in Witney. This 12-month contract offers an exceptional opportunity to gain hands-on experience in quality management systems and regulated product manufacturing.
Role Details:
- Location: Witney, Oxfordshire
- Salary: £33,000 - £45,000 per annum
- Hours: Full-Time, 37.5 hours per week (Monday to Friday)
- Contract Length: 12 Months
Key Responsibilities:
- Monitor and ensure compliance within the Quality Management System (QMS) through the review and impact assessment of documentation and process changes.
- Make critical quality and compliance decisions throughout the product life cycle, including development, validation, and manufacturing.
- Collaborate cross-functionally with R&D, Engineering, and Regulatory Affairs to ensure project goals are met to agreed timelines.
- Utilise risk management tools to prioritise activities and drive continuous process improvements.
- Act as a subject matter expert for audits and internal quality projects.
- Maintain rigorous documentation standards to ensure all records are accurate, secure, and procedural compliant.
We think you need these skills to ace Graduate Quality Engineer
Quality Management Systems (QMS)
Compliance Monitoring
Documentation Review
Impact Assessment
Cross-Functional Collaboration
Risk Management
Process Improvement
