Quality Engineer - Process (Secondment Opportunity)

CompanyTerumo Aortic

LocationRenfrew, Scotland, United Kingdom

Posted At1/29/2026

UK Visa Sponsorship Analytics

Analytics are greyed out due to low classification confidence (42.0%).

Occupation Type

Production and process engineers

Occupation Code Skill LevelHigher Skilled

Sponsorship Salary Threshold

£45,000 (£23.08 per hour)

Occupation rate applies

Above analytics are generated algorithmically based on job titles and may not always be the same as the company's job classification. You can also check detailed occupation eligibility, and salary criteria on our UK Visa Eligible Occupations & Salary Thresholds page.

Disclaimer: Hunt UK Visa Sponsors aggregates job listings from publicly available sources, such as search engines, to assist with your job hunting. We do not claim affiliation with Terumo Aortic. For the most up-to-date job details, please visit the official website by clicking "Apply Now."

Description

We’re looking for a driven and detail‑oriented Quality Engineer – Process Quality to join our high‑performing Quality Assurance team on a fixed term contract for 12 months. In this role, you’ll support R&D, Manufacturing, and Quality functions across a wide range of projects, ensuring our products and processes meet the highest global regulatory standards. You’ll play a key part in fostering a culture of continuous improvement, operational excellence, and regulatory compliance.

What You’ll Do

Quality Engineering & Compliance

Support design and manufacturing-led projects with expert Quality Engineering input.
Lead and contribute to CAPA and complaint investigations, including root cause analysis.
Ensure compliance with global regulatory standards (EU MDR, ISO 13485, FDA 21 CFR 820, MHLW Ordinance 169, and others).
Maintain audit readiness across processes, documentation, and facilities.

Cross-Functional Collaboration

Represent Quality on design teams and process improvement initiatives.
Work closely with R&D and Manufacturing to develop test protocols, validation plans, and IQ/OQ/PQ documentation.

Support execution and oversight of validation activities.

Partner with teams to resolve product and process quality issues using structured problem‑solving tools.

Data, Documentation & Systems

Provide trending data and reports to senior management, regulators, and customers.
Support validated test method development and contribute to dFMEA and pFMEA improvements.
Champion the use of MasterControl for managing protocols, reports, validation data, and engineering change records.
Maintain the Computer System Validation inventory list.

Training & Continuous Improvement

Develop training materials for design and manufacturing teams on validation requirements.
Contribute to process-based procedures for design control, V&V, and IQ/OQ/PQ.
Assist with validation of new tools, equipment, and processes.
Build strong internal and external relationships to support quality and regulatory compliance.

What You’ll Bring

A relevant science or engineering degree.
Six Sigma Green Belt (minimum).
Proven experience in Quality Engineering within a medical device or regulated manufacturing environment.

Strong understanding of global medical device regulations and Quality Management Systems.

Experience supporting design and validation teams in a global organisation.

Working knowledge of Minitab or similar statistical tools.

Excellent analytical, problem‑solving, and communication skills.

Ability to manage multiple priorities in a fast‑paced environment.

Strong IT skills, including Microsoft Office and willingness to learn QA systems.

Ability to influence change through clear, structured communication.

A collaborative mindset and the ability to build effective cross‑functional relationships.