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We are currently seeking a highly skilled Quality Engineer to join a global medical devices company in Witney. This 12-month fixed-term contract offers a significant opportunity for an experienced professional to apply their technical expertise within a high-compliance, regulated manufacturing environment. You will play a pivotal role in maintaining the integrity of our Quality Management System (QMS) while driving excellence across our core operations.
Job Responsibility
Monitor and uphold the integrity of the QMS through diligent review, approval, and impact assessment of documentation and process changes
Provide critical compliance oversight for product development, validation, manufacturing, testing, and packaging activities
Serve as a Subject Matter Expert (SME) during internal and external audits, ensuring all records are accurate, secure, and fully compliant
Collaborate cross-functionally with R&D, Engineering, and Regulatory Affairs to achieve project milestones using robust risk management methodologies
Mentor team members on procedures and quality standards to ensure a culture of continuous improvement and regulatory excellence
Requirements
Substantial experience in a quality-focused role, specifically with professional exposure to design, test validation, or calibration processes
Demonstrated familiarity with cGMP and/or ISO quality system requirements within a regulated sector
Strong analytical capabilities and a meticulous approach to technical documentation and process improvement
Proven ability to manage cross-functional projects and foster effective relationships across complex organisational structures