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We are currently seeking a dedicated professional from a science background to transition into a career in Quality Engineering to join a global medical devices company in Witney. This 12-month contract offers a significant opportunity to apply your technical knowledge within a high-compliance, regulated manufacturing environment.
Job Responsibility
Monitor and ensure the integrity of the Quality Management System (QMS) through the diligent review, approval, and impact assessment of documentation and process changes
Provide critical compliance oversight for products during development, validation, manufacturing, and packaging phases
Collaborate cross-functionally with departments including R&D, Engineering, and Regulatory Affairs to ensure project milestones are achieved
Utilise risk management methodologies to prioritise activities and drive continuous improvement of quality processes
Serve as a subject matter expert during audits and internal quality-focused initiatives
Maintain rigorous documentation standards, ensuring all records are accurate, secure, and fully compliant with procedural requirements
Requirements
Experience in a science-related field with a demonstrated interest in moving into Quality Engineering
Prior experience working within the development or manufacture of regulated products, providing familiarity with cGMP and/or ISO quality system requirements
Strong analytical capabilities and a meticulous approach to technical detail
Ability to foster effective professional relationships across multiple departments
Commitment to maintaining high standards of workplace safety and regulatory excellence