Quality Engineer | Medical Device Are you an experienced Quality Engineer looking to take the next step in your career? A leading medical device manufacturer is seeking an experienced Quality Engineer to join their team on a 12 month contract This role offers the opportunity to lead key quality initiatives, drive product and process improvements, and ensure compliance with ISO standards. You will play a critical role in maintaining quality systems, supporting audits, and managing investigations to enhance product reliability and customer satisfaction. Key Responsibilities: Lead and coordinate quality-related activities to ensure compliance with ISO. Analyse quality data, investigate customer complaints, and implement corrective actions. Manage product/process quality improvement programmes. Support internal and external audits, including unannounced audits. Oversee CAPA investigations, non-conformances, and effectiveness monitoring. Collaborate cross-functionally to enhance quality processes and standards. Provide updates and escalate risks to the Quality Manager. Train and develop direct reports while fostering a culture of continuous improvement. Requirements: Third-level qualification in Science or Engineering. Minimum 2 years' experience in Quality Engineering within a manufacturing environment. Experience in an ISO-certified environment. Strong analytical, planning, and coordination skills. Excellent communication and problem-solving abilities. Previous people management experience is an advantage. Ability to multitask and work effectively in a fast-paced environment. This is an exciting opportunity to join a company committed to high-quality standards, innovation, and professional development. Interested? Apply today or contact Kerry Rickard for more details! Skills: Quality Medical Device ISO 13485 ISO 14971