Senior QA Engineer | Medical Device | Co. Offaly Are you an experienced Quality Engineer looking to take the next step in your career? A leading medical device manufacturer in Co. Offally is seeking a Senior QA Engineer to join their team. 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 3 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 Kerrr Rickard for more details! Skills: Quality Medical Device ISO 13485 ISO 14971 Benefits: Pension Healthcare