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 ISO13485:2016 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 ISO13485:2016.
- 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 ISO13485:2016-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!
