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