Job Description
A Quality Engineer is required to work with a medical device manufacturing client in Limerick. This role involves ensuring the quality and compliance of all production processes.
Key Responsibilities:
* Investigate quality issues, analyze results, make recommendations, and develop reports based on engineering principles.
* Collaborate with operations to develop controls and improvements.
* Develop training materials for production staff to enable knowledge transfer of project and manufacturing processes.
* Assign support tasks, train technicians, and provide feedback.
* Investigate customer complaints and participate in internal audit and supplier audit programs for ISO 13485 and ISO 14001.
* Lead defect resolution, root cause investigation, and continuous improvement activities.
Requirements:
* Bachelor's degree in science, quality, engineering, or related discipline.
* At least 2 years of industry experience.
* Strong written and oral communication skills.
* Experience working with medical device regulations.