Quality Engineer II The Quality Engineer (QE) shall be responsible for monitoring the production and release of finished parts and ensuring quality policies and procedures are adhered to daily, following the requirements of the Quality Management System.
This includes but is not limited to:
Interfacing with the customer to realise customer satisfaction.
Responsibility for production GMP standards Investigation of root cause and following through on effective corrective actions to prevent re-occurrence for customer and internal quality issues.
Initiating and completing CAPA actions as required. Initiating and completing engineering change request and action as required. Initiating and completing non-conformance reports (NCRs) as required, co-ordinating product/production related NCRs to closure in a timely manner. Establishing and monitoring inspection standards, plans, frequencies, and test methods Establishing and maintaining FMEAs. Preparing and updating quality system documentation Supporting customer and surveillance accreditation audits. The quality engineer will perform an active role in quality planning and new product introduction from a quality perspective. Have a good working knowledge of quality management systems (Ideally ISO13485) and other product related regulatory requirements. Develop strong links with customer organisations and other project stakeholders. Validation experience would be advantageous. Performing an active role in further development and continuous improvement of the quality management system. Support Operations area projects and initiatives.
The training of new or existing personnel on quality procedures and documentation; ensuring that production personnel are trained for their tasks and that procedures are in place.
Understanding of customer documents i.e.
Drawings, Purchase Specification, Quality Agreements etc Ensuring that on hold material is dispositioned and actioned from QAHOLD in a timely manner.
Ensuring that all retained samples are stored correctly, and that sample storage area is maintained. Ensuring that all quality records are completed as per company procedures comply with GDP. Adherence to incoming control requirements and supporting the SCAR process when required. Audit experience is advantageous. Perform additional duties at the request of the Quality Operations Manager.
The Ideal Candidate will:
Hold a relevant 3rd-level qualification and 3+ yrs equivalent quality experience in high-volume manufacturing. Have good communication and interpersonal skills. Be a team player with the ability to work independently. Be proactive and solutions-driven in their approach. The must-haves: An existing work permit/ visa for working in Ireland. Experience working in a Quality Department in an injection moulding, high-volume manufacturing, medical device environment. As this is a client-facing role, fluent written and verbal English, paired with a customer-friendly personality is essential. This onsite support role is based in Kildare- you must be within a commutable distance of the site. This role is 5 days per week on site. Do you fit the requirements above? If so, reach out to Niamh at or for more details.
Skills:
Quality Engineering Injection Moulding Medical Device.