Our client, a multinational medical devcie manufacturing company based in Athlone, is hiring for a 9-month contract for the role of Quality Technician.
The role is full-time on-site.
This role is a great opportunity for someone to get experience in a well established Quality team.
Responsibilities: Responsible for providing Quality support to processes, materials, and products, ensuring that Quality standards are upheld.
Assist with the implementation and adherence to the Quality Management program and support the achievement of company goals, objectives, policies, procedures, quality systems, and compliance with regulatory requirements (ISO, FDA, JPAL, and other applicable agencies).
Conducting DHR Reviews Executing Product Release procedures Performing Internal/GMP Audits Reviewing complaint documentation Assisting in the development, analysis, and enhancement of site Quality Metrics Presenting data during Quality Metrics reviews Generating and issuing Certificates of Conformity as needed Conducting Environmental testing when required Requirements: A third-level qualification in Quality, Science, or Engineering A minimum 2 years of experience in a Medical Device or similar regulated environment Exceptional attention to detail Proficiency in computer skills, including MS Excel, PowerPoint, and Word Familiarity with statistical tools like Pareto charts and trend charts Proficiency in problem-solving techniques Experience working in a regulated environment, particularly in medical devices, FDA, or ISO registered work environments The ability to effectively communicate highly technical information, both verbally and in writing, to both non-technical and technical colleagues If you would like more information on this role you can contact Paul Dunican Skills: Quality Technician QC Technician Quality Control