We are seeking a Manufacturing Engineer with a strong background in polymer and injection moulding, validation, and quality compliance. This position supports process improvement, validation projects, and the digitalisation of quality records. It offers an exciting opportunity to contribute to a high-performing team within a regulated environment. This is a 12-month fixed-term contract, based onsite the manufacturing facility in Athlone, Co. Westmeath. Key Responsibilities: Support process validation activities and continuous improvement projects. Assist with the digitalisation of quality records, especially batch records. Contribute to the design and improvement of manufacturing layouts and procedures. Perform root cause analysis and apply statistical tools (SPC, DOE) to resolve production issues. Develop and maintain manufacturing documentation (MP, IP, BOM, IQ/OQ/PQ). Ensure compliance with internal and regulatory quality standards. Collaborate with cross-functional teams including Quality, Engineering, and Production. Key Requirements: Level 8 Degree in Mechanical, Polymer, Biomedical Engineering, or related field. Minimum 4 years' experience in a regulated manufacturing environment (MedTech/Pharma). Experience in injection moulding, polymer processing, and process validation. Familiarity with digital quality systems and batch documentation. Working knowledge of Lean, Six Sigma, SPC, and DOE methodologies. Proficiency in AutoCAD and SolidWorks is an advantage. Strong attention to detail, communication, and problem-solving skills. For a confidential discussion about this opportunity, please contact Ranait Coughlan Skills: injection moulding polymer manufacturing Engineer project engineer quality engineer