Collins McNicholas is seeking a Manufacturing Engineer to support process improvement, validation projects, and digitalisation of quality records in our regulated manufacturing environment.
About the Role
This is an exciting opportunity to contribute to a high-performing team and join our company for a 12-month fixed-term contract based onsite at our 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.
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.
About Us
Collins McNicholas is a leading recruitment and employment agency providing expert advice and solutions to clients across various sectors including pharmaceuticals and medtech.