Job Summary
A cutting-edge medical device manufacturer based in Waterford is seeking a highly skilled Manufacturing Engineer to join their team. This is an excellent opportunity for a qualified engineer with 3–5 years' experience in medical devices or regulated sectors to step into a varied and progressive role.
About the Role
The successful candidate will play a key role in process development, validations, and continuous improvement initiatives within a highly technical production environment. Key responsibilities include leading validation activities, overseeing visual inspection processes, and providing CAD support using SolidWorks.
Key Responsibilities:
* Lead validation activities and ensure timely implementation of Engineering Change Notes (ECNs)
* Oversee Visual FAIR inspection process and complete First Article reports
* Act as project lead for assigned NPIs, liaising with customers and internal teams
* Provide CAD support using SolidWorks (or equivalent) for jigs, fixtures, and engineering documentation
* Define and own manufacturing and assembly processes, including process routings and SOPs
* Support operational teams to meet project milestones and goals
* Drive continuous improvement and waste reduction initiatives
* Stay current with SOPs, safety policies, and modern manufacturing practices
Requirements:
* Bachelor's degree in Engineering (or equivalent)
* 3–5 years' experience in medical devices or similar regulated manufacturing environment
* Proficiency in CAD software (SolidWorks or similar)
* Knowledge of Minitab or equivalent statistical analysis tools (preferred)
* Experience in validation, process engineering, and technical support