Process Engineer

Mergon; Inishcrone; On-site; EUR 45,000 - 65,000; Full time

Job summary

INMO TECH, part of mergon Group, in Enniscrone, Ireland, seeks a Process Engineer to lead the introduction, validation and improvement of medical-device processes, concentrating on injection moulding and related production activities.

The role spans engineering, production, quality and maintenance, driving process qualification, CAPA, and equipment validation to ensure high-quality, efficient manufacturing.

Qualifications

• Bachelor's degree in Mechanical Engineering, Polymer Engineering or related field.
• Experience with injection moulding processes and tooling.
• Medical-device process validation and ISO 13485 familiarity.
• Pneumatic, hydraulic and electrical principles.
• Experience with PLCs and CAD systems (SolidWorks).

Responsibilities

• Manage engineering projects for new product and process introductions in medical-device applications.
• Lead or support process qualification activities (IQ, OQ, PQ) and prepare technical reports.
• Set up and validate new machinery, moulds, automation, and auxiliary equipment.
• Deliver continuous-improvement projects improving quality, productivity, OEE, energy efficiency.
• Maintain engineering records in accordance with ISO 13485.
• Support root-cause analysis, NCR investigations and CAPA reporting.

Skills

Process engineering

Continuous improvement

Cross-functional collaboration

Project management

Education

Bachelor's degree in Mechanical Engineering

Tools

SolidWorks

RJG eDART/CoPilot

Kistler systems

Job description

Due to continued growth in its injection moulding business, INMO TECH part of mergon Group, is recruiting a Process Engineer to join its team in Enniscrone. This is an excellent opportunity for an Engineer who wants to work on technically challenging projects within a high-quality manufacturing environment.

The role

As Process Engineer, you will support the introduction, validation and continuous improvement of products and processes. You will work across engineering, production, quality and maintenance activities, with a particular focus on injection moulding and medical-device manufacturing.

Key responsibilities

• Manage engineering projects, including new product and process introductions for medical-device applications.
• Lead or support process qualification activities, including IQ, OQ and PQ, and prepare the associated technical reports.
• Set up and validate new machinery, moulds, automation and auxiliary equipment.
• Deliver continuous-improvement projects focused on product quality, productivity, OEE, sustainability and energy efficiency.
• Maintain comprehensive engineering records in accordance with ISO 13485.
• Support root-cause analysis, NCR investigations and CAPA reporting.
• Use process-control technologies, including RJG eDART/CoPilot and Kistler systems to achive process capability and efficiency.
• Support maintenance activities involving moulds and manufacturing equipment

Qualifications & Experience

You should ideally hold a minimum of a bachelor’s degree in Mechanical Engineering, Polymer Engineering or a related engineering discipline. Experience in the following areas would be a distinct advantage:

• Injection moulding processes and tooling
• Medical-device process validation
• High-volume medical manufacturing
• Pneumatic, hydraulic and electrical principles
• PLCs,SolidWorks or other CAD systems
• ISO 13485 requirements