Process Engineer

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

Job summary

INMO TECH, part of mergon Group, in Enniscrone seeks a Process Engineer to drive injection-moulding and medical-device manufacturing projects. You will work across engineering, production, quality and maintenance with a focus on continuous improvement.

You will lead process qualification activities, set up new machinery and tooling, and implement improvements to quality, productivity and energy efficiency while maintaining ISO 13485 records.

Qualifications

• Bachelor’s degree in Mechanical or Polymer Engineering or related field.
• Experience in injection moulding and medical-device manufacturing.
• Familiarity with ISO 13485 requirements.

Responsibilities

• Manage engineering projects including new product and process introductions.
• Lead or support process qualification activities (IQ/OQ/PQ).
• Set up and validate new machinery, moulds, automation and equipment.
• Deliver continuous-improvement projects to improve quality, productivity and OEE.
• Maintain engineering records per ISO 13485.
• Support root-cause analysis and CAPA reporting.

Skills

Process engineering

Cross-functional teamwork

Continuous improvement

Project management

Education

Bachelor's degree in Mechanical or Polymer 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