Injection Molding Process Engineer
Dublin
Contract
Negotiable
Manufacturing
CR/605173_1786436942
Injection Molding Process Engineer
Overview
We are seeking an experienced Process Engineer (Injection Moulding) to join a leading Medical Device manufacturer. The successful candidate will be responsible for developing, optimising, validating, and sustaining injection moulding processes used in the manufacture of high-quality medical devices. This role will play a key part in supporting production, driving continuous improvement initiatives, and ensuring compliance with regulatory and quality requirements.
Working within a cross-functional engineering team, you will collaborate with Manufacturing, Quality, Tooling, Automation, Validation, and R&D functions to deliver robust and efficient manufacturing processes.
Key Responsibilities
- Develop, optimise, and maintain injection moulding processes to achieve targeted quality, yield, and throughput objectives.
- Lead process characterisation activities using scientific molding principles and statistical techniques.
- Troubleshoot process, equipment, and quality issues to identify root causes and implement sustainable corrective actions.
- Support the introduction of new products and technologies from development through to commercial production.
- Execute process validations including IQ, OQ, and PQ activities in accordance with regulatory requirements.
- Generate and maintain process documentation, protocols, reports, SOPs, and technical specifications.
- Drive continuous improvement projects focused on scrap reduction, cycle time improvements, and increased equipment efficiency.
- Analyse process data and identify opportunities to improve process capability and product quality.
- Collaborate with toolmakers, machine suppliers, and automation teams to optimise manufacturing performance.
- Support equipment qualifications, preventive maintenance programs, and process monitoring activities.
- Participate in risk assessments, FMEAs, DOE studies, and Root Cause Analysis investigations.
- Ensure compliance with GMP, FDA, ISO 13485, and company quality standards.
- Support internal and external audits as required.
- Provide technical support and training to production and engineering personnel.
