Manufacturing Engineer – Cork (Hybrid)

• Analyse processes, product, material or equipment specifications and performance requirements.
• Responsible for the introduction/transfer and validation of new equipment.
• Troubleshoots new products / process working closely with product development.
• Continuous Improvement & Yield Analysis.
• Continually seeks to drive / improvements in process design, layout and operational performance.
• Engaging with technicians, operators, and other cross-functional teams to ensure business process success.
• Contribution in NPI (New Product Introduction) development
• Execute new equipment introductions and carry out validations.
• Root cause analysis using Lean tools and techniques.
• Writing and improving process procedures.
• PCA (Process Change Analysis) From Documentation to Implementation
• Demonstrates good working knowledge and application of validation techniques and associated regulatory requirements.

• NFQ Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.)
• Minimum 2-5 years' experience working at an Engineering level, ideally in Medical Device industry or other highly regulated environment desirable.
• Project Planning/Management experience highly desirable.
• Automated Manufacturing equipment experience advantageous but not essential
• Process & Equipment validations IQ/OQ/PQ desirable

CREGG Recruitment