Manufacturing (Projects) Engineer- Hybrid

• Analyse processes, product, material or equipment specifications and performance requirements.
• Under broad supervision / guidance compiles and analyses operational, test and experimental data to establish performance standards for newly implemented or modified products / processes.
• Process & Equipment validations – IQ OQ PQ
• Troubleshoots new products / process working closely with product development.
• Continuous Improvement & Yield Analysis, LEAN Mfg.
• 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.
• Process & Equipment validations desirable IQ/OQ/PQ

CREGG Recruitment