Manufacturing Engineer – Projects (Hybrid)

CREGG; Galway; On-site; EUR 50,000 - 70,000; Full time

Job summary

A leading Medical Device company in Galway is looking for a Manufacturing Engineer to join their projects team in a hybrid role. The successful candidate will provide support for production goals and lead manufacturing improvement initiatives. Responsibilities include process analysis, product validation, and collaboration with diverse teams. Candidates should have a NFQ Level 8 qualification in a technical discipline and 2-5 years of engineering experience, ideally in regulated environments. This role offers significant career development opportunities.

Qualifications

• Strong expertise in process validation techniques and regulatory requirements.
• Experience in the Medical Device industry or similar highly regulated sectors.
• 2-5 years of engineering experience in relevant fields.

Responsibilities

• Analyze processes, products, materials or equipment specifications.
• Compile and analyze operational and test data.
• Conduct process validations and troubleshooting for new products.
• Drive continuous improvements and yield analysis.
• Engage with teams to ensure business success.

Skills

Process & Equipment validations

Continuous Improvement

Root cause analysis

Lean tools and techniques

Collaboration with cross-functional teams

Education

NFQ Level 8 in a Technical Discipline

Job description

Manufacturing Engineer – Projects (Hybrid)

Manufacturing Engineer – Galway (Hybrid)

About the role:

Our Galway based client are now hiring for a Manufacturing Engineer (Hybrid) to join their projects team. An excellent opportunity to work with a leading Medical Device company offering great career progression opportunities. The successful candidate will provide daily support of products, processes, materials, and equipment in order to achieve production goals along with develop and implement manufacturing business improvement projects and processes. Hybrid role offering 2 days work from home.

Responsibilities:

• 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.
• 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.

Qualifications and Experience:

• 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.