Manufacturing Engineer – Cork (Hybrid)

CREGG; Cork; Hybrid; EUR 45,000 - 65,000; Full time

Job summary

A leading Medical Device company in Cork is hiring a Manufacturing Engineer. This hybrid role offers opportunities in process improvement and NPI development. The successful candidate will analyze and validate equipment, collaborate with cross-functional teams, and drive operational performance improvements. A Level 8 qualification and relevant experience in engineering, preferably in a regulated environment, are required.

Qualifications

• Minimum 2-5 years’ experience in Engineering, ideally in the Medical Device industry.
• Experience with Process & Equipment validations (IQ/OQ/PQ) desirable.

Responsibilities

• Analyse processes, product, material or equipment specifications.
• Introduce/transfer and validate new equipment.
• Troubleshoot new products/process working closely with product development.
• Drive improvements in process design, layout, and operational performance.
• Engage with cross-functional teams to ensure process success.

Skills

Process Improvement

Lean tools and techniques

Cross-functional collaboration

Root cause analysis

NPI development

Education

NFQ Level 8 in a Technical Discipline

Tools

Automated Manufacturing Equipment

Job description

Our Cork based client are now hiring for a Manufacturing Engineer (Hybrid) to join their team. An excellent opportunity to work with a leading Medical Device company offering great career progression opportunities. The successful candidate will provide daily support and work on projects, NPI, processes, materials, and equipment in order to achieve production goals along with develop and implement manufacturing process improvement projects, liaising with suppliers on materials and working with the latest technologies and equipment.

Responsibilities:

• 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.

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.
• Automated Manufacturing equipment experience advantageous but not essential
• Process & Equipment validations IQ/OQ/PQ desirable

Contact Information:

Please contact Gary Keane for more details: [e-mail], 086-1030418 / 091-700814