Job Description
Manufacturing Engineer in Galway: Analyze and improve production processes, troubleshoot issues, and drive business growth in a medical devices company.
About the Role: Our client, a thriving medical devices company, is seeking a Manufacturing Engineer to join their team in Galway. This role offers an excellent opportunity to work with a dynamic company and develop your skills in a highly regulated environment.
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Responsibilities:
- Analyze process, product, material, or equipment specifications and performance requirements.
- Compile and analyze operational, test, and experimental data to establish performance standards for newly implemented or modified products/processes.
- Summarize, analyze, and draw conclusions from test results to achieve effective technical resolution.
- Troubleshoot new products/processes, working closely with product development.
- Drive continuous improvement and yield analysis.
- Engage with technicians, operators, and other cross-functional teams to ensure business process success.
- Contribute to NPI (New Product Introduction) development and root cause analysis using Lean tools and techniques.
- Write and improve process procedures.
- Perform PCA (Process Change Analysis) from documentation to implementation.
- Demonstrate good working knowledge and application of validation techniques and associated regulatory requirements.
- Promote and participate in a cross-functional teamwork environment.
- Evaluate new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
- Provide technical guidance to Associate Engineers and technicians.
- Be an influential team member, fully motivated to achieve and demonstrate best practices in line with the department and site objectives.
- Demonstrate a primary commitment to patient safety and product quality.
- Understand and comply with all regulations governing the quality systems.
- Ensure all direct reports are aware of their commitment to patient safety and product quality, are current with their training requirements, and understand and comply with all other regulations governing their work.
Qualifications and Experience: NFQ Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.) Minimum 3-5 years experience working at an Engineering level, ideally in Medical Device industry or other highly regulated environment. Project Management experience highly desirable.
Benefits: Paid Holidays Canteen