Description:
Job Purpose:
- Provides daily support of products, processes, materials, and equipment in order to achieve production goals (i.e., quality, delivery, cost, productivity, and safety).
Responsibilities:
- Analyses process, 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.
- Summarises, analyses and draws conclusions from test results leading to effective technical resolution.
- Troubleshoots new products / process working closely with product development.
- Continually seeks to drive improvements in process design, layout and operational performance.
- Demonstrates good working knowledge and application of validation techniques and associated regulatory requirements.
- Actively promotes and participates in a cross -functional teamwork environment.
- Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
- Gives technical guidance to Associate Engineers and technicians.
- Is 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.
- Understands and comply with all the regulations governing the quality systems.
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
- Six Sigma qualification desirable