Job Title: Manufacturing Engineer
Location: Clonmel, Tipperary
Industry: Medical Devices
Role Profile
Responsible for the introduction and validation of new equipment. Analyzes process, product, material or equipment specifications and performance requirements.
Works with cross-functional teams to identify and resolve production/engineering issues.
Sums up, analyzes, and draws conclusions from test results leading to effective technical resolution.
Transfers and validates equipment from one clean room to another.
Continuously seeks to drive improvements in process equipment design, layout and operational performance.
Engages with technicians, operators, and other cross-functional teams to ensure business process success.
Contributes to NPI (New Product Introduction) development
Performs root cause analysis using Lean tools and techniques.
Writes and improves process procedures.
Conducts PCA (Process Change Analysis) From Documentation to Implementation
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.
Understands and complies with all regulations governing the quality systems.
Ensures all direct reports are aware of their commitment to patient safety and product quality, are current with their training requirements and that they understand and comply with all other regulations governing their work.
Qualifications / Professional Skills / Knowledge
A level 8 bachelors related engineering degree: mechanical, manufacturing etc is required.
Proven experience of at least 2-3 years minimum experience, automated manufacturing experience an advantage.
Main skills or qualifications: Lean skills Continuous improvements Six Sigma 5s Project Management Leadership