Manufacturing Engineer (Medical Devices)
Manufacturing Engineer II – Cork (Hybrid)
Our Cork based world leading medical device multinational have an opening on their team for an experienced Manufacturing Engineer. An excellent Hybrid working opportunity. Please reach out to rachel@cregg.ie to discuss.
About the Role
The role involves working in our pharmaceutical quality system supporting commercial production of our pharma product. The successful candidate will be responsible for providing daily support of and equipment, processes, materials, in order to achieve production goals along with develop and implement manufacturing business improvement process improvement projects and processes working with Automated Equipment. The role is heavily involved with equipment line moves, equipment validation, equipment qualification, process improvements, line upgrades.
Responsibilities
Responsible for the introduction and validation of new equipment.
Analyses process, product, material or equipment specifications and performance requirements.
Work with cross-functional teams to identify and resolve production/engineering issues.
Summarises, analyses, and draws conclusions from test results leading to effective technical resolution.
Transfer and validation of equipment from one clean room to another.
Continuous Improvement & Yield Analysis.
Continually seeks to drive / improvements in process equipment 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
Root cause analysis using Lean tools and techniques.
Writing and improving process procedures.
PCA (Process Change Analysis) From Documentation to Implementation.
Gives technical guidance to Associate Engineers and technicians
Qualifications and Experience
NFQ Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.)
Minimum 2+years’ experience working at an Engineering level, ideally in Medical Device industry or other highly regulated environment.
Automated Manufacturing equipment experience advantageous.
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