Manufacturing Engineer II – Cork (Hybrid)About the role:Our Cork based client are now recruiting for a Manufacturing Engineer to join their team. An excellent Hybrid working opportunity to work with a thriving medical devices company. The role would involve working in their 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.Contact Mark 086 190 1346 or markhalligan@cregg.ie for more informationResponsibilities: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) developmentRoot cause analysis using Lean tools and techniques.Writing and improving process procedures.PCA (Process Change Analysis) From Documentation to ImplementationDemonstrates 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.Understandsand complywith all the regulations governing the quality systems.Ensures alldirect 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 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.Automated Manufacturing equipment experience advantageous.Yes please, create an account so that I can apply faster next timeCREGG is currently looking for Automation Engineers with PLC programming experience for a client based in Dublin on a permanent basis. This is a great opportunity to join a veryAutomation Sales Engineer – Dublin 12. As a leading provider of Robotic and Automation solutions, my client wishes to recruit an experienced, results-driven Sales Engineer for a largely external position,CREGG are currently seeking a detail-oriented and highly organised Accounts Receivable Associate to join a large & well-known employer based at their offices in Shannon, Co. Clare. Please note thisCREGG is delighted to be recruiting a Commercial Property Asset Specialist for a well-known property group in Shannon, Co. Clare. As the Commercial Property Asset Specialist, you will be responsibleCREGG is currently recruiting a Documentation Specialist for a client based in East Cork on a permanent basis Role Overview The Documentation Specialist is responsible for supporting the commercial andManufacturing Engineer - Hybrid CREGG are hiring for a Manufacturing Engineer to work with a large Medical Device company in Galway. Hybrid role For more information contact Mark: 086 1901346
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