Job Title: Manufacturing Engineer II (Hybrid) Location: Tipperary (Clonmel) Industry: Medical Device Manufacturing Company information: A world leading medical device multinational Hours: Hybrid role requiring 3 days onsite. 39hr week with a 1pm Friday finish. Role Profile CREGG are seeking experienced Manufacturing Engineers to join Clonmel's world leading medical device manufacturer. The ideal candidate will have strong equipment validation background as the predominant function will be executing validations on duplicate sets of equipment. To discuss call or email Rachel Responsibilities: Equipment Validation Analyses process, product, material or equipment requirements and performance requirements. Under broad supervision / guidance compiles and analyses operational, test and experimental data to verify performance standards for newly implemented or modified products / processes. Troubleshoots new products / process working in conjunction with product development. 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 assistance to Associate Engineers and technicians Qualifications / Professional Skills / Knowledge Level 7 or 8 degree from a STEM discipline 2 years experience at Engineer level Contact Information For a confidential discussion or to find out more, please contact: Rachel McMahon Email: Phone: INDCRG Skills: IQ OQ PQ