ELECTRO-MECHANICAL ENGINEER II Apply Locations: IE-xx-Tullamore-610-Facility Time type: Full time Posted on: Posted 12 Days Ago Job requisition id: JR-4049 Changing lives. Building Careers. Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes. Are you an Electro-Mechanical Engineer looking for an exciting opportunity to work with cutting-edge medical device technology ? Do you thrive in a collaborative environment where innovation, quality, and problem-solving are at the heart of what you do? If so, this could be the perfect role for you! About the Role: As part of our Sustaining Engineering Team , you’ll play a key role in ensuring the continued excellence of our medical devices. You’ll work on component obsolescence projects, production support, failure investigations, and process improvements , all while collaborating with cross-functional teams to enhance product compliance and quality. What You’ll Be Doing: Technical Expertise: Design, debug, and improve electro-mechanical systems. Problem-Solving: Investigate failures, conduct root cause analysis, and identify alternative components. Continuous Improvement: Drive process enhancements and technology implementation for production. Collaboration: Work closely with R&D, Quality, and Manufacturing teams to ensure seamless product lifecycle management. Compliance & Quality: Contribute to ISO 13485 and 21 CFR 820 initiatives, and support regulatory audits. What We’re Looking For: Degree in Engineering (Mechanical, Mechatronic, Electronics, or similar) – NFQ Level 8 or higher. 2-5 years of relevant experience in electro-mechanical systems, manufacturing, or medical devices. Knowledge of ISO 13485, 21 CFR 820, and process validation. Strong skills in problem-solving, planning, and communication. Ability to work both independently and collaboratively in a dynamic environment. Willingness to travel occasionally to partner sites. #J-18808-Ljbffr
Are you an Electro-Mechanical Engineer looking for an exciting opportunity to work with cutting-edge medical device technology ? Do you thrive in a collaborative environment where innovation, quality, and problem-solving are at the heart of what you do? If so, this could be the perfect role for you! About the Role: As part of our Sustaining Engineering Team , you’ll play a key role in ensuring the continued excellence of our medical devices. You’ll work on component obsolescence projects, production support, failure investigations, and process improvements , all while collaborating with cross-functional teams to enhance product compliance and quality. What You’ll Be Doing: Technical Expertise: Design, debug, and improve electro-mechanical systems. Problem-Solving: Investigate failures, conduct root cause analysis, and identify alternative components. Continuous Improvement: Drive process enhancements and technology implementation for production. Collaboration: Work closely with R&D, Quality, and Manufacturing teams to ensure seamless product lifecycle management. Compliance & Quality: Contribute to ISO 13485 and 21 CFR 820 initiatives, and support regulatory audits. What We’re Looking For: Degree in Engineering (Mechanical, Mechatronic, Electronics, or similar) – NFQ Level 8 or higher. 2-5 years of relevant experience in electro-mechanical systems, manufacturing, or medical devices. Knowledge of ISO 13485, 21 CFR 820, and process validation. Strong skills in problem-solving, planning, and communication. Ability to work both independently and collaboratively in a dynamic environment. Willingness to travel occasionally to partner sites. Why Join Us? Work on life-saving medical technology that makes a real impact. Be part of an innovative and growing company in the medical device industry. Collaborative culture with great learning and development opportunities. Hybrid work options available. Changing lives. Building Careers. Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes. Ready to take the next step? Apply today or reach out for more details! #J-18808-Ljbffr
Changing lives. Building Careers. Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes. We are seeking a detail-oriented Quality Assurance Inspector to join our team and ensure the accuracy and compliance of medical devices and components processed in a GMP-rated, FDA, and MOD-regulated environment . The ideal candidate thrives in a meticulous role, possesses excellent organizational skills, and understands the critical importance of inspection, testing, and data integrity in medical device manufacturing. You will play a vital role in upholding quality standards, maintaining compliance, and supporting operational efficiency. In this role, you will: Perform inspections and tests of finished devices, sub-assemblies, and components using appropriate inspection, measurement, and test (IMT) equipment. Review and interpret engineering drawings, material specifications, and test documents (training in technical drawing interpretation will be provided). Support incoming inspection processes using various metrology equipment to ensure compliance with specifications. Collaborate with supply chain and manufacturing teams to plan inspection activities and ensure priorities are achieved. Manage non-conforming materials and communicate issues to management promptly. Analyze trends in failures or anomalies, implement immediate corrective actions, and ensure follow-up measures are executed. Maintain accurate, compliant documentation and records in accordance with cGMP and medical device regulations. Perform additional tasks as directed by the QA Manager . Minimum 2 years of experience in an FDA and ISO 13485 regulated manufacturing facility. Previous experience in a quality inspection role, preferably in a medical device manufacturing environment. Strong attention to detail, data accuracy, and document control. Ability to effectively communicate with management, peers, and cross-functional teams. Preferred Skills Familiarity with metrology tools, IMT equipment, and technical drawing interpretation. Experience conducting failure trend analysis and implementing corrective actions. Knowledge of cGMP and FDA/ISO standards. Soft Skills Strong planning, organizational, and time-management abilities. Effective interpersonal communication and the ability to work both collaboratively and independently. About Us Changing Lives. Building Careers. Integra LifeSciences, a world leader in medical technology, is dedicated to limiting uncertainty for surgeons, so they can concentrate on providing the best patient care. Integra offers innovative solutions in neurosurgery, reconstructive and general surgery, and regenerative wound care. Founded in 1989 Integra is headquartered in Princeton, New Jersey and has more than 4,000 employees worldwide. Integra’s common stock is listed on The NASDAQ Stock Market under the symbol “IART.” #J-18808-Ljbffr
