Share this job as a link in your status update to LinkedIn. Category: For Job Seekers Location: 34501 - EMS FERMOY IRE - Fermoy, CO IE (Primary) Job Description: Remuneration: A competitive salary + shift premiums apply. There is also healthcare and pension. Our Fermoy, Ireland, facility is FDA registered and certified to ISO ISO13485:2016 for the manufacture of high-quality PCBAs, subassemblies and complete devices up to and including Class III medical devices. Sanmina Fermoy’s core specialization is manufacturing automation. We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping and process validation to complex volume manufacturing & test, shipping and repair. We create a state-of-the-art environment for manufacturing medical and other high-quality devices. The facility has a track record of 30 years of outstanding operational performance and customer service, backed by a highly experienced workforce. We hire people with a range of skills, experience, and backgrounds to fulfill roles in careers such as engineering, quality and manufacturing to name just a few. RESPONSIBILITIES: To maintain automation equipment of a Class III Medical Device in excellent condition ensuring consistent quality, output and yield. Follow systematic root cause problem solving and troubleshooting to resolve issues. Carry out preventative and corrective maintenance, completing all associated paperwork and records. Lead and implement process improvements to achieve more efficient operations, while adhering to change management and cGMP (Good Manufacturing Practice) requirements. Assist with the commissioning of new equipment/projects. Order and maintain appropriate stock of spare parts. Cross Train technicians as required. Flexible to travel to support new equipment buy-offs/training. ESSENTIAL REQUIREMENTS: Minimum Level 6 qualification (or close to completing) in Manufacturing Technology, Mechanical/Automation Engineering, Electrical, Electronics, Mechatronics or qualified trade personnel. 2 years experience as an SMT Technician. Experience in high volume automation/robotics. Good communication and influencing skills. Ability to work under own initiative. Availability to work shift patterns. DESIRABLE: Experience in Pneumatics, Electronics, Hydraulics, Programmable Controllers, Servo Motor drives, Vision systems, Ultrasonic welding, workshop machining. Understanding of Process Capability. Understanding of MSA (Measurement System Analysis) & GR&R (Gauge Repeat & Reduction). Experience in FAT (Factory Acceptance Test), SAT (Site Acceptance Test), IOPQ (Installation, Operation, Performance Qualification) automated assembly lines. Experience in leading process improvement projects in medical device environment. #J-18808-Ljbffr
Category (For Job Seekers) Engineering, Manufacturing/Operations, Quality Location 34501 - EMS FERMOY IRE - Fermoy, CO IE (Primary) Job Description As a medical device company, we help people in a truly tangible way. We are one of the most modern electronics factories, which gives us the opportunity to develop and build a career working with the latest technologies. The knowledge and skills you'll gain here are unique, and you'll find new challenges and endless opportunities along the way. Our Fermoy, Ireland, facility is FDA registered and certified to ISO for the manufacture of high-quality PCBAs, subassemblies and complete devices up to and including Class III medical devices. Sanmina Fermoy’s core specialization is manufacturing automation. We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping and process validation to complex volume manufacturing & test, shipping and repair. We create a state-of-the-art environment for manufacturing medical and other high-quality devices. The facility has a track record of 30 years of outstanding operational performance and customer service, backed by a highly experienced workforce. Quality Engineer OBJECTIVES OF POSITION: Primary objective is to ensure customer satisfaction by monitoring, controlling and improving all related customer processes. Principal customer interface for Quality metrics and improvement initiatives. Identifies, plans, and organizes regulatory affairs for ensuring compliance with the FDA’s Quality System Regulations, ISO 9000, ISO 13485:2003, JPAL as well as all international standards relevant to customer products for Sanmina-SCI manufacturing facility. RESPONSIBILITIES: Management of closed loop customer complaints and improvement processes. Generation and review of Quality Metrics System. Overall responsibility for DMR/DHR and Technical Files. Data collection, analyzing and reporting. Pareto and trend analysis. Initiate and drive Continuous Improvement programs. NPI Approval including First Article Inspections and Reporting. CAPA, NCM and RMA analysis and Improvement. QSR Validation protocols and report (IQ, OQ & PQ). Conducting Audits to ensure conformance and effectiveness of the Quality System. MEASUREMENTS: Yields at Key Process Steps Customer Return % and Cost (RMA) Scrap % Outgoing Inspection DPM & Customer Incoming Quality Levels PERSONNEL SPECIFICATIONS ESSENTIAL: University Degree in Science or Engineering. At least 2 years of Quality Assurance experience in a similar Quality Engineering role. Sound understanding and utilization of Problem Solving Techniques. Proficient in the use of Microsoft Word, PowerPoint and Excel. Good communication and influencing skills. Ability to respond to common inquiries or complaints from internal customers and regulatory agencies. Ability to write standard operating procedures, training documents, and regulatory responses. DESIRABLE: Experience in working within a Medical Device Manufacturing Environment or similar. Six Sigma Green or Black Belt Certified Experience in New Product Introduction Processes #J-18808-Ljbffr
Share this job as a link in your status update to LinkedIn. Category: Materials/Planning/Procurement/SCM Location: 34501 - EMS FERMOY IRE - Fermoy, CO IE (Primary) Job Title: Warehouse Lead Department: Materials Reporting To: Warehouse Manager Direct Reports: Yes Objectives of Position: Managing the daily activities of the Stockroom, Receiving, and Shipping functions to achieve customer delivery expectations and support the Company’s inventory control policies. Assist the Warehouse Manager in maintaining the smooth operation of a fast-moving environment. Responsible for the day-to-day management of people within the warehouse function to ensure company targets and objectives are met, ensuring that staff comply with health, safety, and standard operating procedures. Responsible for housekeeping standards and continuous improvement within the warehouse. Responsibilities: Managing Operations: Overseeing the day-to-day operations of a warehouse, measuring and reporting the effectiveness of warehousing activities and employee performance. Inventory Management: Managing inventory levels and ensuring the timely dispatch and receipt of goods, organizing and maintaining inventory and storage areas. Ensure accuracy of inventory transactions for incoming and outbound shipments. Complete Cycle count process of all Stores stock to schedule. Safety: Maintaining a safe working environment adhering to Health, Safety and Environmental procedures and ensuring they are understood and practiced by the team at all times. Training and Supervision: Training, supervising, and evaluating the performance of warehouse employees. Workload Distribution: Assigning workloads to employees to ensure they complete tasks efficiently. Coordination: Coordinating with other departments to streamline warehouse activities and improve efficiency. Communication: Maintaining communications with carriers, suppliers, warehouses, and customs brokers. Logistics: Identifying and planning improvements to logistics processes. Improvement: Identifying areas of improvement and establishing innovative or adjusting existing work procedures and practices. Quality: Ensure ongoing compliance with quality and industry regulatory requirements. Health & Safety: Provide a safe working environment, adhering to Health, Safety and Environmental procedures and ensuring they are understood and practiced by the team at all times. Instill compliance with Health & Safety Legislation and Regulations. Measurements: Measurements will be tracked against plant metrics and MBOs tracked as per the annual appraisal process. Personnel Specifications: Essential: Strong leadership and supervisory skills with experience in managing people to achieve results. Excellent verbal and written communication skills. Ability to anticipate and solve problems, proven ability to direct and coordinate operations. Excellent organizational skills and attention to detail. Ability to meet deadlines. Proficiency with data entry and inventory software and systems. Hands-on commitment to getting the job done. Computer literacy with particular emphasis on Excel and web-based systems (e.g., Oracle & Warehouse Management System). Knowledgeable in materials movement and management. Desirable: Completion of professional examinations such as IPICS or IIPMM. Previous experience in a similar role. #J-18808-Ljbffr
Manufacturing Engineering Technician – Sanmina – Fermoy (Cork) Role Type: 12 hour day/night shifts Remuneration: A competitive salary + shift premiums apply. There is also healthcare and pension. Sanmina Fermoy Our Fermoy, Ireland, facility is FDA registered and certified to ISO 13485:2016 for the manufacture of high-quality PCBAs, subassemblies and complete devices up to and including Class III medical devices. Sanmina Fermoy’s core specialization is manufacturing automation. We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping and process validation to complex volume manufacturing & test, shipping and repair. We create a state-of-the-art environment for manufacturing medical and other high-quality devices. The facility has a track record of 30 years of outstanding operational performance and customer service, backed by a highly experienced workforce. We hire people with a range of skills, experience, and backgrounds to fulfill roles in careers such as engineering, quality and manufacturing to name just a few. RESPONSIBILITIES: To maintain automation equipment of a Class III Medical Device in excellent condition ensuring consistent quality, output and yield. Follow systematic root cause problem solving and troubleshooting to resolve issues. Carry out preventative and corrective maintenance, completing all associated paperwork and records. Lead and implement process improvements to achieve more efficient operations, while adhering to change management and cGMP (Good Manufacturing Practice) requirements. Assist with the commissioning of new equipment/projects. Order and maintain appropriate stock of spare parts. Cross Train technicians as required. Flexible to travel to support new equipment buy-offs/training. ESSENTIAL REQUIREMENTS: Minimum Level 6 qualification (or close to completing) in Manufacturing Technology, Mechanical/Automation Engineering, Electrical, Electronics, Mechatronics or qualified trade personnel. 2 years experience as an SMT Technician. Experience in high volume automation/robotics. Good communication and influencing skills. Ability to work under own initiative. Availability to work shift patterns. DESIRABLE: Experience in Pneumatics, Electronics, Hydraulics, Programmable Controllers, Servo Motor drives, Vision systems, Ultrasonic welding, workshop machining. Understanding of Process Capability. Understanding of MSA (Measurement System Analysis) & GR&R (Gauge Repeat & Reduction). Experience in FAT (Factory Acceptance Test), SAT (Site Acceptance Test), IOPQ (Installation, Operation, Performance Qualification) automated assembly lines. Experience in leading process improvement projects in medical device environment. #J-18808-Ljbffr
Category (For Job Seekers) Engineering, Manufacturing/Operations, Quality Location 34501 - EMS FERMOY IRE - Fermoy, CO IE (Primary) Job Description As a medical device company, we help people in a truly tangible way. We are one of the most modern electronics factories, which gives us the opportunity to develop and build a career working with the latest technologies. The knowledge and skills you'll gain here are unique, and you'll find new challenges and endless opportunities along the way. Our Fermoy, Ireland, facility is FDA registered and certified to ISO for the manufacture of high-quality PCBAs, subassemblies and complete devices up to and including Class III medical devices. Sanmina Fermoy’s core specialization is manufacturing automation. We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping and process validation to complex volume manufacturing & test, shipping and repair. We create a state-of-the-art environment for manufacturing medical and other high-quality devices. The facility has a track record of 30 years of outstanding operational performance and customer service, backed by a highly experienced workforce. Quality Engineer OBJECTIVES OF POSITION: Primary objective is to ensure customer satisfaction by monitoring, controlling and improving all related customer processes. Principal customer interface for Quality metrics and improvement initiatives. Identifies, plans, and organizes regulatory affairs for ensuring compliance with the FDA’s Quality System Regulations, ISO 9000, ISO 13485:2003, JPAL as well as all international standards relevant to customer products for Sanmina-SCI manufacturing facility. RESPONSIBILITIES: Management of closed loop customer complaints and improvement processes. Generation and review of Quality Metrics System. Overall responsibility for DMR/DHR and Technical Files. Data collection, analyzing and reporting. Pareto and trend analysis. Initiate and drive Continuous Improvement programs. NPI Approval including First Article Inspections and Reporting. CAPA, NCM and RMA analysis and Improvement. QSR Validation protocols and report (IQ, OQ & PQ). Conducting Audits to ensure conformance and effectiveness of the Quality System. MEASUREMENTS: Yields at Key Process Steps Customer Return % and Cost (RMA) Scrap % Outgoing Inspection DPM & Customer Incoming Quality Levels PERSONNEL SPECIFICATIONS ESSENTIAL: University Degree in Science or Engineering. At least 2 years of Quality Assurance experience in a similar Quality Engineering role. Sound understanding and utilization of Problem Solving Techniques. Proficient in the use of Microsoft Word, PowerPoint and Excel. Good communications and influencing skills. Ability to respond to common inquiries or complaints from internal customers and regulatory agencies. Ability to write standard operating procedures, training documents, and regulatory responses. DESIRABLE: Experience in working within a Medical Device Manufacturing Environment or similar. Six Sigma Green or Black Belt Certified Experience in New Product Introduction Processes #J-18808-Ljbffr
Graduate Manufacturing Engineer- Sep 2025 Start date - (93297) Location: 34501 - EMS FERMOY IRE - Fermoy, CO IE (Primary) Job Description Who is Sanmina? Sanmina is a Fortune 500 company with revenues of over $8bn in 2022, where over 35,000 employees are working to deliver to our customers every day. For our customers, we design, manufacture, and repair some of the most complex and innovative optical, electronic, and mechanical products in the world. Recognized as a technology leader, Sanmina provides end-to-end design, manufacturing, and logistics solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the industrial, medical, defense and aerospace, automotive, communications networks, and cloud solutions sectors. The successful candidate will be responsible for providing engineering support for a range of products from class 3 medical devices to automotive and consumer products within highly automated production lines. Engineering support would include working in cross-functional teams and could range from supporting new product development, capacity expansion to maintaining and improving production performance. Responsibilities: Support new product developments as required and capacity expansions. Understand, learn, and develop in-depth knowledge for a range of equipment and become the Subject Matter Expert (SME) for specific assigned processes and equipment. Support ongoing PM activities & techniques to minimize lost time. On a daily basis, support the manufacturing engineering requirements and respond in a timely manner to maintain and support production. Monitor machine performance in real time to maximize production output. Develop and improve current standard operating procedures (SOP). Prepare detailed technical reports on process and quality issues. Work effectively within a team and cross-functionally to expedite completion of critical tasks. Ensure Quality standards are maintained and improved. Who we’re looking for? We are looking for highly qualified graduates in Engineering including Manufacturing, Industrial, Biomedical Engineering, Electrical or similar fields. Have you recently completed a degree or are you in the process of finishing your studies? The participants of the Sanmina Graduate programme are passionate, dynamic young graduates with the energy and ability to join our high-performing team. #J-18808-Ljbffr
Share this job as a link in your status update to LinkedIn. Category: For Job Seekers Location: 34501 - EMS FERMOY IRE - Fermoy, CO IE (Primary) Job Description: Remuneration: A competitive salary + shift premiums apply. There is also healthcare and pension. Our Fermoy, Ireland, facility is FDA registered and certified to ISO ISO13485:2016 for the manufacture of high-quality PCBAs, subassemblies and complete devices up to and including Class III medical devices. Sanmina Fermoy’s core specialization is manufacturing automation. We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping and process validation to complex volume manufacturing & test, shipping and repair. We create a state-of-the-art environment for manufacturing medical and other high-quality devices. The facility has a track record of 30 years of outstanding operational performance and customer service, backed by a highly experienced workforce. We hire people with a range of skills, experience, and backgrounds to fulfill roles in careers such as engineering, quality and manufacturing to name just a few. Responsibilities: To maintain automation equipment of a Class III Medical Device in excellent condition ensuring consistent quality, output and yield. Follow systematic root cause problem solving and troubleshooting to resolve issues. Carry out preventative and corrective maintenance, completing all associated paperwork and records. Lead and implement process improvements to achieve more efficient operations, while adhering to change management and cGMP (Good Manufacturing Practice) requirements. Assist with the commissioning of new equipment/projects. Order and maintain appropriate stock of spare parts. Cross Train technicians as required. Flexible to travel to support new equipment buy-offs/training. Essential Requirements: Previous relevant experience within Sanmina (e.g. Process Technician). Minimum Level 6 qualification (or close to completing) in Manufacturing Technology, Mechanical/Automation Engineering, Electrical, Electronics, Mechatronics or qualified trade personnel. Must have completed (or close to completing) the internal Simutech training. Industrial/manufacturing environment experience. Experience in high volume automation/robotics. Good communication and influencing skills. Ability to work under own initiative. Availability to work shift patterns. Desirable: Experience in Pneumatics, Electronics, Hydraulics, Programmable Controllers, Servo Motor drives, Vision systems, Ultrasonic welding, workshop machining. Understanding of Process Capability. Understanding of MSA (Measurement System Analysis) & GR&R (Gauge Repeat & Reduction). Experience in FAT (Factory Acceptance Test), SAT (Site Acceptance Test), IOPQ (Installation, Operation, Performance Qualification) automated assembly lines. Experience in leading process improvement projects in medical device environment. #J-18808-Ljbffr
Graduate Manufacturing Engineer - Sep 2025 Start date - (93297) Location: 34501 - EMS FERMOY IRE - Fermoy, CO IE (Primary) Job Description Who is Sanmina? Sanmina is a Fortune 500 company with revenues of over $8bn in 2022, where over 35,000 employees are working to deliver to our customers every day. For our customers, we design, manufacture, and repair some of the most complex and innovative optical, electronic, and mechanical products in the world. Recognized as a technology leader, Sanmina provides end-to-end design, manufacturing, and logistics solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the industrial, medical, defense and aerospace, automotive, communications networks, and cloud solutions sectors. The successful candidate will be responsible for providing engineering support for a range of products from class 3 medical devices to automotive and consumer products within highly automated production lines. Engineering support would include working in cross-functional teams and could range from supporting new product development, capacity expansion to maintaining and improving production performance. RESPONSIBILITIES: Support new product developments as required and capacity expansions. Develop in-depth knowledge for a range of equipment and become the Subject Matter Expert (SME) for specific assigned processes and equipment. Support ongoing PM activities & techniques to minimize lost time. Respond in a timely manner to manufacturing engineering requirements to maintain and support production. Monitor machine performance in real-time to maximize production output. Develop and improve current standard operating procedures (SOP). Prepare detailed technical reports on process and quality issues. Work effectively within a team and cross-functionally to expedite completion of critical tasks. Ensure Quality standards are maintained and improved. Who we’re looking for? We are looking for highly qualified graduates in Engineering including Manufacturing, Industrial, Biomedical Engineering, Electrical or a similar field. Have you recently completed a degree or are you in the process of finishing your studies? The participants of the Sanmina Graduate programme are passionate, dynamic young graduates with the energy and ability to join our high-performing team. #J-18808-Ljbffr
Location: 34501 - EMS FERMOY IRE - Fermoy, CO IE (Primary) Job Description: Our Fermoy, Ireland, facility is FDA registered and certified to ISO13485:2016 for the manufacture of high-quality PCBAs, subassemblies and complete devices up to and including Class III medical devices. Sanmina Fermoy’s core specialization is manufacturing automation. We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping and process validation to complex volume manufacturing & test, shipping and repair. We create a state-of-the-art environment for manufacturing medical and other high-quality devices. The facility has a track record of 30 years of outstanding operational performance and customer service, backed by a highly experienced workforce. We hire people with a range of skills, experience, and backgrounds to fulfill roles in careers such as engineering, quality, and manufacturing to name just a few. Remuneration: A competitive salary + shift premiums apply. There is also healthcare and pension. RESPONSIBILITIES: To maintain automation equipment of a Class III Medical Device in excellent condition ensuring consistent quality, output, and yield. Follow systematic root cause problem solving and troubleshooting to resolve issues. Carry out preventative and corrective maintenance, completing all associated paperwork and records. Lead and implement process improvements to achieve more efficient operations, while adhering to change management and cGMP (Good Manufacturing Practice) requirements. Assist with the commissioning of new equipment/projects. Order and maintain appropriate stock of spare parts. Cross Train technicians as required. Flexible to travel to support new equipment buy-offs/training. ESSENTIAL REQUIREMENTS: Minimum Level 6 qualification (or close to completing) in Manufacturing Technology, Mechanical/Automation Engineering, Electrical, Electronics, Mechatronics or qualified trade personnel. 2 years experience as an SMT Technician. Experience in high volume automation/robotics. Good communication and influencing skills. Ability to work under own initiative. Availability to work shift patterns. DESIRABLE: Experience in Pneumatics, Electronics, Hydraulics, Programmable Controllers, Servo Motor drives, Vision systems, Ultrasonic welding, workshop machining. Understanding of Process Capability. Understanding of MSA (Measurement System Analysis) & GR&R (Gauge Repeat & Reduction). Experience in FAT (Factory Acceptance Test), SAT (Site Acceptance Test), IOPQ (Installation, Operation, Performance Qualification) automated assembly lines. Experience in leading process improvement projects in medical device environment. #J-18808-Ljbffr
Share this job as a link in your status update to LinkedIn. Category (For Job Seekers) Manufacturing/Operations Location 34501 - EMS FERMOY IRE - Fermoy, CO IE (Primary) Job Description DIRECT REPORTS: Yes *Please note that this is a shift based position (12 hour shifts which includes days and nights inclusive of weekends). A competitive basic salary + shift allowances and benefits package provided! About the company: Our Fermoy, Ireland, facility is FDA registered and certified to ISO 13485 for the manufacture of high-quality PCBAs, subassemblies and complete devices up to and including Class III medical devices. Sanmina Fermoy’s core specialization is manufacturing automation. We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping and process validation to complex volume manufacturing & test, shipping and repair. We create a state-of-the-art environment for manufacturing medical and other high-quality devices. The facility has a track record of 30 years of outstanding operational performance and customer service, backed by a highly experienced workforce. OBJECTIVES OF POSITION: Quality: Ensure production operators assemble, test and handle all products in line with the documented specification and processes, ensuring that all products supplied to our customers are to the highest possible quality levels and conform to all specification requirements. Productivity: Work as part of the manufacturing team to produce the correct number of products in line with the production plans communicated by Supervisors, ensuring correct levels of delivery performance to our customers. Teamwork: Participate as a team member committed to total customer satisfaction during each day of employment. RESPONSIBILITIES: Output Target Achieve hourly and daily targets. Ensure team is busy 100% of shift. Quality Counsel/retrain operators on quality issues. Ensure immediate communication on fails. Monitor scrap levels from area daily and reduce accordingly. Attendance / Timekeeping Monitor/feedback on a daily basis. Meet employees on day of return from absence. Counsel/discipline as required in consultation with Supervisor/HR. Report weekly to Supervisor on absence. Conduct counseling sessions and complete file note. Issue disciplinary action (Verbal warning) with Supervisor and/or HR. Induction of new employees Ensure new employees are “buddied up” during transition. Ensure new employees know product, process. Ensure new employees are familiar with work instructions, DDS, etc. Grievance Report grievances to Supervisor. Documentation Ensure Operators are aware of and adhere to all relevant procedures. Process Adherence Ensure all work instructions are followed. Ensure employees are trained continually/recertification as necessary. Counsel/discipline on non-adherence. Be familiar with SANM Safety policy. Ensure all PPE is worn. Ensure all employees follow safety guidelines. Counsel/discipline on non-conformance/adherence. Ensure working area is orderly and organized. Communications Conduct “Start up meeting” on every shift (quality, targets, safety, other). Support and facilitate team meetings. Ensure effective communications within own team and with other sections of the company. Shipment Updates Flag potential shipment delays to Supervisor. Training Define training requirements by process/product. Achieve training plan. Participate actively in the Section Leader development program and complete successfully. Performance Reviews Monitor/assess employee performance on an ongoing basis. Complete 3 month/6 month/annual appraisals on time. Holidays Ensure adequate shift coverage. Ensure no more than -39 hours holiday balance. Payroll Spend 5 mins every day checking and updating system where necessary. Ensure 100% accuracy. Recruitment Advise Supervisor of requirements. Ensure all new employees are inducted. Overtime Minimize need for overtime and advise in advance of any requirement. Reports – Key Metrics Report on absence. Encourage and support equal opportunity practices. ESSENTIAL SPECIFICATIONS: Team lead experience in a fast-paced and heavily regulated manufacturing facility. A results-driven & quality-conscious individual. A sound understanding of Standard Operating Procedures, line documentation, and customer-specific requirements. #J-18808-Ljbffr
