Find your next tech and IT Job or contract in Ireland

A global medical device company are looking for a Senior Packaging Engineer to join their Research and Development team on a contract basis. The role is to procure and develop packaging for new and existing products across multiple projects. You will lead packaging activities with a cross-functional team including Product Management, Operations, Quality Assurance, Regulatory Affairs and, including New Product and Sustaining Engineering. You will also review, plan and execute packaging efforts for current and potential sterilization modalities. This will tie into development of global packaging processes too. Responsibilities include: * Develop global packaging processes and libraries * Work directly on global new product development * Apply packaging design principles from the pharmaceutical/medical device field to maintain and develop appropriate packaging solutions * Develop and maintain department standards in packaging. Inclusive of environmental and regulatory standards related to medical packaging design and test (e.g. ASTAM F1886, F88, F2096, D4169 and ISO 11607) * Ability to lead multiple projects to successful completion with tight timelines and critical deliverables * Ensure compliance of equipment and packaging designs with company quality system * Perform verification and validation testing of packaging designs and manufacturing methods Essential Skills: * Master of Science in Packaging Science, or closely related field and 3 years experience; or Bachelor's degree in Mechanical Engineering, Packaging Science or closely related field and 5 years experience; or experience of such kind and amount as to provide a comparable background * Product and packaging stability and/or accelerated aging testing a plus * Experience with medical packaging materials (Tyvek, PE/PET films, PETG trays, etc.) * Experience with environmental and regulatory requirements and standards that relate to medical packaging design and testing (i.e. ASTM F1886, F88, F2096, D4169, and ISO 11607) The start date is for ASAP. The initial contract length is for 12 months, with options to extend after. The role is based in Limerick and will not always require weekly visits. Generally once a week would be good but not necessary if the project does not require. At other times you may be required for 2-3 days every few weeks as the projects requires. The rate is EUR55-63 per hour, depending on experience, if you have any expenses please let me know and I can factor that into the rate for you. If you are interested in the role please send me your latest CV and I will call you to discuss the further details. Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Real, please visit XX XX XX XX XX Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

A global medical device company are looking for an Electro-Mechanical Engineer to join their Process Development team on a contract basis. The role will help set up new manufacturing lines, they need someone with a sub speciality in electromechanical Catheter devices for cardiovascular applications. Essential skills: - Electro-mechanical Catheter experience • Problem solving & analytical skills • Mechanical design skills • Fluid dynamics experience (Pressure, Flow, Temperature) • Ability to setup equipment and manufacturing lines (hands on) • Electro-mechanical experience The start date is for ASAP. The initial contract length is for 12 months, with options to extend after. The role is based in Galway. The rate is EUR40-55 per hour, depending on experience, if you have any expenses please let me know and I can factor that into the rate for you. If you are interested in the role please send me your latest CV and I will call you to discuss the further details. Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Real, please visit XX XX XX XX XX Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

A global medical device company are looking for a Senior Packaging Engineer to join their Research and Development team on a contract basis. The role is to procure and develop packaging for new and existing products across multiple projects. You will lead packaging activities with a cross-functional team including Product Management, Operations, Quality Assurance, Regulatory Affairs and, including New Product and Sustaining Engineering. You will also review, plan and execute packaging efforts for current and potential sterilization modalities. This will tie into development of global packaging processes too. Responsibilities include: * Develop global packaging processes and libraries * Work directly on global new product development * Apply packaging design principles from the pharmaceutical/medical device field to maintain and develop appropriate packaging solutions * Develop and maintain department standards in packaging. Inclusive of environmental and regulatory standards related to medical packaging design and test (e.g. ASTAM F1886, F88, F2096, D4169 and ISO 11607) * Ability to lead multiple projects to successful completion with tight timelines and critical deliverables * Ensure compliance of equipment and packaging designs with company quality system * Perform verification and validation testing of packaging designs and manufacturing methods Essential Skills: * Master of Science in Packaging Science, or closely related field and 3 years experience; or Bachelor's degree in Mechanical Engineering, Packaging Science or closely related field and 5 years experience; or experience of such kind and amount as to provide a comparable background * Product and packaging stability and/or accelerated aging testing a plus * Experience with medical packaging materials (Tyvek, PE/PET films, PETG trays, etc.) * Experience with environmental and regulatory requirements and standards that relate to medical packaging design and testing (i.e. ASTM F1886, F88, F2096, D4169, and ISO 11607) The start date is for ASAP. The initial contract length is for 12 months, with options to extend after. The role is based in Limerick and will not always require weekly visits. Generally once a week would be good but not necessary if the project does not require. At other times you may be required for 2-3 days every few weeks as the projects requires. The rate is EUR55-63 per hour, depending on experience, if you have any expenses please let me know and I can factor that into the rate for you. If you are interested in the role please send me your latest CV and I will call you to discuss the further details. Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Real, please visit XX XX XX XX XX Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

Senior Electronics Design Engineer An exciting opportunity as a Senior Electronics Design Engineer is available at an innovative and exciting medical device start-up based in Dublin. Ambitious engineers looking to work on cutting-edge tech will be responsible for the design and development of embedded hardware systems for medical devices and will be heavily involved in all aspects of the development cycle. The ideal Senior Electronics Design Engineer will have; • Proven experience in embedded hardware development. • Background in electrical or computer engineering • PCB and EMC design experience For more information or to apply for the position of Senior Electronics Design Engineer please contact Michael Burns-Peake or find me on Linkedin or email

Job Description Service Integration Manager - Dublin Support the maturation of IT Service Management within their aligned customer group in line with IT Strategic direction to standardize and align to one way of delivering IT Service Excellence: • Assure ITTP delivery towards the assigned business area(s) - work in close partnership with aligned customer group and ITTP teams to ensure that project progress, quality and budget is aligned across all relevant ITTP deliverables. • Oversee onboarding of aligned customer group to ITTP services ensuring that changes to customer operations are understood and onboarding projects are scoped and delivered to support the wider IT strategy of a single way for managing IT service delivery. This will involve being able to co-ordinate the activities of significant numbers (20-40) external resources engaged in the execution of onboarding and ongoing exploitation. • Build strong business relationship with stakeholder groups through leadership of regularly scheduled governance meetings • Act as initial contact point for business needs; evaluate feasibility of potential projects in coordination with relevant customer. • Serve as focal / escalation point for the ITTP initiatives within his/her area of responsibility, partner with the business to add value when preparing business cases. • Provide ITSM consulting expertise towards the relevant business area(s). • Lead solution visioning sessions, including requirement gathering and rationalization. • Support the understanding and alignment of standard operating processes (SOPs) across relevant customers. • Support the establishment and management of the yearly budget review demonstrating efficiency initiatives with positive budget impact for the relevant business area(s), ITTP and IT. • Ensure adherence to financial processes to support ITTP Projects and IT Operations activities for the relevant business area(s) - e.g. Service Level Targets, CARs • Bachelor's degree in a computer science, engineering or information technology discipline. An advanced degree and related accreditations a plus. • 7+ years of experience within IT, ITIL and Service Management • 3+ years of experience within the Pharma / Life Science industry preferable • 5+ years demonstrated experience managing IT services or delivering IT service improvement initiatives. This is a 6 month contract in Dublin. Please forward your CV in Word format.

A global medical device company are looking for an Electro-Mechanical Engineer to join their Process Development team on a contract basis. The role will help set up new manufacturing lines, they need someone with a sub speciality in electromechanical Catheter devices for cardiovascular applications. Essential skills: - Electro-mechanical Catheter experience • Problem solving & analytical skills • Mechanical design skills • Fluid dynamics experience (Pressure, Flow, Temperature) • Ability to setup equipment and manufacturing lines (hands on) • Electro-mechanical experience The start date is for ASAP. The initial contract length is for 12 months, with options to extend after. The role is based in Galway. The rate is EUR40-55 per hour, depending on experience, if you have any expenses please let me know and I can factor that into the rate for you. If you are interested in the role please send me your latest CV and I will call you to discuss the further details. Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Real, please visit XX XX XX XX XX Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

Are you an experienced Programme Manager with experience in the Semiconductor industry? Do you have a background in IC design, physical layout, or silicon validation? Are you ready to take the next big step in your career and join one of the major players in the industry? If so, we have an exciting opportunity for you! As the Project Manager, you will take responsibility for driving internal teams in delivering IP based products. You will create project plans, manage the project life-cycle end to end and manage external stakeholders. This Project Manager position offers you the opportunity to play a key role in the companies growth, with a salary of up to £120,000 (based on experience) as well as being based in a vibrant city known for its rich history, cultural heritage, and high quality of life. Experience Required • Proven experience in Programme or Project Management within the Semiconductor industry. • Strong background in IC design, physical layout, and/or silicon validation. • Excellent leadership and team management skills. • Outstanding communication and interpersonal abilities. If you are interested in this Project Management position and willing to relocate to Cork, Ireland. Please contact Emily Click here to contact this recruiter Resources

Working for a leader in the Semi's industry, I am looking to recruit a high-level, Senior SOC Architect. This position can be based in Edinburgh or Cork. You will be tasked with the definition and development of existing and new SOC product architecture - across a variety of complex digital and high-speed products and applications. The main focus are the technical requirements, but this position also offers the opportunity for team leadership and management. Key skills / requirements: • BSc / MSc / PhD in Micro-electronics, physics, or similar filed • 10+ years' experience in complex SOCs • Deep understanding of Subsystems, Memory Controllers, and memory architectures (e.g., SRAM, ROM, eFuse) • Extensive experience with the Digital ASIC Flow, RTL design (verilog), synthesis, timing closure and Debug methodologies (e.g., DFT, JTAG, Scan, BIST). • Extensive knowledge of SOC architecture, set-up / silicon bring-up, validation and all it's associated processes. • SOC design, system design, architecture and IP selection & integration • DSP / signal processing / communication and interconnect protocols - AXI, AMBA, CHI • Digital-AMS chip development - digital to analog interfaces • low-power, performance and optimisation • low level software, firmware and embedded requirements - drivers, controllers etc. • Confident knowledge of a variety of coding languages - C, C++, system C, TcL, python • Excellent communications, and ability to work across software and hardware teams Nice to have skills • Team leadership / management • SOC performance & modelling - C, C++, system C • UVM verification - at IP & SOC level - system verilog • FPGA architecture • Simulation, emulation Visa sponsorship and relocation support can be offer for the right candidate

Job Description Years of relevant experience 7+ years Education Level Bachelor's Degree About the Job Our Client is seeking to recruit a Service Integration Manager with at least 5 to 10 years expertise. Support of the IT Service Management within their aligned customer group in line with company IT Strategic direction to standardize and align to one way of delivering IT Service Excellence: • Assure IT delivery towards the assigned business area(s) - work in close partnership with aligned customer group and IT teams to ensure that project progress, quality and budget is aligned across all relevant IT deliverables. • Oversee onboarding of aligned customer group to IT services ensuring that changes to customer operations are understood and onboarding projects are scoped and delivered to support the wider company IT strategy of a single way for managing IT service delivery. This will involve being able to co-ordinate the activities of significant numbers (20-40) external resources engaged in the execution of onboarding and ongoing exploitation. • Build strong business relationship with stakeholder groups through leadership of regularly scheduled governance meetings • Act as initial contact point for business needs; evaluate feasibility of potential projects in coordination with relevant customer. • Serve as focal / escalation point for the ITP initiatives within his/her area of responsibility, partner with the business to add value when preparing business cases. • Provide ITSM consulting expertise towards the relevant business area(s). • Lead solution visioning sessions, including requirement gathering and rationalization. • Support the understanding and alignment of standard operating processes (SOPs) across relevant customers. • Support the establishment and management of the yearly budget review demonstrating efficiency initiatives with positive budget impact for the relevant business areas • Ensure adherence to financial processes to support IT Projects and IT Operations activities for the relevant business area(s) - e.g. Service Level Targets, CARs Direct the planning phase of relevant IT projects and manage the IT portfolio for the relevant business area • Initiate or act as initial contact point for project proposals; evaluate feasibility of potential projects in coordination with the associated IT department. Collaborate with the business lead to develop business cases for projects. • Analyze IT requirements for input to the budgeting process. • Assist in compiling, justifying and getting approval for project proposals. • Ensure all requests are documented, screened and scheduled according to designated service offerings. • Ensure effective IT project mandate is developed. • Ensure the business requirements are clearly defined, approved, communicated and understood. • Ensure the impact of IT initiatives from other areas are assessed, aligned and communicated, and requirements are incorporated into plans as needed. • Ensure resources, either internal from associated IT department or external are secured to meet business demands. EDUCATION / EXPERIENCE • Bachelor's degree in a computer science, engineering or information technology discipline. An advanced degree and related accreditations a plus. • 7+ years of experience within IT, ITIL and Service Management • 3+ years of experience within the Pharma / Life Science industry preferable • 5+ years demonstrated experience managing IT services or delivering IT service improvement initiatives. This is a 3 to 6 month contract which will based in Dublin Ireland. Please forward your CV in Word format, along with your availability and salary expectations.

Title: Seeking a Senior Project Engineer for Automation and Validation in Cork Principal Project Engineer - This role is part of the global engineering team. The Project Engineer will oversee all validation activities for automated production lines for a design transfer, ensuring timely and budget-compliant delivery. Key Responsibilities: Lead validation activities (IQ, OQ, PQ) for automated production lines. Develop and maintain project documentation (PDD, URS, test scripts, CQA). Manage contractors and ensure service standards. Collaborate with cross-functional teams for smooth production line transitions. Communicate project status through meetings and reports. Drive project achievements and share best practices. * The individual is required to have strong experience in automation and validation. Qualifications & Experience: Bachelor's degree in engineering, automation, or related field. 3-5 years in validation of automated production lines. Proficiency in validation protocols and project documentation. Project Management experience. Experience in manufacturing, technology, supply chain, and medical device validation. Knowledge of cGMP and industry regulations. Lean Six Sigma Green/Black Belt or equivalent. Other Details: Hybrid working - flexible Based in Cork 12 month contract with likely extension Offering up to 60 euros per hour (depending on experience). If you are interested, please send me your latest CV and we can arrange a call. Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Real, please visit XX XX XX XX XX Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

Title: Seeking a Senior Project Engineer for Automation and Validation in Cork Principal Project Engineer - This role is part of the global engineering team. The Project Engineer will oversee all validation activities for automated production lines for a design transfer, ensuring timely and budget-compliant delivery. Key Responsibilities: Lead validation activities (IQ, OQ, PQ) for automated production lines. Develop and maintain project documentation (PDD, URS, test scripts, CQA). Manage contractors and ensure service standards. Collaborate with cross-functional teams for smooth production line transitions. Communicate project status through meetings and reports. Drive project achievements and share best practices. * The individual is required to have strong experience in automation and validation. Qualifications & Experience: Bachelor's degree in engineering, automation, or related field. 3-5 years in validation of automated production lines. Proficiency in validation protocols and project documentation. Project Management experience. Experience in manufacturing, technology, supply chain, and medical device validation. Knowledge of cGMP and industry regulations. Lean Six Sigma Green/Black Belt or equivalent. Other Details: Hybrid working - flexible Based in Cork 12 month contract with likely extension Offering up to 60 euros per hour (depending on experience). If you are interested, please send me your latest CV and we can arrange a call. Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Real, please visit XX XX XX XX XX Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

Title: Seeking a Senior Project Engineer for Automation and Validation in Cork Principal Project Engineer - This role is part of the global engineering team. The Project Engineer will oversee all validation activities for automated production lines for a design transfer, ensuring timely and budget-compliant delivery. Key Responsibilities: Lead validation activities (IQ, OQ, PQ) for automated production lines. Develop and maintain project documentation (PDD, URS, test scripts, CQA). Manage contractors and ensure service standards. Collaborate with cross-functional teams for smooth production line transitions. Communicate project status through meetings and reports. Drive project achievements and share best practices. * The individual is required to have strong experience in automation and validation. Qualifications & Experience: Bachelor's degree in engineering, automation, or related field. 3-5 years in validation of automated production lines. Proficiency in validation protocols and project documentation. Project Management experience. Experience in manufacturing, technology, supply chain, and medical device validation. Knowledge of cGMP and industry regulations. Lean Six Sigma Green/Black Belt or equivalent. Other Details: Hybrid working - flexible Based in Cork 12 month contract with likely extension Offering up to 60 euros per hour (depending on experience). If you are interested, please send me your latest CV and we can arrange a call. Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Real, please visit XX XX XX XX XX Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

Junior ASIC Design Engineer - Cork or Dublin Our client is seeking a Junior ASIC Design Engineer to join a market leading EDA company in Ireland. The ideal candidate will have a Bachelor’s degree in electrical engineering or a related subject, strong communication skills, and experience with VHDL or Verilog. As a Junior ASIC Design Engineer, you will be responsible for assisting in the design and development of Application-Specific Integrated Circuits (ASICs) for various electronic devices. Responsibilities would include: • Collaborate with senior engineers to design and implement ASIC solutions • Work on RTL coding, simulation, and verification using VHDL or Verilog • Assist in the debugging and testing of ASIC designs • Contribute to the documentation and reporting of ASIC development activities Requirements: • Bachelor’s degree in electrical engineering or a related subject • Strong communication skills • Familiarity with VHDL or Verilog • Knowledge of ASIC design methodologies and tools is a plus For more information on this role or others then please contact Jordan Browne.