Find your next tech and IT Job or contract in Ireland

Senior Embedded Firmware Engineer - Contract Location: Limerick, Ireland (Hybrid - 4 days onsite) Contract: 6 months (potential extension) Rate: Competitive About the Role We are seeking a Senior Embedded Firmware Engineer to join a team developing advanced medical device technology. This role focuses on embedded firmware development , secure systems , and hardware integration in a regulated environment. If you have strong C/C++ programming skills , experience with microcontrollers , and knowledge of medical device compliance , this is your opportunity to make an impact. Key Responsibilities Develop embedded firmware in C/C++ for 8/16/32-bit microcontrollers (Atmel, TI, ST). Design and implement secure bootloaders and robust software architecture . Integrate hardware interfaces ( RS232, RS485, SPI, I2C ) and peripherals ( RTC, LCD, EEPROM, micro-SD ). Perform unit and integration testing using automation and static code analysis tools. Debug hardware using oscilloscopes and logic analyzers. Ensure compliance with IEC 62304 , FDA , EU MDR , and ISO 13485 throughout development. Collaborate with multi-disciplinary teams in an Agile environment. Essential Skills Embedded firmware development experience (7+ years) with C/C++ for microcontrollers. Strong C/C++ programming skills for 8/16/32-bit microcontrollers (Atmel, TI, ST). Expertise in hardware interfaces (RS232, RS485, SPI, I2C) and peripheral integration (RTC, LCD, EEPROM, micro-SD). Knowledge of secure bootloaders , firmware updates , and software architecture principles. Familiarity with IEC 62304 , FDA , EU MDR , and ISO 13485 compliance requirements. Ability to debug hardware using oscilloscopes and logic analyzers. Desirable Skills Experience with CI/CD pipelines , configuration management, and cloud-based tools. Exposure to Agile/Scrum methodologies. Background in medical device development or other safety-critical systems. Why Apply? This is a chance to work on cutting-edge medical technology , applying your embedded firmware expertise , C/C++ programming skills , and regulatory compliance knowledge to projects that improve lives globally. Please click 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

Automation Project Manager - Contract Role (Pharma) Location: Grangecastle, Ireland (Hybrid) Duration: 6-12 months (potential extension) Real Life Science is currently recruiting an Automation Project Manager for a global pharma manufacturer based their Grangecastle site. The Automation Project Manager will lead multiple automation and digital integration projects within a regulated pharmaceutical environment. Key Responsibilities Manage automation and digital integration projects across the site, ensuring delivery on scope, schedule, budget, and quality . Lead major initiatives including: Installation of an offline DCS control system for training/validation. Upgrade of Yokogawa DCS software and OT network infrastructure. Replacement of legacy control systems and lifecycle upgrades. Act as primary liaison with automation, IT/OT, and control system vendors. Drive integration of plant automation with manufacturing OT/IT systems for data integrity and performance management . Prepare and manage project documentation: URS, design specs, RFPs, risk assessments, and business cases. Oversee FAT/SAT, commissioning, qualification, and validation activities. Ensure compliance with GMP, 21 CFR Part 11, Annex 11 , and company standards Coordinate training and handover to operations and support teams. Requirements 5+ years' experience in project management within pharmaceutical or biopharma environments. Strong knowledge of automation/control systems (DCS/PCS/SCADA - Yokogawa experience desirable). Proven ability to manage full project lifecycle: feasibility, design, vendor selection, implementation, and handover. Familiarity with OT network infrastructure, system security, and data integration concepts. Excellent stakeholder management, communication, and leadership skills. Why Join? Work on high-impact automation projects in a global pharma environment. Collaborate with cross-functional teams and cutting-edge technologies. Competitive contract terms with potential for extension. Please click 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

Senior Embedded Firmware Engineer - Contract Location: Limerick, Ireland (Hybrid - 4 days onsite) Contract: 6 months (potential extension) Rate: Competitive About the Role We are seeking a Senior Embedded Firmware Engineer to join a team developing advanced medical device technology. This role focuses on embedded firmware development , secure systems , and hardware integration in a regulated environment. If you have strong C/C++ programming skills , experience with microcontrollers , and knowledge of medical device compliance , this is your opportunity to make an impact. Key Responsibilities Develop embedded firmware in C/C++ for 8/16/32-bit microcontrollers (Atmel, TI, ST). Design and implement secure bootloaders and robust software architecture . Integrate hardware interfaces ( RS232, RS485, SPI, I2C ) and peripherals ( RTC, LCD, EEPROM, micro-SD ). Perform unit and integration testing using automation and static code analysis tools. Debug hardware using oscilloscopes and logic analyzers. Ensure compliance with IEC 62304 , FDA , EU MDR , and ISO 13485 throughout development. Collaborate with multi-disciplinary teams in an Agile environment. Essential Skills Embedded firmware development experience (7+ years) with C/C++ for microcontrollers. Strong C/C++ programming skills for 8/16/32-bit microcontrollers (Atmel, TI, ST). Expertise in hardware interfaces (RS232, RS485, SPI, I2C) and peripheral integration (RTC, LCD, EEPROM, micro-SD). Knowledge of secure bootloaders , firmware updates , and software architecture principles. Familiarity with IEC 62304 , FDA , EU MDR , and ISO 13485 compliance requirements. Ability to debug hardware using oscilloscopes and logic analyzers. Desirable Skills Experience with CI/CD pipelines , configuration management, and cloud-based tools. Exposure to Agile/Scrum methodologies. Background in medical device development or other safety-critical systems. Why Apply? This is a chance to work on cutting-edge medical technology , applying your embedded firmware expertise , C/C++ programming skills , and regulatory compliance knowledge to projects that improve lives globally. Please click 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

Our client is looking for a Scrum Master/PM for one of our clients based in Cork, Ireland, this role would be require working three days a week onsite at the Cork location. Mandatory Skill sets: * 3+ years Scrum Master/Agile Lead experience with proven track record of successful sprint delivery * Certified Scrum Master (CSM) or equivalent agile certification * Deep expertise in agile frameworks (Scrum, Kanban, SAFe) and tools (Jira, Azure DevOps, Confluence) * Strong facilitation, conflict resolution, and servant leadership skills * Experience with software development lifecycle and technical project management Activities to be performed: Sprint Leadership: Facilitate all Scrum ceremonies (daily standups, sprint planning, retrospectives, reviews) ensuring timely, focused, and productive sessions. Team Enablement: Remove impediments, coach team members on agile practices, and foster self-organizing, high-velocity teams. Stakeholder Management: Bridge communication between product owners, development teams, and business stakeholders to ensure alignment and transparency. Process Optimization: Continuously refine team processes, implement best practices, and drive adoption of agile tools and methodologies. Metrics & Reporting: Track sprint metrics, burndown charts, velocity trends, and team performance indicators to drive data-driven improvements. Risk Mitigation: Proactively identify and address project risks, dependencies, and blockers before they impact delivery timelines. LA International is a HMG approved ICT Recruitment and Project Solutions Consultancy, operating globally from the largest single site in the UK as an IT Consultancy or as an Employment Business & Agency depending upon the precise nature of the work, for security cleared jobs or non-clearance vacancies, LA International welcome applications from all sections of the community and from people with diverse experience and backgrounds. Award Winning LA International, winner of the Recruiter Awards for Excellence, Best IT Recruitment Company, Best Public Sector Recruitment Company and overall Gold Award winner, has now secured the most prestigious business award that any business can receive, The Queens Award for Enterprise: International Trade, for the second consecutive period.

SAP ISU IDE Consultant 6 Month contract initially Based: Hybrid - Max 1 day p/w onsite in Ireland (Flexible) Rate: £Market rates p/d - (via Umbrella company) We have a great opportunity with a world leading organisation where you will be provided with all of the support and development to succeed. A progressive organisation where you can really make a difference. We have a great opportunity for a SAP ISU IDE Consultant to join the team. We are seeking an experienced SAP ISU IDE Consultant to join our dynamic IT Service Delivery team. In this role, you will be responsible for the ISU IDE/Meterworks/Device/Workflow areas of SAP systems that support critical business functions. You will collaborate closely with IT and business stakeholders for day-to-day operations and projects. Key Responsibilities: * Provide subject matter expertise and support for the ESB's SAP System's in the area of IDE, Device, Meterworks and Workflow. * Experience with SMART projects and/or AMI/MDMS * Provide end user support for SAP ISU. * Investigate and resolve support calls raised by the business * Work on internal SAP projects and Change Requests as required. * Identify potential process improvements opportunities across the SAP landscape. * Liaise with a variety of stakeholders in the specification, development and testing of enhancements / modifications to the SAP solution. * Complete knowledge transfer for respective application areas to other members of the ESB team. * Work alongside Team Leads, Delivery Leads, Functional SME's and Solution Architects to Identify and manage risks. * Managing change request scoping to include: Estimation and design - preparing functional specifications Implementation - completing system configuration Liaising closely with ABAP / Basis and Security teams during build phase Key Skills & Experience: * Hands-on Functional experience in SAP ISU area of IDE, Device, Meterworks and Workflow. * Knowledge of Meter works and Service Orders, Notifications and tasks, Hands-on experience with Workflow Configuration desirable. Bulk creation of service orders. * Experience in functional specification writing, functional/ integration/ performance testing/ regression testing etc. * Reporting and documentation/ writing for audit reasons and for smooth transition of projects to support. * Stakeholder management, negotiation and communication * Excellent communication/interpersonal skills are mandatory for interaction with different stakeholders involved in the Projects (i.e. in the business process definition stages, design, testing etc. with technical and non-technical people). This is an excellent opportunity on a great project of work, If you are looking for your next exciting opportunity, apply now for your CV to reach me directly, we will respond as soon as possible. LA International is a HMG approved ICT Recruitment and Project Solutions Consultancy, operating globally from the largest single site in the UK as an IT Consultancy or as an Employment Business & Agency depending upon the precise nature of the work, for security cleared jobs or non-clearance vacancies, LA International welcome applications from all sections of the community and from people with diverse experience and backgrounds. Award Winning LA International, winner of the Recruiter Awards for Excellence, Best IT Recruitment Company, Best Public Sector Recruitment Company and overall Gold Award winner, has now secured the most prestigious business award that any business can receive, The Queens Award for Enterprise: International Trade, for the second consecutive period.

R&D Electronics Engineer - Medical Devices (Freelance) Location: Limerick, Ireland (4 days onsite) Contract: 6 months (scope Rate: Competitive dependant on experience Our client, a leader in the medical devices sector, is seeking an R&D Electronics Engineer to join their team in Limerick on a contract basis. This role offers the opportunity to contribute to cutting-edge advancements in medical technology, collaborating with a dynamic team to design and develop innovative solutions. Key Responsibilities: Design and develop embedded software in C/C++ for medical devices Integrate hardware and electronics systems for robotic medical platforms Ensure compliance with FDA 21 CFR Part 11, MDR, and ISO 13485 standards Collaborate on hardware-software integration and troubleshooting Support verification, validation, and risk management activities Document design history and technical files per regulatory requirements Essential Skills & Experience: Minimum 5 years' experience in embedded systems Strong proficiency in C/C++ Electronics and hardware design experience Experienced with integrated systems Desirable: Familiarity with IEC 60601 and related safety standards Experience with FDA and EU MDR regulatory frameworks Please click 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

Purpose Assist in the development and maintenance of test systems for new product introductions and production. Learn and apply basic engineering principles to support product quality and reliability. Key Responsibilities Support the setup and maintenance of test equipment. Assist with prototype testing and basic troubleshooting. Prepare simple documentation and keep accurate records. Collaborate with engineers to implement improvements. Learn test automation tools and electronics fundamentals on the job. Qualifications Bachelor's degree in Electronic Engineering, Computer Engineering, or related field. No prior experience required; willingness to learn is essential. Basic understanding of electronics and programming concepts (academic level). Strong problem-solving skills and attention to detail. Good communication and teamwork abilities. Please click 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

A global medical device company is seeking a Senior Process Engineer to join their Process Development team. You'll lead the design, optimisation, and scaling of electrical test systems for both prototype and production phases. This includes building new systems, improving existing ones, and ensuring they're robust and production-ready. Key responsibilities include hardware/software integration, automation, root cause analysis, and supporting manufacturing transfer. LabVIEW expertise is essential. Key Skills: LabVIEW experience Test system development & debugging Electrical/PCBA knowledge Design-for-test & scalability planning Root cause analysis & validation Support for pre-production/production environments Clear documentation & cross-functional collaboration Details: Start: ASAP Duration: 12 months (extension opportunities) Location: Galway (3 days onsite/week, remote flexibility) Rate: €40-60/hr Please click 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

A global medical device company is seeking a Senior Process Engineer to join their Process Development team. You'll lead the design, optimisation, and scaling of electrical test systems for both prototype and production phases. This includes building new systems, improving existing ones, and ensuring they're robust and production-ready. Key responsibilities include hardware/software integration, automation, root cause analysis, and supporting manufacturing transfer. LabVIEW expertise is essential. Key Skills: LabVIEW experience Test system development & debugging Electrical/PCBA knowledge Design-for-test & scalability planning Root cause analysis & validation Support for pre-production/production environments Clear documentation & cross-functional collaboration Details: Start: ASAP Duration: 12 months (extension opportunities) Location: Tipperary (4 days onsite/week, remote flexibility) Rate: €45-70/hr Please click 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

A global medical device company are looking for a Materials Lab Scientist to join their team on a contract basis. You will provide support in materials science, process development, failure analysis, and new product development. This role is central to enabling high product performance, supporting manufacturing and quality teams, and accelerating innovation through advanced materials and process characterisation. Key Responsibilities: Conduct advanced materials and process characterization to support new product development, R&D, manufacturing, and quality initiatives. Perform failure analysis, contamination investigations, material supplier comparisons, and integrity assessments. Operate, maintain, and interpret results from a broad range of analytical and testing equipment, including but not limited to: Imaging and microscopy systems (CT/SEM) Spectroscopy and compositional analysis tools (EDX/FTIR) Mechanical and physical property testing instruments Thermal analysis equipment (DSC) Surface and dimensional measurement systems Prepare and analyse samples according to best practices, ensuring accurate and reliable results. Document and communicate findings through technical reports and presentations. Collaborate with cross-functional teams to support product development, manufacturing, and quality improvement. Ensure compliance with lab safety, quality, and data integrity standards. Key skills required: Degree in Materials Science, Chemistry, Physics, or a related field. Hands-on experience with a variety of analytical and testing techniques relevant to materials science. Strong analytical and problem-solving skills, especially in failure analysis and process optimization. Ability to interpret complex data and communicate findings clearly to technical and non-technical audiences. Experience working in a regulated manufacturing or R&D environment is highly desirable. Familiarity with relevant standards and calibration/validation of lab equipment is a plus. Excellent organizational, documentation, and teamwork skills. Desirable skills: Commitment to innovation, high performance, and continuous improvement. Strong attention to detail and a proactive approach to troubleshooting. Ability to work independently and as part of a multidisciplinary team. Appreciation for diversity, collaboration, and knowledge sharing. The start date is ASAP. The initial contract is for 12 months, with multiple extension options. The role is based in County Tipperary and will require 5 days onsite per week, remote work can be honoured were possible (for example report writing). The rate is €25-30 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 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

A global medical device company are looking for Mechanical Design and Process Development Engineer with equipment design and prototyping experience. The ideal candidate will have experience designing medical mechanical equipment, as part of a new exploratory project, with some exposure to electronics. This role requires a hands-on, self-driven individual who is comfortable managing the full equipment lifecycle, from concept through to validation. A solid understanding of mechanical design principles and process development within the medical device sector is essential. Candidates should demonstrate a proactive approach to learning, adaptability, and the ability to work independently while valuing the importance of validation and quality standards. This role will focus on design initially and the role will expand as you get embedded into the project. You'll need an attitude to learn new areas quickly, proactively and often autonomously, there will be support still. Essential skills required: Mechanical Design Passion for prototyping Process development experience Qualifying equipment and tooling instruments Medical devices experience The start date is ASAP. The initial contract is for 12 months, with multiple extension options. The role is based in Galway and will require 5 days onsite per week, remote work can be looked at after the first 6 months. The rate is €45-55 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 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

Automation Engineer - Ignition SCADA - Remote - Contract Contract: 6 months (potential to go permanent) Experience: 3-5 years We're looking for an Automation Engineer with hands-on Ignition SCADA expertise to drive global pharmaceutical projects. You'll lead deployments, optimise systems, and ensure seamless integration with enterprise platforms, while championing best practices and compliance. What You'll Do Deploy and standardise Ignition SCADA solutions across multiple sites. Maintain global templates for consistent, efficient rollouts. Integrate SCADA with ERP, MES, LIMS, and other enterprise systems. Troubleshoot, optimise, and keep systems running at peak performance. Train local teams and enforce engineering standards. What You Bring Degree in Engineering, Computer Science, or related field. 3-5 years in pharma automation projects with Ignition SCADA expertise. Knowledge of GMP/FDA regulations. Experience linking SCADA to enterprise platforms (ERP, MES, SQL). Strong communication and collaboration skills. Why Join? Initial 6-month contract with potential for permanent placement. Occasional travel for global site support. Please click 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

Purpose Assist in the development and maintenance of test systems for new product introductions and production. Learn and apply basic engineering principles to support product quality and reliability. Key Responsibilities Support the setup and maintenance of test equipment. Assist with prototype testing and basic troubleshooting. Prepare simple documentation and keep accurate records. Collaborate with engineers to implement improvements. Learn test automation tools and electronics fundamentals on the job. Qualifications Bachelor's degree in Electronic Engineering, Computer Engineering, or related field. No prior experience required; willingness to learn is essential. Basic understanding of electronics and programming concepts (academic level). Strong problem-solving skills and attention to detail. Good communication and teamwork abilities. Please click 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

Key Responsibilities Process Development : From concept to market release Conduct feasibility studies. Apply Lean and process improvement tools. Validation & Compliance : Use IQ, OQ, PQ, PFMEA, and regulatory frameworks. Document validation builds and results. Design & Innovation : Develop mechanical/electro-mechanical components and equipment. Innovate tooling, automation, and procedures. Collaboration : Work with Process Development and machine vendors. Oversee equipment design, build, testing, and handover. Coordinate vendor activities Please click 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

A global medical device company are looking for Mechanical Design and Process Development Engineer with equipment design and prototyping experience. The ideal candidate will have experience designing medical mechanical equipment, as part of a new exploratory project, with some exposure to electronics. This role requires a hands-on, self-driven individual who is comfortable managing the full equipment lifecycle, from concept through to validation. A solid understanding of mechanical design principles and process development within the medical device sector is essential. Candidates should demonstrate a proactive approach to learning, adaptability, and the ability to work independently while valuing the importance of validation and quality standards. This role will focus on design initially and the role will expand as you get embedded into the project. You'll need an attitude to learn new areas quickly, proactively and often autonomously, there will be support still. Essential skills required: Mechanical Design Passion for prototyping Process development experience Qualifying equipment and tooling instruments Medical devices experience The start date is ASAP. The initial contract is for 12 months, with multiple extension options. The role is based in Galway and will require 5 days onsite per week, remote work can be looked at after the first 6 months. The rate is €45-55 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 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

A global medical device company are looking for a Materials Lab Scientist to join their team on a contract basis. You will provide support in materials science, process development, failure analysis, and new product development. This role is central to enabling high product performance, supporting manufacturing and quality teams, and accelerating innovation through advanced materials and process characterisation. Key Responsibilities: Conduct advanced materials and process characterization to support new product development, R&D, manufacturing, and quality initiatives. Perform failure analysis, contamination investigations, material supplier comparisons, and integrity assessments. Operate, maintain, and interpret results from a broad range of analytical and testing equipment, including but not limited to: Imaging and microscopy systems (CT/SEM) Spectroscopy and compositional analysis tools (EDX/FTIR) Mechanical and physical property testing instruments Thermal analysis equipment (DSC) Surface and dimensional measurement systems Prepare and analyse samples according to best practices, ensuring accurate and reliable results. Document and communicate findings through technical reports and presentations. Collaborate with cross-functional teams to support product development, manufacturing, and quality improvement. Ensure compliance with lab safety, quality, and data integrity standards. Key skills required: Degree in Materials Science, Chemistry, Physics, or a related field. Hands-on experience with a variety of analytical and testing techniques relevant to materials science. Strong analytical and problem-solving skills, especially in failure analysis and process optimization. Ability to interpret complex data and communicate findings clearly to technical and non-technical audiences. Experience working in a regulated manufacturing or R&D environment is highly desirable. Familiarity with relevant standards and calibration/validation of lab equipment is a plus. Excellent organizational, documentation, and teamwork skills. Desirable skills: Commitment to innovation, high performance, and continuous improvement. Strong attention to detail and a proactive approach to troubleshooting. Ability to work independently and as part of a multidisciplinary team. Appreciation for diversity, collaboration, and knowledge sharing. The start date is ASAP. The initial contract is for 12 months, with multiple extension options. The role is based in County Tipperary and will require 5 days onsite per week, remote work can be honoured were possible (for example report writing). The rate is €25-30 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 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 Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales