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Senior Process Development Engineer - Medical Devices (Contract) Location: Co. Tipperary, Ireland Contract: 12+ months | Onsite minimum 4 days/week | 40 hours/week About the Role Our client is seeking a Senior Process Development Engineer to join their team on a long-term contract in Co. Tipperary. This is an exciting opportunity to work on advanced process development , particle size distribution analysis , and material science projects within the medical device sector. Essential Requirements Expertise in particle size distribution analysis and ensuring material consistency. Strong skills in data interpretation and reporting of experimental results. Proven experience in process development and manufacturing process optimisation in a regulated environment. Solid knowledge of material science and its application in product performance. Hands-on experience with IQ/OQ/PQ validation protocols and GMP compliance. Level 8 Engineering degree or equivalent. Minimum 5-6 years in medical device or pharmaceutical process development. Desirable Requirements Familiarity with metal additive manufacturing , 3D printing , and advanced manufacturing technologies . Advanced chemical analysis techniques for material characterisation. Exposure to laser systems , CNC machining , and CAD/CAM tools . Application of Lean Six Sigma methodologies for process optimisation. Strong understanding of ISO 13485 , FDA regulations , and quality systems compliance. Why Apply? Work on cutting-edge medical device innovations . Join a dynamic, forward-thinking team . Competitive contract opportunity with 12+ months duration and onsite collaboration . Process Engineer | Validation Engineer | Manufacturing Engineer | Medical Device Engineer | GMP | IQ/OQ/PQ | Process Development | Particle Size Analysis | Material Characterisation | Additive Manufacturing | 3D Printing | Lean Six Sigma | ISO 13485 | FDA Compliance | Chemical Analysis | CNC | CAD/CAM 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

Senior System Development Engineer - Medical Devices (Contract) Location: Limerick, Ireland (Hybrid - 4 days onsite) Contract: 6 months (potential extension) Rate: Competitive About the Role We are seeking a Senior System Development Engineer to join a team developing advanced medical device technology. This role focuses on integrating embedded firmware, hardware, and secure systems within a regulated environment. If you have strong C/C++ and C# programming skills, experience with microcontrollers and embedded systems, and knowledge of medical device compliance standards (ISO 13485, IEC 60601, FDA 21 CFR Part 11), this is your opportunity to make a significant impact. Key Responsibilities: Lead integration of embedded software and hardware systems for advanced medical devices Develop and maintain software in C++, C#, and embedded C Manage bug fixes, patch deployment, and feature enhancements under strict timelines Collaborate with a team of engineers on system-level troubleshooting and network safety Ensure compliance with ISO 13485, IEC 60 Maintain design history files and technical documentation per regulatory requirements Essential Skills & Experience: Strong proficiency in C++, C#, and embedded C Minimum 5 years' experience in embedded systems and system integration Exposure to regulated environments (medical devices preferred; aerospace/automotive acceptable) Ability to work under pressure and deliver from month one Familiarity with hardware-software integration and troubleshooting Desirable: Experience with IEC 60601 safety standards Knowledge of FDA and EU MDR frameworks Why Apply? This is a chance to work on cutting-edge medical technology, applying your expertise in system integration, embedded software development (C/C++ and C#), and regulatory compliance to deliver solutions 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