Sustaining Mechanical Engineer (Contract/Freelance) A high number of candidates may make applications for this position, so make sure to send your CV and application through as soon as possible. Contract Duration: 12 months (40 hours/week) Location: County Galway, Ireland - On-site with hybrid flexibility (4 days on-site / 1 day remote) Start Date: January Sector: Medical Devices About the Role Lead sustaining and cost-saving initiatives within a Value Improvement Process (VIP) framework. This is a hands-on, cross-functional role where you will define scope, drive execution, and close projects end-to-end without a dedicated project manager. Key Responsibilities Own and deliver multiple sustaining/VIP projects focused on cost reduction and product/value improvements. Define scope, timelines, resources, and success criteria; ensure effective execution and formal project closure. Lead cross-functional collaboration (Engineering, Quality, Manufacturing, Supply Chain). Identify savings/efficiency opportunities and implement robust, compliant, sustainable solutions. Prepare project documentation, regular updates, and status reports for stakeholders and HR/TA. Champion continuous improvement and risk mitigation across the product portfolio. Required Experience & Skills Proven track record delivering sustaining engineering projects with measurable cost savings. Strong mechanical engineering background in medical devices or other regulated manufacturing. End-to-end project ownership: scoping, execution, validation/verification, close-out. Effective stakeholder management and clear, professional communication. Practical problem-solving, data-driven decision-making, and familiarity with change control. Preferred Qualifications Experience with VIP frameworks or formal value engineering methodologies. Exposure to small-to-mid-sized multinational environments. Knowledge of DFM (Design for Manufacturability), supplier optimisation, and lifecycle management. How to Apply Apply via this platform and include a short paragraph insert detailing the cost-saving projects you have worked on and sustaining experience. Applications with this will be prioritised. Please click to find out more about our Key Information Documents. Please note that the documents provided contain generic information. xsokbrc 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 | OC(phone number removed) England and Wales
Senior Embedded Firmware Engineer - Contract Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully. 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. xsokbrc 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 | OC(phone number removed) England and Wales
