Find your next tech and IT Job or contract Integration in Ireland

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.

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 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