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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

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