Hero Recruitment is seeking a Buyer Planner to support production planning and supply chain efficiency in Athlone, Ireland. This role requires a Bachelor's degree and at least 5 years of experience in supply chain planning or procurement. The ideal candidate will manage inventory and supply risks while collaborating with internal stakeholders and driving continuous improvement initiatives. This position offers a hybrid working model, requiring onsite presence at least three days per week. #J-18808-Ljbffr
Hero Recruitment is looking for an Engineering Manager in Galway. The role involves leading and developing a team of engineers to deliver quality products and systems. Responsibilities include managing workloads, fostering a culture of continuous improvement, and ensuring alignment with business objectives. The ideal candidate has at least 5 years of experience in a similar role and a degree in Engineering. This position operates in a standard office environment with potential for site visits and on-call support. #J-18808-Ljbffr
Hero Recruitment is looking for an Engineering Manager in Galway. The role involves leading and developing a team of engineers to deliver quality products and systems. Responsibilities include managing workloads, fostering a culture of continuous improvement, and ensuring alignment with business objectives. The ideal candidate has at least 5 years of experience in a similar role and a degree in Engineering. This position operates in a standard office environment with potential for site visits and on-call support. #J-18808-Ljbffr
HERO Recruitment seeks a Senior Packaging Engineer in Ireland to join a global team delivering innovative medical products. This role involves leading packaging projects, developing sterile and non-sterile systems, and ensuring compliance with global regulations. The ideal candidate will have over 6 years in packaging for medical devices, possess expertise in ISO and ASTM standards, and demonstrate strong technical and collaborative skills. A competitive salary and benefits package is offered. #J-18808-Ljbffr
Contract role Galway Job Purpose Develop internal capabilities to support the assessment, design, installation, and maintenance of automated inspection solutions using Machine Vision and Image Processing technologies. The role involves contributing to research initiatives and assisting in the development of innovative production solutions under guidance from senior engineers. Build collaborative relationships through strong teamwork across the organization while supporting existing manufacturing equipment to investigate and resolve machine vision–related issues. This role has a hands‑on focus in equipment development, including exposure to automation and controls, electro‑mechanical systems, industrial and collaborative robots, and computer hardware and software support. Key Responsibilities Vision System Design & Development Contribute to the design of machine vision system architectures to meet defined requirements, including assisting with hardware selection (cameras, lighting, lenses) and software tools. Develop and configure vision applications using established platforms under guidance, ensuring alignment with defined functional requirements. Apply structured problem‑solving techniques to support equipment technology development and continuous improvement initiatives. Commission, test, troubleshoot, and support new and existing manufacturing equipment with integrated vision systems. Provide day‑to‑day technical support for vision hardware and software on production machines. Assist with fault investigation and root cause analysis of vision‑related production issues. Software & Algorithm Development Develop and modify vision applications using Cognex (In‑Sight, VisionPro) and/or Keyence XG/XGX platforms (or equivalent systems). Support software development activities that may include C#, VB, C/C++ and communication with PLC- or PC‑based control systems. Implement basic algorithms for image processing tasks such as measurement, feature detection, OCR, pass/fail logic, and data acquisition. Support the storage, organisation, and retrieval of image and video data used for system development, testing, and troubleshooting. Assist with performance optimisation activities to ensure vision systems meet defined speed and reliability requirements. Participate in testing, validation, and benchmarking activities to verify vision system accuracy and robustness. Collaboration, Compliance & Development Work as part of a cross‑functional team with manufacturing, quality, automation, and engineering partners to resolve technical issues. Follow defined divisional and corporate procedures, including change control, validation, and safety requirements for vision‑related updates. Maintain documentation related to vision system configurations, testing, and changes. Seek to develop technical capability by staying informed of advancements in machine vision technologies and best practices. Apply agreed machine vision standards and practices to support equipment effectiveness and maintainability. Required Qualifications Level 8 NFQ qualification or equivalent in Electronic Engineering or a related technical discipline. Candidates are required to have 3+ years’ experience in machine vision, automation, or equipment engineering roles (graduate‑level experience will be considered). Experience or practical exposure to machine vision systems, ideally using Keyence XG/XGX or Cognex (In‑Sight, Designer, VisionPro) platforms. Foundational understanding of mathematical and image processing concepts. Ability to work effectively both independently and as part of an engineering team. Good written and verbal communication skills with a practical, solution‑focused mindset. Preferred Qualifications Experience working in a regulated manufacturing environment (e.g. medical devices, pharmaceuticals). Exposure to equipment validation, commissioning, or structured problem‑solving methodologies. Familiarity with industrial automation, robotics, or PLC‑based systems. Working Conditions The role is primarily site‑based in a manufacturing and/or laboratory environment. Occasional travel to other company sites may be required. Standard working hours are Monday to Friday; occasional out‑of‑hours or weekend support may be required to support production activities. #J-18808-Ljbffr
Perform Duties of Research & Development Engineer 2 Design development, prototyping, test method design, design evaluation, design reviews, design specifications, design verification and validation, design protocols and reports, transfer to production activities in a timely effective manner. Product testing and evaluation, completion of test reports to support design selection. Preparation and presentation of design reviews. Product risk analysis and risk management. Contribute towards process development during introduction /development of new equipment and production processes as required for any new manufacturing techniques. Source new materials components and equipment. Development of component specifications, inspection methods, bills of materials and manufacturing processes. Introduction of new equipment, materials and technologies. As required work closely with Key Opinion Leaders, physicians, product managers and team to develop innovative medical devices to improve patient care. Work closely with Project Lead and take responsibility for assigned research and development project tasks: Manage and drive assigned project tasks to ensure timely completion of project milestones. Work closely with cross functional groups to achieve project and company goals. Product performance evaluations. Contribute to innovation and creativity within team through filing of disclosures and patents. Hold regular project meetings and document minutes and actions. Ensure project milestones are achieved to meet business metrics. Communications: Regular communication to cross-functional teams and senior management. Project status communications and reporting. Remain on the forefront of emerging industry practices. Educating oneself in the medical area for which the new devices are being developed in order to have an appreciation for what needs to be achieved with these products. Support other cross functional groups to deliver company goals. Qualifications Bachelor’s degree is required, preferably in engineering or a related field. Minimum of 3 years’ relevant experience is desired. Execution of project in a timely effective manner. Knowledge of anatomy and physiology. Good mechanical design and understanding of engineering fundamentals with medical device materials knowledge. Statistical understanding and experience. Manufacturing design and process understanding. Good working knowledge of Solidworks and/or Pro Engineer CAD. Strong technical writer. Knowledge of relevant ISO, EU, FDA medical device standards regulations is required. #J-18808-Ljbffr
Are you a packaging expert ready to make a global impact? My client is looking for a Senior Packaging Engineer to join a Global Packaging team and help us deliver life‑changing medical products with precision, safety, and innovation. In this role, you’ll lead packaging development and will be driving excellence from concept through commercialization. You’ll collaborate cross‑functionally, mentor peers, and influence packaging decisions that ensure compliance, optimize performance, and enhance patient outcomes. In this role you will: Lead packaging projects for new product development and changes to existing products Develop and validate sterile and non‑sterile packaging systems Drive cost savings and continuous improvement initiatives Ensure global regulatory compliance Ideally you will have: 6+ years of packaging experience in medical devices or related industries Expertise in ISO 11607, ASTM, ISTA, and EU MDR/FDA guidance Strong technical writing, validation, and statistical analysis skills A passion for innovation, collaboration, and making a difference Competitive salary and benefits package #J-18808-Ljbffr
Our Renewable Energy client in Galway is seeking a Quantity Surveyor to support the pricing, cost control, and commercial analysis of electrical infrastructure projects. While primarily an internal role, the QS will play a key enabling role in client development and new business growth, ensuring proposals are accurate, competitive, and commercially robust. Key Responsibilities Prepare detailed cost estimates for industrial and commercial renewable energy projects. Develop Bills of Quantities (BoQs) and pricing schedules. Analyse supplier and subcontractor pricing. Maintain cost databases and historical pricing benchmarks. Supporting Client & Business Development Support tender submissions that help win new clients and repeat business. Provide cost insights to support client discussions and value engineering. Assist in responding to client technical-commercial queries during tender stage. Support pricing strategies that align with client budgets and project objectives. Technical & Commercial Coordination Review drawings, specifications, and scope documents. Work closely with Engineering and Procurement teams to ensure pricing accuracy. Assist with risk identification, contingency planning, and post-tender reviews. Experience & Skills Experience in QS within renewable energy or construction industries Strong numerical, analytical, and Excel skills. Ability to interpret technical drawings and specifications. Understanding of EPC project cost structures. Experience with renewable energy systems Quantity Surveying or Engineering qualification. Exposure to commercial or client-facing tender environments. Personal Attributes Detail-focused and methodical. Commercially aware and cost-conscious. Collaborative and supportive of wider business goals. Comfortable working to tender deadlines. #J-18808-Ljbffr
Design and Development Engineer I/II Contract Role Onsite - Galway Our Purpose Coronary & Renal Denervation therapies are a vital component of our client's interventional cardiology portfolio. In addition to our core products that treat blocked coronary arteries, we are seeking to solve unmet needs in the rapidly growing field of complex Percutaneous Coronary Intervention (PCI). We are also leading the way with the transformational Blood pressure reduction therapy, which has the potential to be a powerful tool in battling the global hypertension epidemic. A Day in the Life Of Actively participate in all areas of new product development including process design, process characterisation, technology development & advancement, automation, vendor, sub‑tier supplier management & project management. Collaborate with cross‑functional teams to define, execute and deliver on requirements in the pre and post‑market space. Lead and support the process development, process characterisation, and process validation activities to support new product introduction. Excellent statistical capabilities, utilisation of design of experiments and engineering studies to coach team members on developing engineering DOE’s, transfer functions and build on our team’s capabilities to root cause issues whilst defining robust process windows. Take initiative & lead, innovate and develop best‑in‑class process technology with emphasis on improving quality, reducing variation and developing state‑of‑the‑art automated and semi‑automated systems. Identify and mitigate technology and process risks through the design process. Collaborate with team members on Design, Reliability & Manufacturability methodology (DRM), utilise 3‑D drawing/printing and Augmented Reality to develop our best solutions that will allow us to manufacture devices that positively impact healthcare of millions. Identify and carry out practical actions to solve technical problems using project management, six sigma tools, process characterisation and technology development. Collaborate, document and present all learnings to project and functional teams. Key Skills & Experience Third level 8 degree or higher in Electronic, Electrical, Mechanical, Biomedical Engineering, Science or related discipline with minimum 2 years direct science/engineering experience within a medical device environment. Advanced degree advantageous. Dynamic team player with ability to collaborate effectively within talented team and work proactively on cross‑functional teams. Experience in process validation protocol and report writing. Ability to identify and resolve issues without direct supervision. Working knowledge of statistical tools such as DOE, SPC, hypothesis testing and process capability studies. Experience developing and validating medical device manufacturing processes (IQ, OQ, PQ and PPQ). Knowledge of medical device processes with good understanding of product and process design. Good communicator and fluent in English, with high level of enthusiasm and motivation. Good organisational, presentation and project management skills desirable. #J-18808-Ljbffr
Responsibilities may include the following and other duties may be assigned: Support routine Sterility Assurance activities e.g GMP, Standards Compliance, Cleanroom Risk Assessment, Limits review, Dose Audit activity, Cycle Requalification, Supplier Change control etc Support sterility assurance activities for new products and change control , developing strong partnering relationships with these groups, at both manufacturing and design sites Participate in root cause investigations and continuous improvement in day-to-day activity, initiating appropriate corrective actions and following through to implementation Support cross functional teams in design protocols to ensure that new products/ product changes are adequately evaluated/tested to guarantee compliance to all regulatory standards Collaborates with engineering and manufacturing functions to ensure quality standards are in place Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements. Performs calculations, data integrity checks, technical and record keeping duties in conformance with company and regulatory policies and standards to meet quality and accuracy requirements SPECIALIST CAREER STREAM Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects from design to implementation while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education (typically University). DIFFERENTIATING FACTORS Autonomy Entry level individual contributor on a project or work team. Works with close supervision. Organizational Impact Delivers work of limited scope, typically smaller, less complex projects or related activities. Innovation and Complexity: Identifies, defines and addresses problems that are not immediately evident but typically not difficult or complex. Makes minor changes in systems and processes to solve problems. Communication and Influence Communicates primarily with internal contacts within immediate group. Contacts others to gather, confirm and convey information. Leadership and Talent Management N / A job at this level is focused on self development . Required Knowledge and Experience Requires broad theoretical job knowledge typically obtained through advanced education. Requires a University Degree, 1-2 years of experience required. #J-18808-Ljbffr
