Manufacturing Technician&nbsp; Galway Evenings - The evening shift hours will be 2pm-10pm Monday to Friday. Job Spec:&nbsp; The role is within the balloon manufacturing area and I am looking for the following expertise:<ul><li>Someone with previous experience as a process/manufacturing technician</li><li>Someone with equipment troubleshoot/repair experience</li><li>Someone with Mechanical/pneumatic/electrical experience</li><li>Someone with strong process troubleshooting experience (troubleshooting settings/materials/equipment to reduce scrap)</li><li>Medical device experience desirable</li><li>Polymer processing knowledge also desirable.</li></ul>The evening shift hours will be 2pm-10pm Monday to Friday.

Process Technician - Evenings

Senior Project Manager Department: Research and Development Reporting to: Manager, Research and Development / Senior Manager, Research and Development / Director, Research and DevelopmentResponsibilities:<ul><li>Perform Duties of Senior Project Manager, Research and Development:</li><li>Project management lead for assigned projects. Project management of projects and coordinate with technical leads to progress projects.</li><li>Establishment and management of routine team meetings to facilitate plan updates, decision-making, problem solving, escalations e.g. resourcing gaps, mitigations vs non-adherence to plan.</li><li>Assist with the introduction of best practice project management methodologies.</li><li>Maintains oversight on Project budget; manages project risks i.e. leads the development of risk register and mitigations with the project team.</li><li>Manage the key activities of the project and drive project tasks to ensure timely completion of project milestones</li><li>Generate and monitor project metrics, including ownership of communicating to team/s and senior management.</li><li>Responsible for realising business metrics within projects.</li><li>Work closely to build effective relationships with cross functional groups to achieve project and company goals.</li><li>Work closely with vendors as required to facilitate, plan development, monitoring and controlling.</li><li>Retrospective project reviews to understand lessons learned.</li><li>Compliance with Quality, Regulatory and company policies and systems.</li><li>Mentoring, coaching and development of direct reports if required.</li><li>Foster innovation and creativity within team and perform disclosure reviews.</li><li>Compliance with Quality, Regulatory and company policies and systems.Communications:</li><li>Development, update and utilisation of the project stakeholder register.</li><li>Regular communication to cross-functional teams, senior management and business unit leaders.</li><li>Project status communications and reporting.</li><li>Ensure effective reporting to all relevant stakeholders.</li><li>Remain on the forefront of emerging industry practices.</li><li>Instrumental in driving and implementing change to improve departmental and company performance.</li><li>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.</li><li>Support other cross functional groups to deliver company goals.</li><li>Act as a delegate for the Manager, Research and Development. Qualifications / Requirements:</li><li>Bachelor&rsquo;s degree required, preferably in engineering or a related field.</li><li>Minimum of 5 years&rsquo; relevant experience is required.</li><li>Proven Project Management methodology and skills.</li><li>Certified in Project management is essential.</li><li>Agile methodology is preferred but not essential</li><li>Proven Project Leadership abilities.</li><li>Proven track record in delivering quality results in a timely effective manner.</li><li>Good presentation skills (working knowledge of MS PowerPoint).</li><li>Attention to detail and Quality focus.</li><li>Knowledge of relevant ISO, EU, FDA medical device standards regulations is required.</li><li>Good problem-solving skills.</li><li>An ability to think and plan strategically.</li><li>Highly motivated individual, self-starter with a passion for excellence.</li><li>Must be able to work in a fast paced environment.</li><li>Ability to foster relationships with key stakeholders required to ensure on time project delivery.</li><li>Experience of medical device development from concept through to commercialisation.</li><li>Ability to effectively translate needs of clinicians and SBU into project inputs is preferred but not essential.</li><li>Willingness and availability to travel on company business.</li></ul> <p style="box-sizing: border-box; margin-top: 0px; margin-bottom: 1rem; font-family: Barlow, sans-serif; font-size: 16px; color: #212529; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: #ffffff; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;">Our Vision: To be recognised as the best STEM Contracting &amp; Permanent Recruitment company and the Employer of Choice for top performing Recruiters.<p style="box-sizing: border-box; margin-top: 0px; margin-bottom: 1rem; font-family: Barlow, sans-serif; font-size: 16px; color: #212529; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: #ffffff; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;">For further information on this role please contact Geraldine Gormally on 0861071395&nbsp;&nbsp;<a style="box-sizing: border-box; color: inherit; text-decoration: underline; font-family: inherit !important; font-size: inherit !important;" href="mailto:/%C2%A0recruit@hero.ie">/&nbsp;recruit@hero.ie</a><p style="box-sizing: border-box; margin-top: 0px; margin-bottom: 1rem; font-family: Barlow, sans-serif; font-size: 16px; color: #212529; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: #ffffff; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;">Check out all our open jobs on our HERO Recruitment website &ndash;&nbsp;<a style="box-sizing: border-box; color: inherit; text-decoration: underline; font-family: inherit !important; font-size: inherit !important;" href="https://www.hero.ie/">https://www.hero.ie/</a>&nbsp;&nbsp;<p style="box-sizing: border-box; margin-top: 0px; margin-bottom: 1rem; font-family: Barlow, sans-serif; font-size: 16px; color: #212529; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: #ffffff; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;">Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.<p style="box-sizing: border-box; margin-top: 0px; margin-bottom: 1rem; font-family: Barlow, sans-serif; font-size: 16px; color: #212529; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: #ffffff; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;">Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review your data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

Senior Project Manager 

Senior Embedded Software Engineer &ndash; Embedded Systems (C/C++)&#55357;&#56525; Location: LimerickAbout the RoleWe are seeking a highly motivated and experienced Senior Embedded Software Engineer to join a global R&amp;D team, developing embedded software for optoelectronic and electromechanical devices used across consumer, industrial, and medical applications.This role offers the opportunity to design, implement, and document board-level firmware in C/C++, contributing across the full software development lifecycle while ensuring adherence to quality and regulatory standards. You will collaborate with multidisciplinary teams throughout the entire product lifecycle&mdash;from concept development to commercialization and post-market support&mdash;delivering high-performance, reliable, and scalable embedded software solutions.This is an exciting opportunity to work in a regulated, fast-paced environment and directly influence the development of life-changing technologies.Key ResponsibilitiesTranslate system-level requirements into embedded system requirements and interface definitions.Assess technical feasibility and contribute to embedded system architecture and design.Establish embedded hardware and firmware architecture, decomposing systems into lower-level building blocks.Design, implement, and maintain real-time embedded software using C/C++ for safety-critical applications.Lead software architecture and design reviews, ensuring reliability, testability, and scalability.Collaborate closely with electrical, mechanical, systems, quality, and regulatory teams.Drive and perform verification and validation strategies, including unit, integration, and system testing.Author and maintain documentation for software architecture, design specifications, and risk analysis.Support regulatory submissions and audits when required.Maintain traceability between requirements, verification protocols, and test reports.Contribute to configuration management and technical/design/milestone reviews.Apply Agile and CI/CD principles to maximize quality, performance, and compliance.Qualifications &amp; Experience:Bachelor&rsquo;s or Master&rsquo;s degree in Computer Engineering, Electrical Engineering, or related discipline.Minimum 7 years of experience in embedded software development, ideally in medical device or other regulated industries.Strong proficiency in C; working knowledge of C++ and Python desirable.Experience with microcontrollers, RTOS, low-level drivers, and embedded Linux.Familiarity with IEC 62304, ISO 13485, ISO 14971, or similar safety-critical standards.Skilled in hardware abstraction layers, bootloaders, BSP, and driver development.Hands-on debugging using oscilloscopes, logic analyzers, and similar tools.Experience with communication protocols (SPI, I2C, UART, CAN, USB).Proficiency with unit testing and test automation frameworks (CPPUnit, LDRA, Coverity, Parasoft).Familiarity with Agile/Scrum methodologies and tools (e.g., Jira, Azure DevOps).Knowledge of CI/CD pipelines and build/test infrastructures (e.g., Jenkins, Git, Make, GCC).Preferred:Experience with Xilinx FPGA/SoC programming.Knowledge of cybersecurity requirements for connected embedded systems.Experience implementing automated CI/CD testing for embedded environments.What&rsquo;s on OfferCompetitive salary and benefits package.Opportunity to work on safety-critical, innovative technologies with global impact.Professional development, training, and career growth opportunities.Collaborative international team environment.

Senior Embedded Software Engineer

About the role: The R&amp;D Tech Lead / Staff Engineer plays a critical role in driving innovation and excellence in the development of cutting-edge medical products and technologies. This position blends deep technical expertise with leadership and systems engineering, guiding cross-functional teams through every stage of the product lifecycle&mdash;from initial concept and design to commercialization and post-market support. The role demands a strong understanding of regulatory compliance, ensuring that all documentation and traceability requirements are met for successful submissions. With a focus on shaping product architecture and defining system and sub-system requirements, the Tech Lead is instrumental in delivering safe, effective, and transformative healthcare solutions. In this dynamic and regulated environment, the Tech Lead also serves as a mentor and technical authority, fostering growth and collaboration across engineering teams. Their influence extends beyond technical execution, helping to cultivate a culture of innovation and continuous improvement. By aligning engineering efforts with strategic goals, they ensure that the organization remains at the forefront of medical technology development. This is a unique opportunity for a highly motivated individual to make a meaningful impact on patient lives while advancing their career in a fast-paced and purpose-driven setting.Main responsibilities will include:<ul><li>System Design &amp; Development: Lead system-level design and development for new and existing medical products, ensuring alignment with stakeholder needs.</li><li>Requirements &amp; Architecture: Define product architectures and translate stakeholder inputs into clear, traceable system requirements.</li><li>Integration &amp; Testing: Oversee system integration and testing activities, supporting verification and validation across hardware, software, UX, and systems.</li><li>Technical Leadership: Provide mentorship and technical guidance to cross-functional teams, promoting engineering excellence.</li><li>Documentation &amp; Tools: Own and maintain design control documentation, SOPs, and requirements using tools like DOORS and Modern Requirements.</li><li>Lead configuration/change control processes (e.g., CCB, CIT) and find opportunities for development optimisation.</li><li>Regulatory Compliance: Ensure compliance with ISO 13485, ISO 14971, FDA QSR, and support FDA submissions through collaboration with quality and regulatory teams.</li><li>Risk Management: Conduct risk assessments and implement mitigation strategies, contributing to activities like dFMEA and hazard analysis.</li><li>Multi-functional Collaboration: Work closely with Engineering, Quality, Regulatory, Manufacturing, and Marketing to ensure smooth project execution and post-market support.</li><li>Project Execution &amp; Tools Development: Develop project plans, technical documents, and Excel- based toolsets to streamline workflows and support design control processes. About you:</li><li>Proven experience in leading technical project teams (HW, SW, UX, Systems) through the product lifecycle and phase-gate approach.</li><li>Strong ability to lead large teams and communicate technical deliverables effectively.</li><li>Experience in writing SOPs, guidance, and technical documentation.</li><li>Proficiency in Microsoft Project, Excel, especially in writing macros.</li><li>Experience in cross-functional product development.</li></ul>Preferred Qualifications<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Engineering, Systems Engineering, Biomedical Engineering, or related field.</li><li>5+ years of progressive experience as a senior/lead engineer in product development.</li><li>Creative problem solver with the ability to resolve conflicting requirements and technical risks.</li><li>Practical experience in configuration management and change control processes.</li><li>Familiarity with tools like DOORS, Modern Requirements, SolidWorks, MATLAB, LabVIEW, Minitab.</li></ul>

R&D Tech Lead Engineer

Lead Mechanical Design Engineer We are seeking a highly skilled Lead Mechanical Design Engineer to take a central role in the creation, development, and validation of advanced medical technologies, spanning both equipment and disposable components. This position requires a broad technical background, bringing together expertise in mechanical, mechatronic, electronic, and manufacturing disciplines to deliver innovative, compliant, and high-performing solutions. The role will involve shaping product requirements into detailed design specifications, selecting optimal materials and manufacturing methods, and carrying out feasibility assessments and proof-of-concept builds. A key focus will be driving continuous improvements in design and production processes to ensure product quality, reliability, cost-effectiveness, and scalability. Beyond technical leadership, this position includes managing multi-disciplinary project teams, applying structured project management practices, and leading risk management activities such as PHA, FTA, and FMEA. The engineer will also oversee problem-solving activities, supplier engagement, and provide guidance across the full product lifecycle. Leadership responsibilities will include team development, performance management, and the coordination of daily activities to achieve successful project delivery. The ideal candidate will be a confident communicator, experienced in leading design reviews and presenting technical insights to both internal teams and external partners, while maintaining an active interest in emerging technologies and industry best practices Main Responsibilities<ul><li>Lead and manage the design, development, and validation of assemblies, sub-assemblies, components, and packaging.</li><li>Define product specifications based on requirements and intended use.</li><li>Select suitable materials, processes, tooling, automation, and equipment.</li><li>Conduct engineering studies and proof-of-concept testing to evaluate feasibility.</li><li>Drive improvements in design and processes to strengthen quality, performance, and cost-efficiency.</li><li>Perform and lead risk management activities (PHA, FTA, DFMEA/UFMEA).</li><li>Carry out root cause analysis and corrective actions following failures or non-conformances.</li><li>Partner with manufacturing teams to resolve technical challenges and optimize processes.</li><li>Manage projects and sub-projects, assigning tasks and providing guidance to cross-functional teams.</li><li>Apply structured project management methods and report effectively to stakeholders.</li><li>Investigate and integrate new technologies and engineering tools.</li><li>Oversee recruitment, mentoring, and performance management of direct reports.</li><li>Organize and prioritize daily team activities to ensure timely outcomes.</li><li>Provide technical support to suppliers and external partners.</li><li>Lead technical reviews and deliver presentations to stakeholders.</li></ul>Qualifications &amp; Experience <ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Mechanical or Biomedical Engineering (or equivalent).</li><li>6&ndash;9 years&rsquo; experience in medical device design, including at least 5 years leading mechanical design teams.</li><li>Experience working on both capital equipment and disposable components within medical technology.</li><li>Strong knowledge of engineering principles, root cause analysis, and design documentation.</li><li>Skilled in GD&amp;T, Design for Six Sigma (DfSS), DOE, and statistical analysis.</li><li>In-depth understanding of materials, manufacturing processes, and design for manufacturability/assembly.</li><li>Demonstrated leadership with clear accountability for deliverables and team outcomes.</li><li>Excellent analytical, problem-solving, and decision-making skills.</li><li>Strong communicator with experience leading cross-functional project teams.</li><li>Knowledge of quality and regulatory standards (EN ISO 13485, MDR, FDA CFR 820).</li><li>Familiar with product development processes such as Stage-Gate or PDLC.</li><li>High attention to detail, quality mindset, and strong documentation practices.</li></ul>For further information on this role in please contact on Gavin Moran on 087 4108620 or connect@hero.ie Check out all our open jobs on our HERO Recruitment website &ndash; <a href="https://www.hero.ie/">https://www.hero.ie/</a> Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review

Lead Mechanical Design Engineer 

Purpose Statement Leads a dynamic team of engineers and technicians in a fast-paced manufacturing environment with a strong focus on automation, digital transformation, and operational excellence. Provides technical and people leadership to deliver on key business metrics, drive innovation in automation systems, and build team capability for sustained long-term success. Key Responsibilities<ul><li>Leadership &amp; Team Development - Provides guidance, coaching, and structured development opportunities to staff; fosters a culture of accountability, collaboration, and continuous improvement. - Recruits, retains, and develops top talent with a strong focus on automation and digital skillsets. - Motivates individuals and teams to achieve ambitious goals in a fast-paced, results-driven environment.</li><li>Strategic &amp; Technical Execution - Partners with senior management to establish departmental goals, budgets, and resource plans aligned to business priorities. - Leads and supports manufacturing engineering projects with a focus on automation, smart manufacturing, and process optimization. - Prioritizes and manages multiple projects to ensure timely, high-quality delivery of results.</li><li>Automation &amp; Innovation - Champions the adoption of advanced automation technologies (PLC, SCADA, robotics, IIoT, Industry 4.0) to improve efficiency, safety, and quality. - Collaborates cross-functionally to implement automation solutions, resolve complex technical issues, and enable digital manufacturing capabilities. - Partners with vendors and external stakeholders to assess and deploy new automation technologies.</li><li>Cross-Functional Collaboration - Represents Manufacturing Engineering on cross-functional teams, including new product development and strategic initiatives. - Builds and strengthens collaborative relationships with operations, quality, IT/OT, and global engineering groups.</li><li>Compliance &amp; Standards - Ensures policies, procedures, and quality system requirements are adhered to at all times. - Promotes a safe and compliant work environment aligned to EHS and Energy policies.</li></ul>Experience/Requirements <ul><li>Hons BSc degree in an Engineering/Science discipline required.</li><li>5+ years relevant experience.</li><li>Previous experience in automation highly desired.</li><li>Experience within Manufacturing environment is essential, Med Device/Pharma would be advantageous but not required.</li><li>Previous People Supervision experience is required</li></ul>

Associate Engineering Manager

I specialise in talent acquisition for diverse industries across Ireland. With a robust experience spanning over three decades, HERO Recruitment has earned a stellar reputation for our unwavering passion and commitment to excellence.
Our client portfolio is broad, covering sectors such as medical devices, pharmaceuticals, manufacturing, IT, and more. Armed with extensive connections, I can confidently locate the perfect match for you.
However, let's shift the focus to you &ndash; your dreams and goals are my driving force. Beyond being a recruiter, I am your dedicated partner, ready to guide you through every step of your journey. Together, we will navigate through various opportunities and transform your career aspirations into reality.
Join the HERO Recruitment family today, and let's co-create a success story that is uniquely yours. Together, we will make a substantial impact in the industry. Are you ready? Let's make it happen.

Job Details

Process Technician - Evenings

Recruitment Consultant

Process Technician - Evenings

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