The Senior R&amp;D Program Manager is a cross-functional business leader responsible for driving decision- making, and execution within development projects. You will be accountable for the product development cycle, starting with forming high-performing teams that ensure the successful and predictable delivery of solutions for commercial release. Additionally, you will formulate partnerships with cross functional Core Team members to foster collaboration and cross-functional effectiveness. You will be the key champion in overcoming barriers, driving decisions, and cultivating a culture of empowerment across the organization.This position will be on-site (minimum 4 days per week) based out of our Parkmore, Galway, Ireland site.A Day in The Life Of:<ul><li>Responsibilities may include the following and other duties may be assigned.</li><li>Responsible for driving cross-functional core team and working directly with functional leaders, regional leaders, and extended teams to ensure Senior R&amp;D Program Manager &ndash; Cardiac Ablation Solutions clear communication of program objectives, deliverables, and timing of key milestones.</li><li>Lead team members for on-time, on-budget, within scope project completion, while managing stakeholder and business expectations.</li><li>Accountable for the product development budget and schedule.</li><li>Use of critical thinking and problem-solving skills as a leader of cross functional teams through the intricate details of development projects; from scope definition, cost management to schedule development and risk management.</li><li>Regular communication and presentation to CAS leadership team through program updates at the program review committee meetings</li><li>Mentor team members to ensure each team member is fully engaged and contributing to project success.</li><li>Champion product development best practices such as collecting high-quality Voice of Customer inputs, early risk burn-down and Design for Reliability and Manufacturability (DRM).</li><li>25% or less domestic travel. Key Skills &amp; Experience</li><li>Bachelor's degree in a technical discipline with a minimum of 7 years of relevant experience or advanced degree and a minimum of 5 years of relevant experience</li></ul>Nice to Have: Preferred Qualifications<ul><li>Advanced degree such as MS or MBA</li><li>Medical device industry experiences including new product development, released product management, clinical trials and regulatory submissions</li><li>DRM Blackbelt</li><li>Experience managing complex cross-department and/or cross-functional project teams</li><li>Experience leading collaboratively in a diverse, global, matrixed organization</li></ul>

Senior R&D Program Manager

Shift Technician&nbsp; Main Responsibilities<ul><li>To work with the Shift Supervisors to start and stop machines and troubleshoot day-to-day processing problems to maximize machine up time;</li><li>Execution of other relevant technical tasks on-shift to maintain production at optimal performance;</li><li>Carry out regular services on machines;</li><li>Provide cover for the Shift Supervisor where appropriate and required;</li><li>Participate in continuous improvement or new product introduction projects</li><li>To maintain high standards of safety and housekeeping to ensure area, machines and equipment are maintained in a safe and clean conditions;</li><li>Ensure compliance with Quality and GMP requirements and adherence to all Mfg. Group policies and procedures.</li><li>Perform orientations and oversee training for new employees.</li><li>Communication effectively with all departments.</li></ul>Ideal Candidate <ul><li>The ideal candidate will be able to work on a four-cycle shift basis, to include nights and weekends.</li><li>The individual will have knowledge of the mechanical and electronic systems associated with high volume manufacturing; hold a relevant qualification in one of those disciplines and/or have additional specialised training and industrial experience.</li><li>The individual will have good communication and interpersonal skills and the ability to work well as part of a team.</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

Shift Technician

C&amp;Q Engineer (Cork) Contract Role (6 months)Job Summary:Role will be responsible for the Generation, Execution and Approval of Qualification documents for Direct Impact Systems (Facility, Utility and Equipment) and the generation of Commissioning Test documents for Not direct Systems. Requirements:<ul><li>BS Degree in engineering, science or technical discipline required. </li><li>3 years of Commissioning and Qualification experience, ideally working in OSD or pharmaceutical organization. </li><li>Previous experience with clean utility tie-ins to existing systems is desirable.</li><li>Previous experience with clean utilities, hygienic piping, process instrumentation, controls and TOPs is advantageous.</li><li>Familiarity with the risk-based approach to commissioning and qualification preferred. Familiarity with project management tools is advantageous.</li><li>Previous experience with Clean Utility tie-ins to existing systems is desirable (i.e Upgrading existing purified water skid to support a new tank). </li><li>Working knowledge of sanitary equipment, hygienic piping, process instrumentation and controls is desired </li><li>Familiarity with the risk-based approach to commissioning and qualification preferred.</li><li>Familiarity with project management tools is advantageous.</li><li>Adherence to cGMP and cGDP is mandatory. Strong technical writing skills are essential. The candidate must have a proven track record working within a fast paced GMP environment. </li><li>The candidate must be able to work independently with limited supervision &ndash; self-sufficiency is critical. </li><li>They must demonstrate strong interpersonal &amp; teamwork skills. </li><li>Must be flexible to support unexpected project demands and maintain the overall program schedule. </li></ul>Systems experience:<ul><li>Facility/Qualification</li><li>Dispensing Equipment including down flow booth, matcom stations, PTS powder systems</li><li>Tumble mixer equipment including CIP SKID</li><li>Utilities &ndash; compressed air</li></ul>

CQV Engineer

Automation Technician&nbsp; We are seeking an experienced Automation Technician to maintain, troubleshoot, and improve automated machinery and processes. This role involves programming, validating, and commissioning new equipment, supporting continuous improvement, and ensuring equipment reliability and compliance with quality standards. Main Responsibilities<ul><li>Maintain and troubleshoot automation equipment, robotics, and vision systems.</li><li>Support design, programming, testing, and validation of new equipment (IQ/OQ/PQ).</li><li>Carry out FAT/SAT at automation vendors and integrate equipment into production.</li><li>Analyse processes and develop automation solutions to improve efficiency and quality.</li><li>Perform repairs, calibration, and regular maintenance of automation systems.</li><li>Collaborate with cross-functional teams and provide technical support/training.</li><li>Document processes, write validation reports, and support audits.</li></ul>Key Requirements <ul><li>Bachelor&rsquo;s degree in Electrical, Mechanical, Mechatronics, Computer Science, or related field.</li><li>5+ years&rsquo; automation experience (preferably in injection moulding).</li><li>Proficiency with PLCs, SCADA, HMIs, APIs, SQL, Python, C, Java.</li><li>Experience with robotics, machine vision, and validation protocols.</li><li>Strong problem-solving, communication, and organizational skills.</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

Automation Technician

Senior R&amp;D EngineerRole Overview: We are seeking a Senior R&amp;D Engineer to join our team on a permanent basis. In this key role, you will provide electrical and electronic engineering expertise to support the design, development, and testing of medical devices, specifically focusing on catheter-based ablative therapies such as Renal Denervation (RDN). You will lead the design and troubleshooting of integrated hardware/software systems for single-use devices (SUDs), ensure regulatory and safety compliance, and contribute to innovation and intellectual property efforts to develop safe and effective therapy delivery systems.Primary Responsibilities:<ul><li>Design, develop, debug, modify, and test electrical circuits and systems for therapeutic ablation catheters and their consoles using modern tools and techniques.</li><li>Lead root cause analysis and troubleshooting of electronic failures at the component and system level, driving corrective solutions.</li><li>Manage development and evaluation of new catheter prototypes and console interfaces from concept through product launch in collaboration with cross-functional teams.</li><li>Analyze, verify, and validate requirements, circuits, and integrated systems, ensuring seamless hardware, firmware, and physiological signal acquisition.</li><li>Research, select, and implement electronic circuits, components, tools, and methodologies suitable for advanced ablative therapy devices.</li><li>Maintain comprehensive documentation of electrical development activities in accordance with quality system standards (protocols, technical reports, change requests, design history files).</li><li>Ensure all designs and products comply with medical device safety and electromagnetic compatibility (EMC) standards such as IEC60601.</li><li>Mentor and guide junior engineers and technicians, fostering their technical growth and contributing to a high-performing team.</li><li>Translate clinical requirements into robust engineering solutions, identifying innovative opportunities and contributing to intellectual property generation.</li><li>Communicate project status, risks, and milestones clearly to project leaders and senior management during regular meetings.</li><li>Uphold a strong commitment to patient safety and product quality by strict adherence to the Quality Policy and all relevant quality procedures.</li><li>Ensure availability of appropriate personnel, tools, and resources to maintain compliance with the Quality Management System and organizational policies.</li></ul>Qualifications &amp; Experience:Essential:<ul><li>Level 8 Honours Bachelor's Degree in Electrical Engineering.</li><li>At least 5 years&rsquo; experience in medical devices or similarly regulated industries, with preference for work on catheter-based or implantable systems.</li><li>Demonstrated skills in circuit and system design, troubleshooting, and root cause analysis.</li><li>Proven knowledge of regulatory and safety standards, including IEC60601 series and EMC requirements.</li><li>Excellent communication, technical documentation, and project management capabilities. Desirable:</li><li>Experience with ablative energy modalities such as RF, ultrasound, IVL, or PFA.</li><li>Familiarity with firmware debugging, digital logic design, FPGA technology, and system integration principles.</li><li>Competence in data analysis tools such as LabVIEW, MATLAB, Python, and automated testing frameworks.</li><li>Experience in intellectual property activities such as patent writing and disclosures.</li><li>Proven leadership and mentoring experience within multidisciplinary teams.</li></ul>

Senior Research & Development Engineer

<h1 data-start="181" data-end="211">Principal Systems Engineer Location: Galway</h1><h3 data-start="264" data-end="278">The Role</h3>We are seeking a Principal Systems Engineer to join a leading medical device manufacturer. This role will involve applying systems engineering expertise to new product development, collaborating with cross-functional teams, and supporting the integration of products into hospital environments. You will also contribute to system interface testing and provide technical support for commercial activities.<h3 data-start="691" data-end="717">Key Responsibilities</h3><ul data-start="718" data-end="1041"><li data-start="718" data-end="822">Lead and support cross-functional teams in integration, troubleshooting, testing, and documentation.</li><li data-start="823" data-end="888">Coach and mentor engineers in systems engineering principles.</li><li data-start="889" data-end="975">Provide technical support to marketing, field engineering, and training functions.</li><li data-start="976" data-end="1041">Identify and implement improvements to systems and processes.</li></ul><h3 data-start="1043" data-end="1068">Skills &amp; Experience</h3>Required<ul data-start="1085" data-end="1181"><li data-start="1085" data-end="1181">Bachelor&rsquo;s degree with 7+ years of relevant experience, or an advanced degree with 5+ years.</li></ul>Preferred<ul data-start="1199" data-end="1522"><li data-start="1199" data-end="1304">Experience in systems engineering and systems architecture within medical device product development.</li><li data-start="1305" data-end="1358">Knowledge of design controls for medical devices.</li><li data-start="1359" data-end="1424">Ability to develop strategies and influence across functions.</li><li data-start="1425" data-end="1472">Proven leadership and mentoring experience.</li><li data-start="1473" data-end="1522">Comfortable working in hospital environments.</li></ul><h3 data-start="1524" data-end="1545">What&rsquo;s on Offer</h3><ul data-start="1546" data-end="1693"><li data-start="1546" data-end="1590">Competitive salary and benefits package.</li><li data-start="1591" data-end="1693">Opportunity to work on innovative medical technologies in a collaborative, fast-paced environment.</li></ul>

Principal Systems Engineer

When it comes to my work, I'm all about attention to detail and delivering outstanding results. I believe in going that extra mile to make sure every candidate experience flawless. It's just how I roll! One thing I'm really proud of is my ability to communicate effectively and collaborate with others. I love being part of a team and inspiring my colleagues to bring their A-game. And you know what? I thrive under pressure! No challenge is too big for me.
I have big dreams and I'm confident I'll achieve great things in my career, that&rsquo;s why I believe I can do the same for you. I've got 11 years of experience in fast-paced environments. Talk about hustle! I love working and collaborating with others and together, we can achieve some incredible things. Consistently achieving goals and delivering top-notch quality is what I'm all about.
So, if you're looking for someone who's hardworking, enthusiastic, and a total team player, look no further! I've got your back and together, we'll make it happen
<span data-sheets-value="{&quot;1&quot;:2,&quot;2&quot;:&quot;When it comes to my work, I'm all about attention to detail and delivering outstanding results. I believe in going that extra mile to make sure every candidate experience flawless. It's just how I roll! One thing I'm really proud of is my ability to communicate effectively and collaborate with others. I love being part of a team and inspiring my colleagues to bring their A-game. And you know what? I thrive under pressure! No challenge is too big for me.\r\n \r\nI have big dreams and I'm confident I'll achieve great things in my career, that&rsquo;s why I believe I can do the same for you. I've got 11 years of experience in fast-paced environments. Talk about hustle! I love working and collaborating with others and together, we can achieve some incredible things. Consistently achieving goals and delivering top-notch quality is what I'm all about.\r\n \r\nSo, if you're looking for someone who's hardworking, enthusiastic, and a total team player, look no further! I've got your back and together, we'll make it happen\r\n&quot;}" data-sheets-userformat="{&quot;2&quot;:513,&quot;3&quot;:{&quot;1&quot;:0},&quot;12&quot;:0}">&nbsp;

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Automation Technician

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Automation Technician

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