R&amp;D Engineer <ul><li>Location: Galway</li><li>Contractor Role</li></ul>We are seeking a skilled Research and Development Engineer with a strong focus on data analytics and statistics to join our team. This position primarily involves desk-based work with a key emphasis on supporting laboratory teams, conducting data analysis, problem-solving, and contributing to the development of a new balloon on a catheter. Some of the Key Responsibilities: <ul><li>You will work collaboratively with manufacturing to ensure alignment between print requirements and process validations.</li><li>Demonstrate design control knowledge through generation of high quality deliverables.</li><li>You will maintain product performance through Quality Investigations and ensuring rigorous support for design changes.</li><li>Perform troubleshooting on products/process problems as related to design, material or process.</li></ul>Your Background:<ul><li>Primary Degree in Biomedical Engineering. Min. FETAC level 8.</li><li>Proven ability to work within a regulated industry environment and with a track record of accomplishments.</li><li>Experience in a post-commercial R&amp;D role is essential (1 year +).</li><li>Experience with post-commercial product support is an advantage.</li><li>Experience with PTA Balloons and/or Self-Expanding Stents is an advantage.</li><li>Familiarity with requirements and procedures that govern medical device Design Control, Risk Management and Post Market Surveillance. Knowledge of EU MDR is an advantage.</li><li>Self-Starter with the ability to work independently to plan, schedule and execute activities necessary to meet project timelines to schedule.</li><li>Excellent interpersonal and communication skills with good leadership abilities.</li><li>Excellent analytical and problem-solving skills.</li></ul> For more information on this role please contact Emma Griffin on 086 0334325/quality@hero.ie Check out all our open jobs on our HERO Recruitment website &ndash; https://www.hero.ie/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 you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

R&D Engineer

Control Systems Engineer (R&amp;D)Our HVAC client in Cork is seeking a Control Systems Engineer with strong software development experience to join our R&amp;D team focused on advanced cooling technologies for data centre applications. You&rsquo;ll work as part of a cross-functional team designing and testing control systems that power our next-generation heat rejection products, including passive and hybrid thermosyphon-based solutions.This role bridges the gap between control theory and real-world application. You&rsquo;ll be hands-on with both software and hardware, helping to develop and implement control logic that is critical to the performance of highly efficient, low-energy cooling systems.Key Responsibilities:<ul><li>Design and develop control logic using Function Block Diagram (FBD) and structured programming methods</li><li>Integrate and test control software on prototype systems in our R&amp;D lab environment</li><li>Collaborate closely with mechanical and electrical engineers to define system behaviour</li><li>Tune and refine control loops (PID, cascaded control, etc.) based on experimental results</li><li>Contribute to test planning and support data acquisition and analysis for control validation</li><li>Assist with documentation, version control, and handover to production where needed</li></ul>What You Bring:<ul><li>Degree in Control Systems, Mechatronics, Software Engineering, or a related field</li><li>3+ years of experience in software development for control systems, ideally in HVAC, refrigeration, or process environments</li><li>Proficiency in Function Block Diagram (FBD) programming</li><li>Understanding of control system fundamentals and real-world system dynamics</li><li>Experience with industrial sensors, PLCs, and automation hardware</li><li>Ability to troubleshoot, iterate, and collaborate in a hands-on lab setting</li></ul>Nice to Have:<ul><li>Familiarity with Carel and/or Automated Logic Controls (ALC) platforms, though not required</li><li>Experience working with industrial protocols (Modbus, BACnet, etc.)</li><li>Background in data centre cooling, refrigeration, or thermal systems</li><li>Experience in R&amp;D or prototype development environments</li></ul>

Control Systems Engineer (R&D)

Project Manager - Automation Our medical device client are looking to hire an automation engineer who has had experience delivering automation projects from generation through to development and implementation. This role will be based on their site in ClonmelJob Description:<ul><li>Design and develop&nbsp;automation systems&nbsp;and processes to improve efficiency and productivity.</li><li>Collaborate with project managers, engineers, and other stakeholders to define project requirements and objectives.</li><li>Create detailed project plans, including timelines, budgets, and&nbsp;resource allocation.</li><li>Conduct feasibility studies and risk assessments for proposed automation solutions.</li><li>Oversee the installation, testing, and commissioning of&nbsp;automation systems.</li><li>Troubleshoot and resolve technical issues related to automation equipment and software.</li><li>Ensure compliance with industry standards, safety regulations, and company policies.</li><li>Provide training and support to end-users on the operation and maintenance of&nbsp;automation systems.</li><li>Prepare&nbsp;technical documentation, including user manuals, maintenance procedures, and project reports.</li><li>Stay updated with the latest advancements in automation technology and industry trends.</li></ul>Qualifications:<ul><li>Bachelor&rsquo;s degree in&nbsp;Electrical Engineering,&nbsp;Mechanical Engineering,&nbsp;Automation Engineering, or a related field.</li><li>Minimum of 5-7 years of experience in&nbsp;automation engineering, with a proven track record of successful automation projects in the medical device industry</li><li>Strong knowledge of&nbsp;automation systems,&nbsp;PLC programming, HMI development, and&nbsp;SCADA&nbsp;systems.</li><li>Proficiency in&nbsp;CAD software&nbsp;and other relevant engineering tools.</li><li>Excellent problem-solving skills and attention to detail.</li><li>Strong communication and interpersonal skills.</li><li>Ability to work independently and as part of a team.</li><li>Project management certification (e.g.,&nbsp;PMP) is a plus.</li></ul>&nbsp;

Project Manager - Automation 

We are seeking an experienced Automation Project Engineer to provide technical leadership and project management across manufacturing operations and new product introductions (NPIs) in a GMP-regulated, pharmaceutical environment. This role will focus on the design, implementation, and lifecycle management of control systems, and requires collaboration across engineering, IT, and quality teams.KEY RESPONSIBILITIES:<ul><li>Provide technical support and lead control system projects for manufacturing and NPIs.</li><li>Drive qualification and validation activities for control systems during project start-up.</li><li>Collaborate with IT to integrate new automation systems into existing network infrastructure.</li><li>Lead control system aspects of capital and continuous improvement projects.</li><li>Develop and manage future control system integrations with MES, ERP, and data historian platforms (e.g., OSI PI).</li><li>Ensure lifecycle compliance of control systems with internal procedures and regulatory standards.</li><li>Troubleshoot, optimize, and maintain control systems, ensuring proper documentation and system integrity.</li><li>Identify vendor improvement opportunities, support vendor qualification, and review technical documentation.</li><li>Comply with EHS policies and promote best safety practices on-site.</li></ul>QUALIFICATIONS &amp; EXPERIENCE:<ul><li>NFQ Level 8 Bachelor&rsquo;s Degree or Higher Diploma in a relevant engineering discipline.</li><li>2+ years of automation experience in a pharmaceutical or medical device environment.</li><li>Proficient in PLC, HMI, and SCADA system development within GMP settings.</li><li>Strong understanding of 21 CFR Part 11 compliance requirements.</li><li>Demonstrated experience with plant start-ups and NPIs in regulated industries.</li><li>Proven capability in the qualification and validation of control systems.</li><li>Familiarity with internal auditing and inspection processes is an advantage.</li></ul>&nbsp;KEY COMPETENCIES:<ul><li>Strong analytical and problem-solving skills with a structured approach to issue resolution.</li><li>Innovative thinker with a proactive mindset for identifying and implementing new solutions.</li><li>High attention to detail and strong commitment to quality and compliance.</li><li>Excellent written and verbal communication skills</li><li>Strong interpersonal skills and the ability to collaborate across functions.</li><li>Self-starter with a results-driven attitude and ability to work independently.</li><li>Demonstrates integrity, professionalism, and a high standard of work.</li></ul>Our Vision:&nbsp;To be recognised as the best STEM Contracting &amp; Permanent Recruitment company and the Employer of Choice for top performing Recruiters For further information on this role please contact&nbsp;R&oacute;is&iacute;n Vaughan&nbsp;on&nbsp;086 440 3742 /&#8239;consult@hero.ie Check out all our open jobs on our HERO Recruitment website -&nbsp;<a href="https://hero.ie/">HERO Recruitment: Leading STEM Recruitment Agency</a>&#8239; 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 your data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel. Apply Now <a href="https://hero.ie/jobs/?sector=c2ce20a6-e260-445c-87b5-fdd10b9592e8&amp;role_type=0b03e526-12a7-4e6f-ad0b-71db88f03371">Share Jobs</a>

Automation Project Engineer

Technical Operations Specialist - Vaccines IPT Location: Cork | Department: Vaccines IPT An exciting opportunity has become available for a Technical Specialist &ndash; Operations to join the Vaccines IPT team for an 11-month contract. This role is ideal for someone passionate about biopharmaceutical innovation and process excellence, with strong technical expertise in vaccine manufacturing. As a Technical Specialist, you will play a critical role in supporting operations, driving technical investigations, and leading continuous improvement initiatives across the site. KEY RESPONSIBILITIES: As a Technical Specialist, you will bring energy, technical acumen, and leadership to:<ul><li>Provide day-to-day technical support for vaccine manufacturing processes.</li><li>Troubleshoot process-related issues and lead root cause investigations using structured problem-solving tools (DMAIC, A3, OPPS).</li><li>Lead and support cross-functional technical projects to enhance process performance and robustness.</li><li>Manage and coach on EHS and quality investigations; review and oversee batch records.</li><li>Act as a site point of contact for compliance initiatives related to Vaxneuvance.</li><li>Drive process improvements using Lean Six Sigma and other lean methodologies.</li><li>Support material management, with a focus on cost efficiency and supply continuity.</li><li>Represent the Vaccines IPT team on cross-functional site projects.</li><li>Ensure strict adherence to compliance, quality, and safety standards in line with the site's Quality Management System (QMS).</li></ul> QUALIFICATIONS AND EXPERIENCE: To succeed in this role, you will ideally have:<ul><li>An Honours Degree or Master&rsquo;s in Science or Engineering (preferably in Biotechnology).</li><li>4+ years of experience in a biopharmaceutical or vaccine manufacturing environment.</li><li>Expertise in drug substance manufacturing processes such as UF/DF, lyophilisation, bottle filling, and PAT.</li><li>Hands-on experience with single-use technologies, including troubleshooting and vendor interaction.</li><li>Proven track record in leading or contributing to cross-functional technical teams.</li><li>Familiarity with material management systems and cost optimization.</li><li>Solid understanding of FDA/HPRA regulations and quality standards in the pharmaceutical sector.</li><li>Strong problem-solving skills and the ability to apply existing knowledge creatively to complex challenges.</li><li>Excellent interpersonal and stakeholder management skills across diverse teams.</li><li>Demonstrated independence in decision-making and project execution.</li></ul>

Technical Operations Specialist - Vaccines

Maintenance Supervisor - Tipperary&nbsp;Our client is a global healthcare leader with a portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices,&#8239;nutritional&#8239;and branded generic medicines. They are looking for a Maintenance Supervisor who manages the activities, manpower and resources within their Maintenance area to ensure support is provided to meet the department and company goals.Main Responsibilities&#8239;:<ul><li>Supervises the activities, manpower and resources within the Maintenance area to ensure support is provided to meet the department and company goals.</li><li>Manages a Team of 10 experienced technicians across a 3-shift cycle</li><li>Responds to complaints on equipment, work orders, equipment availability and downtime due to equipment issues, plans and implements projects and processes needed to ensure equipment availability runs to agreed target, and that supplies, and spare parts are kept to agreed levels</li><li>Co-ordinates with engineers to facilitate research, development and/or product and process improvements and enhancements to support business needs.</li><li>Implements policies and procedures to maintain production equipment compliance and financial compliance.</li></ul>Ideally you will have:&nbsp;<ul><li>Bachelor's degree, preferably in Manufacturing/Engineering/Science (NFQ) level 7 qualification in a relevant discipline</li><li>4+ years of related work experience, or an equivalent combination of education and work experience. Maintenance leadership experience (people &amp; equipment management)</li><li>Strong understanding of high-precision, non-automated manufacturing equipment</li><li>Mechanical or electrical background &ndash; no requirement to be a certified electrician/fitter</li><li>Automation experience desirable</li><li>Experience with Maximo (Maintenance Management System) is a plus</li><li>Must be strategic-minded and comfortable with a planned, structured maintenance environment</li><li>Used to working with high standards (e.g., 99.9% uptime)</li></ul>For more on this contact Regina at HERO 086 0100903 or jobs@hero.ieCheck out all our open jobs on our HERO Recruitment website &ndash; <a href="https://www.hero.ie/">https://www.hero.ie/</a>&nbsp;Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval&nbsp;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. &nbsp;You have supplied us with your personal data in the process of applying for a position. &nbsp;Our client company may have personnel outside of the EEA who will review you data. &nbsp;We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

Maintenance Supervisor 

Hey there! As an experienced recruitment consultant with a solid track record in the industry. I've got the skills and expertise to make those perfect connections. My experience spans various industries, such as medical devices, pharmaceuticals, Fintech, Medtech, IT, and automotive. Talk about a wide range! My passion for learning knows no bounds. I'm always seeking new knowledge and continuously studying to stay ahead of the game. Because let's face it, staying up-to-date is crucial in this fast-paced world.
As someone who values hard work, I understand the importance of finding a place that respects not only your professional expertise but also who you are as a person. It's all about finding that perfect match where you feel valued and appreciated.
Outside of work I love music and festivals. You might be wondering how that ties into my recruitment work, but here's the thing&mdash;music and festivals are all about creating incredible experiences, bringing people together, and fostering a sense of community. These values align perfectly with my approach to recruitment. I believe in creating meaningful connections, understanding the unique qualities and passions of candidates, and finding the perfect fit where they can thrive and contribute.
If you have any questions about the roles I'm advertising or need assistance with your hiring needs, don't hesitate to reach out. I'm here to guide you, connect the dots, and make your recruitment journey smooth and successful.

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Control Systems Engineer (R&D)

Recruitment Consultant

Control Systems Engineer (R&D)

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