Staff Automation Controls EngineerLocation:&nbsp;County Clare, IrelandTravel:&nbsp;Up to 25% (Europe)Industry:&nbsp;Life SciencesType:&nbsp;Full-time | On-siteJoin a cutting-edge life sciences team transforming healthcare through innovative automation! We&rsquo;re hiring a&nbsp;Staff Automation Controls Engineer&nbsp;to support high-speed filling and packaging operations at our state-of-the-art facilities in&nbsp;County Clare, Ireland&nbsp;and EuropeAbout the RoleAs a Staff Automation Controls Engineer, you&rsquo;ll lead the&nbsp;design, development, programming, and validation&nbsp;of advanced automation systems. You&rsquo;ll collaborate cross-functionally with Operations, Engineering, and Maintenance teams, as well as external vendors, to deliver robust and compliant equipment solutions &mdash; from concept through commissioning and validation.<ul><li>Lead specification, installation, and validation of automation and control systems.</li><li>Design and program&nbsp;PLC (Rockwell/Siemens), HMI, and&nbsp;SCADA&nbsp;for new and existing lines.</li><li>Implement advanced automation strategies involving&nbsp;motion control, robotics, and&nbsp;vision systems.</li><li>Troubleshoot complex automation challenges and minimize downtime.</li><li>Oversee system integration,&nbsp;IQ/OQ/PQ validation, and ensure regulatory compliance (GMP, FDA, ISO).</li><li>Collaborate with equipment vendors for installations, upgrades, and ongoing support.</li></ul>Required<ul><li>Bachelor&rsquo;s degree in&nbsp;Electrical, Automation, Mechanical Engineering, or related discipline.</li><li>10+ years of automation and controls experience in&nbsp;regulated manufacturing&nbsp;(e.g., medical devices, pharma, biotech).</li><li>Expertise in&nbsp;PLC programming (Rockwell/Siemens)&nbsp;and&nbsp;HMI development.</li><li>Strong background in&nbsp;servo motion, robotics, and vision systems.</li><li>Proven ability to create&nbsp;User Requirement Specifications (URS)&nbsp;and execute validation (IQ, OQ, PQ).</li><li>Excellent troubleshooting, communication, and project management skills.</li><li>Willingness to travel up to&nbsp;25%, supporting our German operations.</li></ul><ul><li>Be part of a high-impact engineering team shaping the future of automated manufacturing.</li><li>Gain international exposure and support strategic projects across Europe.</li><li>Competitive compensation and growth opportunities in a collaborative environment.</li></ul>

Staff Automation Controls Engineer

The Technical Engineer (Electrical) plays a vital role in coordinating, facilitating, and executing maintenance activities, minor repairs, relocations, and logistics. The role ensures compliance with health, safety, security, and environmental (HSSE) standards, as well as adherence to Safe Systems of Work across the managed property portfolio.Key Responsibilities:<ul><li>Escort and brief engineers and supplier maintenance staff as required.</li><li>Contribute to continuous improvement of preventive maintenance programs.</li><li>Maintain effective, asset-specific maintenance and safety procedure manuals, ensuring compliance.</li><li>Coordinate maintenance activities with external contractors, tenant project teams, and internal engineers.</li><li>Assist in overseeing building systems including fire/life safety, plumbing, HVAC, and electrical systems.</li><li>Administer equipment and construction warranties during the defect liability period.</li><li>Respond promptly to emergency situations (e.g., fire, evacuation, equipment failures) and address customer concerns.</li><li>Support engineering and maintenance issues as needed.</li><li>Implement and manage inventory control systems for parts and supplies.</li><li>Ensure compliance with relevant codes, regulations, and directives regarding building operations.</li><li>Conduct routine inspections of mechanical, electrical, and equipment systems; recommend and oversee necessary adjustments.</li><li>Drive improvements in technical service delivery and contribute to a high-quality workplace experience.</li><li>Support utility savings, service enhancements, and operational efficiencies.</li><li>Remain adaptable and responsive to changing client needs.</li></ul>Electrical Duties:<ul><li>Install, maintain, and repair electrical systems, wiring, fixtures, and equipment in compliance with applicable codes and safety standards.</li><li>Diagnose faults using appropriate testing equipment and troubleshooting methods.</li><li>Read and interpret electrical blueprints, schematics, and technical drawings.</li><li>Conduct regular preventive maintenance on electrical systems and components.</li><li>Install lighting systems, power panels, and control systems.</li><li>Test systems for voltage, continuity, and functionality.</li><li>Maintain clear records of all work performed, including materials used and system modifications.</li><li>Respond promptly to electrical emergencies.</li><li>Ensure compliance with local, national, and international electrical standards.</li><li>Recommend energy-efficient solutions and improvements.</li><li>Collaborate with other disciplines on multi-technical projects.</li><li>Keep updated with advancements in electrical technology and safety practices.</li></ul>Skills and Experience:<ul><li>Proven experience in general maintenance, engineering, or handyman-type roles.</li><li>Knowledge of Predictive, Preventive, and Protective Maintenance methodologies.</li><li>Solid understanding of building systems and troubleshooting techniques.</li><li>Ability to onboard, supervise, and assess contractor performance.</li><li>Electrical competency for installation and repairs.</li><li>Strong knowledge of safety and environmental regulations related to equipment and facilities.</li><li>Proficient in computerised systems such as Building Management Systems (BMS) and Computerized Maintenance Management Systems (CMMS).</li></ul>Apply today!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.

Technical Engineer (Electrical)

The Project Engineer is responsible for the safe coordination and execution of projects related to new product introductions, process improvements, automation, aseptic processing, and new processing equipment - along with associated facility and utilities modifications. The primary focus is to ensure that all projects are delivered on time, within budget, and to agreed quality standards. The Project Engineer reports to the Senior Manager of Aseptic Engineering, receiving guidance and support to meet technical and project goals.KEY RESPONSIBILITIES:People &amp; Project Leadership:<ul><li>Lead cross-functional project teams to deliver processing equipment to site per timelines and scope.</li><li>Write User Requirement Specifications (URS).</li><li>Select and evaluate vendors; complete vendor evaluation matrices.</li><li>Manage project lifecycle: write capital requests (RCEs), place orders, lead project meetings, and participate in design reviews.</li><li>Work to ASME BPE 2019 standards and relevant ISPE guidelines.</li><li>Oversee installation and utility hook-up of processing equipment in collaboration with vendors and internal engineering staff.</li><li>Lead Factory Acceptance Testing (FAT) efforts.</li><li>Ensure all equipment documentation is compiled and maintained.</li><li>Support commissioning and assist in qualification activities.</li><li>Coordinate operator training, O&amp;M manuals, spare parts, and preventive maintenance (PM) schedules.</li></ul>Product &amp; Process Improvement:<ul><li>Collaborate in problem-solving forums focused on product manufacturing and aseptic filling.</li><li>Lead and contribute to process improvement and cost-reduction initiatives.</li></ul>Project &amp; Team Communication:<ul><li>Organize and lead regular project review meetings (weekly/bi-weekly).</li><li>Attend Tier 1 meetings with the reporting manager.</li></ul>KEY REQUIREMENTS:Education &amp; Experience:<ul><li>Bachelor's degree (or equivalent) in Engineering or related discipline.</li><li>4+ &nbsp;years of experience in the biologics, pharmaceutical, or medical device industry.</li><li>Demonstrated project engineering &amp; management experience.</li><li>Technically confident self-starter with strong initiative.</li><li>Proven ability to work cross-functionally in team-based environments.</li><li>Strong leadership and interpersonal skills.</li></ul>Technical &amp; Soft Skills:<ul><li>Strong written and verbal communication skills.</li><li>Ability to organise, plan, and allocate resources efficiently.</li><li>Sound decision-making capabilities in team environments.</li><li>Flexibility to adapt in dynamic, fast-paced conditions.</li><li>Results-driven approach with a high level of energy and persistence.</li><li>Open to feedback and receptive to others&rsquo; ideas.</li></ul>Apply today!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.

Project Engineer

An exciting opportunity is available for an experienced Isolator Validation Engineer to join a high-performing team in a dynamic cGMP regulatory environment. This role focuses on the qualification of isolator systems, including Airflow Visualisation, Vaporised Hydrogen Peroxide (VHP), and HVAC components.Key Responsibilities:As an Isolator Validation Engineer, you will:<ul><li>Design, author, review, approve, and execute qualification and validation documentation.</li><li>Develop and execute cycle development studies in alignment with internal approval processes.</li><li>Support and manage change control documentation and execution.</li><li>Troubleshoot and resolve technical issues during validation studies.</li><li>Collaborate closely with Production, Maintenance, and Quality teams during validation activities.</li><li>Provide technical input into deviations and quality investigations.</li><li>Conduct root cause analysis using standard tools and methodologies.</li><li>Apply Lean Six Sigma principles to drive continuous improvement.</li><li>Represent the validation team in cross-functional projects and global forums.</li><li>Ensure compliance with all regulatory requirements, GMP standards, and company procedures.</li><li>Complete risk assessments, address corrective actions, and support inspections and audits.</li><li>Contribute to a culture of safety, compliance, and performance.</li><li>Perform additional duties as required.</li></ul>Required Experience &amp; Skills:To succeed in this role, you should have:<ul><li>Direct experience with Isolator Airflow Visualisation, VHP, and HVAC Qualification.</li><li>Solid background in a GMP-regulated pharmaceutical or biotechnology manufacturing environment.</li><li>Experience in writing and executing validation protocols, reports, and change controls.</li><li>Proven ability to lead validation efforts independently and as part of a team.</li><li>Knowledge of deviation management and CAPA processes.</li><li>Understanding of regulatory standards applicable in Ireland, the EU, and internationally.</li><li>Strong analytical skills, with the ability to interpret complex data and identify trends.</li><li>Proficiency in Microsoft Office and relevant job-related applications.</li><li>Excellent communication, collaboration, and documentation skills.</li></ul>Preferred Qualifications &amp; Skills:The following additional experience is advantageous but not necessary:<ul><li>Filter Validation</li><li>Container Closure Integrity (CCI) Qualification</li><li>Shipping Qualification</li><li>Equipment Lifecycle Validation</li><li>Autoclave / SIP Sterilisation Validation</li><li>Dry Heat Sterilisation</li><li>Cleaning Validation</li><li>Controlled Temperature Equipment Qualification</li><li>Vial and Syringe Processing Technologies</li><li>Knowledge of DeltaV, Pi System, or other automation/data systems</li><li>Project Management skills or certification</li></ul>Education &amp; Qualifications:<ul><li>A relevant technical qualification in Applied Pharmaceutical, Biological, or Chemical Sciences, or Engineering.</li></ul>Apply today!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.

Isolator Validation Engineer

VALIDATION ENGINEER &ndash; CARLOW, IRELAND Location: Carlow, Ireland Job Type: Full-time&nbsp; Senior and P2 Roles available About the Role A leading biopharmaceutical company is seeking a talented Validation Engineer to join their high-performing team in Carlow, Ireland. This is an exciting opportunity to advance your career in a world-class manufacturing environment that is focused on cutting-edge innovation, patient safety, and continuous improvement.The Validation Engineer will be responsible for ensuring all equipment, systems, and processes meet regulatory compliance standards and function as intended. Working cross-functionally with Quality Assurance, Engineering, and Manufacturing teams, the successful candidate will lead and execute validation activities across the site in alignment with GMP, FDA, and EU regulations.Key Responsibilities<ul data-start="1004" data-end="1679"><li data-start="1004" data-end="1125">Develop, review, and execute Validation Protocols (IQ/OQ/PQ) for equipment, facilities, utilities, and processes.</li><li data-start="1126" data-end="1269">Collaborate with cross-functional teams to deliver validation projects on time and in compliance with internal and regulatory requirements.</li><li data-start="1270" data-end="1388">Generate and maintain validation documentation in accordance with site procedures and regulatory expectations.</li><li data-start="1389" data-end="1473">Support investigations and non-conformance reports related to validation issues.</li><li data-start="1474" data-end="1572">Participate in audits and inspections, ensuring validation readiness and robust documentation.</li><li data-start="1573" data-end="1679">Drive continuous improvement initiatives to optimise validation processes and enhance product quality.</li></ul>Candidate Requirements<ul data-start="1710" data-end="2141"><li data-start="1710" data-end="1781">Bachelor&rsquo;s degree in Engineering, Science, or a related discipline.</li><li data-start="1782" data-end="1896">3+ years&rsquo; experience in a regulated manufacturing environment, preferably pharmaceutical or biotechnology.</li><li data-start="1897" data-end="1988">Strong knowledge of GMP, FDA, and EU validation regulations and guidelines.</li><li data-start="1989" data-end="2059">Excellent communication, documentation, and organisational skills.</li><li data-start="2060" data-end="2141">Ability to work effectively both independently and in a team-focused setting.</li></ul>Why Apply?<ul data-start="2160" data-end="2404"><li data-start="2160" data-end="2257">Join a global leader in the life sciences industry with career development opportunities.</li><li data-start="2258" data-end="2337">Be part of a collaborative and dynamic team where innovation is encouraged.</li><li data-start="2338" data-end="2404">Competitive salary and comprehensive benefits package offered.&nbsp; For further information on this role please contact Hannah Talbot&nbsp; Phone:&nbsp;086 107 0950 Email:&nbsp;engineering@hero.ieCheck out all our open jobs on our HERO Recruitment website &ndash;&nbsp;<a href="https://www.hero.ie/">https://www.hero.ie/</a>&nbsp;&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.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. </li></ul>

Validation Engineer 

Project Manager &ndash; MedTech | KildareLocation:&nbsp;Kildare, IrelandIndustry:&nbsp;MedTech / Medical DevicesFunction:&nbsp;Project Management / Engineering / OperationsAre you a dynamic Project Manager ready to lead cutting-edge projects in the MedTech space? Our client, a leading medical technology company based in Kildare, is seeking an experienced&nbsp;Project Manager&nbsp;to drive the successful development, commercialisation, and delivery of new and existing projects across cross-functional teams.Key Responsibilities:<ul><li>Plan, schedule, and manage project activities in alignment with business and quality objectives.</li><li>Lead and coordinate cross-functional project teams, ensuring timely delivery of milestones.</li><li>Develop and maintain strong relationships with stakeholders through structured communication plans.</li><li>Track project progress, costs, and budgets; provide accurate status updates and ensure ROI targets are met.</li><li>Drive compliance with regulatory standards (e.g. GMP, ISO13485) and internal quality management systems.</li><li>Coach and mentor team members on project management best practices.</li><li>Proactively manage project risks, issues, and change requests.</li><li>Conduct post-project reviews and contribute to continuous improvement initiatives.</li><li>Ensure compliance with all company policies, including H&amp;S, financial controls, and QMS requirements.</li></ul>Your Profile:<ul><li>Bachelor&rsquo;s degree (or equivalent) in Engineering, Project Management, or related field;&nbsp;PMP certification preferred.</li><li>Extensive experience managing full project life cycles in a GMP-compliant, high-volume manufacturing environment.</li><li>Proven track record in budget management, process improvement, and project delivery.</li><li>Strong leadership, interpersonal, and stakeholder management skills.</li><li>Excellent communication abilities &ndash; both verbal and written.</li><li>Solid understanding of QMS principles (ISO13485 preferred).</li><li>Proficiency in Microsoft Office, Gantt charts, and other project tracking tools.</li><li>Detail-oriented with excellent analytical and organisational skills.</li><li>Self-motivated team player, capable of managing multiple priorities in a fast-paced setting.</li><li>Flexibility to travel occasionally as required.</li></ul>Why Join Us?<ul><li>Join an innovative MedTech company making a real difference in patient lives.</li><li>Be part of a collaborative, forward-thinking team.</li><li>Gain exposure to global projects and continuous learning opportunities.</li><li>Enjoy a competitive salary and comprehensive benefits package.</li></ul>

Project Manager  - MedTech

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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Staff Automation Controls Engineer

Recruitment Consultant

Staff Automation Controls Engineer

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