Facilities Technician (Electrical)&nbsp;We are seeking an experienced Facilities Technician (Electrical) to maintain and operate plant, utilities, and equipment, ensuring smooth and safe operations at our Kilkenny site. This role is ideal for a proactive professional with strong technical expertise and a commitment to maintaining high operational standards.<h3>Key Responsibilities</h3><ul data-spread="false"><li>Perform maintenance, repairs, and troubleshooting of plant equipment.</li><li>Respond to helpdesk requests and conduct daily equipment checks.</li><li>Coordinate and oversee external contractors performing maintenance work.</li><li>Ensure all equipment operates safely and meets regulatory standards.</li><li>Maintain compliance with EHS laws and technical guidelines.</li><li>Support operations by resolving technical issues efficiently.</li></ul><h3>Person Specification</h3><ul data-spread="false"><li>Experience working with plant equipment such as boilers, chillers, HVAC, and water systems.</li><li>Strong problem-solving skills and the ability to troubleshoot technical issues effectively.</li><li>Excellent communication and customer service skills.</li><li>Proactive and detail-oriented approach to work.</li></ul><h3>Qualifications &amp; Experience</h3><ul data-spread="false"><li>Engineering qualification or Level 6 trade certification.</li><li>Experience in medical, pharmaceutical, or production environments preferred.</li><li>Knowledge of Maximo and a GMP background is an advantage.</li></ul>For further information on this role in please contact on Gavin Moran on 087 4108620 or <a href="mailto:connect@hero.ie">connect@hero.ie</a> 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

Facilities Technician - Electrical 

Facilities Technician (Mechanical)We are seeking an experienced Facilities Technician (Mechanical) to maintain and operate plant, utilities, and equipment, ensuring smooth and safe operations at our Kilkenny site. This role is ideal for a proactive professional with strong technical expertise and a commitment to maintaining high operational standards.<h3>Key Responsibilities</h3><ul data-spread="false"><li>Perform maintenance, repairs, and troubleshooting of plant equipment.</li><li>Respond to helpdesk requests and conduct daily equipment checks.</li><li>Coordinate and oversee external contractors performing maintenance work.</li><li>Ensure all equipment operates safely and meets regulatory standards.</li><li>Maintain compliance with EHS laws and technical guidelines.</li><li>Support operations by resolving technical issues efficiently.</li></ul><h3>Person Specification</h3><ul data-spread="false"><li>Experience working with plant equipment such as boilers, chillers, HVAC, and water systems.</li><li>Strong problem-solving skills and the ability to troubleshoot technical issues effectively.</li><li>Excellent communication and customer service skills.</li><li>Proactive and detail-oriented approach to work.</li></ul><h3>Qualifications &amp; Experience</h3><ul data-spread="false"><li>Engineering qualification or Level 6 trade certification.</li><li>Experience in medical, pharmaceutical, or production environments preferred.</li><li>Knowledge of Maximo and a GMP background is an advantage </li></ul>

Facilities Technician - Mechanical 

Facilities ManagerWe are seeking a highly motivated Facilities Manager to oversee operations at our Ballyogan site while also managing other contracts and remote sites. This role offers a dynamic opportunity to lead facility services, ensure seamless operations, and maintain strong client relationships. The ideal candidate will be responsible for planned preventative maintenance, security, caretaking, and cleaning services, ensuring all functions run smoothly and efficiently.<h3>Key Responsibilities</h3><ul data-spread="false"><li>Oversee all aspects of the contract, ensuring service delivery meets expectations and remains within budget.</li><li>Ensure the Planned Preventative Maintenance (PPM) plan is executed in accordance with the contract.</li><li>Manage contract budgets, attend commercial meetings, and oversee financial planning across multiple sites.</li><li>Provide leadership and guidance to Facilities Managers at remote sites.</li><li>Drive service excellence, ensuring compliance with industry regulations and company quality standards.</li><li>Monitor and control costs, ensuring all expenditures remain within budget.</li><li>Ensure Service Level Agreements (SLAs) are met across all contracts.</li><li>Manage utility billing, liaising with tenants/clients regarding usage and costs.</li><li>Review and manage Work in Progress (WIP) and aged debt reports, ensuring timely clearance.</li><li>Oversee statutory inspections and ensure compliance with health, safety, and quality standards.</li><li>Develop and implement strategies for continuous improvement and cost-effective service delivery.</li><li>Manage security, cleaning, and caretaking teams, ensuring smooth daily operations.</li><li>Act as the primary point of contact for on-site tenants, providing guidance and support.</li><li>Lead and oversee projects and additional works, liaising with stakeholders as needed.</li><li>Promote environmental and waste management best practices.</li><li>Ensure safe systems of work are in place and adhered to across all sites.</li><li>Coordinate and manage contractors, ensuring compliance with all necessary documentation.</li><li>Support the company&rsquo;s security function when required.</li></ul><h3>Qualifications &amp; Experience</h3><ul data-spread="false"><li>Proven experience in site or facilities management.</li><li>Strong financial and budgetary management skills.</li><li>Excellent computer literacy and proficiency in relevant software.</li><li>Experience in project management and team leadership.</li><li>Strong problem-solving and decision-making abilities.</li><li>Ability to foster a customer-focused, solution-driven approach.</li><li>Excellent communication and people management skills.</li><li>Self-motivated with the ability to motivate and manage others.</li><li>Flexible, proactive, and committed to continuous improvement.</li></ul><h3>Why Join Us?</h3>We pride ourselves on delivering excellence in facility management. This role offers a fantastic opportunity for a proactive professional to take ownership of a key site while also influencing operations across multiple locations. If you thrive in a fast-paced environment and are passionate about delivering high-quality facility services, we&rsquo;d love to hear from you!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

Facilities Manager

Reliability Engineer &ndash; Drive Excellence and Innovation in Equipment Performance! Job Type: Contract Location: Westport, Mayo, Ireland. Industry: Biopharmaceutical The Reliability Engineer is responsible for leading continuous improvement initiatives to minimise risks related to equipment and utility issues on-site. The role ensures compliance with engineering standards and supports the Maintenance Excellence Program (MEP) by optimising critical equipment assets and driving ongoing improvements. <h4 class="" data-start="1366" data-end="1397">KEY RESPONSIBILITIES </h4><ul><li class="" data-start="86" data-end="164">Integrate the Maintenance Excellence Program (MEP) into company culture.</li><li class="" data-start="165" data-end="240">Develop programs and procedures for compliant maintenance activities.</li><li class="" data-start="241" data-end="305">Monitor and optimize equipment and system performance.</li><li class="" data-start="306" data-end="398">Analyze and improve key MEP KPIs (e.g., asset utilisation, maintenance costs).</li><li class="" data-start="399" data-end="478">Prevent and reduce system failures using best practices and technologies.</li><li class="" data-start="479" data-end="555">Implement predictive maintenance and optimize preventive measures.</li><li class="" data-start="556" data-end="655">Lead root cause failure analysis (RCFA), RCM, FMEA, FTA, and PM optimisation.</li><li class="" data-start="656" data-end="738">Train employees on reliability processes and supervisor impact on equipment.</li><li class="" data-start="739" data-end="811">Review work orders and promote ongoing preventive maintenance.</li><li class="" data-start="812" data-end="873">Analyze failure history to develop long-term solutions.</li><li class="" data-start="874" data-end="956">Ensure reliability and maintainability specifications for new equipment.</li><li class="" data-start="957" data-end="1044">Conduct internal and external audits, ensuring safety and compliance.</li><li class="" data-start="1045" data-end="1120">Utilise Maximo and manage the Engineering Change Control process.</li><li class="" data-start="1121" data-end="1175">Collaborate and share expertise within the team.</li></ul><h4 class="" data-start="1366" data-end="1397"> KEY REQUIREMENTS </h4><ul><li>Third-level qualification&nbsp;in&nbsp;Engineering&nbsp;or relevant discipline, or&nbsp;Trade qualification&nbsp;with 6+ years of experience.&nbsp;</li><li>Minimum 3 years of relevant experience, with strong&nbsp;IT skills&nbsp;(Maximo&nbsp;preferred).&nbsp;</li><li>Proven&nbsp;problem-solving skills&nbsp;under pressure and&nbsp;innovative thinking.&nbsp;</li><li>Strong&nbsp;attention to detail, with a&nbsp;results-driven&nbsp;mindset.&nbsp;</li><li>Excellent&nbsp;communication&nbsp;and&nbsp;interpersonal skills&nbsp;for cross-functional collaboration.&nbsp;</li><li>Ability to work&nbsp;autonomously&nbsp;and adhere to "Right First Time" principles.&nbsp;</li><li>Knowledge of&nbsp;cGMP,&nbsp;FDA/HPRA regulations, and&nbsp;regulatory compliance&nbsp;</li><li>Leadership skills&nbsp;for managing&nbsp;projects,&nbsp;teams, and&nbsp;cost improvements.&nbsp;</li></ul> Ready to make an impact? Join our team and help drive excellence in equipment reliability and performance. Apply today and be part of our innovative journey! 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.

Reliability Engineer

Job Title:&nbsp;Chemist Work Type:&nbsp;Contract Location:&nbsp;Limerick Role Overview:&nbsp;This is an exciting opportunity for a skilled Chemist to take on a key role in supporting the development of combination drug devices. The successful candidate will oversee process development, validation, and regulatory compliance, ensuring the highest standards in chemistry, manufacturing, and controls (CMC). This position is ideal for those looking to make an impact in the pharmaceutical and medical device industries while working in a collaborative, innovative, and supportive environment.&nbsp; <h3 class="" data-start="636" data-end="666">Key Responsibilities</h3><ul data-start="667" data-end="2182"><li class="" data-start="667" data-end="841">Support New Product Introduction: Assist in assessing and implementing proposed manufacturing processes, offering guidance throughout product development and changes.</li><li class="" data-start="842" data-end="995">Collaboration Across Functions: Work closely with R&amp;D, Production, Quality, and Regulatory teams to ensure the smooth implementation of projects.</li><li class="" data-start="996" data-end="1163">Data and Report Review: Technically review data and reports (e.g., stability data, lot release data) for accuracy and consistency with regulatory expectations.</li><li class="" data-start="1164" data-end="1320">CMC Expertise: Provide specialist knowledge in CMC, supporting the selection, qualification, and auditing of contract manufacturers and API vendors.</li><li class="" data-start="1321" data-end="1493">Regulatory Strategy: Contribute to the development of CMC strategies for global regulatory submissions and interact with global teams to implement these strategies.</li><li class="" data-start="1494" data-end="1633">Compliance with Global Standards: Maintain high-level expertise in FDA, US Pharmacopeia, European Pharmacopeia, and ICH guidelines.</li><li class="" data-start="1634" data-end="1777">Investigation and Root Cause Analysis: Support OOS investigations, ensuring consistency with methodologies and regulatory expectations.</li><li class="" data-start="1778" data-end="1933">Cross-functional Interaction: Work with Post Market and Manufacturing Engineering teams to achieve objectives and ensure smooth project completion.</li><li class="" data-start="1934" data-end="2039">Reporting: Provide regular updates to the Engineering management team on progress and activities.</li><li class="" data-start="2040" data-end="2182">Compliance and Quality: Ensure all activities align with Cook&rsquo;s Code of Conduct, Quality System requirements, and Company HR policies.</li></ul><h3 class="" data-start="2184" data-end="2225">Qualifications and Requirements</h3><ul data-start="2226" data-end="3017"><li class="" data-start="2226" data-end="2335">Education: Bachelor&rsquo;s degree (Master&rsquo;s or PhD preferred) in Engineering, Science, or a related field.</li><li class="" data-start="2336" data-end="2458">Experience: A minimum of 3 years&rsquo; relevant experience in CMC within the pharmaceutical or medical device industry.</li><li class="" data-start="2459" data-end="2645">Knowledge: Strong understanding of medical device quality standards (ISO 13485, FDA practices), GMP, GLP, and relevant regulatory guidelines (FDA, US/European Pharmacopeia, ICH).</li><li class="" data-start="2646" data-end="2780">Skills: Excellent problem-solving, analytical, and interpersonal skills with the ability to work effectively across functions.</li><li class="" data-start="2781" data-end="2882">Technical Expertise: Familiarity with statistical methods, data analysis, and interpretation.</li><li class="" data-start="2883" data-end="2948">Software Skills: Proficient in Microsoft Office software.</li><li class="" data-start="2949" data-end="3017">Travel: Willingness to travel on company business as needed. Limerick, IrelandLimerick, Ireland, offers an excellent quality of life, blending rich history, scenic landscapes, and a thriving business environment, making it an ideal place to live and work. <div><div class="py-5 container"><div class="mx-3 mx-md-0"><div class="styles_description__GuR03 px-3 px-md-0">Our Vision: 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 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.</div><div class="flex-xl-row flex-wrap d-flex justify-content-center vstack gap-3"><button class="btn btn-dark" type="button">Apply Now</button><a class="py-1 btn btn-outline-dark" tabindex="0" role="button" href="https://www.hero.ie/jobs/?sector=ce7b03ff-2643-4cf8-9a78-4840ac5202a8&amp;role_type=0b03e526-12a7-4e6f-ad0b-71db88f03371">Share Jobs</a></div></div></div></div><div><div><div class="styles_root__6iuYk px-3 px-md-0 pt-4 pb-3 py-md-5"><div class="container"><div class="text-md-center mb-3 mb-md-5">&nbsp;</div></div></div></div></div>&nbsp;&nbsp;</li></ul>

Chemist

Process Engineer III - Lead the Expansion of Cutting-Edge Vaccine Manufacturing! A leading biopharmaceutical company is seeking a Process Engineer III to provide process engineering services in support of the design, commissioning, and qualification of an expansion to an existing bulk vaccine processing facility. The Process Engineer III will work closely with the process engineering team as a client owner representative to deliver the project objectives.This role involves leading cross-functional teams to manage the following:<ul><li>Equipment package design, factory acceptance testing, installation, and commissioning</li><li>Equipment packages may include Product Vessels, Single Use Mixers, Single Use UFDF skids, and CIP/SIP skids.</li></ul>Located in Brinny, Cork a thriving town known for its scenic landscapes, and welcoming community, this position provides an excellent environment for professional and personal growth. <h4 class="" data-start="1366" data-end="1397">KEY RESPONSIBILITIES </h4><ul><li>Support the process lead to implement process design based on project scope and requirements.</li><li>Lead and manage cross-functional project teams to ensure project goals are met and stakeholders' requirements are reflected in C&amp;Q (Commissioning &amp; Qualification) deliverables.</li><li>Ensure all project stakeholders are informed and consulted on key process activities and decisions.</li><li>Monitor progress, milestones, and provide regular status updates to project tiers and stakeholders.</li><li>Oversee C&amp;Q progression in collaboration with partner firms.</li><li>Ensure adherence to engineering standards, procedures, and best practices.</li><li>Support and, at times, lead the preparation and execution of C&amp;Q field activities.</li><li>Develop and/or review system lifecycle documents, including Criticality and Risk assessments, FAT (Factory Acceptance Testing) documentation, and C&amp;Q documentation.</li><li>Manage installation, startup, and testing of process systems through OQ (Operational Qualification) completion. Interface with cross-functional teams to ensure readiness for systems post-OQ (e.g., PQ, PPQ).</li><li>Liaise with stakeholders, equipment vendors, business partners, and subject matter experts at other facilities as required.</li><li>Prepare project-related deliverables, including schedules, work plans, and equipment cost tracking.</li><li>Coordinate project activities and ensure smooth collaboration between various stakeholders.</li></ul><h4 class="" data-start="1366" data-end="1397">KEY REQUIREMENTS</h4><ul><li>Minimum qualification: B.Sc., M.Sc., or M.Eng degree in Chemical Engineering, Biochemical Engineering, or a related field (e.g., Biotechnology or Industrial Chemistry)</li><li>5 - 8 years experience in biopharmaceutical process engineering, specifically in the design, construction, and startup of relevant facilities.</li><li>Demonstrated ability to lead and influence teams in a matrix team environment.</li><li>Excellent communication, presentation, and organizational skills.</li><li>In-depth understanding of process engineering and technologies specific to bulk vaccine or biologics processing facilities.</li><li>Knowledge and experience in applying single-use technologies in biopharmaceutical manufacturing.</li><li>Familiarity with DCS/PLC process control platforms and industry SDLC methodologies such as Delta V.</li><li>Proven ability to coordinate large-scale projects and ensure they are completed on time and within budget.</li></ul> Our Vision: 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 R&oacute;is&iacute;n Vaughan on 086 440 3742 /&#8239;consult@hero.ie Check out all our open jobs on our HERO Recruitment website - <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.

Process Engineer III

Exciting Project Engineer III Opportunity - Westport, Mayo! We are seeking a skilled and motivated Project Engineer to join our client's&nbsp; dynamic Engineering &amp; Technology team. In this role, you will lead and manage critical projects related to process improvements, automation, aseptic processing, and the introduction of new processing equipment. You will also be involved in facility and utility modifications to support the integration of these systems. Your primary responsibility will be to ensure that projects are executed efficiently, meeting all objectives within the agreed timelines and budget. You will work closely with a variety of cross-functional teams to deliver results, reporting directly to the Senior Manager of Engineering.Key Responsibilities:Project Leadership<ul><li>Lead and coordinate cross-functional teams to deliver processing equipment, ensuring projects are completed within scope, timeline, and budget. Equipment includes packaging, inspection, assembly equipment, autoclaves, RABS, Isolator filling machines, LAF units, compounding skids, and vessels.</li><li>Develop, review, and manage User Requirement Specifications (URS).</li><li>Perform vendor selection and evaluation, managing the entire vendor relationship.</li><li>Prepare and review RCEs, manage orders, and facilitate design review and project management meetings.</li><li>Ensure compliance with industry standards (ASME BPE 2019, ISPE guidelines, etc.) throughout the project lifecycle.</li><li>Manage the installation of processing equipment and oversee the connection of services, working closely with equipment vendors and internal engineering teams.</li><li>Lead the Factory Acceptance Testing (FAT) process and coordinate all necessary documentation.</li><li>Support commissioning and qualification activities, collaborating with cross-functional teams to ensure the project&rsquo;s success.</li><li>Oversee handover procedures, including training, O&amp;M manuals, spare parts, and preventive maintenance schedules.</li></ul>Product Development &amp; Process Improvements:<ul><li>Actively contribute to technical problem-solving in the areas of product manufacturing and aseptic filling.</li><li>Identify and drive process improvement initiatives and cost reduction projects.</li></ul>Meetings &amp; Reporting:<ul><li>Lead regular project review meetings with your project team to track progress and address any concerns.</li><li>Participate in bi-weekly Engineering &amp; Technology Tier 2 meetings with the Senior Manager of Engineering.</li></ul>Education &amp; Experience:<ul><li>Bachelor&rsquo;s degree in Engineering or related discipline (or equivalent experience).</li><li>Minimum of 2-5 years&rsquo; experience working in the Biologics, Pharmaceutical, or Medical Device industry.</li><li>Proven track record in project management, with demonstrable success in delivering complex projects on time and within budget.</li><li>Strong technical background with the ability to work independently and collaborate effectively with cross-functional teams.</li><li>Excellent communication and interpersonal skills, with the ability to work in a multi-functional team environment.</li></ul>Key Skills &amp; Competencies:<ul><li>Strong leadership skills with the ability to motivate and guide team members.</li><li>Problem-solving and decision-making abilities, with a focus on practical and efficient solutions.</li><li>Well-organized, able to plan and prioritize tasks effectively.</li><li>Ability to adapt to a fast-paced, changing environment while meeting deadlines.</li><li>High level of energy and passion for delivering results.</li><li>Open to receiving and acting on constructive feedback.</li><li>Ability to build strong working relationships with stakeholders at all levels.</li></ul>Additional Information:Occasional travel (up to 4 times per year) may be required for design review meetings, build inspections, Factory Acceptance Tests (FAT), etc.This is an onsite role based in Westport.If you're passionate about working in a collaborative environment and leading impactful projects in aseptic processing and automation, we'd love to hear from you! Apply below or contact R&oacute;is&iacute;n Vaughan at 086 440 3742.

Project Engineer III

Job Title:&nbsp;Project Engineer Work Type:&nbsp;Contract Location:&nbsp;Dublin Role Overview: Are you a talented Project Engineer looking to make an impact in an innovative and dynamic environment? This role offers an exciting opportunity to lead and manage capital and expense projects that involve the implementation, installation, commissioning, and qualification of new facilities, utilities, and manufacturing equipment. As a Project Engineer, you will play a pivotal role in coordinating and executing projects while ensuring compliance with all safety, regulatory, and quality standards. This is a fantastic opportunity for an individual seeking to work in a supportive, collaborative, and forward-thinking team environment.<article class="w-full text-token-text-primary" dir="auto" data-testid="conversation-turn-12" data-scroll-anchor="true"><div class="text-base my-auto mx-auto py-5 px-6"><div class="mx-auto flex flex-1 text-base gap-4 md:gap-5 lg:gap-6 md:max-w-3xl group/turn-messages focus-visible:outline-none" tabindex="-1"><div class="group/conversation-turn relative flex w-full min-w-0 flex-col agent-turn @xs/thread:px-0 @sm/thread:px-1.5 @md/thread:px-4"><div class="relative flex-col gap-1 md:gap-3"><div class="flex max-w-full flex-col flex-grow"><div class="min-h-8 text-message relative flex w-full flex-col items-end gap-2 whitespace-normal break-words text-start [.text-message+&amp;]:mt-5" dir="auto" data-message-author-role="assistant" data-message-id="dae92040-0cc9-4d11-95dc-5fd38c978846" data-message-model-slug="gpt-4o-mini"><div class="flex w-full flex-col gap-1 empty:hidden first:pt-[3px]"><div class="markdown prose w-full break-words dark:prose-invert light">Key Responsibilities: Project Development &amp; Execution<ul data-start="762" data-end="1024"><li class="" data-start="762" data-end="911">Manage the full lifecycle of projects from planning to execution, including change control, and coordination of both internal and external teams.</li><li class="" data-start="912" data-end="1024">Ensure projects are completed on time, within budget, and in line with all safety and regulatory requirements.</li></ul>&nbsp;Process &amp; Equipment Reviews<ul data-start="1063" data-end="1228"><li class="" data-start="1063" data-end="1228">Conduct thorough reviews of processes and equipment, preparing detailed technical reports and recommending improvements for quality enhancement and cost reduction.</li></ul>Specifications &amp; Design<ul data-start="1263" data-end="1461"><li class="" data-start="1263" data-end="1461">Develop comprehensive user requirement specifications, technical specifications, and design specifications for new or upgraded equipment, ensuring optimal design concepts and technology selection. &nbsp;Equipment Qualification</li></ul><ul data-start="1496" data-end="1609"><li class="" data-start="1496" data-end="1609">Plan and execute equipment qualification protocols (IQ/OQ) to ensure full compliance and operational readiness.</li></ul>Cross-Functional Collaboration<ul data-start="1651" data-end="1817"><li class="" data-start="1651" data-end="1817">Work closely with departments such as operations, maintenance, quality assurance, and EHS to minimise disruptions to ongoing production while meeting project goals.</li></ul>Compliance &amp; Safety<ul data-start="1848" data-end="1998"><li class="" data-start="1848" data-end="1998">Observe and adhere to all safety procedures and actively identify opportunities for improving safety practices, reducing incidents or near-misses.</li></ul>Reporting &amp; Continuous Improvement<ul data-start="2044" data-end="2186"><li class="" data-start="2044" data-end="2186">Provide regular updates on project progress and challenges, ensuring all issues are addressed according to established escalation processes.</li></ul>&nbsp;Travel &amp; Equipment Selection<ul data-start="2226" data-end="2391"><li class="" data-start="2226" data-end="2391">Travel as required for equipment selection and participation in Factory Acceptance Tests (FATs), ensuring that chosen equipment meets all necessary specifications. </li></ul>Requirements:<ul><li>&nbsp;Bachelors Degree in Engineering or equivalent combination of education and work experiences required.</li><li>3-5 years related experience and nor training; or equivalent combination of education and experience.</li><li>Experience in pharmaceutical manufacturing and packaging equipment and/or pharmaceutical processing equipment design, evaluation, and specification is an advantage.</li><li>Detailed understanding of P&amp;IDs, process flow diagrams, and all related pharmaceutical commissioning and qualification documentation.</li><li>Experience working with pharmaceutical processing technologies and good understanding of 2ICFR cGMP documentation and electronic systems requirements.</li><li>&nbsp;Demonstrated experience applying sound engineering principals and critical reasoning to troubleshoot complex process and engineering challenges.</li><li>&nbsp;Proficiency of computer skills with Microsoft Word, Excel, Outlook, CAD.</li></ul> Why Dublin? Dublin is a city known for its welcoming community, vibrant cultural scene, and high quality of life. Enjoy a mix of urban energy and beautiful natural surroundings, with access to excellent public services, recreational spaces, and a thriving economy.<hr class="" data-start="2939" data-end="2942">This role offers an exciting opportunity for an experienced Project Engineer who is eager to make an impact. If you&rsquo;re passionate about engineering, project management, and working in a fast-paced environment, apply today to join this dynamic team.</div></div></div></div><div class="flex justify-start"><div class="-me-1 -ms-2.5 flex select-none items-center p-1 touch:-me-2 touch:-ms-3.5 -mt-1 duration-[1.5s] focus-within:transition-none hover:transition-none pointer-events-none [mask-image:linear-gradient(to_right,black_33%,transparent_66%)] [mask-position:100%_0%] [mask-size:300%_100%] motion-safe:transition-[mask-position] group-hover/turn-messages:pointer-events-auto group-hover/turn-messages:[mask-position:0_0] group-focus-within/turn-messages:pointer-events-auto group-focus-within/turn-messages:[mask-position:0_0] has-[[data-state=open]]:pointer-events-auto has-[[data-state=open]]:[mask-position:0_0]">&nbsp;</div></div></div><div class="absolute"><div class="flex items-center justify-center">&nbsp;</div></div></div></div></div></article><div class="pointer-events-none h-px w-px" aria-hidden="true" data-edge="true">&nbsp;</div>

Project Engineer

Our medical device client is hiring a Line Support Technician to join their Operations Team in Galway. In this hands-on role, you'll play a key part in optimizing production performance, improving processes, and ensuring top-quality standards in a fast-paced medical device manufacturing environment.<h3 class="" data-start="402" data-end="427">What You'll Do:</h3>&#9989; Monitor and maintain line performance to maximize efficiency &#9989; Implement daily process improvements (Kaizen mindset) &#9989; Train and upskill operators to the highest quality standards &#9989; Conduct audits to ensure compliance with GMP &amp; EH&amp;S &#9989; Work with Engineering &amp; Production teams on new product introductions<h3 class="" data-start="767" data-end="791">What You Need:</h3>&#55357;&#56633; Experience in medical device manufacturing (cleanroom environment) &#55357;&#56633; Knowledge of &nbsp;catheters and stents &#55357;&#56633; Strong problem-solving &amp; organizational skills &#55357;&#56633; Proficiency in Microsoft Office (Word, Excel, PowerPoint) &#55357;&#56633; Commitment to quality, safety, and continuous improvement<h3 class="" data-start="1103" data-end="1125">Why Join Us?</h3>&#55357;&#56481; Competitive Salary &amp; Benefits Package &#55356;&#57317; Healthcare &amp; Dental Plan &#55357;&#56496; Pension &amp; Life Assurance &#55357;&#56538; Learning &amp; Development Support &#55356;&#57291;&#65039; Corporate Discounts, Social Club &amp; Wellbeing Events &#55357;&#57010; Bike-to-Work Scheme &amp; Free ParkingIf you&rsquo;re ready to take your career to the next level in a dynamic, innovative environment, apply today!

Line Support Technician

JOB DESCRIPTIONROLE TITLE: EHS SPECIALIST/ ADVISORPOSITION SUMMARY:Provide EH&amp;S support for major projects at the Cork site with a focus on EH&amp;S by Design. As a member of the site EH&amp;S Projects team, you will act as an SME and advisor to selected project teams in relation to EHS legislation, J&amp;J EH&amp;S Standards, relevant engineering standards &amp; industry norms.Mainly onsite, minimal WFH (1 day a week)Need a technical tertiary and EHS experience (not construction safety) in a regulated manufacturing environment, ideally pharma.Machine safety experience would be advantageous.GENERAL SCOPE OF RESPONSIBILITIES:Primary role<ul><li>Conduct EHS Impact Assessments (IA) as part of Management of Change process to ensure that all EHS requirements and J&amp;J standards are incorporated</li><li>Implement J&amp;J &lsquo;EH&amp;S by Design&rsquo; as required for selected projects</li><li>Participate in design reviews, HAZOPs &amp; 3D model reviews</li><li>In addition support JSAs, noise /IH/ergonomics / WRAPs (machine safety) assessments</li><li>Support FATs / SATs as required</li><li>Participate in W1 / W3 / Care Custody &amp; Control walkdowns as part of project closeout</li><li>Support IA action closure &amp; tracking</li><li>Perform periodic walkdowns / audits / programme reviews to ensure compliance with IED licence, SOPs &amp; regulatory requirements.</li></ul>This is not an exhaustive, comprehensive listing of job functions. May perform other duties as assigned.<ul><li>Candidate must have a strong EHS general/technical knowledge and experience in the Bio/Pharma industry, MedTech or equivalent, be a strong effective communicator with all stakeholders.</li><li>Candidate must be a strong collaborator with a proven track and a strong networker able of leveraging EHS&amp;S expertise on and off site.</li></ul>KEY COMPETENCIES REQUIRED:<ul><li>Excellent interpersonal skills</li><li>Ability to operate as part of a team is critical.</li><li>Customer focus</li><li>Innovative</li><li>Excellent communication skills both written and verbal</li><li>Excellent presentation and training skills</li><li>Strong Influencing skills<ul><li>Attention to detail</li><li>Good problem-solving skills</li><li>Results and performance driven</li><li>Adaptable and flexible</li><li>Ability to maintain confidentiality</li><li>Availability and willingness to travel on company business</li><li>Ability to exercise tact and diplomacy when dealing with colleagues regarding EHS issues</li></ul></li></ul>QUALIFICATIONS AND EXPERIENCE:<ul><li>Previous experience working to ISO14001 and ISO45001 international standards, preferably</li><li>within a Biopharma/pharmaceutical or related environment is required.</li></ul>ESSENTIAL:<ul><li>A relevant third level qualification in Science, Engineering or EHS, with at least 5 years&rsquo; experience in the environment, health and safety area is a prerequisite for the position.</li><li>Good overall knowledge of legal requirements and best practices in both Environment and Safety</li><li>Creates dashboards, power-point presentations and can track and trend KPI&rsquo;s, assembling information into clearly written reports, documented findings or recommendations and communicate this progress in easily understandable manner to all stakeholders.</li></ul>DESIRABLE:<ul><li>Machine safety experience/qualification would be a distinct advantage</li><li>Excellent communication, presentation, and training skills</li><li>A flexible approach, good priority setting skills and ability to deal with multiple tasks</li></ul>KEY INDIVIDUAL LEADER COMPETENCIES:<ul><li>A strong communicator &amp; influencer who is credible, self-assured and highly capable of negotiating successful outcomes with site stakeholders (managers, leads, contractors, front line workers).</li><li>Demonstrates ability to work with teams and individuals</li><li>Proven track record of delivering agreed-upon expectations.<ul><li>Builds strong productive lasting relationships</li><li>Strong technical skills and the ability to explain complex issues and requirements in an easily understood manner</li><li>Excellent problem-solving skills and the necessary capabilities to understand and find solutions for complex technical/regulatory issues</li><li>Asserts personal ideas and opinions using persuasion to influence others</li><li>Seeks opportunities to grow and develop professionally</li><li>Uses best practices to improve business operations</li><li>Holds self-accountable for compliant and flawless execution</li><li>Takes personal responsibility for decisions that successfully build customer value</li><li>Effectively manages and adapts to change</li><li>Demonstrates the courage to stand alone on ideas and opinions that differ from others</li><li>Listens effectively and remains open to other&rsquo;s ideas.</li><li>Works effectively with people that have diverse styles, talents and ideas</li><li>Maintains the highest standards of ethical behaviour</li><li>Treats people with dignity and respect</li><li>SIGNIFICANT SAFETY OR WORKING CONSIDERATIONS:</li><li>Comply with the requirements of the company&rsquo;s Environmental, Health &amp; Safety Policy, Safety</li><li>Statement, associated EHS Procedures and duties outlined in the site EHS Manual.</li></ul></li></ul> Our Vision: 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 Geraldine Gormally on 0861071395&nbsp;&nbsp;<a href="mailto:/%C2%A0recruit@hero.ie">/&nbsp;recruit@hero.ie</a>Check 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.

EHS Specialist 

<div>I&rsquo;ve gained experience in various environments, and I&rsquo;m ready to bring my dedication and efficiency to the recruitment process. As a recruitment consultant, I&rsquo;m eager to learn and partner with candidates to provide a positive and effective experience. I&rsquo;m always focused on helping teams hit their goals and contributing to recruitment strategies that work.</div>
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<div>My communication skills are strong, and I stay updated on the latest trends and developments in the STEM industry, ensuring I can support candidates and clients effectively. You can trust me to assist you throughout the recruitment process, and I&rsquo;m excited to be part of the journey with you!</div>

Contracting Recruitment Consultant

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