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

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

Validation Engineer - Exciting Opportunity in Carlow, IrelandJob Type: Contract Location: Carlow, Ireland Industry: Pharmaceutical / Biotechnology / cGMP Regulatory EnvironmentAre you ready to take on a rewarding challenge in the dynamic pharmaceutical and biotechnology industry?We are currently seeking a passionate and driven Validation Engineer to join a team committed to ensuring the highest standards of quality and compliance in a cGMP manufacturing environment. This is an excellent opportunity for professionals with experience in validation to enhance their career while working on cutting-edge technology in the heart of Ireland.<h3 class="" data-start="670" data-end="700">Key Responsibilities</h3>As a Validation Engineer, you will play a key role in ensuring validation and qualification activities are performed to the highest standards. Your responsibilities will include, but are not limited to:<ul data-start="911" data-end="2042"><li class="" data-start="911" data-end="1105">Design &amp; Documentation: Author, review, approve, and execute qualification/validation documentation and cycle development studies, ensuring compliance with cGMP and regulatory standards.</li><li class="" data-start="1106" data-end="1291">Change Control Management: Oversee the development and execution of change controls, ensuring that any modifications meet the required standards and are validated appropriately.</li><li class="" data-start="1292" data-end="1473">Technical Troubleshooting: Resolve any technical issues that arise during the execution of validation studies, using root cause analysis to find and address system failures.</li><li class="" data-start="1474" data-end="1678">Collaboration: Work closely with cross-functional teams, including Production, Maintenance, and Quality, to ensure seamless execution of cycle development and performance qualification activities.</li><li class="" data-start="1679" data-end="1873">Compliance &amp; Audits: Play an active role in maintaining compliance with global policies, GMP guidelines, and regulatory requirements, while supporting audits and inspections as required.</li><li class="" data-start="1874" data-end="2042">Continuous Improvement: Drive continuous improvement initiatives through Lean Six Sigma methodologies, contributing to the enhancement of processes and systems.</li></ul><h3 class="" data-start="2049" data-end="2077">What You Will Need</h3>To succeed in this role, you should possess a strong technical background and relevant experience in the pharmaceutical or biotechnology sectors. The ideal candidate will have:<ul data-start="2258" data-end="3405"><li class="" data-start="2258" data-end="2377">Education: A relevant Level 8 technical qualification in Pharmaceutical, Biological, Chemical sciences, or Engineering.</li><li class="" data-start="2378" data-end="2521">Experience: A proven track record in validation and qualification within a GMP environment, with hands-on experience in a similar role.</li><li class="" data-start="2522" data-end="3170">Key Skills:<ul data-start="2544" data-end="3170"><li class="" data-start="2544" data-end="2655">Extensive knowledge of equipment validation, process validation, and sterilisation technologies</li><li class="" data-start="2658" data-end="2733">Experience with CTU equipment qualification and thermal mapping</li><li class="" data-start="2736" data-end="2833">Strong technical troubleshooting abilities, especially in resolving deviations and exceptions</li><li class="" data-start="2836" data-end="2927">Familiarity with automation systems (e.g., DeltaV, Pi System) would be an advantage</li><li class="" data-start="2930" data-end="3013">Excellent proficiency in Microsoft Office and related software applications</li><li class="" data-start="3016" data-end="3092">Project management skills and the ability to lead technical projects</li><li class="" data-start="3095" data-end="3170">A solid understanding of regulatory requirements and GMP guidelines</li></ul></li><li class="" data-start="3171" data-end="3405">Personal Attributes: Strong communication skills, with the ability to engage with cross-functional teams and external stakeholders. A collaborative mindset and ability to work both independently and within teams are essential.</li></ul><h3 class="" data-start="3412" data-end="3442">Desirable Experience</h3>In addition to the core qualifications, the following experience will be beneficial:<ul data-start="3531" data-end="3870"><li class="" data-start="3531" data-end="3593">Sterile Fill-Finish processes and associated equipment</li><li class="" data-start="3594" data-end="3655">Filter Validation and Container Closure Integrity</li><li class="" data-start="3656" data-end="3702">Autoclave/SIP Sterilisation Validation</li><li class="" data-start="3703" data-end="3773">Isolator Qualification (Filling, Sterility, Material Transfer)</li><li class="" data-start="3774" data-end="3829">Temperature Mapping and Cleaning Validation</li><li class="" data-start="3830" data-end="3870">Project Management Certification 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 &ndash;&#8239;https://www.hero.ie/ &#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. </li></ul>

Validation Engineer 

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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Line Support Technician

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Line Support Technician

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