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 

Engineer Manager We are seeking an experienced Engineering Manager to lead and develop a high-performing engineering team. This role focuses on people development, coaching, and mentoring, while driving continuous improvement initiatives through Lean Six Sigma methodologies. A key responsibility is optimizing production lines to enhance efficiency and ensure best practices in manufacturing operations.<h3 class="" data-start="956" data-end="986">Key Responsibilities</h3><ul data-start="987" data-end="1897"><li class="" data-start="987" data-end="1106">Lead, mentor, and develop the engineering team, fostering a culture of continuous learning and professional growth.</li><li class="" data-start="1107" data-end="1231">Implement Lean Six Sigma principles to drive process improvements, reduce waste, and enhance operational efficiency.</li><li class="" data-start="1232" data-end="1343">Oversee line optimization projects, identifying opportunities to improve productivity and reduce costs.</li><li class="" data-start="1344" data-end="1449">Collaborate with production, quality, and regulatory teams to ensure smooth and compliant operations.</li><li class="" data-start="1450" data-end="1557">Develop and execute engineering strategies aligned with business objectives and long-term growth plans.</li><li class="" data-start="1558" data-end="1638">Manage technical projects, ensuring timely delivery within scope and budget.</li><li class="" data-start="1639" data-end="1733">Promote a culture of innovation, problem-solving, and resourcefulness within the team.</li><li class="" data-start="1734" data-end="1808">Ensure compliance with industry regulations and company standards.</li><li class="" data-start="1809" data-end="1897">Monitor engineering performance KPIs and implement corrective actions as needed.</li></ul><h3 class="" data-start="1899" data-end="1925">Key Requirements</h3><ul data-start="1926" data-end="2700"><li class="" data-start="1926" data-end="2014">Degree in Mechanical, Manufacturing, Biomedical Engineering, or a related field.</li><li class="" data-start="2015" data-end="2139">Proven leadership experience in an engineering role within the medical device or regulated manufacturing sector.</li><li class="" data-start="2140" data-end="2230">Strong people management skills, with experience in coaching and team development.</li><li class="" data-start="2231" data-end="2305">Expertise in Lean Six Sigma methodologies and process improvement.</li><li class="" data-start="2306" data-end="2392">Hands-on experience in line optimization and driving operational efficiencies.</li><li class="" data-start="2393" data-end="2475">Strong problem-solving, decision-making, and project management abilities.</li><li class="" data-start="2476" data-end="2588">Excellent communication and interpersonal skills, with the ability to engage and influence stakeholders.</li><li class="" data-start="2589" data-end="2700">Ability to thrive in a fast-paced, highly regulated environment with a focus on continuous improvement.</li></ul><h3 class="" data-start="2702" data-end="2727">What&rsquo;s on Offer</h3><ul data-start="2728" data-end="2953"><li class="" data-start="2728" data-end="2772">Competitive salary and benefits package.</li><li class="" data-start="2773" data-end="2834">Opportunity to work in a dynamic and growing company.</li><li class="" data-start="2835" data-end="2896">Career development and professional growth opportunities.</li><li class="" data-start="2897" data-end="2953">A collaborative and supportive work environment.</li></ul>If you are a results-driven Engineering Manager with a passion for people development and continuous improvement, we would love to hear from you!For further information on this role in please contact on Gavin Moran on 087 4108620 or connect@hero.ieCheck 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

Engineering Manager 

Role:&nbsp;&nbsp;&nbsp; Senior Lead Engineer MechanicalLocation: Frankfurt am Main, GermanyOur client are pioneers shaping the future of high-tech industries such as semiconductors, batteries, pharmaceuticals, biotechnology, and data centres.Your Role:As a Senior Lead Engineer Mechanical, you will spearhead our Data Centre Business Unit in Frankfurt. Your responsibilities include planning and engineering utilities and HVAC (wet/dry) systems, as well as assembling and leading a new team of Mechanical Engineers. You will play a crucial role in team recruitment, goal setting, and ensuring successful project outcomes. If you possess strong organizational acumen and strategic vision, we eagerly await your application.Key Responsibilities:<ul><li>Plan, project manage, and execute utilities and HVAC (wet/dry) systems.</li><li>Develop detailed execution documents (e.g., drawings, functional descriptions, bill of quantities) for procurement and service planning, addressing any execution phase queries.</li><li>Lead and mentor a team of Mechanical Engineers.</li><li>Ensure projects meet budget, quality, and timeline objectives.</li><li>Support project management by preparing and updating schedules as necessary.</li><li>Coordinate subcontractors to ensure the highest quality execution, adhering to safety, health, and environmental standards.</li><li>Manage trade interfaces effectively.</li></ul>Your Expertise:<ul><li>Degree in Mechanical Engineering or similar field.</li><li>Extensive experience leading mechanical design in major projects, preferably within high-tech or industrial sectors.</li><li>Technical proficiency in Engineering, Design, and Construction of mechanical systems, from Preliminary Design to Commissioning.</li><li>Familiarity with fast-track project execution processes.</li><li>Strong local construction knowledge.</li><li>Proven ability to mentor and motivate teams in challenging technical environments.</li><li>Excellent English skills; German proficiency advantageous.</li><li>Willingness to travel within Central Europe (approximately 10%).</li></ul>For further information on this Senior Mechanical Lead role in Germany please contact Caroline Kingston on +353 868395531 or email caroline@hero.ie Check out all our open jobs on our HERO Recruitment website &ndash; https://www.hero.ie/.Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.Data can only be transferred outside of the EEA based on 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.

Senior Lead Engineer Mechanical 

Are you an experienced Controls Engineer looking for a dynamic role in the Life Sciences, Pharma, or MedTech sector? This is an exciting opportunity to work with a global team, driving automation and control system projects from concept to commissioning.<h3 data-start="343" data-end="374">Key Responsibilities:</h3>&#55357;&#56633; Develop, program, and commission automation and control systems (Levels 1-3 of the ISA pyramid). &#55357;&#56633; Lead PLC programming, HMI/SCADA development, motion control, robotics, and vision system integration. &#55357;&#56633; Work closely with OEMs and project teams to ensure seamless system implementation. &#55357;&#56633; Troubleshoot, test, and validate automation solutions to meet regulatory standards (e.g., FDA, GMP, GAMP). &#55357;&#56633; Stay ahead of emerging control technologies and drive continuous improvement.<h3 data-start="892" data-end="915">Requirements:</h3>&#9989; Bachelor's or Master&rsquo;s degree in Engineering, Manufacturing, or Computer Science. &#9989; 5+ years&rsquo; experience in control systems within Life Sciences, Pharma, or MedTech. &#9989; Expertise in Allen Bradley PLCs &amp; FactoryTalk, with experience in Siemens TIA Portal a plus. &#9989; Strong knowledge of industrial communication protocols (Ethernet/IP, Profibus, Modbus). &#9989; Familiarity with cybersecurity principles for SCADA systems. &#9989; Experience with GAMP 5, validation, and automation change control.<h3 data-start="1450" data-end="1480">The Ideal Candidate:</h3>&#55357;&#56481; A proactive problem-solver with strong technical expertise and a passion for innovation. &#55358;&#56605; A confident team player with excellent communication and organizational skills. &#55357;&#56960; Able to work across multifunctional teams and deliver projects on time and within budget.&#55357;&#56525; Location: Athlone (Hybrid) &#55357;&#56508; Join a cutting-edge team driving automation excellence!

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.

Job Details

Senior Controls Engineer

Recruitment Consultant

Senior Controls Engineer

Key Responsibilities:

Requirements:

The Ideal Candidate:

Similar Jobs