Senior Automation Manager 
Join a global transformation journey to modernize and standardize automation across a network of 18 manufacturing sites. This is a technical leadership role focused on shaping and implementing automation standards and guidelines, with a near-term emphasis on greenfield sites.
Key Responsibilities:
<ul>
<li>Develop and implement automation system standards and guidelines (PLC, SCADA, BMS, EMS, IoT, robotics, and more).</li>
<li>Partner with suppliers to finalize system specifications and oversee FAT/SAT processes.</li>
<li>Support equipment startups, conduct site reviews, and update standards based on learnings and technology advancements.</li>
<li>Drive standardization, share best practices, and evaluate emerging automation technologies across sites.</li>
<li>Provide leadership and guidance to site automation teams and external service providers.</li>
</ul>
Qualifications:
<ul>
<li>Degree in Electrical or Electrical &amp; Electronic Engineering.</li>
<li>5&ndash;7 years of automation/digitalization experience in manufacturing.</li>
<li>Expertise in automation systems, change management, and global project management.</li>
<li>Strong analytical, project management, and communication skills.</li>
</ul>
Additional Details:
<ul>
<li>Location: Ballina, with 50&ndash;75% travel (including extended periods for site commissioning and stabilization).</li>
<li>Reporting to: Senior Director, Automation.</li>
</ul>
For further information, contact Dee Curley at <a rel="noopener">dee@hero.ie</a> or 086-7902191.
Check out more opportunities at <a href="https://www.hero.ie/" target="_new" rel="noopener">HERO Recruitment</a>.

Senior Automation Manager

Quality Engineer (Projects) County Cork, Ireland
Nestled in the heart of County Cork, this role offers the chance to live and work in a region celebrated for its vibrant community, stunning landscapes, and unparalleled quality of life.
Overview:
A leading recruitment agency is delighted to represent a premier client in their search for a Quality Engineer (Projects). This exciting role places a dynamic professional at the forefront of quality assurance for cutting-edge product introductions and manufacturing excellence. With opportunities to shape processes and drive compliance in a GMP-regulated environment, this position is a career-defining opportunity for an experienced engineer.
Key Responsibilities:
Validation Leadership:
<ul>
<li>Drive compliance with validation requirements for new product introductions.</li>
<li>Define and characterise process, product, and test method validation requirements.</li>
<li>Prepare and approve Master Validation Plans, protocols, and reports.</li>
</ul>
Development Support:
<ul>
<li>Provide effective QA support for production line development and ramp-up, focusing on risk mitigation.</li>
<li>Offer quality expertise to ensure production lines meet cGMP requirements, including procedure approvals, FMEAs, and cleanroom practices.</li>
</ul>
Change and Quality Control:
<ul>
<li>Approve change requests for product, process, and quality system updates.</li>
<li>Identify and implement appropriate statistical techniques to monitor process performance, such as SPC, CpK analysis, and sampling techniques.</li>
<li>Provide functional expertise on quality-related issues, including non-conformances, CAPA, regulatory requirements, and statistical approaches.</li>
</ul>
Education &amp; Experience Requirements:
<ul>
<li>Bachelor of Science degree in Engineering or Technology (minimum requirement).</li>
<li>3-4 years of experience in a manufacturing or equivalent environment, with direct QA experience (preferably in a GMP-regulated setting).</li>
</ul>
Why Join? This role is perfect for ambitious professionals looking to make a meaningful impact in a highly supportive environment. It&rsquo;s an opportunity to work on innovative projects while enjoying the unique lifestyle and vibrant culture that County Cork has to offer.
Apply Today! Check out all our open jobs on our HERO Recruitment website &ndash; <a href="https://www.hero.ie/">https://www.hero.ie/</a>  &nbsp;
Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.&nbsp;
&nbsp;
&nbsp;

Quality Engineer (Projects)

Night Shift Technician &ndash; Drug-Eluting Stent (DES) Manufacturing
Location: Galway, Ireland Shift: Night Shift (23:00 &ndash; 07:00, Sunday night to Thursday night) Shift Premium
Are you passionate about cutting-edge medical technology and skilled in troubleshooting? Join a collaborative team in Galway, renowned for its vibrant community, excellent quality of life, and stunning natural surroundings.
This Night Shift Technician role offers the opportunity to support advanced manufacturing lines for drug-eluting stents (DES), combining your technical skills with impactful contributions to life-saving medical devices.
<h3>Key Responsibilities</h3>
<ul>
<li>Equipment Support: Troubleshoot and resolve equipment issues, perform preventative maintenance, and escalate complex problems to Engineering or Maintenance teams when necessary.</li>
<li>Yield Management: Collaborate with Manufacturing Engineers to investigate and resolve scrap and yield issues related to equipment and processes.</li>
<li>Team Collaboration: Work as part of a close-knit team of approximately six Technicians and Production Core Teams across 3&ndash;4 key processes.</li>
<li>System Utilisation: Record maintenance activities in internal systems, use PowerPoint for yield updates, and manage handovers via Teams and Excel.</li>
<li>Database Interaction: Utilise SQL databases (training provided) to interact with equipment data and optimise performance.</li>
<li>Commitment to Safety and Quality: Execute all tasks with the highest regard for safety standards and quality protocols.</li>
</ul>
<h3>Essential Skills and Attributes</h3>
<ul>
<li>Strong problem-solving abilities.</li>
<li>Familiarity with electrical or mechanical troubleshooting is highly advantageous.</li>
<li>A team player with effective communication skills.</li>
<li>Comfortable with learning new systems and tools; SQL training will be provided.</li>
</ul>
<h3>Why Join Us?</h3>
<ul>
<li>Full training and ongoing professional development provided.</li>
<li>Work in a supportive, innovation-driven environment where your skills directly impact healthcare.</li>
<li>Night shift premium to recognise your commitment.</li>
</ul>
<h3>What We&rsquo;re Looking For</h3>
This role is ideal for individuals with a background in technical troubleshooting, maintenance, or manufacturing support. Prior experience in medical device manufacturing is beneficial but not essential, as training will be provided.
<h3>Next Steps</h3>
Interviews will take place in December for a January start date. This opportunity is subject to final confirmation of an existing team member&rsquo;s departure.
Take the next step in your career and become part of a team that makes a difference.
Apply today to join a global leader in medical technology, based in the heart of Galway&rsquo;s thriving innovation hub.
For further information on this role, please contact Diarmuid Lannon on +353 861287246 or email&nbsp;<a href="mailto:consulting@hero.ie">consulting@hero.ie</a>&nbsp;Check out all our open jobs on our HERO Recruitment website &ndash; https://www.hero.ie/
Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.
Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.
&nbsp;

Night Shift - Manufacturing Technician

Design Assurance Engineer
<ul>
<li>Contractor Role</li>
<li>Medical Device</li>
</ul>
This job posting is for a&nbsp;Design Assurance Engineer Contract Role&nbsp;based in&nbsp;Galway, Ireland, with a hybrid working arrangement. The successful candidate will be part of a Sustaining Engineering team responsible for supporting&nbsp;Drug Eluting Stent&nbsp;and&nbsp;Cutting Balloon products, contributing to post-market activities, ensuring compliance, and enhancing product quality. Below is a summary of key information: Job Purpose
The role involves:
<ul>
<li>Ensuring&nbsp;patient safety,&nbsp;customer satisfaction, and&nbsp;product quality.</li>
<li>Compliance with&nbsp;quality systems&nbsp;and applicable regulations.</li>
<li>Risk mitigation in design, use, and manufacturing.</li>
<li>Adherence to training and regulatory requirements.</li>
</ul>
Key Responsibilities
General
<ul>
<li>Work under limited supervision while liaising with cross-functional teams (R&amp;D, Regulatory, Clinical, etc.).</li>
<li>Understand and follow procedures for medical device&nbsp;Design Control,&nbsp;Risk Management, and&nbsp;Post Market Surveillance.</li>
<li>Resolve complex issues, support quality/process improvements, and ensure adherence to quality requirements.</li>
<li>Exhibit strong&nbsp;communication,&nbsp;interpersonal, and&nbsp;leadership skills.</li>
</ul>
Technical
<ul>
<li>Provide&nbsp;design quality support&nbsp;for post-market commercial products.</li>
<li>Address issues like complaints,&nbsp;CAPAs,&nbsp;VIPs, and regulatory changes.</li>
<li>Perform risk management, analyze data, and make informed decisions.</li>
<li>Ensure compliance with regulatory standards.</li>
</ul>
Leadership
<ul>
<li>Actively contribute to the team&rsquo;s success in sustaining engineering and post-market activities.</li>
<li>Promote best practices and support change initiatives within the project/department.</li>
</ul>
&nbsp;
Qualifications &amp; Experience
<ul>
<li>HETAC Level 8&nbsp;in a STEM discipline (240 credits) with 3-4 years of relevant experience.</li>
<li>Strong technical and analytical skills, with proven&nbsp;problem-solving&nbsp;abilities.</li>
<li>Effective communication, teamwork, and the ability to work independently.</li>
<li>Familiarity with medical device quality systems and regulatory requirements.</li>
</ul>

Design Assurance Engineer

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<h3>Supplier Engineer II</h3>
Location: Cork, Ireland
Join a mission-driven team dedicated to transforming lives through innovative medical solutions. This role focuses on collaborating across teams to develop impactful solutions that enhance patient health and support healthcare professionals.
<hr />
<h3>Role Purpose</h3>
As a Supplier Engineer, you will play a key role in driving Material Value Improvement Projects (MVIP) aimed at achieving consistent cost reductions on purchased commodities.
<hr />
<h3>Key Responsibilities</h3>
<h4>Engineering Expertise</h4>
<ul>
<li>Act as a technical team member across multidisciplinary groups, including Purchasing, Supplier Quality, and Business Units.</li>
<li>Apply technical knowledge in commodity management and quality systems to achieve project goals.</li>
</ul>
<h4>Supplier and Quality Management</h4>
<ul>
<li>Support quality, cost, and service objectives across the supply chain.</li>
<li>Promote and enhance quality systems within supplier networks.</li>
<li>Ensure supplier compliance with established requirements and implement corrective actions.</li>
</ul>
<h4>Continuous Improvement and Collaboration</h4>
<ul>
<li>Lead material value improvement projects and supply chain optimizations.</li>
<li>Partner with Procurement, Supplier Quality, and Receiving Inspection teams to develop and implement process improvements.</li>
<li>Communicate effectively with all stakeholders to maintain alignment and progress.</li>
</ul>
<h4>Project Leadership</h4>
<ul>
<li>Plan and manage projects, including product and process transfers.</li>
<li>Develop GMP-compliant documentation with team collaboration.</li>
<li>Identify, resolve, and escalate obstacles impeding project success.</li>
</ul>
<hr />
<h3>Education &amp; Experience</h3>
<h4>Required Qualifications</h4>
<ul>
<li>Bachelor&rsquo;s degree (Level 8) in Engineering or a related discipline.</li>
<li>2&ndash;5 years of experience in supplier engineering or project management roles.</li>
</ul>
<h4>Preferred Skills</h4>
<ul>
<li>Strong project management capabilities and financial process understanding.</li>
<li>Experience in supply chain project management and regulated environments.</li>
<li>Excellent problem-solving, communication, and teamwork skills.</li>
</ul>
<hr />
This role is based in Cork, Ireland, offering an opportunity to innovate, collaborate, and lead improvements across the supply chain while contributing to meaningful projects that make a real difference in patient care.
</div>
</div>
</div>
</div>

Supplier Engineer II

Position Overview The Mechanical Engineer in the R&amp;D team will focus on the design, development, and testing of innovative cooling systems for data centers. This role requires a solid background in mechanical engineering, strong problem-solving abilities, and a collaborative mindset to work effectively within a multidisciplinary team. The successful candidate will contribute to advancing cooling technologies to address the growing demands of data center operations.
Primary Responsibilities
<ul>
<li>Collaborate with cross-functional teams to support the development of new products.</li>
<li>Create and maintain technical documentation, including design specifications, test plans, and user guides.</li>
<li>Provide engineering support during the production and implementation phases of new cooling solutions.</li>
<li>Participate in design reviews and drive continuous improvement efforts within the R&amp;D team.</li>
<li>Work closely with the R&amp;D lab to conduct performance testing and validate prototypes, recording results and refining designs based on outcomes.</li>
<li>Assist with prototype assembly to gain practical insights and drive design enhancements.</li>
</ul>
Key Competencies
<ul>
<li>Proficiency in HVAC system and component knowledge.</li>
<li>Extensive experience in mechanical system design, particularly in an OEM environment.</li>
<li>Strong understanding of thermodynamics, fluid mechanics, and heat transfer principles.</li>
<li>Excellent skills in documentation, project management, and organization.</li>
<li>Hands-on experience in prototype development, testing methods, and data analysis.</li>
<li>Expertise in sheet metal and piping system design.</li>
<li>Familiarity with process cooling water and refrigeration system design (highly desirable).</li>
<li>Proficiency in SolidWorks.</li>
</ul>
Qualifications
<ul>
<li>Bachelor&rsquo;s degree in Mechanical Engineering or a related field.</li>
<li>A minimum of five years of experience in mechanical design and development.</li>
</ul>

Mechanical 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.

Job Details

Senior Automation Manager

Recruitment Consultant

Senior Automation Manager

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