Clinical Laboratory Technician III (Technical Support)
Location: Fully Onsite
Contract Duration: 12 Months
Overview
This role involves performing a range of technical and laboratory procedures to support production, research and development, quality, and compliance activities. The position requires a seasoned technician capable of working with limited supervision while contributing to process improvements and supporting junior staff.
Key Responsibilities
<ul>
<li>Perform routine laboratory procedures, including:</li>
<li>Preparing solutions and reagents</li>
<li>Conducting routine reactions</li>
<li>Make and record observations, perform calculations, and collect data for evaluation</li>
<li>Support laboratory operations by:</li>
<li>Stocking and distributing supplies</li>
<li>Setting up and dismantling equipment</li>
<li>Cleaning and storing glassware</li>
<li>Maintain accurate technical records in compliance with company and regulatory standards</li>
<li>Analyze compounds and manage compound collections (where applicable)</li>
<li>Carry out technical procedures across:</li>
<li style="list-style-type: none;">
<ul style="list-style-type: circle;">
<li>Production</li>
<li>Research &amp; Development</li>
<li>Quality Control / Assurance</li>
<li>Compliance / Environmental</li>
<li>Technical Support Duties</li>
</ul>
</li>
</ul>
Provide technical support across areas such as:
<ul>
<li>Production and operations</li>
<li>Maintenance and safety</li>
<li>Testing and process improvement</li>
<li>Product development</li>
<li>Interpret schematics, diagrams, and technical instructions</li>
<li>Perform testing and troubleshooting on equipment and systems</li>
<li>Gather, format, and analyze technical data using established methods</li>
<li>Conduct detailed mathematical calculations</li>
<li>Identify and suggest improvements to optimize processes</li>
</ul>
 Experience Level &amp; Autonomy 
<ul>
<li>Operates as a seasoned individual contributor</li>
<li>Works with limited supervision</li>
<li>Supports and trains junior team members</li>
<li>Leads minor projects, including:</li>
</ul>
<ul style="list-style-type: circle;">
<li>Testing</li>
<li>Data interpretation</li>
<li>Report development</li>
</ul>
Key Competencies
Organizational Impact
<ul>
<li>Executes technical tasks requiring sound judgment</li>
<li>May own and manage smaller projects</li>
<li>Handles non-routine technical assignments</li>
</ul>
Innovation &amp; Problem Solving
<ul>
<li>Addresses general technical challenges</li>
<li>Analyzes issues and proposes solutions independently</li>
</ul>
Communication
<ul>
<li>Communicates with internal stakeholders</li>
<li>Shares and gathers technical information relevant to the role</li>
</ul>
Leadership
<ul>
<li>Provides guidance, coaching, and training within the team</li>
</ul>
Requirements
<ul>
<li>Minimum of 4 years of relevant experience</li>
<li>Broad knowledge of operational systems, techniques, and practices</li>
<li>Vocational or technical education and/or certification preferred</li>
<li>Strong analytical, technical, and problem-solving skills</li>
</ul>

Clinical - Lab Technician III

Design and Development Engineer I/II&nbsp; Contract Role Onsite - Galway Our Purpose
Coronary &amp; Renal Denervation therapies are a vital component of our clients interventional cardiology portfolio. In addition to our core products that treat blocked coronary arteries, we are seeking to solve unmet needs in the rapidly growing field of complex Percutaneous Coronary Intervention (PCI). We are also leading the way with the transformational Blood pressure reduction therapy, which has the potential to be a powerful tool in battling the global hypertension epidemic.
Our team support the creation our market-leading portfolio of innovations. Combine the best of your experience with training and mentorship to move forward. If you want a challenging, energizing, rewarding career that changes lives, join us. Help us bring the next generation of life-changing medical technology to patients worldwide.
A Day in The Life Of:
<ul>
<li>As a Design &amp; Development Engineer II, you will actively participate in all areas of new product development including the following: Process design, Process characterisation, Technology development &amp; advancement, Automation, Vendor, Sub Tier supplier management &amp; Project management.</li>
<li>Collaborate with cross functional teams to define, execute and deliver on requirements in the Pre and Post market space.</li>
<li>Lead and support the process development, process characterisation, and process validation activities to support new product introduction. You should have excellent statistical capabilities and utilise design of experiments and engineering studies to coach team members on developing engineering DOE&rsquo;s, transfer functions and build on our teams capabilities to root cause issues whilst defining robust process windows.</li>
<li>Take initiative &amp; lead, innovate and develop best in class process technology with emphasis on improving quality, reducing variation and developing state of the art automated and semi-automated systems.</li>
<li>Identify and mitigate technology and process risks through the design process.</li>
<li>Collaborate with team members on Design, Reliability &amp; Manufacturability methodology (DRM), utilise 3-D drawing/printing and Augmented Reality to develop our best solutions that will allow us manufacture devices that will positively impact the healthcare of millions.</li>
<li>Identify and carry out practical actions to solve technical problems using your skills in project management, six sigma tools, process characterisation and technology development.</li>
<li>Collaborate, document, and present all learnings to project and functional teams.</li>
</ul>
Key Skills &amp; Experience
<ul>
<li>Third Level 8 Degree or higher in Electronic, Electrical, Mechanical, Biomedical Engineering, Science, or related discipline with a minimum 2 year relevant direct Science/Engineering experience within medical device environment. Advanced degree advantageous.</li>
<li>Dynamic team player with the ability to collaborate effectively within a talented team and can work effectively and proactively on cross-functional teams.</li>
<li>Experience in Process validation protocol and report writing.</li>
<li>Ability to identify and resolve issues without direct supervision.</li>
<li>Working knowledge of statistical tools such as DOE, SPC, Hypothesis Testing and Process Capability Studies.</li>
<li>Experience developing and validating medical device manufacturing processes (IQ, OQ, PQ, and PPQ)</li>
<li>Knowledge of medical device processes with a good understanding of product and process design.</li>
<li>Good communicator and fluent in English, with a high level of enthusiasm and motivation.</li>
<li>Good organizational, presentation and project management skills are desirable</li>
</ul>

Design and Development Engineer I/II

EHS Specialist |&nbsp; MedTech | Co. Mayo
A well-established MedTech manufacturer in Co. Mayo is seeking an experienced EHS Specialist to join their site team on a permanent basis. This is a broad, hands-on role covering the full spectrum of EHS, from regulatory compliance and environmental management through to health &amp; safety risk management and incident response.
The Role
Reporting into the site EHS function, the successful candidate will support the implementation and continuous improvement of EHS policies, procedures, and site programmes. Key areas of responsibility include:
<ul class="[li_&amp;]:mb-0 [li_&amp;]:mt-1 [li_&amp;]:gap-1 [&amp;:not(:last-child)_ul]:pb-1 [&amp;:not(:last-child)_ol]:pb-1 list-disc flex flex-col gap-1 pl-8 mb-3">
<li class="whitespace-normal break-words pl-2">Ensuring compliance with national EHS regulations, corporate standards, and ISO-aligned management systems</li>
<li class="whitespace-normal break-words pl-2">Managing hazardous and non-hazardous waste programmes, including vendor oversight</li>
<li class="whitespace-normal break-words pl-2">Conducting risk assessments, GEMBA walks, internal audits, and EHS change management reviews</li>
<li class="whitespace-normal break-words pl-2">Leading or supporting incident investigations with robust root-cause analysis and CAPA implementation</li>
<li class="whitespace-normal break-words pl-2">Coordinating the Emergency Response Team programme, including drills and readiness</li>
<li class="whitespace-normal break-words pl-2">Maintaining and reporting EHS KPIs and supporting cross-functional improvement projects</li>
</ul>
What They're Looking For
<ul class="[li_&amp;]:mb-0 [li_&amp;]:mt-1 [li_&amp;]:gap-1 [&amp;:not(:last-child)_ul]:pb-1 [&amp;:not(:last-child)_ol]:pb-1 list-disc flex flex-col gap-1 pl-8 mb-3">
<li class="whitespace-normal break-words pl-2">Third-level qualification in EHS, Environmental Science, Environmental Engineering, or a related discipline</li>
<li class="whitespace-normal break-words pl-2">Minimum 5 years' EHS experience in manufacturing or a similarly regulated environment</li>
<li class="whitespace-normal break-words pl-2">Experience with ISO 14001 and ISO 45001 highly desirable</li>
<li class="whitespace-normal break-words pl-2">Strong communicator with the ability to influence at all levels</li>
<li class="whitespace-normal break-words pl-2">Self-motivated, able to manage competing priorities and work independently</li>
</ul>
What's On Offer
<ul class="[li_&amp;]:mb-0 [li_&amp;]:mt-1 [li_&amp;]:gap-1 [&amp;:not(:last-child)_ul]:pb-1 [&amp;:not(:last-child)_ol]:pb-1 list-disc flex flex-col gap-1 pl-8 mb-3">
<li class="whitespace-normal break-words pl-2">Permanent contract with a stable, secure employer</li>
<li class="whitespace-normal break-words pl-2">Comprehensive benefits package including private medical insurance, company pension, and annual bonus</li>
<li class="whitespace-normal break-words pl-2">Collaborative, dynamic working environment with access to state-of-the-art facilities</li>
</ul>

EHS Specialist 

Senior Chemist
Location: Onsite
Contract Duration: 12 Months
Role Overview
We are seeking a highly motivated Analytical Scientist to perform laboratory testing and support analytical method development within a regulated environment. The successful candidate will play a key role in ensuring product quality, compliance, and continuous improvement initiatives.
Key Responsibilities
<ul>
<li>Perform analytical testing on drug and combination products using techniques such as Liquid and Gas Chromatography, spectroscopic methods, elution, and wet chemistry.</li>
<li>Develop and validate analytical test methods in line with regulatory requirements.</li>
<li>Lead and support laboratory investigations, ensuring timely closure and proper documentation.</li>
<li>Accurately interpret and report analytical results, including trending data and generating technical reports.</li>
<li>Collaborate with cross-functional teams including Quality, Supply Chain, Operations, Finance, and Engineering to ensure efficient and compliant processes.</li>
<li>Provide technical expertise for analytical instrumentation and methodologies, including troubleshooting as needed.</li>
<li>Drive continuous improvement initiatives to reduce testing lead times and achieve cost savings.</li>
<li>Independently plan and schedule work to meet project deadlines.</li>
<li>Support the training and onboarding of new team members.</li>
<li>Participate in internal and external audit programs.</li>
<li>Contribute to regulatory submissions and related documentation.</li>
</ul>

Senior Chemist 

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Electrical Design Engineer
&nbsp;
Purpose
To provide Electrical and Safety design expertise in the design, manufacture, documentation, and continuous improvement of equipment to produce medical devices.
Responsibilities
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<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Generation of equipment electrical designs which meet manufacturing, safety, CE, and performance requirements.&nbsp;</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Proactively and continuously ensure potential safety risks are addressed and ensure equipment meets CE marking standards.&nbsp;</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Work closely with internal engineers to understand their equipment requirements.&nbsp;</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Work closely with internal and external machine build vendors in order to ensure that any equipment supplied is built according to compnay specifications and is properly handed over to manufacturing.</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Ensure equipment solutions are delivered within planned schedules and within budget.</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Ensure documentation/drawing standards for equipment meet compnay requirements.&nbsp;</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">As part of the design team, this person is expected to work closely with both internal and external specialists to complete equipment- related projects.</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Build Quality into all aspects of work by maintaining compliance to all quality requirements</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Participates in and leads the use of lean and Continuous Improvement tools in equipment designs and engineering systems.&nbsp;</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Support continuous improvement activities</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Provide technical guidance / leadership to the equipment build team</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">PSPI/CI/VIP opportunity identification and collation</li>
</ul>
&nbsp;
Qualifications
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<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Candidates are required to hold an Engineering qualification equivalent to or above NFQ Level 8 with a minimum of 3 years&rsquo; experience in the design and build of equipment for the medical device industry.</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Proficient in the use of AutoCAD Electrical, and design of pneumatic circuits.&nbsp;</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Proven ability to design and commission electrical and pneumatic control panels for automated equipment.</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Proven ability to assess and remediate equipment safety issues</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Good technical capabilities, teamwork abilities and initiative.&nbsp;</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Proven ability to work well as part of a team &amp; on own with minimum supervision</li>
<li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;">Good communication skills combined with an imaginative and creative approach to problem solving.&nbsp;</li>
</ul>
</div>
</div>
</div>

Electrical Design Engineer

R&amp;D EngineerLocation: GalwayContractor roleOnsiteAbout the RoleWe are seeking a highly motivated R&amp;D Engineer to join the Galway Interventional Cardiology Therapies (ICTx) Sustaining R&amp;D team.This group provides critical design and technical support to a portfolio of commercial products, ensuring safety, compliance, and manufacturing continuity across a range of minimally invasive cardiovascular devices.Job PurposeAs part of a multidisciplinary and dynamic New Product Development (NPD) organisation specializing in coronary intervention systems, you will support the commercialization of next-generation minimally invasive medical devices used in the treatment of coronary artery disease.Working with limited supervision, you will:Compile, analyze, and report operational, test, and research data to ensure design intent is maintained throughout the product lifecycle.Provide essential post-launch support as a key source of product and clinical expertise.This role is ideal for someone who enjoys technical problem-solving, cross-functional collaboration, and direct impact on patient-focused medical technologies.Key Responsibilities● Apply the design change process to ensure proposed modifications are thoroughly evaluated, justified, and verified against design intent.● Collaborate cross-functionally with project management, quality, manufacturing, regulatory, clinical, and marketing teams.● Partner closely with manufacturing teams to reduce product costs through informed design improvements.● Analyze market and clinical feedback, providing design insights on device performance and anatomy interaction; identify opportunities for enhancement and engage with physicians where needed.● Interface with vendors and physicians to support project needs.● Maintain product performance through quality investigations and robust documentation of design changes.● Work independently to plan and schedule activities to meet project timelines.● Troubleshoot product or process issues related to design, materials, or manufacturing processes.● Summarize and interpret test data, preparing clear technical reports and documentation.● Offer technical guidance within multidisciplinary and international teams.● Lead or participate in cross-functional teams resolving design or process issues.● Demonstrate a strong commitment to patient safety and product quality.Qualifications● Level 8 Degree (HETAC) in a relevant technical field: Mechanical, Polymer, Materials, or Biomedical Engineering preferred.● Minimum 3 years&#8217; R&amp;D or technical experience, ideally within the healthcare or medical device sector.● Strong interpersonal and communication skills with proven leadership capability.● Excellent analytical and problem-solving abilities.

Research and Development 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

Quantity Surveyor

Recruitment Consultant