Master Data Management Coordinator (12-Month Contract)Location: Swords, DublinContract Type: 12-Month ContractWorking Pattern: Onsite 4 days per week / Work from Home 1 day per weekReports to: MDM Operations LeaderOur client is a global climate innovator, delivering efficient and sustainable climate solutions for buildings, homes, and transportation. As a leader in climate technology, we create innovative solutions that improve lives and help protect our planet for generations to come.We are currently seeking an experienced Master Data Management Coordinator to join our team on a 12-month contract based in Swords, Dublin. This is an excellent opportunity to join a fast-paced global organisation, working within a collaborative team while enjoying a hybrid working model and plenty of onsite parking.The OpportunityThe Master Data Management Coordinator will play a key role in ensuring the accuracy, integrity, and governance of commercial master data across the business. The successful candidate will have a strong background in Master Data Management, experience working with ERP systems, and the ability to thrive in a high-volume, KPI-driven environment.This position focuses primarily on the creation and maintenance of EMEA customer and supplier master data, while ensuring data quality standards, business rules, and service level agreements are consistently achieved.Key ResponsibilitiesCreate and maintain commercial master data within the Oracle ERP system, including:Customer MasterVendor MasterItem MasterPricing MasterManage daily activity through the team inbox and Teams Workflow system (Mendix).Perform root cause analysis on process issues and data queries.Liaise with Strategic Business Units (SBUs), internal customers, and support teams to ensure Service Level Agreements are achieved.Maintain master data in response to changing business structures and operational requirements.Ensure all data is processed accurately, efficiently, and right first time.Build and maintain strong relationships with stakeholders to drive best practice in data management.Ensure compliance with all Data Management audit requirements.Provide Remedy Ticket support by working with support teams to resolve system and data issues.Assist with the preparation of regular and ad-hoc management reports relating to commercial master data.Maintain and update detailed work instruction procedures.Record and monitor daily performance metrics.Support continuous improvement initiatives, driving Data Management strategy and productivity.Foster trusted, collaborative relationships that enhance the overall employee experience.Skills &amp; ExperienceMinimum of 2 years' experience working within an ERP environment.Oracle ERP experience (preferred but essential)Strong understanding of master data management within an ERP system.Experience working in a high-volume data processing environment.Excellent analytical skills with strong attention to detail.A proactive, self-motivated approach with the ability to work independently.The ability to work effectively in a fast-paced, target-driven environment.Excellent Microsoft Office skills, particularly Excel.

Master Data Management

Process Development Engineer Contracting role Galway
Works closely with R&amp;D and Manufacturing in the development of robust, capable, cost effective &amp; safe manufacturing processes. equipment, materials and products and supports efficient and effective transfer of new products &amp; processes into commercial production.
Key Responsibilities
<ul>
<li>Demonstrates strong technical expertise on process/product technologies to support selection, design, optimisation, validation and troubleshooting of, and can mentor engineers and technicians in problem resolution on, those technologies.</li>
<li>Liases with Equipment Engineering or external equipment/tooling or material vendors in the selection, design &amp; development of new (or upgrades to existing) equipment, tooling and materials.</li>
<li>Demonstrates strong knowledge of DFSS/DMAIC tools and applies these tools in the characterization, optimization and troubleshoooting of process equipment and technology performance.</li>
<li>Leads the development and execution of experimentation and testing to enable characterisation, optimization and troubleshooting of key processes and equipment. and summarises, analyses and draws conclusions from test results leading to effective technical resolution.</li>
<li>Co-ordinates the introduction of new processes, equipment and materials including installation, calibration, EHS assessment debug, and all associated process and quality system documentation requirements including technical and process work instructions.</li>
<li>Demonstrates strong knowledge and application of Lean methodologies, and process improvement tools in identification and elimination of "waste" process steps and development of efficient, cost effective equipment and processes.</li>
<li>Demonstrates strong knowledge and application of Process and equipment validation techniques, PFMEA&#146;s, and associated regulatory requirements and applies this knowledge in the efficient &amp; timely validation of equipment and processes.</li>
<li>Completes or leads the writing and release of process validation documentation including FMEA's, Validation Plans, protocols and reports.</li>
<li>Co-ordinates execution and documentation of validation builds, co-ordinates testing of validation units and the compilation, analysis and reporting of the validation results.</li>
<li>Supervision of one or more Technicians, managing their technical development and facilitating their daily and project tasks.</li>
<li>Demonstrates a primary commitment to patient safety and product quality.</li>
<li>Ensures all direct reports are aware of their commitment to patient safety and product quality, are current with their training requirements and that they understand and comply with all other regulations governing their work.</li>
<li>Understands and complies with all the regulations governing the quality systems.</li>
</ul>

Knowledge
A developing professional. Working knowledge and application of business and technical concepts, procedures and practices. General knowledge of industry practices, techniques, and standards. General understanding of business unit/group function. Exercises judgment when interpreting company policies and procedures to resolve a variety of issues.
Problem Solving
Develops solutions to a variety of problems of moderate scope and complexity where analysis of situations or data requires a review of identifiable factors. Exercises judgment to determine appropriate action. Has knowledge of alternatives and an understanding of their impact on the business or technological environment.
Planning and Organization
Plans, organizes, and prioritizes own daily work routine to meet established schedule.
Discretion/Latitude; Supervision Received; Decision Making
Works under general direction regarding the progress of projects and special assignments. May seek guidance in resolving problems, interpretating established policies, procedures and practices. Work is reviewed for soundness of judgment.
Business Relationships and Project Management
Cultivates a wide range of internal business relationships and begins to develop an external network of resources to facilitate completion of tasks. May lead a project team of small to moderate scope. Influence exerted at peer level and occasionally at first levels of management.
Impact
Contributes to the completion of departmental projects and goals. Errors in judgment, poor recommendations, or failure to achieve results would normally require a moderate expenditure of resources to rectify.
Liaison
Engages with internal company and external contacts. Represents organization on specific projects. Uses diplomacy and tact in interactions and problem solving.
Mentoring
Provides guidance to less experienced staff.

Process Development Engineer

Process Technician (Nights Role) &#150; Galway, Ireland
Overview:
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 Technician role offers the opportunity to support advanced manufacturing lines, combining your technical skills with impactful contributions to life-saving medical devices.
Key Responsibilities
<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&#150;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>
<li>Essential Skills and Attributes</li>
<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 provide</li>
</ul>
What We&#146;re Looking For
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.

Process Technician - Nights

DESCRIPTION: My client is seeking a motivated Design Assurance Engineer to support both commercially released products and ongoing product development activities. This role will work across sustaining engineering projects and&nbsp;new product development initiatives, including support for software and electronics-based medical device&nbsp;systems.
The successful candidate will be responsible for ensuring that design control, risk management, verification&nbsp;and validation, and regulatory requirements are effectively applied throughout the product lifecycle.
Working closely with R&amp;D, Manufacturing Engineering, Quality, and Regulatory Affairs, the Design Assurance
Engineer will support product changes, development activities, compliance initiatives, and continuous&nbsp;improvement of design assurance processes.
KEY RESPONSIBILITIES:
<ul>
<li>Support sustaining and new product development projects from a Design Assurance perspective throughout the product lifecycle.</li>
<li>Ensure compliance with applicable design control, risk management, and quality system requirements, including FDA and international medical device standards.</li>
<li>Contribute to design change activities, including assessment of quality, risk, usability, biocompatibility, manufacturing, software, electronics, and regulatory impacts where applicable.</li>
<li>Plan, execute, and document design verification and validation activities, including generation of protocols, reports, and traceability documentation.</li>
<li>Lead risk management activities, ensuring risks are identified, evaluated, controlled, and maintained throughout the product lifecycle to meet FDA, ISO 14971, and ISO 13485 requirements.</li>
<li>Generate and maintain Design History Files (DHF) and other design and development records.</li>
<li>Plan, prepare, facilitate, and document design reviews, ensuring compliance with design control requirements and effective progression through project milestones.</li>
<li>Collaborate with R&amp;D teams supporting mechanical, software, and electronics development activities, ensuring appropriate application of design assurance principles</li>
<li>Lead complaint investigations and post-market surveillance activities, conducting technical assessments and root cause analysis, and support CAPA development, implementation, and effectiveness reviews.</li>
<li>Provide design assurance input to manufacturing, supplier, and process change activities.</li>
<li>Assist in regulatory submissions, audits, and inspections by providing supporting documentation and technical expertise.</li>
<li>Contribute to continuous improvement initiatives within Design Assurance, Quality, and Product Development processes</li>
<li>Mentor junior engineers as needed.</li>
</ul>
EDUCATION &amp; EXPERIENCE
<ul>
<li>Bachelor's degree (Level 8 NFQ or equivalent) in Engineering, Biomedical Engineering, Science, Software Engineering, Electronics Engineering, or a related technical discipline</li>
<li>Approximately 3+ years of experience in Design Assurance, or a related role within the medical device industry.</li>
<li>Strong knowledge of medical device regulations and standards, including:</li>
<li>ISO 13485</li>
<li>ISO 14971</li>
<li>FDA Quality Management System Regulation (QMSR; 21 CFR Part 820)</li>
<li>Working knowledge of IEC 62304, IEC 60601, and ISO 62366 and their application within software, electronics, and medical device development projects.</li>
<li>Experience supporting design control activities, risk management, and product verification and validation.</li>
<li>Exposure to software and electronics development projects is desirable.</li>
<li>Experience with complaint investigations, CAPA activities, or post-market product support is advantageous.</li>
<li>Strong technical writing, analytical, organisational, and communication skills.</li>
<li>Ability to work effectively as part of cross-functional teams while managing multiple priorities.</li>
</ul>
KEY COMPETENCIES
<ul>
<li>Problem-solving and analytical thinking</li>
<li>Effective communication and collaboration skills</li>
<li>Ability to work independently and as part of a team</li>
<li>Decision-making supported by risk-based thinking</li>
<li>Continuous improvement mindset</li>
<li>Ability to build strong cross-functional relationships across the organisation</li>
<li>Strong attention to detail and quality mindset</li>
</ul>

Design Assurance Engineer (software)

Manufaccturing Engineer - Projects 

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Position: Cleanroom Prototype Technician Location: Eindhoven, Netherlands Employment: Full-time, currently Day Shift (future 2-shift system)
<h3 data-section-id="zmeluu" data-start="294" data-end="312">About the Role</h3>
As a Cleanroom Prototype Technician, you will assemble, test, troubleshoot, and optimize next-generation Atmospheric Wafer Handler (AWH MK9) systems for ASML lithography machines. Working in VDL ETG's Prototype Department, you'll help transition products from prototype to full-scale production while collaborating closely with engineers.
<h3 data-section-id="164ueu3" data-start="661" data-end="685">Key Responsibilities</h3>
<ul data-start="686" data-end="1080">
<li data-section-id="ar07a5" data-start="686" data-end="740">Assemble complex mechanical and mechatronic systems.</li>
<li data-section-id="ajhbk8" data-start="741" data-end="781">Read and interpret technical drawings.</li>
<li data-section-id="8lavr7" data-start="782" data-end="836">Perform testing, qualification, and troubleshooting.</li>
<li data-section-id="14nwrap" data-start="837" data-end="896">Conduct root cause analysis and resolve technical issues.</li>
<li data-section-id="eibfoe" data-start="897" data-end="948">Improve assembly processes and work instructions.</li>
<li data-section-id="7woj14" data-start="949" data-end="981">Record assembly and test data.</li>
<li data-section-id="b88hh4" data-start="982" data-end="1035">Support industrialization and production readiness.</li>
<li data-section-id="1j262uv" data-start="1036" data-end="1080">Work in a high-tech cleanroom environment.</li>
</ul>
<h3 data-section-id="14esvje" data-start="1082" data-end="1098">Requirements</h3>
<ul data-start="1099" data-end="1542">
<li data-section-id="108cb3h" data-start="1099" data-end="1219">Technical qualification (EQF Level 4) in:
<ul data-start="1145" data-end="1219">
<li data-section-id="1byeel0" data-start="1145" data-end="1159">Mechatronics</li>
<li data-section-id="1mt0f6i" data-start="1162" data-end="1186">Mechanical Engineering</li>
<li data-section-id="ky5t1m" data-start="1189" data-end="1219">Or a related technical field</li>
</ul>
</li>
<li data-section-id="1ef3aoj" data-start="1220" data-end="1268">Experience with technical/mechanical assembly.</li>
<li data-section-id="zjcczi" data-start="1269" data-end="1320">Ability to read technical drawings independently.</li>
<li data-section-id="1cyqgag" data-start="1321" data-end="1364">Knowledge of testing and troubleshooting.</li>
<li data-section-id="1mljjrp" data-start="1365" data-end="1401">Good English communication skills.</li>
<li data-section-id="4tr4bx" data-start="1402" data-end="1460">Proactive, quality-focused, and problem-solving mindset.</li>
<li data-section-id="lrflmc" data-start="1461" data-end="1542">Willingness to work in a cleanroom and transition to a future 2-shift schedule.</li>
</ul>
<h3 data-section-id="5y7puq" data-start="1544" data-end="1556">Benefits</h3>
<ul data-start="1557" data-end="2003">
<li data-section-id="1wcy5cg" data-start="1557" data-end="1576">25 paid holidays.</li>
<li data-section-id="l01t9x" data-start="1577" data-end="1600">8% holiday allowance.</li>
<li data-section-id="ismsut" data-start="1601" data-end="1620">5% ADV allowance.</li>
<li data-section-id="1i4sbn4" data-start="1621" data-end="1691">Potential 20% shift allowance when the department moves to 2 shifts.</li>
<li data-section-id="9r89fb" data-start="1692" data-end="1736">Extensive training and career development.</li>
<li data-section-id="1228ngg" data-start="1737" data-end="1767">Modern cleanroom facilities.</li>
<li data-section-id="3ttb60" data-start="1768" data-end="1804">International working environment.</li>
<li data-section-id="33ij9z" data-start="1805" data-end="2003">Relocation support including:
<ul data-start="1839" data-end="2003">
<li data-section-id="14jd9sf" data-start="1839" data-end="1859">Housing assistance</li>
<li data-section-id="to8qp2" data-start="1862" data-end="1880">BSN registration</li>
<li data-section-id="qjjncx" data-start="1883" data-end="1903">Dutch bank account</li>
<li data-section-id="kmua6h" data-start="1906" data-end="1930">Health insurance setup</li>
<li data-section-id="1sagsg9" data-start="1933" data-end="1956">Dutch language course</li>
<li data-section-id="zoy9td" data-start="1959" data-end="2003">Ongoing relocation and integration support</li>
</ul>
</li>
</ul>
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*The 20% shift allowance is not currently applicable because the role is on day shift. It becomes payable if the department transitions to a 2-shift operation.
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Prototype Technician

I specialise in talent acquisition for diverse industries across Ireland. With a robust experience spanning over three decades, HERO Recruitment has earned a stellar reputation for our unwavering passion and commitment to excellence.
Our client portfolio is broad, covering sectors such as medical devices, pharmaceuticals, manufacturing, IT, and more. Armed with extensive connections, I can confidently locate the perfect match for you.
However, let's shift the focus to you &ndash; your dreams and goals are my driving force. Beyond being a recruiter, I am your dedicated partner, ready to guide you through every step of your journey. Together, we will navigate through various opportunities and transform your career aspirations into reality.
Join the HERO Recruitment family today, and let's co-create a success story that is uniquely yours. Together, we will make a substantial impact in the industry. Are you ready? Let's make it happen.

Job Details

Manufaccturing Engineer - Projects

Recruitment Consultant

Manufaccturing Engineer - Projects

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