PROJECT ENGINEER Reporting to: Assoc Director of AutomationJob SummaryThe Project Engineer is responsible for safely coordinating and leading projects associated with Automation, Aseptic processing, new processing equipment, packaging, new Facility builds or modifications/extensions. The primary responsibility of the role is to ensure that the project meets its agreed goals/targets on time and on budget. The engineer reports project progress to the Project Manager to ensure the equipment/facility design and goals/targets are achieved.Responsibilities<ul><li>Safely coordinate the delivery of processing equipment to the site based on planned timelines and scope. Processing equipment would include e.g. autoclaves, LAF units, moulds, extruders, packaging equipment, automated vision inspection systems, lyophilsers, isolators, containment booths, stopper processing equipment and equipment upgrades &ndash; both hardware and SCADA.</li><li>Coordination of equipment installation and services hook up, working with equipment vendors and engineering personnel.</li><li>Lead the Project Team or support the Project Manager in Factory Acceptance Testing program.</li><li>Coordination of all equipment documentation requirements.</li><li>Commissioning of equipment for validation activities.</li><li>Preparation of equipment training and maintenance protocols.</li><li>Report into the Project Manager on project progress and advice/support on key project outcomes</li><li>Contribute in a team environment on specific technical problem solving forums associated with product manufacture, aseptic fill and Packaging.</li><li>Deliver Process improvement projects.</li><li>Work with the relevant Business Unit team leaders to implement improvement opportunities</li><li>Lead regular Equipment/Facility Project review meetings.</li><li>Attend the weekly Tier Meetings.</li><li>Attend monthly Department Meeting</li></ul> Requirements <ul><li>Third level qualification in an Engineering or Science or equivalent discipline/experience (Automation)</li><li>Experience of working within either the medical device or bio/pharmaceutical industry would be an advantage but not necessary. 5 years+ experience.</li><li>Project Management experience is preferable but not necessary</li><li>Interpersonal skills required to operate in a multi-function project team set up.</li><li>Ability to work within a team and on own initiative to articulate and deliver specific functional requirements for all aspects of the project and work with members of various disciplines and functions across the project.Essential Knowledge, Skills &amp; Abilities:</li><li>Experience of working on a team, including strong organizational and time management skills.</li><li>Exposure to process/equipment projects preferred.</li><li>Experience in a GxP regulated environment is preferred.</li><li>Experience with manufacturing systems is preferred.</li><li>Proficient in Windows Operating System, Microsoft Office and a good understand of PLC and Scada systems preferred.</li><li>Flexibility to respond to production issues outside normal business hours.</li><li>Ability to learn new and different technologies.Behaviours/Value:</li><li>Relationship Building: Establishing good working relationships with key contact members within the organisation.</li><li>Communication: Good communication and presentations skills, both written and oral &ndash; ability to present production data in a clear and concise manner to team members and where required, to management.</li><li>Planning &amp; Organising: able to plan activities and tasks whilst ensuring the required number of people are available and in place to perform the task.</li><li>Decision Making: identify and understand issues, problems and opportunities whilst working within a team environment to provide a solution.</li><li>Adaptability; Able to work in a fast, dynamic, environment whilst being able to adjust readily to meet unexpected constraints.</li><li>Passion for results: - Drive, high energy and ability to work under pressure and deliver results; get things done (an action-oriented approach); overcome obstacles.</li><li>Receptivity to feedback - Receptive to the ideas of others and welcome and accept constructive feedback, display humility where appropriate.</li><li>Have a people centred approach in a team environment whilst upholding the values and ethos of the company</li><li>Other requirement (i.e. travel): Undertake any training or travel that the role may require.</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 Geraldine Gormally on 0861071395&nbsp;&nbsp;<a href="mailto:/%C2%A0recruit@hero.ie">/&nbsp;recruit@hero.ie</a>Check out all our open jobs on our HERO Recruitment website &ndash;&nbsp;<a href="https://www.hero.ie/">https://www.hero.ie/</a>&nbsp;&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.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.

Project Engineer 

Lead Packaging Engineer -&nbsp; Co Mayo&nbsp;Are you a packaging expert ready to make a global impact? My client is looking for a Lead Packaging Engineer to join a Global Packaging team and help us deliver life-changing medical products with precision, safety, and innovation.In this role, you&rsquo;ll lead packaging development and will be driving excellence from concept through commercialization. You&rsquo;ll collaborate cross-functionally, mentor peers, and influence packaging decisions that ensure compliance, optimize performance, and enhance patient outcomes.In this role you will:&nbsp;<ul><li>Lead packaging projects for new product development and changes to existing products</li><li>Develop and validate sterile and non-sterile packaging systems</li><li>Drive cost savings and continuous improvement initiatives</li><li>Ensure global regulatory compliance&nbsp; </li></ul>Ideally you will have:&nbsp; <ul><li>6+ years of packaging experience in medical devices or related industries</li><li>Expertise in ISO 11607, ASTM, ISTA, and EU MDR/FDA guidance</li><li>Strong technical writing, validation, and statistical analysis skills</li><li>A passion for innovation, collaboration, and making a difference</li></ul> Benefits:<ul><li>Competitive salary and benefits package</li></ul> To discuss this and other roles call Regina Carroll at 086 0100903 or email <a href="mailto:engineering@hero.ie">jobs@hero.ie</a> Check 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 you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

Lead Packaging Engineer 

Digitalisation Manager &ndash; Medical Device Leader | Co. Mayo (Hybrid)We are seeking a Digitalisation Manager to lead Industry 4.0, IIoT, and smart factory initiatives for a global medical device manufacturer. Based in Co. Mayo, this strategic role will spearhead the digital transformation of manufacturing operations&mdash;driving real-time data enablement, IT/OT convergence, and intelligent automation.Key Responsibilities:<ul data-start="592" data-end="1161"><li data-start="592" data-end="675">Develop and execute a global digitalisation strategy aligned with business goals.</li><li data-start="676" data-end="790">Lead deployment of smart technologies including</li><li data-start="791" data-end="897">Collaborate with IT, OT, engineering, and quality teams to optimize efficiency, quality, and throughput.</li><li data-start="898" data-end="981">Translate operational data into actionable insights that improve decision-making.</li><li data-start="982" data-end="1077">Guide and mentor cross-functional teams on digital literacy and smart manufacturing adoption.</li><li data-start="1078" data-end="1161">Support succession planning by working closely with the existing Digital Manager.</li></ul>What You Bring:<ul data-start="1183" data-end="1622"><li data-start="1183" data-end="1274">7+ years in manufacturing, with strong experience in digital transformation/Industry 4.0.</li><li data-start="1275" data-end="1357">Background in controls engineering, automation, or related technical fields.</li><li data-start="1358" data-end="1460">Hands-on experience with MES, SCADA, IIoT, edge computing, and data visualization platforms.</li><li data-start="1461" data-end="1541">Familiarity with regulated environments (medical devices or pharma preferred).</li><li data-start="1542" data-end="1622">Strong leadership, stakeholder engagement, and change management capabilities.</li></ul>Why Join:<ul data-start="1638" data-end="1922"><li data-start="1638" data-end="1739">Help position this site as a centre of excellence for digitalisation and business transformation.</li><li data-start="1740" data-end="1820">Work on impactful initiatives with global reach and long-term strategic value.</li><li data-start="1821" data-end="1922">&nbsp;</li></ul>

Manufacturing Digitalization Manager

Manufacturing Engineer II&nbsp;Location: GalwayJob Type: Full-Time Contract RoleExperience Level: Mid-Level (Minimum 3 years of relevant experience)Job Summary: As a Manufacturing Engineer II, you will play a crucial role in the production of self-expanding Stents products. You will leverage your technical expertise, problem-solving abilities, and validation experience to ensure the efficiency and quality of our manufacturing processes. Your efforts will directly impact the improvement of our processes and the successful completion of our projects.Key Responsibilities:<ul><li>Technical Expertise: Apply advanced engineering principles to support and improve manufacturing processes within the medical device sector.</li><li>Problem Solving: Identify and resolve manufacturing issues to maintain product quality and production efficiency.</li><li>Validation Experience: Conduct and document validation activities to ensure compliance with regulatory requirements and quality standards.</li><li>Process Improvement: Continuously evaluate and enhance manufacturing processes to optimize productivity and reduce costs.</li><li>Project Management: Lead and participate in project teams, ensuring timely completion of deliverables within budget.</li><li>Teamwork: Collaborate effectively with cross-functional teams including R&amp;D, Quality, and Operations to achieve common goals.</li><li>Communication Skills: Clearly and effectively communicate technical information to team members, stakeholders, and management.</li></ul>Qualifications:<ul><li>Minimum of 3 years of experience in a manufacturing engineering role, preferably within the medical device or related industry.</li><li>Strong technical background with a proven track record in problem-solving and process improvement.</li><li>Hands-on experience with validation processes and documentation.</li><li>Excellent project management skills with the ability to manage multiple projects simultaneously.</li><li>Effective teamwork and interpersonal skills.</li><li>Strong verbal and written communication skills.</li></ul>

Manufacturing Engineer II

Job Purpose:The Process Development Engineer I will support multiple ongoing projects, primarily focusing on process improvement, equipment validation, and technical problem-solving. The current assignment involves working on coating processes within a medical device manufacturing environment. This role will collaborate with cross-functional teams to develop, validate, and optimize manufacturing processes in line with New Product Introduction (NPI) and Continuous Improvement (CI) strategies.Key Responsibilities:<ul><li>Support coating and other manufacturing processes, driving improvements in yield, quality, and throughput.</li><li>Collaborate across departments (e.g., R&amp;D, Quality, Manufacturing) to introduce and integrate new products/processes into production.</li><li>Assist in the programming and maintenance of new equipment sets using both visual and CAD-based approaches.</li><li>Participate in the validation of equipment and processes, ensuring compliance with regulatory standards (Validation experience is desirable but not essential).</li><li>Analyse and troubleshoot technical issues, working from basic to advanced engineering principles.</li><li>Document findings, prepare technical reports, and present results to stakeholders.</li><li>Work with minimal supervision in an independent role, while coordinating with the team for project alignment.</li><li>Contribute to a positive and collaborative team culture - cultural fit is a key hiring criterion.</li></ul>Minimum Qualifications:<ul><li>Level 8 BSc Honours Degree in a relevant engineering discipline (e.g., Mechanical, Electrical, Biomedical, Chemical or Process Engineering).</li><li>1+ years of relevant industry experience (Medical Device experience ideal, but not essential).</li><li>Strong analytical skills with proven problem-solving ability.</li><li>Excellent communication skills and ability to work cross-functionally.</li></ul>Desirable Technical Skills:<ul><li>Experience with coating processes in a manufacturing or R&amp;D setting.</li><li>Exposure to equipment validation and process validation activities.</li><li>Proficiency in CAD and visual programming tools for equipment development.</li></ul>Why Join?<ul><li>Exposure to advanced manufacturing technologies and cross-functional project work.</li><li>Supportive team environment with strong mentorship during onboarding.</li><li>Opportunity to build long-term experience in a globally respected medical device company.</li></ul>Apply today!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.

Process Development Engineer I 

Electrical Design Engineer PurposeTo provide Electrical and Safety design expertise to the Equipment Engineering department in the design, manufacture, documentation, and continuous improvement of equipment to produce medical devices.Responsibilities <ul><li>Generation of equipment electrical designs which meet manufacturing, safety, CE, and performance requirements.&nbsp;</li><li>Proactively and continuously ensure potential safety risks are addressed and ensure equipment meets CE marking standards.&nbsp;</li><li>Work closely with internal engineers to understand their equipment requirements.&nbsp;</li><li>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>Ensure equipment solutions are delivered within planned schedules and within budget.</li><li>Ensure documentation/drawing standards for equipment meet compnay requirements.&nbsp;</li><li>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>Build Quality into all aspects of work by maintaining compliance to all quality requirements</li><li>Participates in and leads the use of lean and Continuous Improvement tools in equipment designs and engineering systems.&nbsp;</li><li>Support continuous improvement activities</li><li>Provide technical guidance / leadership to the equipment build team</li><li>PSPI/CI/VIP opportunity identification and collation</li></ul> Qualifications <ul><li>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>Proficient in the use of AutoCAD Electrical, and design of pneumatic circuits.&nbsp;</li><li>Proven ability to design and commission electrical and pneumatic control panels for automated equipment.</li><li>Proven ability to assess and remediate equipment safety issues</li><li>Good technical capabilities, teamwork abilities and initiative.&nbsp;</li><li>Proven ability to work well as part of a team &amp; on own with minimum supervision</li><li>Good communication skills combined with an imaginative and creative approach to problem solving.&nbsp;</li></ul>Working Conditions <ul><li>Much of the work will be spent on-site in a manufacturing support environment</li><li>There may be a requirement as part of the role to travel to other sites.&nbsp;</li><li>Working times are Monday to Friday; however, weekend work may be required.&nbsp;</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 Geraldine Gormally on 0861071395&nbsp;&nbsp;<a href="mailto:/%C2%A0recruit@hero.ie">/&nbsp;recruit@hero.ie</a>Check out all our open jobs on our HERO Recruitment website &ndash;&nbsp;<a href="https://www.hero.ie/">https://www.hero.ie/</a>&nbsp;&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.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.

Electrical Design Engineer 

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.

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Lead Packaging Engineer

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Lead Packaging Engineer

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