Job Title: Construction Manager Consultant Department: Engineering Location: Limerick&nbsp; Summary: Construction Manager to lead, co-ordinate and deliver projects on-site in Limerick supporting and optimizing throughout. Essential Duties and Responsibilities include, but are not limited to, the following: <ul><li>Oversee day-to-day site operations, ensuring works are carried out safely, efficiently, and to specification.</li><li>Implement and enforce health, safety, and environmental standards in line with company an statutory requirements.</li><li>Demonstrate, promote and acknowledge positive behaviours to develop a proactive safety culture on site, Identify and prevent unsafe behaviors, defects.</li><li>Coordinating with consultants, subcontractors, supervisors, planners, quantity surveyors and the general workforce involved in the project.</li><li>Coordinate with project managers, engineers, and stakeholders to ensure seamless project delivery.</li><li>Monitor progress, identify risks or delay, and implement solutions to keep the project on track.</li><li>Prepare and present regular reports on site performance and progress.</li><li>Review technical drawings and ensure site works align with design specifications and standards.</li></ul>Education and experience: <ul><li>Bachelor&rsquo;s degree in engineering (Construction, Civil or related field).</li><li>Proven experience as a Construction Manager or Site Manager, ideally on ideally in the biopharma or life sciences sector.</li><li>Strong leadership and organisational skills with the ability to coordinate diverse teams.</li><li>Solid understanding of construction processes, safety regulations, and technical drawings.</li><li>Excellent communication skills and the ability to foster strong working relationships.</li></ul>

Construction Manager Consultant 

Senior Chemist Overview We are seeking a Senior Chemist to serve as a subject matter expert (SME) in analytical chemistry in a leading Medical Device company, providing technical leadership and oversight in critical areas of new product development (NPD). The role will involve designing and validating analytical methods, supporting laboratory operations, driving continuous improvements, and ensuring regulatory and quality compliance across projects. Key Responsibilities<ul><li>Act as a subject matter expert in critical NPD areas, including:</li></ul><ul style="list-style-type: circle;"><li>Dissolution/Elution (USP Apparatus II / USP Apparatus VII)</li><li>Liquid/Gas Chromatography</li><li>Analytical test method development</li><li>Analytical test method validation</li></ul><ul><li>Work independently to plan, prioritize, and schedule activities to ensure project milestones are achieved.</li><li>Author and review technical reports, validation documents, and regulatory-supporting documentation.</li><li>Provide guidance and communicate progress to cross-functional and cross-site teams.</li><li>Support laboratory investigations by identifying root causes and implementing meaningful corrective and preventive actions.</li><li>Lead or contribute to continuous improvement projects aimed at reducing testing lead times and achieving cost savings.</li><li>Support onboarding and training of new colleagues in analytical techniques and laboratory practices.</li><li>Participate in and support internal and external audits.</li><li>Provide analytical expertise and documentation for regulatory submissions.</li></ul><h2 data-start="2083" data-end="2115">Qualifications &amp; Experience</h2><ul><li data-start="2118" data-end="2243">Bachelor&rsquo;s or Master&rsquo;s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field; PhD preferred.</li><li data-start="2118" data-end="2243">Proven industry experience in analytical chemistry, preferably within medical devices, pharmaceuticals, or related regulated industries.</li><li data-start="2387" data-end="2476">Strong knowledge of dissolution/elution testing and chromatographic techniques (LC/GC).</li><li data-start="2479" data-end="2567">Experience in analytical method development and validation under GMP/GLP requirements.</li><li data-start="2570" data-end="2662">Demonstrated ability to author and review technical documentation to regulatory standards.</li><li data-start="2665" data-end="2742">Hands-on experience with laboratory investigations and root cause analysis.</li><li data-start="2745" data-end="2825">Familiarity with regulatory requirements (e.g., FDA, ISO) and audit processes.</li></ul><h2 data-start="2827" data-end="2846">Desired Skills</h2><ul><li>Excellent organizational and project management abilities.</li><li>Strong analytical problem-solving skills with attention to detail.</li><li>Effective communicator across teams and at different organizational levels.</li><li>Ability to train, mentor, and influence colleagues in best practices.</li><li>Continuous improvement mindset with focus on efficiency and compliance.</li></ul> <p style="box-sizing: border-box; margin-top: 0px; margin-bottom: 1rem; font-family: Barlow, sans-serif; font-size: 16px; color: #212529; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: #ffffff; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;">Our Vision: To be recognised as the best STEM Contracting &amp; Permanent Recruitment company and the Employer of Choice for top performing Recruiters<span style="box-sizing: border-box; font-family: inherit !important; font-size: inherit !important;" data-ccp-props="{&quot;201341983&quot;:0,&quot;335557856&quot;:16777215,&quot;335559739&quot;:150,&quot;335559740&quot;:240}">&nbsp;<p style="box-sizing: border-box; margin-top: 0px; margin-bottom: 1rem; font-family: Barlow, sans-serif; font-size: 16px; color: #212529; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: #ffffff; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;"><span style="box-sizing: border-box; font-family: inherit !important; font-size: inherit !important;" data-ccp-props="{&quot;201341983&quot;:0,&quot;335557856&quot;:16777215,&quot;335559739&quot;:150,&quot;335559740&quot;:240}">&nbsp;For further information on this role please contact&nbsp;Geraldine Gormally&nbsp;on&nbsp;0861071395&nbsp; /<a style="box-sizing: border-box; color: inherit; text-decoration: underline; font-family: inherit !important; font-size: inherit !important;" href="mailto:recruit@hero.ie">&#8239;recruit@hero.ie</a>&nbsp;<p style="box-sizing: border-box; margin-top: 0px; margin-bottom: 1rem; font-family: Barlow, sans-serif; font-size: 16px; color: #212529; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: #ffffff; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;">Check out all our open jobs on our HERO Recruitment website &ndash;&#8239;<a style="box-sizing: border-box; color: inherit; text-decoration: underline; font-family: inherit !important; font-size: inherit !important;" href="https://www.hero.ie/">https://www.hero.ie/</a>&nbsp;&#8239;<span style="box-sizing: border-box; font-family: inherit !important; font-size: inherit !important;" data-ccp-props="{&quot;201341983&quot;:0,&quot;335557856&quot;:16777215,&quot;335559739&quot;:150,&quot;335559740&quot;:240}">&nbsp;<p style="box-sizing: border-box; margin-top: 0px; margin-bottom: 1rem; font-family: Barlow, sans-serif; font-size: 16px; color: #212529; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: #ffffff; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;">Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.<span style="box-sizing: border-box; font-family: inherit !important; font-size: inherit !important;" data-ccp-props="{&quot;201341983&quot;:0,&quot;335557856&quot;:16777215,&quot;335559739&quot;:150,&quot;335559740&quot;:240}">&nbsp;<p style="box-sizing: border-box; margin-top: 0px; margin-bottom: 1rem; font-family: Barlow, sans-serif; font-size: 16px; color: #212529; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: #ffffff; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;">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.

Senior Chemist 

<h3 data-start="351" data-end="379">Regulatory Affairs Specialist Contract Galway Position Overview:</h3>This role is responsible for planning, coordinating, and executing regulatory submissions for the US FDA, EU notified bodies, and global product registrations. It also involves maintaining ongoing compliance with regulatory approvals and performing change impact assessments.<h3 data-start="664" data-end="695">Key Responsibilities:</h3><ul data-start="697" data-end="1780"><li data-start="697" data-end="808">Support regulatory activities with a focus on Coronary Therapy devices as part of a collaborative team.</li><li data-start="809" data-end="956">Prepare and submit regulatory documentation for U.S. and EU markets, including PMAs, CE Marking submissions, and internal regulatory files.</li><li data-start="957" data-end="1106">Serve as a regulatory representative on cross-functional product development teams, offering strategic guidance throughout the product lifecycle.</li><li data-start="1107" data-end="1210">Review and approve design and manufacturing changes to ensure compliance with relevant regulations.</li><li data-start="1211" data-end="1292">Support product registrations and approvals across international markets.</li><li data-start="1293" data-end="1444">Contribute to continuous improvement initiatives aligned with the organization's Quality Management System and applicable regulatory standards.</li><li data-start="1445" data-end="1551">Collaborate on enhancing team practices and promoting knowledge sharing and regulatory best practices.</li><li data-start="1552" data-end="1638">Participate in sustaining activities under product lifecycle management processes.</li><li data-start="1639" data-end="1780">Assist in preparing for and participating in regulatory inspections and audits (e.g., FDA, EU Notified Bodies, national authorities).</li></ul><h3 data-start="1787" data-end="1825">Qualifications &amp; Experience:</h3><ul data-start="1827" data-end="2347"><li data-start="1827" data-end="1901">Degree (Level 8 or equivalent) in a Science or Engineering discipline.</li><li data-start="1902" data-end="1947">Strong interpersonal and teamwork skills.</li><li data-start="1948" data-end="2032">Excellent verbal and written communication, including technical writing ability.</li><li data-start="2033" data-end="2107">Proven ability to manage multiple priorities and projects effectively.</li><li data-start="2108" data-end="2192">Prior experience in Regulatory Affairs or Design Assurance is desirable.</li><li data-start="2193" data-end="2347">Familiarity with drug-device combination products or manufacturing processes in the medical device or pharmaceutical industry is an advantage.</li></ul>

Regulatory Affairs Specialist

Job Title - Applications Engineer&nbsp; Reports to - Engineering Manager&nbsp; Type: Long Term Contract&nbsp; Summary&nbsp; Your role will encompass maintaining software solutions, fault finding issues, reviewing code, supporting new automated systems and training engineers on code review. Key Areas of Responsibility:&nbsp; <ul><li>Technical Support &amp; Troubleshooting: Provide ongoing support to users, diagnosing and resolving application-related issues promptly.</li><li>Performance Monitoring: Regularly assess application performance, identifying areas for optimization and implementing necessary enhancements.</li><li>Provide Applications Technical leadership from an engineering perspective.</li><li>Review code on old machines and insert comments on blocks.</li><li>Train engineers on code troubleshooting techniques.</li><li>All other duties as assigned</li></ul> Qualifications, Knowledge &amp; Skills:&nbsp; <ul><li>Level 8 Degree in Mechanical Engineering or relevant discipline or equivalent technical experience is required.</li><li>Has minimum of 4 years&rsquo; experience in a manufacturing environment.</li><li>Strong communication and influencing skills with both internal and external.</li><li>Proficiency in programming languages such as Siemens, Allen Bradley, Rockwell Studio, Mitutibi, Beckhoff, Fanuc and ABB controls.</li><li>Capable of working as part of a multi-disciplined team in an aggressive, dynamic and results motivated environment</li><li>Good knowledge on how to access panels and access the software system.</li><li>Demonstrable strong analytical &amp; problem solving skills, a process improvement orientation, and the ability to handle multiple tasks in a fast-paced environment</li><li>Demonstrable ability to work autonomously</li><li>A team player, with a flexible approach.</li></ul>

Applications Engineer - PLC

Electrical Engineering Consultant Limerick&nbsp; Contract role&nbsp; Position Summary: Seeking an experienced Electrical Engineer to provide technical design support for a new Process Area CAPEX project. The role will also involve supporting smaller capital initiatives and ongoing site operations. <h3 data-start="380" data-end="409">Key Responsibilities:</h3><ul data-start="411" data-end="1726"><li data-start="411" data-end="636">Design and maintain Low Voltage (LV) systems (e.g., lighting, general services, UPS, protection settings including arc flash) and Extra-Low Voltage (ELV) systems (e.g., fire alarm, data points, building automation).</li><li data-start="637" data-end="724">Manage and execute small-scale projects focused on electrical systems infrastructure.</li><li data-start="725" data-end="823">Support the design review, site acceptance, and installation processes for electrical equipment.</li><li data-start="824" data-end="903">Prepare and maintain electrical drawings and related technical documentation.</li><li data-start="904" data-end="1008">Specify and design cGMP-compliant electrical and instrumentation (E&amp;I) equipment and process controls.</li><li data-start="1009" data-end="1075">Oversee electrical systems integrated with business IT networks.</li><li data-start="1076" data-end="1183">Collaborate with the validation team by preparing design documentation and supporting protocol execution.</li><li data-start="1184" data-end="1297">Participate in investigations of equipment anomalies, including power quality events and control system issues.</li><li data-start="1298" data-end="1385">Prepare engineering evaluations and manage modification change control documentation.</li><li data-start="1386" data-end="1475">Supervise electrical contractors, ensuring work is completed to the required standards.</li><li data-start="1476" data-end="1571">Prepare risk assessments, method statements, and other Health &amp; Safety-related documentation.</li><li data-start="1572" data-end="1643">Promote and enforce a clean, safe, and compliant working environment.</li><li data-start="1644" data-end="1726">Ensure compliance with applicable regulations, standards, and internal policies.</li></ul><h3 data-start="1733" data-end="1769">Qualifications &amp; Experience:</h3><ul data-start="1771" data-end="1908"><li data-start="1771" data-end="1841">Bachelor&rsquo;s degree in Electrical Engineering or a related discipline.</li><li data-start="1842" data-end="1908">Minimum of 4 years of relevant experience in a similar role.</li></ul>

Electrical Engineer

Project Manager - Castlebar - 12 month contract&nbsp; Our client is a manufacturing provider to medical device and pharma and is looking for a Project Manager for 12 months to plan, lead and execute project's ensuring alignment with organizational goals while managing stakeholder relationships.&nbsp; In this role you will :&nbsp; Lead the planning and execution of projects from initiation to closure. <ul><li>Define project scope, objectives, deliverables, timelines and budgets.</li><li>Develop and maintain detailed project plans, schedules, Gantt charts and documentation.</li><li>Manage relationships with external parties, vendors, contractors and suppliers.</li><li>Co-ordinate and liaise with cross functional teams to ensure project success.</li><li>Identify, assess, and mitigate project risks and issues.</li><li>Monitor project progress, track KPI&rsquo;s and report updates to stakeholders.</li><li>Manage stakeholder communications and ensure alignment across teams.</li></ul>Ideally you will have:&nbsp; <ul><li>Bachelor&rsquo;s degree in Business, Management, Engineering or a related field.</li><li>Proven experience as a Project Manager or similar role (ideally in Manufacturing)</li><li>Strong leadership, organisational and problem-solving skills.</li><li>Proficiency in project management tools, e.g. MS Project, Jira, etc)</li><li>Ability to manage multiple projects simultaneously under tight deadlines.</li><li>Strong financial and budget management skills.</li></ul> For further information on this role in please contact on Regina Carroll&nbsp; on 086 0100 903 or jobs@hero.ie 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

Project Manager

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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