Lead Research and Development Engineer Location: Limerick, Ireland
Overview: The Lead Research and Development Engineer will oversee a team of engineers dedicated to the research, development, and implementation of innovative medical device designs. This role provides technical leadership within project teams, including approving deliverables, mentoring team members, and delegating responsibilities effectively.
Reports to: Manager/Senior Manager, Research and Development
Key Responsibilities:
Project Leadership:
<ul>
<li>Lead medium to large-scale R&amp;D projects, providing technical expertise across multiple projects or specialized areas.</li>
<li>Develop and optimize chemical and physical analytical methods to support early-stage product development.</li>
<li>Drive capacity analysis within the Pharmaceutical Development Formulation team to ensure efficient resource and equipment utilization.</li>
</ul>
Technical Excellence:
<ul>
<li>Collaborate with internal and external teams to identify and evaluate Critical Material Attributes (CMAs).</li>
<li>Champion improvement initiatives, including ownership of departmental processes.</li>
<li>Incorporate lean principles into the design and implementation of new processes where applicable.</li>
</ul>
Project Management:
<ul>
<li>Approve project deliverables and oversee work outputs to meet timelines and quality standards.</li>
<li>Drive project milestones and ensure alignment with business objectives in collaboration with project managers.</li>
<li>Foster effective relationships with cross-functional teams to achieve project and company goals.</li>
</ul>
Design Leadership:
<ul>
<li>Lead technical development efforts and key design decisions to ensure high-quality solutions meet customer needs.</li>
<li>Conduct retrospective reviews of projects to identify lessons learned for future initiatives.</li>
<li>Oversee device evaluations, ensuring compliance with quality and regulatory standards, as well as internal policies.</li>
</ul>
Compliance and Industry Engagement:
<ul>
<li>Ensure all work complies with guidance and best practices, such as USP, Ph. Eur., and ICH.</li>
<li>Represent the company in industry standards committees, working groups, and conferences. Mentorship:</li>
<li>Act as a mentor to department personnel, fostering their technical and professional growth.</li>
<li>Support training initiatives to strengthen team capabilities.</li>
</ul>
Qualifications and Experience:
<ul>
<li>Bachelor&rsquo;s degree in Engineering (preferably Polymer Science, Industrial Chemistry, or Pharmaceuticals) or a related field, with 7+ years of relevant experience, OR</li>
<li>Master&rsquo;s degree with 5+ years of relevant experience, OR</li>
<li>PhD with 4+ years of relevant experience.</li>
<li>Extensive experience in product development for medical devices, including combination product development.</li>
<li>Deep understanding of technologies and challenges related to formulation and product development.</li>
<li>Competence in chemical and physical analytical methodologies and testing procedures for formulation approval.</li>
<li>Proven knowledge of technical transfer processes to manufacturing operations.</li>
</ul>
Leadership Skills:
<ul>
<li>Demonstrated technical and project leadership experience.</li>
<li>Strong project management skills, with experience collaborating closely with project managers.</li>
<li>In-depth knowledge of ISO, EU, and FDA medical device standards and regulations.</li>
</ul>
&nbsp;

Lead Research & Development Engineer

<h2 class="css-7papts" data-automation-id="jobPostingHeader">Mechanical Technician Location: Limerick, Ireland Contract: Fixed Term Contract (12 months)</h2>
Are you a skilled&nbsp;with a passion for supporting cutting-edge medical technology? A leading global healthcare company, renowned for its innovative medical devices, is looking for a dedicated Maintenance Technician to join their team in Limerick. This is a fantastic opportunity to work in a highly collaborative and dynamic environment, contributing to the advancement of healthcare solutions.
About the Role
The Mechanical Technician&nbsp;will be an integral part of the Mechanical &amp; Test team, providing vital support in a wide range of activities, from design verification and validation to reliability testing and root cause analysis. The role is hands-on and offers the chance to work with state-of-the-art equipment while making a meaningful impact on the development of life-changing medical devices.
Key Responsibilities
<ul>
<li>Laboratory and Project Support: Assist with fixture development, testing, and reporting. Contribute to the documentation of test results and support ongoing projects.</li>
<li>Execution of Day-to-Day Tasks: Conduct analytical testing on medical devices to generate data that enhances product design and supports design verification.</li>
<li>Documentation &amp; Reporting: Help in the creation of product development documentation, including test methods, test protocols, and test reports.</li>
<li>Data Management: Maintain precise data records, prepare reports, and communicate technical challenges with solutions to the team.</li>
<li>Laboratory Equipment: Assist in the installation, validation, and maintenance of R&amp;D laboratory equipment.</li>
<li>Collaboration &amp; Communication: Participate in technical review meetings and collaborate with cross-functional teams to drive progress on project activities.</li>
</ul>
About You
The ideal candidate will have a technical qualification in Mechanical Engineering, Mechatronics, Manufacturing, or a similar field, either through an apprenticeship or third-level education. You should have hands-on experience in an R&amp;D environment and be comfortable working independently with minimal supervision. Familiarity with laboratory equipment, including analytical balances, pressure sensors, and Instron UTM, will be advantageous. Additionally, you should be proficient in standard office software (Microsoft Word, Excel, PowerPoint) and possess excellent communication skills to liaise effectively with all levels of technical and management teams.
Key Skills and Qualifications
<ul>
<li>Technical Qualification: Mechanical Engineering, Mechatronics, Manufacturing, or similar (apprenticeship or third-level education).</li>
<li>Industry Experience: Previous experience in an R&amp;D environment is desirable.</li>
<li>Laboratory Skills: Experience with laboratory equipment such as analytical balances, vernier calipers, micrometers, pressure sensors, and Instron UTM.</li>
<li>Software Skills: Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).</li>
<li>Communication Skills: Strong verbal and written communication skills.</li>
<li>Independence and Time Management: Ability to prioritise tasks and work independently in a fast-paced environment.</li>
</ul>
Why Join This Company?
This is more than just a job &ndash; it&rsquo;s an opportunity to be part of a company that is at the forefront of transforming healthcare. You&rsquo;ll have the chance to collaborate with inspiring leaders, gain exposure to world-class projects, and make a real difference in people&rsquo;s lives. The company fosters a growth-focused, inclusive culture where learning and professional development are encouraged every step of the way.
Our Vision: To be recognised as the best STEM Contracting &amp; Permanent Recruitment company and the Employer of Choice for top performing Recruiters&nbsp;
&nbsp;For further information on this role please contact Edward Britton on 0864403742&nbsp;/<a href="mailto:hire@hero.ie"> hire@hero.ie</a>&nbsp;&nbsp;
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;
 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.&rdquo;&nbsp;
&nbsp;

Mechanical Technician

Global Project Manager Our client is dedicated to transforming lives through innovative medical solutions that improve the health of patients around the world.&nbsp; They are seeking a Global Sourcing Technical Project Manager .&nbsp;
The job: The Global Project Manager will be responsible for the leadership of the Operations portion of new product development projects, site transfers, acquisition integrations and other complex manufacturing project initiatives associated with Sourced Finished Medical Device products. Responsibilities:
<ul>
<li>Lead teams consisting of Supplier resources.</li>
<li>Assemble the cross functional resources required to drive project completion.</li>
<li>Identify, coordinate, and ensure completion all activities required to for an assigned project or task while confirming current policies and best practices.</li>
<li>Prioritize projects and activities based on business need, timing, and financial risk.</li>
<li>Ensure successful execution of projects using various tool kits, work instructions and best practices.</li>
<li>Create project tracking plans, schedules, and risks for projects and communicate across the organization as applicable</li>
</ul>
You will have:&nbsp; 
<ul>
<li>12+ years engineering experience (manufacturing, process development or related)</li>
<li>Level 8 Bachelor&rsquo;s degree required, preferably in engineering&nbsp;</li>
<li>5+ years technical project management experience.</li>
<li>Strong communication skills.</li>
<li>2+ years experience working with external manufacturing partners.</li>
<li>Ability to travel up to 25% of the time regional and international. </li>
</ul>
 
For more on this contact Regina at HERO 086 0100903 or <a href="mailto:jobs@hero.ie">jobs@hero.ie</a> 
HERO Recruitment website &ndash; <a href="https://www.hero.ie/" target="_blank" rel="noopener">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.

Global Project Manager - Operations

Principal Instrumentation Engineer - Limerick This role is to provide support, direction and subject matter expertise on electrical &amp; instrumentation issues. Primarily focused on the instrumentation / calibration / regulatory side of the discipline. Understand and own all aspects of our site calibration program and be able to talk to the site calibration programme to health authorities and regulatory bodies during audits. The principal engineer will also own and be responsible for all aspects of the instrumentation equipment installed on site.&nbsp; Key Responsibilities:&nbsp; - Own the site calibration program.&nbsp; - Own and be responsible for all aspects of the instrumentation equipment installed on site, examples working on RCAi, Safety / quality deviations, equipment upgrades, obsolescence, project support, MTBF etc. - Initiate and roll out new site calibration strategies and directives. &middot; - Provide engineering support to both maintenance and equipment owners in your area of expertise. Ideally you will have : - 5+years experience in a maintenance/engineering role, ideally within the pharmaceutical industry. - Demonstrated ability to act independently using good organisational skills. - Proven ability to make good use of systems, procedures &amp; processes. - Working knowledge of relevant EU directives (e.g. ATEX, etc). - Familiarity with the relevant national/international engineering standards (e.g. NSAI, NECI, NEC, IEC, ISO, CEN, ISA, CENELEC etc). - Level 8 Degree in Electrical &amp; Instrumentation Engineering or equivalent 
For more on this contact Regina at HERO 086 0100903 or jobs@hero.ie
For more information on this role please contact Regina Carroll &nbsp;086 0100901 or jobs@hero.ie&nbsp;&nbsp;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;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. &nbsp;You have supplied us with your personal data in the process of applying for a position. &nbsp;Our client company may have personnel outside of the EEA who will review you data. &nbsp;We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

Principal Instrumentation Engineer

<h3>Principal Process Automation Engineer</h3>
Location: Limerick Type: Full-time &amp; Onsite
Join our client a global healthcare leader committed to improving lives through innovative medical solutions. As a Senior Principal Engineer &ndash; Process Automation, you will provide technical leadership and expertise in automation to support manufacturing operations. This role involves mentoring a team of engineers, designing automation solutions, ensuring compliance with GMP and safety guidelines, and driving continuous improvement in pharmaceutical manufacturing processes.
Key Responsibilities:
<ul>
<li>Lead and mentor process automation engineers.</li>
<li>Design and implement automation solutions, including DCS, PLC, HMI, and SCADA systems.</li>
<li>Manage process control system changes, execute Computer System Validation (CSV) activities, and resolve automation-related issues.</li>
<li>Identify opportunities for process optimization and continuous improvement.</li>
<li>Support troubleshooting and maintenance of automation systems.</li>
<li>Provide technical oversight on engineering projects and collaborate with cross-functional teams.</li>
<li>Research and implement new control strategies and technologies.</li>
</ul>
What We&rsquo;re Looking For:
<ul>
<li>Degree in Chemical Engineering, Computer Science, Electronic Engineering, or related field.</li>
<li>7+ years of experience in configuring and troubleshooting automation systems (e.g., DeltaV, Siemens, OSI PI).</li>
<li>Experience in mentoring and providing technical guidance.</li>
<li>Strong skills in communication, teamwork, and project management.</li>
<li>Knowledge of GMP and regulated environments.</li>
</ul>
Additional Preferences:
<ul>
<li>Familiarity with Manufacturing Execution Systems (e.g., Syncade).</li>
<li>Expertise in change control, deviation processes, and storage/retrieval systems.</li>
</ul>
For further information on this Senior Automation role in Limerick please contact Dee Curley on 086 7902191 /&nbsp;<a href="mailto:dee@hero.ie">dee@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: HERO Recruitment will not forward your details to any company without your prior approval
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. &nbsp;You have supplied us with your personal data in the process of applying for a position. &nbsp;Our client company may have personnel outside of the EEA who will review you data. &nbsp;We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.
&nbsp;

Principal Process Automation Engineer

Manufacturing Engineer II 
Our client, a Medical Device company is looking for a Manufacturing Engineer to join their team in central Galway.&nbsp;
The Manufacturing Engineer will be responsible for providing engineering support to Manufacturing, and the development of existing and new process technologies within the business unit.&nbsp; Key Responsibilities:
<ul>
<li>Provide Manufacturing line support to production.</li>
<li>Lead Improvement Projects addressing yield, efficiency and capacity.</li>
<li>Lead projects for new equipment and process introduction and qualification</li>
<li>Identify and implement solutions to quality and technical issues.</li>
<li>Improve manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing methods and equipment; conferring with equipment vendors.</li>
<li>Responsible for managing the overall equipment performance (OEE) through the appropriate use of Lean Manufacturing tools and techniques.</li>
<li>Investigate new process technologies and evaluate potential competitive advantage and the cost benefit of introduction.</li>
<li>Prepare product and process reports by collecting, analysing, and summarizing information and trends.</li>
</ul>
Qualifications:
<ul>
<li>Must have L8 Bachelors Degree in an Engineering, Science or related discipline.</li>
<li>Minimum 3 years&rsquo; experience in a similar role or more in a Technician Level role.&nbsp;</li>
<li>Previous experience working within Medical Devices industry, Lasers would be an advantage.&nbsp;</li>
<li>Practical understanding of Lean Manufacturing principles</li>
</ul>

Manufacturing 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.

Job Details

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Manufacturing Engineer

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