Manufacturing Engineer II x2&nbsp;Location: GalwayJob Type: Full-Time Contract RoleExperience Level: Mid-Level&nbsp;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>&nbsp;

Manufacturing Engineer II X2 

Design Engineer&nbsp; A leading designer and manufacturer of high-reliability film capacitors for the power electronics market, supplying low- and medium-voltage film capacitors to industries including industrial, medical, aerospace, automotive, and renewable energy. We are seeking a talented Design Engineer with a multi-skilled engineering background to help design and select capacitors that meet customer needs &mdash; and turn technical requirements into practical, high-performance solutions. Main Responsibilities<ul><li>Collaborate with Design, Engineering &amp; Innovation, Operations, and Sales teams to develop solutions for customer projects.</li><li>Select and design capacitors that meet complex technical specifications.</li><li>Communicate directly with customers to understand requirements and present proposed solutions.</li><li>Build strong relationships with both internal teams and external stakeholders.</li><li>Use CAD tools (SolidWorks or similar) to create and adapt designs.</li><li>Contribute to product development and improvement initiatives.</li><li>Extensive on-the-job training will be provided to familiarise you with products, design capabilities, and manufacturing processes.</li></ul>Qualifications &amp; Experience <ul><li>Bachelor&rsquo;s degree in Industrial, Mechanical, or Electrical Engineering.</li><li>5+ years&rsquo; industry experience in an engineering role.</li><li>Strong technical ability and problem-solving skills.</li><li>Confident communicator with excellent presentation skills.</li><li>Proficiency in MS Office and CAD software (SolidWorks or equivalent).</li><li>Ability to work effectively in a team environment and manage multiple priorities.</li><li>A genuine drive to deliver results and exceed expectations.</li></ul>Why Join <ul><li>Be part of a company with over 40 years of technical expertise and innovation.</li><li>Work on projects across diverse industries including aerospace, medical, and renewable energy.</li><li>Enjoy a collaborative environment with direct access to decision-makers.</li><li>Receive extensive product training and opportunities for professional growth.</li></ul>For further information on this role in please contact on Gavin Moran on 087 4108620 or connect@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

Design Engineer

We&rsquo;re looking for an energetic Process Engineer to join our Carlow site and support New Product Introduction (NPI) and commercial manufacturing. You&rsquo;ll work on cross-functional projects, lead technical initiatives, and support continuous improvement across diverse manufacturing operations.What You&rsquo;ll Do:<ul data-start="508" data-end="991"><li data-start="508" data-end="605">Lead or support process development, equipment validation, and change control activities.</li><li data-start="606" data-end="691">Contribute to Kaizen/continuous improvement initiatives using Lean Six Sigma.</li><li data-start="692" data-end="756">Perform root cause analysis of system or process issues.</li><li data-start="757" data-end="826">Represent technical operations in internal and global forums.</li><li data-start="827" data-end="908">Ensure compliance with cGMP, regulatory standards, and internal policies.</li><li data-start="909" data-end="991">Collaborate with teams to drive a safe, compliant, and innovative culture.</li></ul>What You Bring:<ul data-start="1015" data-end="1535"><li data-start="1015" data-end="1095">Bachelor&rsquo;s degree (Science, Engineering, or Technical discipline preferred).</li><li data-start="1096" data-end="1162">Minimum 3 years&rsquo; manufacturing experience, ideally in GMP.</li><li data-start="1163" data-end="1213">Proven ability to lead technical projects.</li><li data-start="1214" data-end="1323">Knowledge of automation systems (DeltaV), process monitoring, and data systems (Pi System) is a plus.</li><li data-start="1324" data-end="1402">Strong skills in documentation, validation, and regulatory compliance.</li><li data-start="1403" data-end="1470">Excellent communication, presentation, and teamwork skills.</li><li data-start="1471" data-end="1535">Hybrid role with occasional shift support post-training.</li></ul> Why This Role: Work in a dynamic environment with opportunities across Biological, Chemical, Automation, Capital Projects, Process Development, and more. Drive innovation, improve processes, and make a tangible impact on manufacturing operations.

Process Engineer II

<h1 data-start="171" data-end="199">ENGINEERING TECHNICIAN</h1><h2 data-start="201" data-end="224">Responsibilities</h2><ul data-start="226" data-end="2335"><li data-start="226" data-end="365">Work as a team member to support engineering in pharma operations in line with all safety, regulatory, and organizational requirements.</li><li data-start="366" data-end="497">Participate in design and process project discussions to ensure reliability by design is integrated prior to equipment arrival.</li><li data-start="498" data-end="627">Own and prepare preventative and predictive maintenance plans for new pharmaceutical equipment; approve procedures in Maximo.</li><li data-start="628" data-end="705">Complete and document PMs and pDMs for manufacturing equipment in Maximo.</li><li data-start="706" data-end="780">Ensure commissioning spare parts are received and cataloged in Maximo.</li><li data-start="781" data-end="847">Identify, receive, and catalog critical spare parts in Maximo.</li><li data-start="848" data-end="994">Actively participate in Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), and the commissioning and qualification of equipment.</li><li data-start="995" data-end="1169">Review and approve process-related commissioning, qualification, and validation protocols for completeness and accuracy; execute protocols in line with project schedules.</li><li data-start="1170" data-end="1258">Review and approve process flow diagrams (PFDs), specifications, layouts, and P&amp;IDs.</li><li data-start="1259" data-end="1388">Ensure high performance in day-to-day preventative and demand maintenance activities for manufacturing and utility equipment.</li><li data-start="1389" data-end="1492">Liaise with operations, quality, and technical teams to maximize equipment and process performance.</li><li data-start="1493" data-end="1597">Maintain records and documentation according to Engineering Procedures and maintenance requirements.</li><li data-start="1598" data-end="1760">Collaborate with internal/external engineering personnel and contract maintenance providers for troubleshooting, installation, and commissioning of equipment.</li><li data-start="1761" data-end="1814">Complete instrument calibrations as per schedule.</li><li data-start="1815" data-end="2008">Take ownership of the site&rsquo;s Predictive Maintenance program, including managing and developing outsourced condition monitoring contracts, implementing recommendations, and tracking closure.</li><li data-start="2009" data-end="2089">Implement equipment/process upgrades in a culture of continuous improvement.</li><li data-start="2090" data-end="2177">Support production teams in maintaining equipment to meet output and yield targets.</li><li data-start="2178" data-end="2224">Adhere to all quality and safety policies.</li><li data-start="2225" data-end="2289">Support successful external inspections and internal audits.</li><li data-start="2290" data-end="2335">Supervise external contractors as required.</li></ul><h2 data-start="2342" data-end="2361">Requirements</h2><h3 data-start="2363" data-end="2397">Education &amp; Qualifications</h3><ul data-start="2398" data-end="2528"><li data-start="2398" data-end="2480">Relevant Trade Qualification or Engineering Certificate (minimum requirement).</li><li data-start="2481" data-end="2528">Diploma or Degree in Engineering (preferred).</li></ul><h3 data-start="2530" data-end="2566">Technical/Business Knowledge</h3><ul data-start="2567" data-end="2801"><li data-start="2567" data-end="2681">Minimum 3 years&rsquo; experience in a highly regulated manufacturing environment (Pharma/Biologics/Medical Device).</li><li data-start="2682" data-end="2735">Proven ability to troubleshoot complex equipment.</li><li data-start="2736" data-end="2801">Strong experience with instrumentation and PLC troubleshooting.</li></ul><h2 data-start="2808" data-end="2832">Core Competencies</h2><h3 data-start="2834" data-end="2858">Cognitive Skills</h3><ul data-start="2859" data-end="3324"><li data-start="2859" data-end="2901">Proven problem-solving under pressure.</li><li data-start="2902" data-end="2960">Ability to propose and implement innovative solutions.</li><li data-start="2961" data-end="3016">High attention to detail and procedural compliance.</li><li data-start="3017" data-end="3055">Results-driven and target-focused.</li><li data-start="3056" data-end="3112">Commitment to quality and consistent high standards.</li><li data-start="3113" data-end="3162">Demonstrates strong integrity and work ethic.</li><li data-start="3163" data-end="3217">Excellent verbal and written communication skills.</li><li data-start="3218" data-end="3263">Strong interpersonal and teamwork skills.</li><li data-start="3264" data-end="3324">Understands and applies continuous improvement principles.</li></ul><h3 data-start="3331" data-end="3365">Ownership &amp; Accountability</h3><ul data-start="3366" data-end="3786"><li data-start="3366" data-end="3441">Personally committed to organizational goals and strategic imperatives.</li><li data-start="3442" data-end="3502">Supports a positive and compliant developmental culture.</li><li data-start="3503" data-end="3557">Knowledgeable of internal policies and procedures.</li><li data-start="3558" data-end="3616">Works autonomously with initiative and sound judgment.</li><li data-start="3617" data-end="3658">Maintains a &ldquo;Right First Time&rdquo; ethos.</li><li data-start="3659" data-end="3727">Ensures adherence to all GMP, ISO, FDA, and company regulations.</li><li data-start="3728" data-end="3786">Demonstrates persistence in resolving issues to closure.</li></ul><h3 data-start="3793" data-end="3823">Influence &amp; Leadership</h3><ul data-start="3824" data-end="4056"><li data-start="3824" data-end="3893">Supports cross-functional teams and cost improvement initiatives.</li><li data-start="3894" data-end="3958">Provides technical leadership and stakeholder collaboration.</li><li data-start="3959" data-end="4012">Contributes to site goals and change initiatives.</li><li data-start="4013" data-end="4056">Leads and delivers new training programs.</li></ul><h3 data-start="4063" data-end="4095">Decision Making &amp; Impact</h3><ul data-start="4096" data-end="4351"><li data-start="4096" data-end="4143">Works independently with minimal direction.</li><li data-start="4144" data-end="4203">Exercises judgment in determining technical objectives.</li><li data-start="4204" data-end="4294">Handles day-to-day training and development queries; escalates major issues as needed.</li><li data-start="4295" data-end="4351">Presents technical data to facilitate decision-making.</li></ul><h3 data-start="4358" data-end="4377">Supervision</h3><h4 data-start="4379" data-end="4396">Received</h4><ul data-start="4397" data-end="4466"><li data-start="4397" data-end="4466">Operates in a largely self-managed environment with some oversight.</li></ul><h4 data-start="4468" data-end="4485">Provided</h4><ul data-start="4486" data-end="4744"><li data-start="4486" data-end="4508">No direct reports.</li><li data-start="4509" data-end="4638">Interfaces with external contractors, service engineers, commissioning personnel, safety inspectors, and equipment engineers.</li><li data-start="4639" data-end="4698">May provide training or mentorship to new team members.</li><li data-start="4699" data-end="4744">May lead projects and training initiatives.</li></ul><h2 data-start="4751" data-end="4778">EHS Responsibilities</h2><ul data-start="4780" data-end="5175"><li data-start="4780" data-end="4844">Comply with all EHS policies and demonstrate best practices.</li><li data-start="4845" data-end="4927">Be vigilant of personal and team safety; follow all safety signs and barriers.</li><li data-start="4928" data-end="5009">Report all incidents and near-misses promptly and log them in the EHS system.</li><li data-start="5010" data-end="5090">Promote a culture of EHS excellence by submitting improvement opportunities.</li><li data-start="5091" data-end="5150">Attend mandatory EHS training and medical surveillance.</li><li data-start="5151" data-end="5175">Wear all required PPE.</li></ul>

Engineering Technician

<h1 data-start="273" data-end="326">Discover Top Process Engineering Jobs in Cork</h1>
Cork is one of Ireland&rsquo;s leading hubs for process engineering jobs, offering exciting opportunities in pharmaceutical, biotech, chemical, and medical device industries. At HERO Recruitment, we connect skilled process engineers with innovative companies across Cork and Munster, from global multinationals to fast-scaling local firms.
If you're looking for a permanent role, contract position, or project-based opportunity, explore the latest process engineering jobs available right now.
<h2 data-start="860" data-end="923">Why Choose Cork for Your Next Process Engineering Role?</h2>
Cork is home to world-class manufacturing and life sciences operations, making it a hotspot for:
<ul data-start="1027" data-end="1249">
<li data-start="1027" data-end="1082">
Process optimisation and continuous improvement roles
</li>
<li data-start="1083" data-end="1137">
Scale-up of production in pharma and medtech sectors
</li>
<li data-start="1138" data-end="1187">
Regulatory compliance and validation activities
</li>
<li data-start="1188" data-end="1249">
Cutting-edge automation and lean manufacturing environments
</li>
</ul>
Major employers include Pfizer, Johnson &amp; Johnson, Stryker, and AbbVie, among many others.
<h2 data-start="1364" data-end="1423">Explore the Latest Process Engineering Jobs in Cork</h2>
We&rsquo;re actively hiring for roles such as:
<ul data-start="1467" data-end="1775">
<li data-start="1467" data-end="1537">
<a href="https://www.hero.ie/jobs/15075-process-development-engineer/" data-start="1469" data-end="1537">Process Development Engineer</a>
</li>
<li data-start="1538" data-end="1621">
<a href="https://www.hero.ie/jobs/15112-process-development-engineer-i/" data-start="1540" data-end="1621">Process Development Engineer I</a>
</li>
<li data-start="1622" data-end="1701">
<a href="https://www.hero.ie/jobs/15101-maintenance-engineer/" data-start="1624" data-end="1701">Maintenance Engineer</a>
</li>
</ul>
<h2 data-start="1896" data-end="1958">Contract or Permanent Process Engineering Jobs in Cork</h2>
Looking for contract work or flexibility? We support both:
<ul data-start="2020" data-end="2189">
<li data-start="2020" data-end="2112">
<a href="https://www.hero.ie/jobs/?query=cork&amp;role_type=%2C0b03e526-12a7-4e6f-ad0b-71db88f03371" data-start="2022" data-end="2112">Contracting Jobs in Cork &raquo;</a>
</li>
<li data-start="2113" data-end="2189">
<a href="https://www.hero.ie/contracting/" data-start="2115" data-end="2189">STEM Contracting Services in Ireland &raquo;</a>
</li>
</ul>
Prefer something permanent? <a href="https://www.hero.ie/permanent/">💼 Explore Full-Time STEM Roles &raquo;</a>
<h2 data-start="2297" data-end="2364">Start Your Process Engineering Career with HERO Recruitment</h2>
With over 20 years of experience placing STEM talent, we offer:
<ul data-start="2435" data-end="2679">
<li data-start="2435" data-end="2487">
Access to unadvertised roles in top Cork companies
</li>
<li data-start="2488" data-end="2547">
Specialist knowledge of engineering and regulatory hiring
</li>
<li data-start="2548" data-end="2608">
Support with CV advice, interviews, offers, and onboarding
</li>
<li data-start="2609" data-end="2679">
Expertise in both permanent recruitment and STEM contracting
</li>
</ul>
 <a href="https://www.hero.ie/about-us/">👥 Meet Our Recruitment Experts &raquo;</a>
<h2 data-start="3598" data-end="3642">FAQs &ndash; Process Engineering Jobs Cork</h2>
Are there contracting opportunities for process engineers in Cork? Yes. We support both contract and permanent hires for Cork&rsquo;s top employers.
Do you need industry-specific experience? Most roles require experience in pharma, biotech, medtech, or manufacturing, depending on the job level.
Can international candidates apply? Yes. We support relocation and provide guidance for international applicants.

Process Engineering Jobs Cork | HERO Recruitment

Discover Top Process Engineering Jobs in Cork

Why Choose Cork for Your Next Process Engineering Role?

Explore the Latest Process Engineering Jobs in Cork

Contract or Permanent Process Engineering Jobs in Cork

Start Your Process Engineering Career with HERO Recruitment

FAQs – Process Engineering Jobs Cork

Engineering Jobs

Manufacturing Engineer II X2

Design Engineer

Process Engineer II

Engineering Technician