CREGG Recruitment are looking for a full time Store Assistant for long term/permanent work in Mervue, Galway . Our client is a company specialized in providing services and goods for the industrial sector, looking to grow and expand their business. Job description – Store Assistant Greeting customers entering the shop & assisting shoppers to find the goods they are seeking Inform customers on technical benefits of our product selection and have the confidence to discuss these Merchandising in retail unit & locating stock in warehouse Reporting discrepancies & issues to Business Manager Balancing cash registers with receipts & dealing with customer refunds €14.50 per hour (€29,500 per year) Hours of Work Monday – Saturday (5 days a week) 08:30– 17:30 Job requirements – Store Assistant Min 1 year of experience in retail (preference hardware or technical background). Polite, patient & helpful, excellent interpersonal skills – with a friendly & engaging personality. Ability to work as part of a team- with good communication, organisational and administration skills. Flexible, reliable and Pro-active attitude with ability to bring new ideas / initiatives. Contract type Full time / Permanent (39 hours a week) Long term (6 month probation, followed by long term/permanent) Notice required We are considering candidates, who have to give up to 2 weeks notice. Application Please apply with your CV, if interested in Store Assistant role. #J-18808-Ljbffr
Project Manager – Galway Job Title: Project Manager Location: Galway, Ireland Industry: Medical Device Manufacturing About the Company: We are now hiring for a Project Manager for a leading medical device manufacturing company based in Galway, committed to delivering innovative and life‑enhancing solutions in healthcare. We are currently seeking an experienced Project Manager to join our dynamic team and play a pivotal role in the successful execution of cross‑functional projects. About the role: As a Project Manager, you will lead cross‑functional teams in the planning, execution, and delivery of complex and CAPEX projects within our manufacturing operations. You will be responsible for managing the full project lifecycle, from initial scoping through to execution and close‑out, with a focus on equipment introduction, process improvements, and supplier/vendor coordination. Responsibilities Project Leadership: Lead the planning, coordination, and execution of manufacturing and engineering projects, ensuring alignment with strategic goals. Scoping & Planning: Define project scope, objectives, deliverables, and timelines in collaboration with stakeholders. Cross‑functional Collaboration: Work closely with internal departments (R&D, Quality, Manufacturing, Regulatory, and Supply Chain) to drive project success. Equipment Introduction: Manage the introduction and qualification of new manufacturing equipment and technologies, including FAT, SAT, IQ/OQ/PQ processes. Stakeholder Management: Interface with internal and external stakeholders to ensure alignment, clear communication, and timely updates on project progress. Supplier & Vendor Management: Source, evaluate, and manage relationships with suppliers and vendors to ensure timely delivery of project‑related equipment and materials. Risk Management: Identify project risks and develop mitigation plans to ensure on‑time and within‑budget delivery. Reporting: Provide regular project updates, KPIs, and dashboards to senior management. Compliance: Ensure all activities adhere to company policies, industry standards, and applicable regulatory requirements (e.g., ISO 13485, FDA, MDR). Requirements Bachelor’s degree in Engineering, Science, or a related technical field. Minimum of 5 years of experience in project management within a regulated manufacturing environment, preferably medical devices. Proven experience managing cross‑functional projects including equipment introduction and supplier/vendor coordination. Strong understanding of GMP, ISO 13485, and FDA requirements. Project Management certification (e.g., PMP, PRINCE2) is an advantage. Experience with project management tools (e.g., MS Project, Smartsheet, JIRA). Excellent leadership, communication, and problem‑solving skills. Ability to manage multiple priorities and work under pressure in a fast‑paced environment. For more information on this opportunity please reach out or send your CV to garykeane@cregg.ie Contact Gary Keane garykeane@cregg.ie - 086-1030418 INDCRG #J-18808-Ljbffr
CREGG are looking for Electronic Device Product Builders , for long term work in Parkmore area of Galway City. Our client is a growing electronic and medical device production company, looking to add more staff for their day shift production requirements. Job Description – Product Builder: Read and interpret drawings, diagrams, blueprints, specifications, work orders, or reports. Review work activities with supervision. Inspect wiring installations, assemblies, and circuits. Pack finished products for shipment. Adjust or repair electrical equipment. Test product to ensure conformance to specifications. Hours of work: Monday – Thursday, 08:00 – 16:25 Friday, 08:00 – 15:00 Total 38.5 hours per week Rate of Pay: €14.10 per hour Job requirements – Product Builder: Previous experience in relevant production industry – min 1 year. Experience with soldering/crimping is a bonus. Excellent attention to details. Ability to work well as a team. Contract Type: Full time Availability: We are looking for candidates who are available with 2 weeks' notice. Please apply with your CV, if interested in Product Builder role. #J-18808-Ljbffr
CREGG is delighted to be recruiting a Technical Sales Manager to join one of Ireland's leading renewable energy/solar solutions companies based in Shannon, Co. Clare. Reports to: Sales Director Location: Hybrid role – 2-3 days based in Shannon office. Company Description: Our client is Ireland’s largest solar products distributor, servicing over 50% of Irish solar installers with market-leading products from world-class manufacturers. With headquarters in Shannon, Co. Clare and offices in Spain, the UK, and Italy, they are committed to providing top-notch support, service, and delivery for their customers. Role Summary: The Technical Sales Manager bridges the gap between commercial sales and engineering expertise. This role is responsible for supporting sales with deep product knowledge , designing solutions that meet installer and end-user needs, and providing technical guidance pre- and post-sale. The ideal candidate is both technically competent and customer-focused , capable of building trust with installers, electrical contractors, and commercial clients, while supporting internal teams in delivering solar energy solutions. Key Responsibilities: Solution Design & Consultation Support sales and account teams by designing solar system layouts and advising on product selection for residential, commercial, and agricultural projects. Technical Sales Support Join sales meetings to explain system performance, compatibility, and installation requirements to clients. Training & Education Deliver product training to installers and staff (in-person or virtual), ensuring correct use of inverters, batteries, and monitoring systems. Product Demonstrations Conduct on-site or online demos for new product lines and technologies, highlighting key features and benefits. Assist with troubleshooting, product warranties, and system configuration queries after installation. Work closely with Procurement and Technical Directors to feedback on installer challenges, emerging needs, and competitor product gaps. CRM & Reporting Log technical support activity, training sessions, and solution proposals in Odoo CRM. Contribute to monthly sales and product performance reports. Skills & Experience Required: Prior experience in technical sales , solar system design , or electrical engineering . Strong knowledge of solar PV systems , inverters , batteries , and monitoring platforms. Excellent communication skills, with the ability to explain technical topics clearly to non-technical clients. Familiarity with CRM systems (Odoo or similar), layout tools (e.g. PV*SOL, Helioscope), and inverter platforms. Ability to work independently and collaborate across departments. Full clean driver’s licence and willingness to travel within Ireland. Offer: Competitive salary on offer commensurate with the skills & experience of the successful candidate. You will also be entitled to excellent benefits including: Company Pension Company vehicle Competitive bonus structure tied to personal and team success. Laptop, Company Phone Collaborative, growth-focused company culture Be part of Ireland’s leading solar distributor, driving the country’s renewable energy transition. This is an exciting opportunity to join a growing & progressive company at a pivotal time in their journey. For a confidential chat, feel free to get in contact with me directly: Barry Dolan Phone: 061 363 318 #J-18808-Ljbffr
CREGG Recruitment are hiring for a Quality Engineer to join a leading Medical Device company in Galway For more information contact Mark: markhalligan@cregg.ie or 0861901346 About the Role We are seeking a highly motivated Quality Engineer to join our world-class medical device team in Galway. This is an exciting opportunity to contribute to the development and manufacture of life-changing products that improve patient outcomes worldwide. The successful candidate will play a key role in ensuring compliance with quality standards, driving continuous improvement, and supporting the delivery of safe, effective, and reliable medical devices. Key Responsibilities Ensure compliance with applicable regulations (ISO 13485, FDA 21 CFR Part 820, MDR, etc.) and company quality management systems. Provide quality engineering support for new product development, manufacturing, and post-market activities. Participate in risk management activities, including FMEAs, hazard analysis, and control strategies. Drive root cause analysis and implement effective corrective and preventive actions (CAPA). Support validation and qualification activities (process, equipment, software, and test methods). Partner with cross-functional teams (R&D, Manufacturing, Regulatory, and Supply Chain) to ensure robust design transfer and product lifecycle management. Conduct internal audits and support external regulatory and notified body inspections. Identify opportunities for continuous improvement in processes, systems, and quality culture. Qualifications & Experience Bachelor’s degree in Engineering, Science, or related discipline. 2+ years of experience in quality engineering, ideally in the medical device, pharmaceutical, or regulated industry. Strong knowledge of ISO 13485, FDA regulations, and EU MDR. Experience with risk management, validation, and statistical analysis tools. Demonstrated problem-solving skills with experience in CAPA, root cause analysis, and process improvement. Excellent communication and interpersonal skills, with the ability to work in cross-functional teams. Detail-oriented, organized, and self-driven with a commitment to quality and compliance. #J-18808-Ljbffr
3 days ago Be among the first 25 applicants Workshop Manager CREGG are exclusively recruiting for an experienced and hands‑on Workshop Manager to join our client’s team in East Limerick. This is a full‑time permanent position. The Workshop Manager will have end‑to‑end responsibility for the management, optimisation, and leadership of all workshop activities, ensuring vehicles are maintained to the highest standards of safety, reliability, and compliance. Key Responsibilities Lead and manage the daily operations of the in‑house garage, ensuring efficient servicing, repair, and maintenance of all fleet vehicles, trailers, and equipment. Develop, implement, and maintain structured preventative maintenance systems to minimise downtime and optimise fleet performance. Ensure full compliance with all RSA (Road Safety Authority) and CVRT (Commercial Vehicle Roadworthiness Testing) requirements, maintaining accurate documentation and inspection records within robust compliance systems. Monitor and analyse workshop performance using KPIs, ensuring jobs are completed on time, within budget, and to the highest quality standards. Ensure strict adherence to approved budgets while driving initiatives to achieve financial targets and optimise resource allocation. Provide clear leadership and direction to the team of mechanics and fitters, fostering a high‑performance culture through training, mentoring, and regular performance feedback. Ensure all workshop activities adhere to health and safety regulations and company policies, embedding a culture of safety and accountability. Lead the development and expansion of a commercial third‑party service offering, complementing in‑house fleet maintenance operations to drive new revenue streams and strengthen market presence. Qualifications and Skills Proven experience as a Workshop Manager, Workshop Supervisor, or similar role within a commercial vehicle or logistics environment, with a track record of managing systems and leading teams. Strong technical knowledge of HGVs, trailers, and associated mechanical/electrical systems is advantageous. In‑depth understanding of RSA regulations, vehicle inspection requirements, and compliance processes, with the ability to implement effective compliance systems. Strong communication skills with the ability to liaise effectively across departments, with drivers, suppliers, and regulatory bodies. Proficiency in using computer‑based job tracking, maintenance scheduling, and performance reporting systems. Full, clean driver’s licence (HGV licence advantageous but not essential). For more information, please contact Gary (garycusack@cregg.ie) with your CV. Please be aware that your CV will not be shared with anyone outside of CREGG without your express permission. #J-18808-Ljbffr
Manufacturing Operative – Day Shift – Shannon CREGG Recruitment are working along side our client in Shannon in hiring a on Manufacturing Operativeday shift. * MUST HAVE 1 YEARS PRODUCTION EXPERIENCE Monday- Friday Hours of work: 7am- 3.30pm €13.50/hr Duties and Responsibilities include the following. Other duties may be assigned. The Manufacturing Operative will be Running Reader and Card Machine processes and able to perform efficiently with training. Be able to identify inefficiencies in a process and be able to make suggestions on how to improve it. TheManufacturing Operative will Take responsibility for parts and inventory which is used in the day-to-day running of Machine. Proactively escalate potential issues in order to minimize safety, quality and delivery issues. Be involved in 5S / Housekeeping and other continuous improvement activities To be a team player and support investigations into issues and support actions which will prevent them in the future. To be able to work with people outside of Machine cell (e.g. Warehouse (3PL), Material Replenishment, Purchasing, Quality, Manufacturing Engineering) Maintain compliance to all Site policies and procedures (in particular Health & Safety and Quality). Ability to learn and understand processes quickly Able to work in an efficient manner Aware of when to ask for help and when to use their own initiative to solve a problem. Though primarily running Machine processes, motivated to identify and get involved in other activities to help improve the Operations environment. Considers themselves a team player and willing to help out with whatever is needed. Must be familiar with routing slips, material requisitions, and job / work orders. Must have flexibility to work overtime as required (including weekends) and periodically work a different shift. Able to manage time and priorities in a fast paced Operations environment #J-18808-Ljbffr
Job Title: Manufacturing Engineer (Med Device Manufacture) Hours: Hybrid role 3 days on site with a 1pm Friday finish and free on-site gym. 39hr week offering flexitime Location: Galway Industry: Medical Devices Company information: Galway's world leading multi-national Medical device company Contact: rachel@cregg.ie or call 0860127415 Manufacturing Engineer: Medical Devices Galway's world leading medical device manufacturing company have available opportunities for EXPERIENCED Manufacturing Engineers to join their team. Please send CV to rachel@cregg.ie to apply. About the role To support a critical site-wide remediation program following an FDA 483 observation. This role offers a fantastic opportunity to work directly onsite, collaborating closely with manufacturing and quality teams to drive compliance improvements and process validation initiatives. Hours of work: Monday-Friday 39hr week with a 1pm Friday finish. Key Responsibilities Identify and remediate compliance gaps. Support manufacturing process validation activities (IQ/OQ/PQ). Drive closure of CAPAs and NCRs with effective corrective actions. Provide clear and concise technical writing for quality and manufacturing procedures. Collaborate cross-functionally with Quality, Manufacturing, and Regulatory teams to implement compliant solutions. Qualifications & Experience Bachelor’s degree in Engineering or related discipline. 2–5 years of experience in medical device manufacturing, quality, or remediation projects. Strong knowledge of process validation (IQ/OQ/PQ) and CAPA/NCR management. Proven technical writing and documentation skills. Familiarity with 21 CFR Part 820 and ISO 13485 quality standards. Excellent problem-solving skills with the ability to take a problem statement through to a compliant solution. Must be available to work onsite in Galway. Contact: Rachel Mc Mahon for more information. Email: rachel@cregg.ie / 0860127415 #J-18808-Ljbffr
Our client is a large Construction contractor who are currently looking for an experienced Project Manager/Foreman for projects in Limerick . Responsibilities Manage the construction of civil engineering projects to ensure they are completed on time, within budget and to the highest quality standards. Oversee the work of engineers, supervisors and laborers. Develop and implement project plans, schedules and budgets. Ensure all health and safety regulations are adhered to. Liaise with clients, subcontractors and suppliers. Requirements At least 5 years of experience managing the construction of civil engineering projects. Strong leadership and management skills. Excellent communication and interpersonal skills. Knowledge of health and safety regulations. #J-18808-Ljbffr
Our client is a large Construction contractor who are currently looking for an experienced Site Manager for projects in the Carrick on Shannon area, Co Leitrim. Responsibilities Manage the construction of civil engineering projects to ensure they are completed on time, within budget and to the highest quality standards. Oversee the work of engineers, supervisors and laborers. Develop and implement project plans, schedules and budgets. Ensure all health and safety regulations are adhered to. Liaise with clients, subcontractors and suppliers. Requirements At least 5 years of experience managing the construction of civil engineering projects. Strong leadership and management skills. Excellent communication and interpersonal skills. Knowledge of health and safety regulations. #J-18808-Ljbffr
