Cpl Healthcare has an exciting opportunity for an experienced Registered Nurse. Our client is a well established private Cork city hospital, who as a result of continuing expansion has a requirement for a Clinical Nurse Manager 2 –Surgical Ward to join the team. The successful candidate will play a pivotal role within the multidisciplinary team to lead a team of staff in the implementation and provision of the highest quality patient care coordination and drive the management of activity and resources within the clinical area. To be considered for the role, the following criteria will apply: Registered General Nurse on the live register with The NMBI Demonstrable commitment to patient Safety & Quality Minimum 5 years post graduate acute care nursing experience essential. Flexibility and demonstrable experience in meeting the challenges of coordinating and delivering acute surgical services. Management qualification/educational preparation to degree level desirable. Proven leadership and change management skills Excellent knowledge of contemporary nursing practice and skills Ability to make decisions with excellent organisational skills Vision of development of service Eligible to work in Ireland. For further details on this role, please contact Catherine Hoban: T: + 353 21 4626138 E: catherine.hoban@cplhealthcare.com #J-18808-Ljbffr
Facilities Coordinator – Limerick Our client, a well-respected charitable organisation with tangible social impact based in Limerick, is now seeking an experienced Facilities Coordinator to join the team. So, if you have experience working in multi-stakeholder projects and commercial property management and want to work in an environment that combines social purpose with innovation then please apply today!! The Role As Facilities Coordinator you will manage the day-to-day operations, maintenance, and administration of our client’s campus services, ensuring building systems, services, compliance, and tenant needs are efficiently delivered in a safe, clean, and compliant environment. Acts as a key liaison between tenants, contractors, and the CEO. Operations & Maintenance Manage building services: HVAC, electrical, plumbing, waste management, security/CCTV Log and track reactive and preventative maintenance via app-based systems Coordinate contractors for maintenance, repairs, and projects Conduct regular property inspections to ensure safety, cleanliness, and compliance. Lead scheduling, tracking, and documentation of planned maintenance programmes Prepare annual minor capital works plan for the Campus Tenant Liaison First point of contact for tenant queries Manage Spark Hub (co-working space for hot desking and meeting rooms) Communicate maintenance updates, disruptions, and works notices Support tenant onboarding, move-in, and move-out coordination Health, Safety & Compliance Ensure adherence to regulatory and company policies. Maintain risk assessments, incident reports, and compliance documentation Lead emergency preparedness, fire drills, and contractor safety inductions Support sustainability and environmental initiatives Project & CEO Support Assist with capital works and refurbishment projects Track project budgets, timelines, and completion reports Deputise for the CEO in meetings and support stakeholder engagement Skills & Qualifications Minimum 3 years’ experience in facilities, property, or building management Knowledge of building systems (HVAC, electrical, plumbing, BMS) and service coordination. Familiarity with health, safety, and compliance requirements (risk assessments, fire safety) Proficient in Microsoft Office Suite and comfortable adopting new technology Strong organisational, communication, and problem-solving skills Strong attention to detail and prioritisation skills Excellent interpersonal and stakeholder management skills Ability to work independently and as part of a team Flexible and adaptable to operational needs Strong work ethic and alignment with company’s mission Desirable Experience with facilities management software Experience in multi-tenant office buildings or mixed-use developments First Aid, Fire Warden, or H&S certification Interest in process improvement through technology adoption The Offer This is a permanent fully onsite role based in Limerick with excellent negotiable salary depending on the candidates’ qualifications and experience. #J-18808-Ljbffr
Cpl Healthcare is seeking a motivated individual for a customer service role at Bank of Ireland located in Loughrea, County Galway. This 12-month position involves engaging with customers, handling their inquiries, and facilitating their experience within the branch. Ideal candidates are those with strong communication skills and a passion for customer service, willing to learn and adapt to new technologies. No essential qualifications are required, making this a great opportunity for career progression. #J-18808-Ljbffr
Job Title: Production Operative Location: Naas, Co. Kildare About the Role Flexsource is currently seeking a number of Production Operatives to join a well-known international company within the agri-food industry, based in Naas. This is a great opportunity to become part of a reputable organisation offering long-term career potential. Key Duties & Responsibilities Loading and unloading deliveries, grain handling, and general yard work (including lifting bags up to 20kg) Operating production line and warehouse machinery Receiving, inspecting, and verifying incoming goods against documentation Ensuring proper storage and handling of materials Maintaining cleanliness and organisation across the work area Adhering strictly to all health and safety regulations Requirements Previous experience in a warehouse or production environment is essential Ability to perform physically demanding tasks (lifting, bending, kneeling) Good command of English, both written and spoken Basic computer literacy Comfortable working in varying conditions (indoor/outdoor, dust, noise, and temperature changes) Shift Pattern Rotating weekly shifts (Monday to Friday) Morning: 6:00am – 2:00pm Evening: 2:00pm – 10:00pm Pay Rate €16.98 per hour (€14.15 base rate + 20% shift allowance) #J-18808-Ljbffr
Cpl Healthcare is seeking an experienced Clinical Nurse Manager 2 for a private hospital in Cork. The successful candidate will lead a multidisciplinary team, ensuring the highest quality of patient care coordination. Applicants must be a Registered General Nurse and have a minimum of 5 years of post-graduate acute care nursing experience. This role requires flexibility and strong leadership skills. Further details can be obtained by contacting Catherine Hoban at +353 21 4626138 or catherine.hoban@cplhealthcare.com. #J-18808-Ljbffr
Cpl Healthcare is seeking a Graphic Designer for their Galway office. In this permanent role, you will work closely with the creative team to develop innovative design concepts across various digital and print materials, ensuring brand consistency. The ideal candidate should have over 5 years of professional design experience, strong proficiency in Adobe Creative Suite, and a robust portfolio demonstrating diverse design skills. This role also requires clear communication and the ability to juggle multiple projects effectively. #J-18808-Ljbffr
Process Engineer (Level I/II) Provides technical and sustaining engineering support focused on process development, optimisation, and control within a production environment. The role can be tailored to either entry-level or experienced candidates, depending on demonstrated capability, with scope ranging from supported learning to independent project ownership. Responsibilities Provides technical support for existing manufacturing processes, ensuring consistent performance and output Identifies and implements process improvements to enhance quality, efficiency, and yield Develops, optimises, and troubleshoots processes to meet product and technology specifications Reviews product development requirements to ensure compatibility with process capabilities, cost, and timelines Collaborates with design and development teams to align product and process requirements Supports or leads the development and optimisation of new process concepts, including feasibility, material selection, and process design Supports process transfer activities from development into manufacturing operations Defines or supports definition of process parameters, critical inputs/outputs, and alignment to performance requirements Applies statistical process control methods and supports or develops measurement systems Ensures all processes comply with regulatory and quality standards Contributes to or leads projects from concept through implementation across cross‑functional teams Provides guidance to junior staff (Level II) or actively develops technical capability (Level I) Requirements Bachelor’s degree in Engineering or a related technical discipline 0–3+ years’ relevant process engineering experience, with level determined based on experience and capability Understanding of process development, optimisation, and continuous improvement methodologies Exposure to or experience with statistical analysis, process control, and validation techniques Ability to work under supervision (Level I) or independently on moderately complex assignments (Level II) Strong communication and cross‑functional collaboration skills Working knowledge of regulatory requirements within a manufacturing or regulated environment Demonstrated problem‑solving ability with a willingness to learn and develop (Level I) or proven track record of delivering process improvements (Level II) Experience supporting projects (Level I) or leading initiatives and mentoring others (Level II) #LI-MS2 #J-18808-Ljbffr
On behalf of our client, we are currently recruiting for a Pharmacovigilance Officer for a part‑time role of approximately 10‑15 hours per week. This will be an ongoing contract. This position can be remote, hybrid or office based, depending on the preference of the candidate; however, the candidate must be based in Ireland. Role Overview Reporting jointly to the Qualified Person for Pharmacovigilance (QPPV) and the CEO (or their delegate), the Pharmacovigilance Officer will join the pharmacovigilance team and will be responsible for the day‑to‑day maintenance and documentation of ongoing compliance of the pharmacovigilance system and related administrative duties. Roles & Responsibilities Under the oversight of the QPPV, the Pharmacovigilance Officer will carry out the following responsibilities and duties with and along with the assistance of contract service providers supported by service level agreements in the following areas: Maintain a pharmacovigilance system (cGPV) in accordance with EU and international legislation to handle Adverse Event Reports (AER’s), Periodic Reports () with overall responsibility for the processing and reporting of safety information to Regulatory Authorities, Licensees, and Distributors. Document and process all safety information, ensuring that serious adverse event reports are processed and reported according to ICH/EU guidelines, regulatory requirements, and company SOPs or procedures. Manage all weekly routine PV activities, monitoring the PV mailbox, literature screening, and ICSR download processes. Manage all reconciliation activities with partners and tracking of Regulatory intelligence. Manage the review of safety data. Ensure timely lifecycle maintenance of PV periodic documents such as PBER’s, PSUR’s, DSUR'S, Signal, and Annual Summary Reports. Assist the external company medical doctor/physician in the review and follow‑up of safety information. Design and implement process improvements, including procedural documents (SOPs) with QPPV support to ensure the smooth and successful running of the Pharmacovigilance system. Review monthly and maintain and update as required the EU and UK Project System Master Files (PSMFs) and periodically review the KH Pharmacovigilance Management Plan (PMP) as required. Under the guidance of the QPPV, oversee and maintain Safety Data Exchange Agreements with a small number of partners and distributors. Prepare PV monthly report and organise the PV meetings as per agreed timelines. Person Profile The ideal candidate will have at least 1‑2 years of PV experience in the pharmaceutical industry and have a life science or pharmacy degree. Skills & Competences The successful candidate will possess the following: Knowledge and understanding of the EU regulatory frameworks for medicinal products. Knowledge of medical device quality standards would be of distinct advantage. Knowledge and understanding of the food supplement legislation would be advantageous. International experience in registrations/variations/significant changes of Medicinal Products. Proven experience within Regulatory Strategy and its execution. Good understanding of the content and format of MA registration files (CTD and eCTD) with the ability to prepare high‑quality submissions. Previous experience with the preparation and submission of new MAAs, life cycle maintenance in the EU (national/MRP/DCP), and non‑EU markets. Awareness or knowledge of the EU Guidelines on Good Pharmacovigilance Practices (GVP). Excellent interpersonal skills. An excellent level of attention to detail and accuracy. Proven organisational and planning skills. Strong verbal and written communication skills. Enjoy and thrive in a fast‑paced environment. Good interpersonal skills, ability to work with others and independently. Self‑motivated, self‑driven, and "can‑do" attitude. Excellent IT skills in word processing, Excel, PDF software such as Adobe, document management. Proficiency in speaking, comprehending, reading, and writing English is required. Must hold a valid work permit to work in Ireland. #J-18808-Ljbffr
Cpl Healthcare is seeking a Principal Verification Engineer in Ireland to join a leading semiconductor organization. This senior role involves ownership of verification architecture and execution, with responsibilities including the design of verification environments and collaboration with design engineers. Candidates should have 10–15 years of experience in the semiconductor field, a degree in a relevant area, and strong communication skills. The position offers competitive salary, flexible working arrangements, and opportunities for long-term career progression. #J-18808-Ljbffr
Cpl are partnering with a market leading semiconductor organisation to appoint an experienced Principal Verification Engineer. This is a senior technical role within a high‑performing IP development team, focused on the verification of advanced DDR memory controllers used in next‑generation systems across datacenter, AI, automotive, and edge computing markets. The Role The successful candidate will take ownership of verification architecture and execution for complex controller IP, contributing at both a hands‑on and strategic level. Key responsibilities include: Architecture and development of verification environments for complex IP Design and implementation of UVM‑SV scoreboards and self‑checking testbenches Creation of functional coverage models within metric‑driven verification frameworks Development of SystemVerilog Assertions (SVAs) for simulation and formal verification Definition and management of verification plans (vPlans) using industry‑standard tools Setup and maintenance of automated regression flows (e.g. Jenkins) Participation in technical reviews, checklist reviews, and formal quality processes Close collaboration with design engineers to debug and resolve complex issues Candidate Profile Degree in Electrical / Electronic Engineering, Microelectronics, or a related field 10–15 years’ experience in the semiconductor, microelectronics, or EDA industry Strong background in Verilog RTL design Proven expertise in Metric Driven Verification (MDV) Excellent communication skills and the ability to operate at a senior technical level Self‑driven, organised, and comfortable working in globally distributed teams What’s on Offer Competitive salary and benefits package Flexible working arrangements and multiple Irish locations Opportunity to work on market‑leading IP used in high‑volume, mission‑critical products Long‑term career progression within a technically strong organisation If you believe you have the above experience and are interested in hearing more, then reach out to Killian O’Callaghan @Cpl Cork on 021 4944867 for a confidential conversation #J-18808-Ljbffr
