Beginn Join Lufthansa Technik Turbine Shannon’s Finance team! Support accurate reporting, optimise processes, and drive innovation in grants and R&D projects while gaining hands‑on experience in a dynamic, international finance environment. Assist in month-end accounts, post and review journal entries Analyse expenses, reconcile balance sheets, and monitor variances Support annual audits and liaise with external auditors Maintain, update, and track fixed asset register to ensure accuracy Grants Identify national, EU, and private funding opportunities aligned with LTTS strategy Build and maintain strong relationships with funding agencies and organisations Monitor deadlines, prepare, coordinate, and submit grant proposals Ensure compliance with funding requirements and maximise financial benefit Research & Development Collaborate with Engineering to identify R&D projects eligible for tax credits Prepare, file, and track all submissions with Revenue Ensure compliance, maintain documentation, and maximise tax credit benefits Ihr Profil: We are seeking a highly skilled and motivated finance professional who thrives in a dynamic environment, demonstrates strong analytical thinking, and collaborates effectively across teams and projects. +7 years PQE. Experience with accounting software and systems. Strong written and verbal communication skills Experience in preparing and filing grant claims would be desirable but training will be given if required. Previous experience in managing and filing research and development tax claims is desirable. Strong analytical and problem solving skills. Team player and ability to collaborate effectively with other teams and stakeholders. Proficient in Microsoft Excel, Word and PowerPoint. #J-18808-Ljbffr

A recruitment firm specializing in clinical roles is seeking a Senior Clinical Affairs Specialist for a 9-month contract in Shannon, County Clare. This position involves supporting clinical projects, ensuring compliance with EU medical device regulations, and managing client communications. The ideal candidate will possess at least a bachelor’s degree and 5 years of experience in the medical devices industry, alongside strong communication and analytical skills. #J-18808-Ljbffr

A financial services company in Ireland is seeking a finance professional with over 7 years of post-qualification experience. The role includes responsibilities such as assisting in month-end accounts, identifying funding opportunities, and collaborating on R&D tax credits. Ideal candidates will have strong analytical skills, proficiency in accounting software, and experience with grant claims. This position offers a dynamic international finance environment. #J-18808-Ljbffr

A leading recruitment firm is seeking an experienced Senior Buyer in Shannon, County Clare. This full-time position focuses on electronics procurement and involves strategic supplier management and negotiation. Ideal candidates have at least 7 years of procurement experience and a relevant degree. Join a dynamic team to drive cost reduction and supply chain efficiency while promoting sustainability initiatives. #J-18808-Ljbffr

A healthcare company in Shannon, Ireland is seeking a Senior Clinical Affairs Specialist regarding medical writing activities. The successful candidate will ensure compliance with EU regulations, prepare clinical documents, and collaborate with project teams. Excellent communication skills and a background in medical writing are essential for this role, along with 5+ years of experience in a related field. #J-18808-Ljbffr

1 day ago Be among the first 25 applicants Direct message the job poster from Collins McNicholas Recruitment & HR Services Group An exciting opportunity has arisen for an experienced Senior Buyer with a strong background in electronics procurement to join a growing supply chain function. This newly created role will support an expanding team and work closely with a recently promoted Senior Buyer, reporting into the Head of Sustainability & Supply Chain. This position is ideal for a driven procurement professional who thrives in a fast-paced environment, enjoys building strategic supplier relationships, and is motivated by continuous improvement and sustainability-focused initiatives. Key Responsibilities Supplier Management: Identify, evaluate, and develop global suppliers for electronic components, ensuring reliability, quality, and long‑term value. Strategic Negotiation: Lead commercial negotiations using market intelligence and commodity analysis to secure competitive pricing, favourable terms, and optimal lead times. Procurement Strategy: Align sourcing activities with wider business and supply chain objectives, contributing innovative ideas to strengthen overall procurement strategy. Cost & Risk Management: Drive continuous cost‑reduction initiatives while proactively managing supply risks to ensure material availability and minimise disruption. Internal Collaboration: Partner with production, engineering, and quality teams to meet operational requirements and support key projects. Market & Technical Expertise: Stay informed on industry trends, electronic component markets, and emerging technologies. Process Improvement: Support ongoing enhancements in purchasing processes, systems, and supplier engagement tools while upholding ethical procurement standards. Skills & Experience Required Strong knowledge of the electronics supply chain, component categories, and supplier landscape. Proven negotiation skills with experience securing cost savings and developing supplier relationships. Excellent analytical and problem‑solving abilities, with confidence interpreting market data. Proficiency in ERP and procurement systems; experience with supplier portals is an advantage. Exceptional communication skills for collaborating with internal teams and global suppliers. Demonstrated leadership qualities and ability to work effectively within a team‑focused environment. Bachelor’s degree in Supply Chain Management, Engineering, Business Administration, or related field. Minimum 7 years’ procurement experience, specifically within electronics. For a confidential discussion and more information, please contact Jessica Kennedy Seniority level Mid‑Senior level Employment type Full‑time Job function Purchasing and Supply Chain Industries Appliances, Electrical, and Electronics Manufacturing, Computers and Electronics Manufacturing, and Electrical Equipment Manufacturing Get notified about new Buyer jobs in Shannon, County Clare, Ireland . #J-18808-Ljbffr

An established industry player is seeking a driven Inside Sales Representative to enhance its global footprint. In this dynamic role, you will build and nurture relationships with end users and channel partners, maximizing revenue opportunities. With a focus on solution selling, you will engage with customers to understand their needs and present tailored solutions. This position offers the chance to work in a fast-paced, goal-oriented environment where your contributions will directly impact the company's success. If you are passionate about sales and eager to succeed, this opportunity is perfect for you. #J-18808-Ljbffr

A leading electronics manufacturer is seeking a Product Regulatory Engineer in Shannon, Ireland. In this pivotal role, you will lead regulatory compliance strategies for international safety and performance standards. The ideal candidate has at least 3 years of regulatory experience, strong project management skills, and a background in engineering or law. Competitive compensation and opportunities for professional development are offered. #J-18808-Ljbffr

Senior Clinical Affairs Specialist- 9 Month Contract This position is responsible for providing support for assigned clinical projects. These projects ensure product conformity of medical devices to EU MDD or MDR. The Senior Clinical Affairs Specialist will provide support to the functional project teams leading to sound clinical documents for new and existing products/indications. Key Responsibilities Preparing, writing, editing, and reviewing Instructions for use (IFUs), Clinical Evaluation Plans (CEPs), Clinical Evaluation Reports (CERs), Post Market Clinical Plans (PMCFPs), Post Market Clinical Follow-up Reports (PMCFRs) and Summary of Safety and Clinical performance (SSCPs) Design, conduct and documentation of systematic literature searches in medical databases on products, specific indications, outcomes, or other topics. Appraisal, grading, analysis and write up of all clinical data obtained through the systematic searches to establish clinical evaluation acceptance criteria and quantitatively compare subject device data to demonstrate compliance to relevant general safety and performance requirements (GSPRs). Knowledge of risk management processes for medical devices (such as ISO 14971) to provide clinical input and review to risk management personnel. Knowledge and understanding of proposed and current global medical device regulations and guidance and the ability to relay the impact of such regulations and guidance internally and to clients. Ensuring documents are produced in accordance with procedures, internal and external guidelines (e.g. MEDDEV 2.7.1 Rev. 4, (EU) MDR 2017/745, relevant MDCGs, ISO standards). Appraising, analysing and summarizing clinical data and preparing reports, figures, and scientific meeting presentations. Client management tasks such as; project scoping and proposal writing, proposal management and scheduling, leading weekly progress calls with clients. Key Requirements At minimum a bachelor's degree or equivalent in medical-related field or life science/healthcare field. Minimum 5 years of experience in a similar role in the medical devices industry Fluent written and spoken English. Excellent communication & interpersonal skills Excellent attention to detail and execution of critical appraisal of information Knowledge of clinical research of medical devices (Good clinical practice principles: ISO 14155 and relevant MDCG guidance) including preparing, writing, editing and reviewing clinical investigation documents such as Clinical investigation plans (CIPs), Investigator Brochure (IB), case report form (CRFs) For further information please contact Loretta Flynn Skills clinical affairs, medical writer, medical devices, ISO 14971, EU MDR 2017/745 #J-18808-Ljbffr

Job Title: Senior Clinical Affairs Specialist (Medical Writing) Contract Type: 9-month contract This position is responsible for providing support for assigned clinical projects. These projects ensure product conformity of medical devices to EU MDD or MDR. The Medical Writer will provide support to the functional project teams leading to sound clinical documents for new and existing products/indications. The role will predominantly involve writing clinical evaluation plans (CEPs) and reports (CERs), participating and interacting with project groups ensuring EU MDD/MDR compliance, assisting with clinical submissions to notified bodies and other regulatory bodies and other departmental projects as assigned. The role may also involve working with clinical investigation project planning teams externally to assist in writing clinical investigation documents in order to gain EU MDR conformity in the future or to generate post-market clinical follow up data. Responsibilities and Accountabilities Preparing, writing, editing, and reviewing Instructions for use (IFUs), Clinical Evaluation Plans (CEPs), Clinical Evaluation Reports (CERs), Post Market Clinical Plans (PMCFPs), Post Market Clinical Follow-up Reports (PMCFRs) and Summary of Safety and Clinical performance (SSCPs) Design, conduct and documentation of systematic literature searches in medical databases on products, specific indications, outcomes, or other topics. Appraisal, grading, analysis and write up of all clinical data obtained through the systematic searches to establish clinical evaluation acceptance criteria and quantitatively compare subject device data to demonstrate compliance to relevant general safety and performance requirements (GSPRs). Knowledge of risk management processes for medical devices (such as ISO 14971) to provide clinical input and review to risk management personnel. Knowledge and understanding of proposed and current global medical device regulations and guidance and the ability to relay the impact of such regulations and guidance internally and with our clients. Ensuring documents are produced in accordance with procedures, internal and external guidelines (e.g. MEDDEV 2.7.1 Rev. 4, (EU) MDR 2017/745, relevant MDCGs, ISO standards). Appraising, analysing and summarizing clinicaldata and preparing reports, figures, and scientific meeting presentations. Establishing and overseeing digital clinical libraries, to ensure evidence is organized and maintained appropriately. Knowledge of clinical research of medical devices (Good clinical practice principles: ISO 14155 and relevant MDCG guidance) including preparing, writing, editing and reviewing clinical investigation documents such as Clinical investigation plans (CIPs), Investigator Brochure (IB), case report form (CRFs) Client management tasks such as; project scoping and proposal writing, proposal management and scheduling, leading weekly progress calls with clients. Qualifications and Education Requirements At minimum a bachelor's degree or equivalent in medical-related field or life science/healthcare field. Post-graduate degree preferred. At least 5 years of documented professional experience in a life science or healthcare field or as a medical writer with good clinical/scientific writing skills. Specific Role Requirements and Skills Medical writing (e.g. post-graduate experience in a relevant science or in medicine; training and experience in medical writing, systematic review and clinical data appraisal), excellent attention to detail and execution of critical appraisal of information Fluent written and spoken English. Excellent verbal and written communication. Full competency and proficiency with Microsoft Word, Excel, SharePoint, Teams and Outlook. Experience with document control within a quality management system is strongly desired. Excellent interpersonal and customer service skills. Knowledge or experience with the following Research methodology (including clinical investigation design and biostatistics); Information management (e.g. scientific background or librarianship qualification; experience with relevant databases such as Cochrane library and PubMed Medline); Regulatory requirements for medical devices in the EU #J-18808-Ljbffr