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

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

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

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

Direct message the job poster from Coopman Search and Selection | B Corp™ Coopman is partnering with a leading international financial services organisation to hire a qualified Senior Financial Accountant for their Shannon based office, with a dedicated focus on aviation finance structures. This is a strong opportunity to join a growing AIFM platform and play a key role in the financial reporting, oversight, and governance of aviation leasing funds, aircraft investment vehicles, and related alternative asset structures. Key Responsibilities Lead the preparation of monthly, quarterly, and annual financial statements for aviation-focused AIFs, aircraft SPVs, and leasing structures under IFRS Support consolidation and group reporting requirements across multiple AIFM and aviation-leasing jurisdictions Oversee NAV reviews, asset-level reconciliations, maintenance reserve accounting, and key financial controls associated with aircraft assets Partner with portfolio management, technical, risk, and operations teams to deliver insightful analysis on aircraft performance, valuation, cashflows, and lease metrics Coordinate with aviation fund administrators, auditors, technical managers, servicers, and other external service providers Ensure compliance with all AIFM regulatory obligations, together with aviation-specific accounting, valuation, and reporting standards Contribute to enhancements in reporting processes, asset-level oversight frameworks, and internal control environments relating to aviation investment structures Requirements ACA / ACCA qualified accountant (Big 4 / Top 10 background advantageous) 3+ years’ PQE in audit or financial reporting within aviation finance, aircraft leasing, investment funds, AIFMs, or administrators Strong IFRS technical skills; exposure to IFRS 16, aircraft classification, leasing structures, SPVs, or US GAAP is beneficial Experience working with aviation fund administrators, leasing platforms, or asset-management teams is a strong advantage Proven ability to manage deadlines and deliver accurate, high-quality reporting in a fast-paced asset-focused environment Advanced Excel capability with strong analytical and problem-solving skills Strong communicator with commercial awareness and the ability to work effectively with cross-functional aviation teams This is an excellent opportunity to deepen your experience within the aviation finance and alternatives sector, gaining exposure to complex aircraft investment structures within a dynamic and expanding organisation. Apply now or contact Aaron.Ryan@Coopman for a confidential discussion. Seniority level Mid-Senior level Employment type Full-time Job function Accounting/Auditing and Finance Industries Financial Services, Funds and Trusts, and Accounting #J-18808-Ljbffr

Direct message the job poster from Ei Electronics We are seeking a highly experienced and proactive Product Regulatory Engineer to lead our efforts in navigating the complex landscape of international regulations and standards. The Product Regulatory Engineer will be responsible for defining, implementing, and maintaining Ei Electronics' global regulatory compliance strategy across all product lines. This pivotal role will ensure that all products meet relevant national and international safety, performance, and environmental standards, facilitate successful product approvals, and manage all interactions with Notified Bodies and other regulatory authorities. Key Responsibilities Develop, implement, and maintain a comprehensive global regulatory compliance strategy for all Ei Electronics products, ensuring alignment with business objectives and market expansion plans. Monitor and interpret new and evolving national, regional, and international regulations, standards, and directives relevant to fire and carbon monoxide detection products (e.g., CPR, RED, LVD, EMC, RoHS, WEEE, UKCA, UL, CE, BSI, VdS, etc.). Provide expert guidance and support to R&D, Quality, Manufacturing, Sales, and Marketing teams on regulatory requirements throughout the product lifecycle, from concept to end-of-life. Proactively identify potential regulatory risks and opportunities, developing mitigation strategies and action plans. Manage and oversee all aspects of product approvals and certifications for new and existing products across various global markets. Prepare and submit comprehensive technical documentation, test reports, and declarations of conformity to Notified Bodies, certification agencies, and regulatory authorities. Coordinate and facilitate all necessary product testing with internal and external laboratories to ensure compliance with relevant standards. Maintain and update all product certifications, licenses, and declarations, ensuring their ongoing validity. Notified Body & Regulatory Authority Interactions Act as the primary point of contact and lead all interactions with Notified Bodies, national regulatory authorities, and other certification bodies. Manage and facilitate audits, inspections, and assessments by Notified Bodies and regulatory agencies. Respond to inquiries, address deficiencies, and negotiate with regulatory bodies to achieve timely product approvals and resolve compliance issues. Build and maintain strong working relationships with key regulatory stakeholders. Documentation & Quality Management Systems Establish and maintain robust regulatory documentation systems, ensuring accurate, complete, and readily accessible records of all approvals, certifications, and compliance activities. Collaborate with the Quality team to integrate regulatory requirements into the company's Quality Management System (QMS) (e.g., ISO 9001, EN13980 for CPR). Develop and deliver training programs to internal teams on regulatory compliance requirements and best practices. Ensure all product labeling, user manuals, and marketing materials comply with relevant regulatory requirements. Post-Market Surveillance & Compliance Maintenance Support post-market surveillance activities, including the review of product complaints and incidents for potential regulatory impact. Manage and track changes to existing products to ensure continued compliance with evolving regulations. Initiate and manage recall activities if required, in collaboration with relevant internal departments and regulatory bodies. Qualifications and Experience Bachelor's degree in Engineering, Science, Law, or a related technical discipline. Minimum of 3 years of experience in a dedicated Product Regulatory role within a manufacturing environment, ideally in electronics, consumer goods, or a similarly regulated industry. Proven in-depth knowledge and practical experience with key international regulatory frameworks and standards relevant to regulated products (e.g., Construction Products Regulation (CPR), Radio Equipment Directive (RED), Low Voltage Directive (LVD), EMC Directive, RoHS, WEEE, REACH, UKCA marking, UL, BSI, VdS standards). Demonstrable experience in managing complex product approval processes from start to finish, including interactions with Notified Bodies. Strong understanding of quality management systems (e.g., ISO 9001) and their application in a regulatory context. Excellent written and verbal communication skills, with the ability to articulate complex regulatory information clearly and concisely to diverse audiences. Highly organized, meticulous, and detail-oriented, with strong project management skills. Proactive, self-motivated, and able to work independently as well as collaboratively within a team. Master's degree or higher in a relevant field. Experience in the fire safety or security industry. Experience with global market access strategies. Legal background or specific qualification in regulatory affairs. Fluency in additional languages relevant to key export markets. Skills and Competencies High level of integrity and ethical conduct. Strong analytical and problem-solving abilities. Ability to influence and persuade stakeholders at all levels. Resilience and adaptability in a fast-paced, evolving regulatory landscape. Commitment to continuous learning and professional development. Limerick, County Limerick, Ireland 3 weeks ago #J-18808-Ljbffr