A leading biotech company in County Clare, Ireland is seeking a QC Specialist to support GMP-compliant activities in Quality Control for gene therapy products. This role involves a variety of responsibilities from equipment qualification to routine testing, promoting communication and data integrity. Suitable candidates must have a degree in Human Health or Sciences, at least 8 years in the pharma or biotech industry, and knowledge of GMP regulations. Strong analytical and communication skills are essential. #J-18808-Ljbffr

A leading technology company in Shannon, County Clare, is seeking a Senior Corporate Accountant. The role requires strong accounting skills and managing the month-end close process in a hybrid environment. Candidates should have significant experience, preferably with a Big 4 background, and proficiency in US GAAP. This role offers interaction across multiple business functions, ensuring compliance and enhancing performance. An excellent opportunity for a self-starter to join an international finance team. #J-18808-Ljbffr

A leading recruitment agency is seeking a skilled Mechanical Design Engineer for a contract role in County Clare, Ireland. The role involves the design and development of mechanical systems and components through the full product lifecycle. Candidates should have experience with 3D CAD tools and a relevant engineering degree. This opportunity offers initial 6-month contract with a competitive rate and potential for permanent employment based on performance. #J-18808-Ljbffr

The Plant Manager is responsible to lead daily operations for the plant and to ensure reliability and consistency on HSE/Compliance and the smooth execution of the production line. Contribute and lead in the development of a business plan for the business unit as a whole. Is involved in discussions with other disciplines about future developments and consequences for the business unit. Develops a strategic midterm plan for the manufacturing unit based upon the agreed strategic plan for the whole unit. Responsibilities, Authorities And Accountabilities Responsible as site leader for the management and overall leadership of the Shannon plant. Lead and manage the manufacturing production facility in order to reach defined targets in HSE, Compliance , revenue, quality, cost, delivery and safety. Lead and develop the plant management team in performance development and career growth and in executing on business strategy goals and objectives. Lead and drive accountability for everyone meeting HSE delivery and execution for manufacturing plant. Deliver best in class OTD target at 100%, zero past dues and overdue backlog. Be responsible for overall cost actions within the plant, focus on VCP, cost management and bullet trains along with tight control for plant po management. Responsible for overall plant backlog integrity and date maintenance. Leads resolution of sales order blocks and assumes complete ownership for backlog. Drive continuous business improvement with focus on lean and additive manufacturing. Lead plant capacity planning and production/manufacturing planning strategy with drive on zero past due orders and leading indicator focus on planned orders. Team management of plant leadership team and site leadership for all plant employees. Management of overall plant P and E, inventory and Obso/scrap execution and strategy. Conduct frequent interactions on strategic level due to complex long term planning activities and/or complex long term sales processes with high degrees of customizations. Handles very complex manufacturing processes. Complexity due to inherent technical variety, interdependency of production cycles, required technical know-how, value of assets or scale of production. Leads a big manufacturing unit. Consistent of several value stream departments and dispersed manufacturing departments. Required Qualifications Engineering or supply chain Bachelor's degree from an accredited university or college. Minimum of 15 additional years of experience ideally in Plant Management and materials management. Experience in planning and materials management leadership roles. Desired Characteristics Strong oral and written communication skills. Strong interpersonal and leadership skills. Demonstrated ability to analyze and resolve problems. Demonstrated ability to lead programs / projects. Ability to document, plan, market, and execute programs. Established project management skills. #J-18808-Ljbffr

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives, and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered, and recognised. What You Can Expect Support the development, implementation, and training of Lean tools and concepts from incoming to shipment at Zimmer Biomet large site or multiple production sites. Responsible for the overall development program which teaches and promotes efficient, quality, lean, and cost‑effective operation and manufacturing processes using Lean Production Methods. Assist in operationalizing the site strategy on the shop floor. Support departments in identifying operational waste and areas for improved operational effectiveness. Working collaboratively with the Engineering Team, assist in determining, deploying, and training the right development plans and corresponding implementation of Lean concepts within the targeted department. Manage and track specific deployment projects, create and modify development procedures, and conduct kick‑off and site activities to maximize deployment effectiveness and to meet stated objectives in the areas of quality, lead time/delivery, and total cost of product/service goals. How You’ll Create Impact Drive continuous improvement, cost savings, and continuous improvement culture across the operations organization. Assist with establishing governance, standards, measurement, and reporting processes to evolve the OPEX infrastructure and systems for the manufacturing organization. Implement Lean Kanban, JIT, Kaizen, Jidoka, Heijunka, 5S, Visual Management, and other lead philosophies at production sites to improve the overall flow of materials and information. Identify and facilitate process improvement projects, trainings, and workshops to drive cultural change. Perform program management activities with site‑specific projects while monitoring operation progress against stated objectives and goals. Conduct operational assessments and identify initial gaps while creating specific development action plans to address the gaps. Support curriculum development and refine training material use to deploy the Lean Manufacturing philosophy. Conduct root cause analysis to determine metrics and to troubleshoot manufacturing, business, and assembly issues as well as material flow, projects plans, production capacity, and facility design. Create process documentation in support of all activities as needed. Drive value stream mapping to define "As‑Is" Analysis and the transition to Future State. Act as a change agent for continuous improvement efforts that cross clients, sites, and processes. Assist with the deployment of mechanisms for knowledge sharing and best practice transfer to replicate and accelerate improvement efforts. Develop, evaluate, and improve manufacturing methods as it relates to both new product and current product. Confer with management and sets standards for efficient production methods. Estimate production times, process efficiencies, and related costs to provide recommendations and direction for change decisions. Coach and mentor plant project and certification candidates to ensure their continued development in Six Sigma, Lean Manufacturing, and other continuous improvement methodologies. Build and lead a strong internal team of results‑driven, continuous improvement facilitators. Continuously challenge team members to find opportunities for continuous improvement and to raise the bar for performance. Partner with other key stakeholders and search for innovative opportunities. Ensure all initiatives and efforts contribute to the company's long‑term goals and objectives. This is not an exhaustive list of duties or functions and might not necessarily comprise all the essential functions for purposes of the Americans with Disabilities Act. What Makes You Stand Out Extensive knowledge of Lean tools, concepts, and plant‑wide application within manufacturing and processing facilities. Demonstrated ability to apply Lean concepts to improve overall manufacturing effectiveness, ensuring that the right quantity of the right parts is delivered at the right time. Advanced knowledge of analytical/statistical problem‑solving tools (DMAIC/PDCA/8 Disciplines). Demonstrated ability to develop and refine training material for maximum effectiveness. Excellent written, presentation, and communication skills with the ability to articulate complex ideas and strategies clearly and persuasively to diverse audiences at various organizational levels. Ability to work with and influence others in a fast‑paced environment. Ability to work across divisions and functions to influence change across the organization and unleash full potential as a company and as individuals. Proven ability to continuously improve processes and profitability through meaningful and appropriate cost reductions. Able to take action in solving problems and making decisions while exhibiting judgement and a realistic understanding of issues, able to use reason, even when dealing with emotional topics. An understanding of and proficiency in Change Management. Your Background Bachelor's Degree in Industrial Engineering, Engineering, Supply Chain Management, Business Administration required. Five years experience in Lean application and/or training in an industrial or manufacturing setting required. Six Sigma, Lean Manufacturing, or equivalent certification required. Experience leading teams required. Advanced skills in statistical software packages (Minitab, Visio, etc.) and MS Office required. Travel Expectations Up to 25% EOE/M/F/Vet/Disability #J-18808-Ljbffr

A leading global medical technology firm in Shannon, Ireland is looking for a dedicated Lean Manufacturing Specialist to support and enhance operational efficiency. Candidates should have a Bachelor's in Engineering or Business, with at least five years of experience in Lean methodologies and team leadership. Responsibilities include supporting Lean training and continuous improvement projects. Strong analytical skills, certification in Six Sigma, and proficiency in statistical software are essential for success. The position offers up to 25% travel. #J-18808-Ljbffr

Join a leading biotech in Ireland as a Bioprocessing Scientist powering GMP-grade productions in a cutting-edge cleanroom. R&D Partners is seeking a Bioprocessing Scientist to join a leading biotechnology company in Ireland. This role focuses on performing production processes in a GMP-compliant cleanroom environment while ensuring compliance with health and safety standards. Please note that to be considered for this role you must have the right to work in this location. Responsibilities Execute production processes using aseptic techniques in a GMP-compliant cleanroom. Monitor and maintain facility cleanliness, safety, and environmental standards. Review and update process documentation and perform routine equipment checks. Manage stock inventory, including ordering, receiving, and storing materials. Identify and report deviations, support investigations, and assist with technology transfers. Ensure timely delivery of products while adhering to health and safety procedures. Key Skills and Requirements Execute production processes using aseptic techniques in a GMP-compliant cleanroom. Monitor and maintain facility cleanliness, safety, and environmental standards. Review and update process documentation and perform routine equipment checks. Manage stock inventory, including ordering, receiving, and storing materials. Identify and report deviations, support investigations, and assist with technology transfers. Ensure timely delivery of products while adhering to health and safety procedures. #J-18808-Ljbffr

Safeguard the quality behind life‑changing gene therapies through GMP‑driven QC excellence. R&D Partners is seeking a QC Specialist to support GMP-compliant activities within Quality Control (QC) for the manufacture and release of plasmids and gene therapy products. This role involves contributing to a GMP facility for gene therapy production, with responsibilities spanning equipment qualification, method transfer, routine in-process and release testing, and other QC-supporting activities. Please note that to be considered for this role you must have the right to work in this location. Responsibilities Support technical transfer of drug substance dilution to QC. Conduct bridging studies for QC dilutions to compare dilution regimes. Execute dilution studies, including equipment installation and qualification. Plan, track, monitor, and execute QC stability studies in accordance with international standards and regulations. Address issues, CAPAs, change controls, action items, and risk assessments within QC. Escalate and resolve QC issues with site leadership. Lead major investigations impacting QC analysis. Author and review scientific and technical documentation. Stay updated on developments in methods and regulations for ATMP analytics. Promote effective communication within the team, across departments, and with external collaborators. Ensure data integrity throughout the data lifecycle. Maintain compliance with GMP, GDP, and GxP guidelines. Support new product introductions and strategic QC-related activities. Key Skills and Requirements Analytical Skills: Ability to synthesize complex information and use data-driven insights. Problem Solving: Timely resolution of issues with alternative solutions. Leadership: Inspire and motivate others while accepting feedback. Cost Consciousness: Work within budgets and implement cost‑saving measures. Planning & Organization: Prioritize tasks and manage time efficiently. Professionalism: Treat others with respect and maintain composure under pressure. Quality Management: Promote quality improvements and ensure accuracy. Communication: Strong oral and written communication skills, including technical writing. Qualifications Degree in Human Health or Sciences, or equivalent relevant work experience. Minimum 8 years of experience in the pharmaceutical or biotech industry. Demonstrated knowledge of GMP environments and quality control. Experience with audits and client-facing interactions. Proficiency in EU/FDA regulations, ICH guidelines, GMP/GLP/GCP, Lean Manufacturing, and Six Sigma. Strong collaboration, communication, and conflict resolution skills. #J-18808-Ljbffr

A well-established organisation in Ireland seeks a Senior Financial Accountant to prepare financial reports and manage compliance with corporate regulations. Candidates must be qualified accountants with strong Excel skills and proficiency in reporting tools. This position requires excellent communication, analytical abilities, and the capacity to work independently. The company offers a competitive salary and strong employment benefits. #J-18808-Ljbffr

A leading aviation services company in Shannon, Ireland, seeks a B1/B2 Licensed Aircraft Engineer for full-time, permanent work. This role involves delivering line maintenance and supporting the organization’s operational integrity while ensuring compliance with safety regulations. Candidates should possess an EASA Part 66 B1/B2 Licence, strong communication skills, and the ability to work under pressure. The position offers a competitive salary, generous holiday allowance, and health benefits. #J-18808-Ljbffr