Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Beckman Coulter Diagnostics, one of 15+ operating companies, our work saves livesand were all united by a shared commitment to innovate for tangible impact. Youll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danahers system of continuous improvement, you help turn ideas into impact innovating at the speed of life. As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratorys role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision makingwe are enabling clinicians to deliver the best possible car to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. The Staff Manufacturing/Projects Engineer is responsible for the delivery of strategic equipment projects to Beckman European sites: Clare and Krefeld. In this role, you will work with Operations, Engineering and External Equipment Vendors to deliver equipment projects, starting with the development of the User Requirements specifications all the way through equipment validation. You will be responsible for driving continuous improvement initiatives and fostering a culture of technical excellence and problem-solving within the team. This is a permanent role. This position will report to the Manager, Manufacturing Process Engineer, and is part of the Global Engineering team and will be an on-site role at our Clare, Ireland site. In this role, you will be responsible for: Manage Large Scale Equipment Engineering Projects: Works with Operations, and Engineering teams on new equipment designs and is the link engineer to external 3rd party equipment builders to manage the full equipment life cycle. Drive Process Improvement: Lead initiatives to enhance efficiency, reduce waste, and improve product quality using Lean and Six Sigma methodologies. Support Production Operations: Provide hands-on engineering support to resolve manufacturing issues, minimize downtime, and ensure smooth operations. Implement Advanced Technologies: Evaluate and deploy new equipment and automation solutions to boost manufacturing capability and scalability. Ensure Quality & Compliance: Partner with Quality teams to maintain process controls, conduct NC/CAPA, and ensure regulatory compliance. Problem Solving: Utilize process PSP / DIVE to troubleshoot new products / process / equipment while working closely with cross functional team and/or external vendors. Communication: Provide regular effective and clear updates on Equipment and process projects, issues. The essential requirements of the job include: Education: Bachelors degree in: Manufacturing, Industrial, Mechanical, Electrical Engineering, or a related technical field. Experience: 9+ years in manufacturing engineering within a GMP environment. Experience of relevant quality systems (e.g., ISO 13485). Process Improvement: Proven success driving Lean Manufacturing and Six Sigma initiatives; Green or Black Belt certification preferred. Technical Knowledge: Strong understanding of manufacturing processes such as assembly, machining, fabrication, automation, and inspection. Leadership & Problem Solving: Excellent team building, coaching, and analytical skills with a data-driven approach to decision-making. Communication Skills: Strong verbal and written communication abilities, capable of conveying complex technical concepts to varied audiences. Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel 20% It would be a plus if you also possess previous experience in: cGMP MedTech experience Experience with CAD software and statistical analysis tools (e.g., Minitab, JMP). Experience in the life sciences or healthcare industry. Experience with industrial automation (e.g., PLCs, SCADA). Knowledge of AI integration with automation. Experience in a regulated industry Proficiency in project management Beckman Coulter Diagnostics, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether its a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at . Skills: Projects Lean Manufacturing Manufacturing Process Engineering Process Improvement Benefits: Pension Fund Medical Aid / Health Care Performance Bonus
Wondering whats within Beckman Coulter Diagnostics? Take a closer look. At first glance, youll see that for more than 80 years weve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. Were building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and youll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, were working at the pace of change to improve patient lives with diagnostic tools that address the worlds biggest health challenges. TheManufacturing Scientist I, Value Assignment for Beckman Coulter Diagnostics is responsible for all testing and laboratory activities required to support value assignment of controls and calibrators for the AU product line. This position is part of the AU Technical Operations/Value Assignment Department located just outside Tulla in O'Callaghan's Mills, Co. Clare and will be an on-site position. This role is a 12-month FTC. Graduates are welcome to apply. You will report to the Supervisor, Value Assignment responsible for value assignment of controls and calibrators for the AU product line. If you thrive in a fast-paced role and want to work to build a world-class Technical Operations organizationread on. In this role, you will have the opportunity to: Perform testing, tabulation, report generation and investigational work in relation to Value Assignment. Any other duties as outlined by the manager. Perform linearity pool production / stock control & maintenance, validation of excel templates and other technical data analysis Perform laboratory maintenance / Equipment calibration & maintenance. The essential requirements of the job include: Level 8 Degree in Chemistry, Biochemistry or equivalent Science discipline. Knowledge of quality assurance, GMP/FDA/ISO regulations. Familiarity with handling chemicals, bio-hazardous materials, enzymes and laboratory equipment and analyzers. It would be a plus if you also possess previous experience in: Clinical Chemistry or Immunology Reagent. Quality assurance, GMP / FDA / ISO regulations. Skills: Laboratory GMP Calibration Analytical Troubleshooting Benefits: Pension Fund Medical Aid / Health Care Performance Bonus
Wondering whats within Beckman Coulter Diagnostics? Take a closer look. At first glance, youll see that for more than 80 years weve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. Were building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and youll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, were working at the pace of change to improve patient lives with diagnostic tools that address the worlds biggest health challenges. The Analyst II, Technical Project Managementfor Beckman Coulter Diagnostics is responsible for managing all aspects of diverse projects which require technical knowledge and expertise. This is a specific purpose contract. This position is part of the AU Technical Operations department located in Lismeehan, O'Callaghan's Mills, Co. Clare and will be an onsite position. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Technical Operations team and report to the Senior Manager, Technical Operations. If you thrive in a multifunctional role and want to work to build a world-class Technical Operations organizationread on. In this role, you will have the opportunity to: Deliver/transfer supply chain projects in line with agreed targets and objectives in support of NPI including coordination and/or facilitation of cross functional technical teams to achieve project goals. Laboratory testing in line with technical operations targets and objectives, including qualification of new raw material/ suppliers for clinical chemistry use and failure investigation into problem products, for root cause determination and corrective action recommendations. Documentation of test results and Report generation for SCM files. Technical support to other BC Ireland Inc departments in their internal problem resolution / product maintenance support where relevant. Support of other technical Operations teams as required. The essential requirements of the job include: Degree or Diploma in Chemistry, Biochemistry or equivalent and/or experience in Clinical Chemistry or Immunology Reagent and a mimimum of 2 years relevant work experience Familiar with handling of chemicals, bio-hazardous materials, enzymes and laboratory equipment and analysers. Skills in handling computer software for calculation of data and record keeping. Quality assurance, GMP / FDA / ISO regulations. It would be a plus if you also possess previous experience in: Preparation of reagents. Failure investigation techniques. Project Management Benefits: Pension Fund Medical Aid / Health Care Performance Bonus
