Cytiva

to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva, you will be able to continuously improve yourself and us - working on challenges that truly matter with people who care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System , which makes everything possible. As the Director Site Quality you will collaborate closely with cross functional leadership and associates to ensure compliant execution, monitoring, and continuous improvement of the implemented QMS in line with certification requirements and customer expectations. This position reports to the Sr Director QA Bioprocess Filtration and leads both the Quality Control and Quality Assurance teams located in Ilfracombe . This is an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Quality Leadership & Compliance: Serve as the Ilfracombe site's Quality Management Representative, leading QA/QC functions, ensuring regulatory compliance, and aligning with organizational quality goals. Quality Management System (QMS): Implement, maintain, and optimize the Cytiva QMS, ensuring procedures, work instructions, and IT systems support site operations and lead with DBS mindset to drive continuous improvement. Strategic Partnership & Advocacy: Collaborate with site and global leadership to address process changes, advocate for site-specific needs, and drive customer-centric solutions during change management initiatives. Team Development & Performance: Build a high-performing quality department, fostering a safe, empowering environment that encourages skill development, psychological safety, and continuous improvement. Audits, Reporting, & Representation: Lead Quality Management Reviews, define and monitor KPIs, host audits, and represent the site in executive discussions and global best practice initiatives. Who you are: Hold a Bachelor's degree, preferably in Science, Business, or Engineering. Have at least 7 years of experience in Quality Assurance, Quality Engineering, or Manufacturing Operations within Life Sciences, Biotechnology, Medical Device, Biopharma, or other FDA/EPA-regulated manufacturing environments. Possess several years of leadership experience, with senior leadership roles in QA, Operations, or Quality Engineering preferred. Regulatory and Quality Expertise: Strong knowledge of ISO standards, FDA regulations, cGMPs, CFR requirements, and quality management practices, including operational controls, CAPA, complaints, audits, and risk management. Analytical and Process Optimization: Proficiency in quality statistical methods, Lean Manufacturing principles, Six Sigma methodologies, and Root Cause Analysis tools to drive data-driven decisions and resource optimization. Leadership and Communication: Proven ability to lead, coach, and mentor teams; manage performance; plan succession; and effectively communicate at all organizational levels, both written and verbal. Strategic and Operational Acumen: Skilled in managing budgets, assessing opportunity costs, and fostering innovative problem-solving, while maintaining exceptional organizational and time management capabilities. Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel 10% of the time to other Cytiva manufacturing locations in Europe and Worldwide, as required. Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info . Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here . We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at to request accommodation. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. Are you our new Senior QA Specialist at Stevenage Site UK, reporting to the Quality Assurance department at Cytiva Uppsala, Sweden. As Senior QA Specialist you will be part of the QA team at site that has the oversight of QMS-management and batch release. You will have supporting function to the organization within Change Control, CAPA, NC (deviation) and complaints handling. You will represent QA in projects and ensure compliance to the design control procedure and QMS. In this role you will work in cross-functional team with the rest of the site as manufacturing and R&D and also teams from Uppsala. This is an on-site role at Stevenage site UK. In this role you will: Represent QA in cross-functional projects as new product- and equipment projects. Represent QA on site to support the organization within the QMS processes; Change Control, CAPA, NC and batch release. Review and approve Change Control, CAPA, NC Perform batch release. Be the QA counter part to approve qualification activities to meet set timelines and project planes, in close collaboration to the rest of the organization. Represent QA in cross functional risk assessments. Review and approve risk assessments and qualification documentation Participate and actively drive improvement activities within the QMS, in projects and processes. Ensure compliance with the Quality Management System (QMS) in close collaboration with the rest of the organization and the Uppsala QA organization. Who you are: Relevant Batchelor degree within chemistry/ Pharmacy or equivalent Experience of similar QA-role within Life Science companies (t.ex ISO 9001, ISO 13485 and/or GMP). Experience of being QA in projects. Experience of Qualification activities within automation, equipment and analytical methods. Earlier experience as QA in risk assessments/FMEA, batch release and deviations/NC. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. We are seeking a Multi Skilled Engineering Technician. This position reports to the Engineering Production Leader and is part of the Manufacturing/Process Engineering Team located in Cardiff, UK and will be an on-site role. At Cytiva, our vision is to advance future therapeutics from discovery to delivery. What you will do Carry out routine / preventative maintenance activities on all production equipment. Be production focused, react to unplanned equipment breakdowns, process changeovers, health and safety actions, and machine setup. Be involved in installation qualifications, risk assessments, PUWER's, and LOTO's. Work with process engineering to monitor equipment performance, and strive for continuous improvement. Who you are Apprenticeship (or equivalent formal qualifications, NVQ 3 / HNC / BTEC) in production maintenance manufacture with an Electrical / PLC background. Works well under time-bound pressure as part of a team, and independently. Highly motivated, with a strong focus on Safety, Quality, and Delivery. It would be a plus if you also possess previous experience in: Experience in mechanical maintenance. Able to interrogate and modify PLC software (Siemens / Mitsubishi) Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. What you'll do: Responsible for individual team members who are supporting related projects (DRA). Provide leadership and support to Engineering and Technical teams for all activities within remit. Ensuring structured and well executed Daily Management of projects through VPM with both the core team and communicating effectively with stakeholders. Provide stakeholder management across multiple functions and business levels. Who you are: Degree in Manufacturing, Mechanical Engineering, Project Mgmt with a technical/operations bias. Hands on experience of delivering Mfg Engineering projects/improvements/experience in managing change within a manufacturing environment. Strong track-record of successfully improving and sustaining Safety, Quality and Performance of our manufacturing equipment. Demonstrated ability to act with urgency, deliver sustained results, work well within a team and demonstrates a commitment to delivering results. Effective planning, ability to make detailed analysis and data-driven decisions, structured approach for both your own work load and also the support of others to enable efficient and effective project execution. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible The Calibration Specialist is responsible for maintaining global calibration programs, ensuring adherence to global requirements and implementing process improvements. This position reports to the Calibration Governance Leader and is part of the Qualification Services team within the Equipment Services Organization. This position will be located in Marlborough, MA and will be an on-site role. In this role, you will have the opportunity to: Review, recommend, and implement improvements to calibration work instructions, procedures, and methods to ensure accuracy and compliance. Audit the calibration program, including evaluation of calibration performance, to ensure adherence to established standards and procedures. Provide technical support and guidance to calibration technicians and other team members. Maintain detailed records of calibration activities and results for audit purposes. Ensure all calibration activities comply with quality standards and regulatory requirements and assist in determining and monitoring Key Performance Indicators (KPIs) related to calibration activities. The essential requirements of the job include: Bachelor's degree in engineering, physics, or a related field with multiple years of experience in metrology related field; or long-standing experience in the Life Science industry with calibration experience. Strong understanding of ISO 17025 standards and requirements. Ability to work collaboratively with team members and lead when necessary. Familiarity with industry standards and regulations related to calibration. Strong organizational and time management skills with the ability to manage multiple tasks and projects simultaneously. Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel up to 10% globally. Must have a valid passport and able to travel internationally It would be a plus if you also possess previous experience in: Proficiency in calibration tools and techniques. Ability to train and assist others in calibration techniques. Experience in developing and implementing Standard Operating Procedures. Excellent analytical and problem-solving skills. Ability to conduct audits and evaluate performance metrics. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here . We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at to request accommodation.

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. This position is part of the Media Engineering Team located onsite in Newquay and will be >. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Drive root-cause analysis and implement permanent countermeasures Provide technical support for relevant processes and products Work with internal and external customers and suppliers Generate, execute and approval of change validation activities Who you are: Team player with drive for improvements and positive change Previous experience in manufacturing processes and practice Posses a degree level qualification in an Engineering related subject Experience in lean manufacturing techniques, preferably six sigma Experienced practitioner in TPM / PPM culture and OEE improvement. It would be a plus if you also possess previous experience in: Industrial electronics and control systems Web-handling systems Hydraulics, pneumatics and mechanical equipment Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we're pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives. What you'll do Reporting to the engineering lead, you will provide all Electrical and Mechanical support within the production area adopting a proactive / reactive mindset whilst resolving equipment breakdowns in a timely manner following all Health and Safety requirements. To ensure maximum machine available uptime through effective planned maintenance schedules and play an active role in the controlling and sourcing of equipment spares Involved with installation qualifications (Risk assessments, PUWER's, LOTO's and Maintenance Instructions). Working with process engineering, to monitor equipment performance, and strive for continuous improvement. Who you are Time served Apprenticeship (or equivalent formal qualifications, NVQ 3 / HNC / BTEC) in an Electrical/Mechanical discipline with PLC experience obtained within a manufacturing environment. Works well under time-bound pressure as part of a team, and independently. Highly motivated, with a strong focus on Safety, Quality, and Delivery. It would be Desirable if you also possess previous experience in: Vison systems (Keyence/Cognex). Maintenance experience working on Pharma production chillers and freeze driers. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Senior Method Development Scientist for Cytiva is responsible for identifying, evaluating, developing, and validating our key methods. This position is part of the Fibro R&D department located in Stevenage and will be on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Work closely with a cross-disciplinary R&D team of Biologists, Chemists, Engineers and Material Scientists to support method development and validation activities. Plan, delegate and develop experiments for process and product characterisation of Fibro materials and devices Review and write reports and interrogate data generated from various analytical methods, or development projects. Help develop the team around you, by delegating and encouraging less senior staff in their duties Prepare and present data internally in the form of presentations, technical reports, memos and eLNs. Who you are: Must have a PhD in a bioscience or analytical chemistry based field 3+ years of industrial experience You will have hands-on experience developing and validating analytical methods in a laboratory environment You will have demonstrable experience of leading a transfer of an analytical method from R&D to Pilot or manufacturing facilities You will have a working knowledge of chromatography for the bioprocess industry, materials science This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off and medical/dental/vision insurance to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Quality Control Technician is responsible for performing routine raw material/finished goods testing and release activities to ensure timely provision of materials to production, and products to customers. They will also control and investigate items that are non-conforming to support manufacturing and the wider business. This position reports to the Quality Control Team Leader and is part of the Quality Control department located in Cardiff and will be an on-site role working on a rotating shift pattern. What you will do: Inspection, measurement and testing of raw materials and finished products Review of batch records and performance of quality release actions, ensuring GDP requirements are adhered to. Ensure non-conformances are reported when they occur, completing thorough investigations when required. Feedback data/results generated from QC activities to relevant stakeholders and recommend actions, where appropriate. Who you are: A formal engineering or scientific qualification is preferred. Ability to interpret engineering drawings is essential. Ability to work with minimal supervision, using own initiative, prioritising work as appropriate whilst maintaining a cross-functional approach. Previous experience within a quality control environment/ ISO 9001/ ISO13485/ Pharma regulated manufacturing environment is an advantage. It would be a plus if you also possess previous experience in: Able to make reasoned and objective decisions where necessary Knowledge and ability to use Microsoft Office applications Experience or knowledge of Lean techniques Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. This job is also eligible for bonus/incentive pay. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is proud to work alongside a community of ten fellow Danaher Life Sciences companies. Together, we're pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives. Position Summary For the Cytiva Discovery & Medical business unit, the Director, Advanced Engineering is responsible for the advancement of quality of our products and productivity within our plants through the identification and deployment of improved technology and automation to meet the needs of our Customers, Associates and Shareholders. In this role, the associate would assess current manufacturing capability and capacity, working alongside Operations Strategy and Plant Teams, deploying technology to bridge gaps as measured through SQDIP. In addition, this role is responsible for creating and successfully deploying a comprehensive OEE mechanism and global Preventive Maintenance and Spares systems within the D&M organization, owning the subsequent actions to close the gaps. In addition, the role will also lead the execution of Strategic Programs and Projects that improve Safety, Quality, Delivery, Inventory, Productivity and Cost through the optimization of manufacturing capacity and capability (PMO). Director, Advanced Engineering - D&M What you'll do Adopt responsibility for identification, governance, development, selection and deployment of Manufacturing Technologies and Processes across the D&M sites, as well as inter-OpCo and CMO supply sites, resulting in improved OEE, reduced cycle times, increased line reliability and improved yields, leading to reliable output and increased customer satisfaction. Lead site-based teams alongside the relevant Plant Leader through the planning and execution of Capital Investment in chosen new technology, or upgraded manufacturing lines for the benefit of Safety, Quality, Delivery or Cost through the expert utilization of DBS tools and techniques Engage & Contribute to Strategy Deployment for the OpCo. Identifying key breakthrough technologies and strategic technical projects with a technology and investment roadmap with a 5 to 7 year view, that will enable growth and improved manufacturing performance. Development and leadership through approval, execution, and sustainment phases of all significant investment proposals for facilities and manufacturing technology programs and projects across D&M and CMO supplying sites Create and implement a business-wide preventative maintenance program using DBS tools Development and leadership through approval of significant investment proposals for facilities and manufacturing technology programs and projects across the D&M sites. Provide functional direction, support and guidance to the site-based ME, PE, Manufacturing Technology and Project Associates for the execution of strategic and tactical programs and projects delivering improvements across SQDIP. Collaborate with central Technical & Digital Operations Teams to adopt best practice processes and procedures. Lead the D&M Digital Operations initiative. Who you are: Bachelor or Masters degree in Engineering or related field (Science / Manufacturing). Minimum of 10 years of progressive leadership in Operations and/or Engineering leadership in a highly automated assembly environment in Life Sciences or similar regulated industry. Recognized Manufacturing Engineering expertise in a Lean Manufacturing environment. Competency with a breadth of technologies. Solid problem-solving skills- ability to resolve complex problems, communicate issues and propose solutions to both external customers and internal team members. Demonstrated experience of successfully delivering concurrent technology programs or projects in a high-volume automated manufacturing environment Ability to operate effectively in a multi-tasking, dynamic environment, while maintaining a forward-thinking and customer-first attitude. Ability to energize, develop and build rapport, collaborate and influence at all levels within an organization. Act as inspirational leader with optimism, highly approachable and humble. Ability to travel up to 50% of the time. High level presentation and interpersonal skills- able to communicate and present ideas to customers in a way that produces understanding and impact that builds effective strategic relationships. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is proud to work alongside a community of ten fellow Danaher Life Sciences companies. Together, we're pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives. Position Summary For the Cytiva Discovery & Medical business unit, the Director, Advanced Engineering is responsible for the advancement of quality of our products and productivity within our plants through the identification and deployment of improved technology and automation to meet the needs of our Customers, Associates and Shareholders. In this role, the associate would assess current manufacturing capability and capacity, working alongside Operations Strategy and Plant Teams, deploying technology to bridge gaps as measured through SQDIP. In addition, this role is responsible for creating and successfully deploying a comprehensive OEE mechanism and global Preventive Maintenance and Spares systems within the D&M organization, owning the subsequent actions to close the gaps. In addition, the role will also lead the execution of Strategic Programs and Projects that improve Safety, Quality, Delivery, Inventory, Productivity and Cost through the optimization of manufacturing capacity and capability (PMO). Director, Advanced Engineering - D&M What you'll do Adopt responsibility for identification, governance, development, selection and deployment of Manufacturing Technologies and Processes across the D&M sites, as well as inter-OpCo and CMO supply sites, resulting in improved OEE, reduced cycle times, increased line reliability and improved yields, leading to reliable output and increased customer satisfaction. Lead site-based teams alongside the relevant Plant Leader through the planning and execution of Capital Investment in chosen new technology, or upgraded manufacturing lines for the benefit of Safety, Quality, Delivery or Cost through the expert utilization of DBS tools and techniques Engage & Contribute to Strategy Deployment for the OpCo. Identifying key breakthrough technologies and strategic technical projects with a technology and investment roadmap with a 5 to 7 year view, that will enable growth and improved manufacturing performance. Development and leadership through approval, execution, and sustainment phases of all significant investment proposals for facilities and manufacturing technology programs and projects across D&M and CMO supplying sites Create and implement a business-wide preventative maintenance program using DBS tools Development and leadership through approval of significant investment proposals for facilities and manufacturing technology programs and projects across the D&M sites. Provide functional direction, support and guidance to the site-based ME, PE, Manufacturing Technology and Project Associates for the execution of strategic and tactical programs and projects delivering improvements across SQDIP. Collaborate with central Technical & Digital Operations Teams to adopt best practice processes and procedures. Lead the D&M Digital Operations initiative. Who you are: Bachelor or Masters degree in Engineering or related field (Science / Manufacturing). Minimum of 10 years of progressive leadership in Operations and/or Engineering leadership in a highly automated assembly environment in Life Sciences or similar regulated industry. Recognized Manufacturing Engineering expertise in a Lean Manufacturing environment. Competency with a breadth of technologies. Solid problem-solving skills- ability to resolve complex problems, communicate issues and propose solutions to both external customers and internal team members. Demonstrated experience of successfully delivering concurrent technology programs or projects in a high-volume automated manufacturing environment Ability to operate effectively in a multi-tasking, dynamic environment, while maintaining a forward-thinking and customer-first attitude. Ability to energize, develop and build rapport, collaborate and influence at all levels within an organization. Act as inspirational leader with optimism, highly approachable and humble. Ability to travel up to 50% of the time. High level presentation and interpersonal skills- able to communicate and present ideas to customers in a way that produces understanding and impact that builds effective strategic relationships. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is proud to work alongside a community of ten fellow Danaher Life Sciences companies. Together, we're pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives. Position Summary For the Cytiva Discovery & Medical business unit, the Director, Advanced Engineering is responsible for the advancement of quality of our products and productivity within our plants through the identification and deployment of improved technology and automation to meet the needs of our Customers, Associates and Shareholders. In this role, the associate would assess current manufacturing capability and capacity, working alongside Operations Strategy and Plant Teams, deploying technology to bridge gaps as measured through SQDIP. In addition, this role is responsible for creating and successfully deploying a comprehensive OEE mechanism and global Preventive Maintenance and Spares systems within the D&M organization, owning the subsequent actions to close the gaps. In addition, the role will also lead the execution of Strategic Programs and Projects that improve Safety, Quality, Delivery, Inventory, Productivity and Cost through the optimization of manufacturing capacity and capability (PMO). Director, Advanced Engineering - D&M What you'll do Adopt responsibility for identification, governance, development, selection and deployment of Manufacturing Technologies and Processes across the D&M sites, as well as inter-OpCo and CMO supply sites, resulting in improved OEE, reduced cycle times, increased line reliability and improved yields, leading to reliable output and increased customer satisfaction. Lead site-based teams alongside the relevant Plant Leader through the planning and execution of Capital Investment in chosen new technology, or upgraded manufacturing lines for the benefit of Safety, Quality, Delivery or Cost through the expert utilization of DBS tools and techniques Engage & Contribute to Strategy Deployment for the OpCo. Identifying key breakthrough technologies and strategic technical projects with a technology and investment roadmap with a 5 to 7 year view, that will enable growth and improved manufacturing performance. Development and leadership through approval, execution, and sustainment phases of all significant investment proposals for facilities and manufacturing technology programs and projects across D&M and CMO supplying sites Create and implement a business-wide preventative maintenance program using DBS tools Development and leadership through approval of significant investment proposals for facilities and manufacturing technology programs and projects across the D&M sites. Provide functional direction, support and guidance to the site-based ME, PE, Manufacturing Technology and Project Associates for the execution of strategic and tactical programs and projects delivering improvements across SQDIP. Collaborate with central Technical & Digital Operations Teams to adopt best practice processes and procedures. Lead the D&M Digital Operations initiative. Who you are: Bachelor or Masters degree in Engineering or related field (Science / Manufacturing). Minimum of 10 years of progressive leadership in Operations and/or Engineering leadership in a highly automated assembly environment in Life Sciences or similar regulated industry. Recognized Manufacturing Engineering expertise in a Lean Manufacturing environment. Competency with a breadth of technologies. Solid problem-solving skills- ability to resolve complex problems, communicate issues and propose solutions to both external customers and internal team members. Demonstrated experience of successfully delivering concurrent technology programs or projects in a high-volume automated manufacturing environment Ability to operate effectively in a multi-tasking, dynamic environment, while maintaining a forward-thinking and customer-first attitude. Ability to energize, develop and build rapport, collaborate and influence at all levels within an organization. Act as inspirational leader with optimism, highly approachable and humble. Ability to travel up to 50% of the time. High level presentation and interpersonal skills- able to communicate and present ideas to customers in a way that produces understanding and impact that builds effective strategic relationships. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is proud to work alongside a community of ten fellow Danaher Life Sciences companies. Together, we're pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives. Position Summary For the Cytiva Discovery & Medical business unit, the Director, Advanced Engineering is responsible for the advancement of quality of our products and productivity within our plants through the identification and deployment of improved technology and automation to meet the needs of our Customers, Associates and Shareholders. In this role, the associate would assess current manufacturing capability and capacity, working alongside Operations Strategy and Plant Teams, deploying technology to bridge gaps as measured through SQDIP. In addition, this role is responsible for creating and successfully deploying a comprehensive OEE mechanism and global Preventive Maintenance and Spares systems within the D&M organization, owning the subsequent actions to close the gaps. In addition, the role will also lead the execution of Strategic Programs and Projects that improve Safety, Quality, Delivery, Inventory, Productivity and Cost through the optimization of manufacturing capacity and capability (PMO). Director, Advanced Engineering - D&M What you'll do Adopt responsibility for identification, governance, development, selection and deployment of Manufacturing Technologies and Processes across the D&M sites, as well as inter-OpCo and CMO supply sites, resulting in improved OEE, reduced cycle times, increased line reliability and improved yields, leading to reliable output and increased customer satisfaction. Lead site-based teams alongside the relevant Plant Leader through the planning and execution of Capital Investment in chosen new technology, or upgraded manufacturing lines for the benefit of Safety, Quality, Delivery or Cost through the expert utilization of DBS tools and techniques Engage & Contribute to Strategy Deployment for the OpCo. Identifying key breakthrough technologies and strategic technical projects with a technology and investment roadmap with a 5 to 7 year view, that will enable growth and improved manufacturing performance. Development and leadership through approval, execution, and sustainment phases of all significant investment proposals for facilities and manufacturing technology programs and projects across D&M and CMO supplying sites Create and implement a business-wide preventative maintenance program using DBS tools Development and leadership through approval of significant investment proposals for facilities and manufacturing technology programs and projects across the D&M sites. Provide functional direction, support and guidance to the site-based ME, PE, Manufacturing Technology and Project Associates for the execution of strategic and tactical programs and projects delivering improvements across SQDIP. Collaborate with central Technical & Digital Operations Teams to adopt best practice processes and procedures. Lead the D&M Digital Operations initiative. Who you are: Bachelor or Masters degree in Engineering or related field (Science / Manufacturing). Minimum of 10 years of progressive leadership in Operations and/or Engineering leadership in a highly automated assembly environment in Life Sciences or similar regulated industry. Recognized Manufacturing Engineering expertise in a Lean Manufacturing environment. Competency with a breadth of technologies. Solid problem-solving skills- ability to resolve complex problems, communicate issues and propose solutions to both external customers and internal team members. Demonstrated experience of successfully delivering concurrent technology programs or projects in a high-volume automated manufacturing environment Ability to operate effectively in a multi-tasking, dynamic environment, while maintaining a forward-thinking and customer-first attitude. Ability to energize, develop and build rapport, collaborate and influence at all levels within an organization. Act as inspirational leader with optimism, highly approachable and humble. Ability to travel up to 50% of the time. High level presentation and interpersonal skills- able to communicate and present ideas to customers in a way that produces understanding and impact that builds effective strategic relationships. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. What you'll do: On site role reporting through to the Cardiff Site Leader and based in Cardiff, this role is responsible for the day-to-day Engineering leadership of our medical facility. Lead a team of Manufacturing Engineers and Technicians, Provide Engineering support and guidance of technical control for Automated Lines. Lead as principle point of contact to resolve technical, validation and quality issues both internally and liaising with suppliers. Purchase and introduce new machinery using validation and mechanical change control demonstrating cost savings to the Business via process improvements and waste reduction initiatives. Project manage capital projects from initial concept through to successful completion and control the budgets. Develop and maintain an engineering Master Plan for the area in terms of understanding the long-term space requirements and facilitate solutions through the integration Danaher Business Systems (DBS) Continuous Improvement philosophy. Generate through leadership quality production documentation including Specifications, Training and Maintenance Guidelines. Who you are: Demonstrated leadership in a position of authority in an Operations Environment Bachelor's Degree in Engineering or equivalent with relevant experience. Experience of implementing change in a regulated industry Experienced practitioner in TPM culture, engagement and improvement. Experience of SPC implementation and adoption to make data driven decisions. Excellent communication skills with direct team members as well as external teams and stakeholders. Ensuring the smooth running of equipment by positioning maintenance priorities with production needs and aligning engineering efforts with the overall business goals. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. What you'll do: Support production teams to hit business KPI targets. Accountable for delivering Projects. Raise and progress purchase orders. Accountable for spares management in relevant area. Accountable for capital approvals and delivery against business objectives. Who you are: Proven technical / engineering knowledge with minimum 3 years' experience. Proven leadership / teamwork skills. Self-motivated, drives change with urgency and control. Data driven decision making and sustainment of improvements. Able to prioritize based on data to leverage benefits to business. Preferable Graduate level educated in a suitable engineering discipline but not essential. It would be a plus if you also possess previous experience in: Electrically qualified to support and maintain manufacturing equipment. Experienced in PLC/HMI Software support and improvement of manufacturing equipment. 6 sigma qualification - ideally to a minimum green belt level. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Are you seeking an opportunity to take your career to the next level? Are you excited by a role that bridges between the worlds of research and industry? Do you have experience in the development and introduction of new manufacturing technologies? If your answers to these questions are "yes", the role of Manufacturing Technology Engineer at Cytiva could be for you: What you'll do: Work in partnership with our manufacturing plants to understand their current and future needs. Use your insights from gemba to identify valuable problems to solve and build compelling cases for investments in improvements. Collaborate across our research and development network to establish state of the art and alternative technology options. Design, build and test innovative solutions, developing these from proof-of-concept through industrialisation. Commission, qualify and validate new manufacturing equipment and processes in full production, managing these changes according to quality and regulatory standards. Ensure that manufacturing plants are prepared for new equipment and processes through documentation and training. Provide expert support to maintain continuity of manufacturing and demonstrate successful sustainment post implementation. Take the overall lead in planning and coordinating cross-functional and multi-locational activities. Apply your management skills to guide projects from launch to handover. Who you are: Bachelor's Degree in a relevant engineering discipline e.g. Manufacturing Engineering, Mechanical Engineering or Electrical Engineering. Practical "hands-on" experience in the development of new technologies, including knowledge of product introduction methodologies and technology readiness levels. Competent in the specification and implementation of equipment, including expertise with at least one of the following systems: mechanical, electrical, pneumatic or controls. Experience with lean and six-sigma tools, as applied to problem solving and continuous improvement in manufacturing applications. Skilled in management of projects, proven via application to individual activities and leadership of cross-functional teams. It would be a plus if you also possess previous experience in: Manufacturing for biotechnology, pharmaceutical or similar regulated industry. Knowledge of GMP would be advantageous. Knowledge of procedures associated with the management of change in a regulated environment and, specifically, commissioning, qualification and validation. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Are you seeking an opportunity to take your career to the next level? Are you excited by a role that bridges between the worlds of research and industry? Do you have experience in the development and introduction of new manufacturing technologies? If your answers to these questions are "yes", the role of Manufacturing Technology Engineer at Cytiva could be for you: What you'll do: Work in partnership with our manufacturing plants to understand their current and future needs. Use your insights from gemba to identify valuable problems to solve and build compelling cases for investments in improvements. Collaborate across our research and development network to establish state of the art and alternative technology options. Design, build and test innovative solutions, developing these from proof-of-concept through industrialisation. Commission, qualify and validate new manufacturing equipment and processes in full production, managing these changes according to quality and regulatory standards. Ensure that manufacturing plants are prepared for new equipment and processes through documentation and training. Provide expert support to maintain continuity of manufacturing and demonstrate successful sustainment post implementation. Take the overall lead in planning and coordinating cross-functional and multi-locational activities. Apply your management skills to guide projects from launch to handover. Who you are: Bachelor's Degree in a relevant engineering discipline e.g. Manufacturing Engineering, Mechanical Engineering or Electrical Engineering. Practical "hands-on" experience in the development of new technologies, including knowledge of product introduction methodologies and technology readiness levels. Competent in the specification and implementation of equipment, including expertise with at least one of the following systems: mechanical, electrical, pneumatic or controls. Experience with lean and six-sigma tools, as applied to problem solving and continuous improvement in manufacturing applications. Skilled in management of projects, proven via application to individual activities and leadership of cross-functional teams. It would be a plus if you also possess previous experience in: Manufacturing for biotechnology, pharmaceutical or similar regulated industry. Knowledge of GMP would be advantageous. Knowledge of procedures associated with the management of change in a regulated environment and, specifically, commissioning, qualification and validation. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. What you'll do: Responsible for individual team members who are supporting related projects (DRA). Provide leadership and support to Engineering and Technical teams for all activities within remit. Ensuring structured and well executed Daily Management of projects through VPM with both the core team and communicating effectively with stakeholders. Provide stakeholder management across multiple functions and business levels. Who you are: Degree in Manufacturing, Mechanical Engineering, Project Mgmt with a technical/operations bias. Hands on experience of delivering Mfg Engineering projects/improvements/experience in managing change within a manufacturing environment. Strong track-record of successfully improving and sustaining Safety, Quality and Performance of our manufacturing equipment. Demonstrated ability to act with urgency, deliver sustained results, work well within a team and demonstrates a commitment to delivering results. Effective planning, ability to make detailed analysis and data-driven decisions, structured approach for both your own work load and also the support of others to enable efficient and effective project execution. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Job Title: Design Engineer II Company: Pall Medical R&D, part of Cytiva Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Design Engineer II, is responsible for creating, modifying, and optimizing detailed 2D and 3D models for our Medical Pall legacy products, components, and systems. This position reports to the Medical R&D Leader and is part of the Medical R&D team, nested within the Discovery & Medical Opco, and will be an on-site role based in Portsmouth. What you will do: Create component drawings and design models using CAD software; developing detailed 2D and 3D models for products, components, and systems. Evaluate and implement design changes for existing products/components. Liaise with production/molding teams to manage support requests; producing and maintaining engineering drawings, specifications, and documentation to support manufacturing and assembly processes. Create mock-ups/prototypes and perform relevant tests. Contribute to completion of Project Design Files. Who you are: Bachelor's degree or equivalent experience. Mechanical Engineering or technical background is an advantage. Over 2 years of experience as a designer/design engineer in the medical or other regulated industry. Proficiency with any relevant drawing tools (SolidWorks and/or CATIA, Creo) and design guidelines. Understanding of manufacturing processes and production knowledge around plastic parts and joining techniques. Experience in designing and producing prototype products for trials. Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role Position will be based at Portsmouth (Harbourgate) however occasionally travel will be required to manufacturing and supplier sites. It would be a plus if you also possess previous experience in: Project management skills New product development experience Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info . At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. Purpose Product Engineering is responsible to drive life cycle management of equipment, being involved in new product development and support the product throughout its entire life cycle, from launch until discontinuation. This includes first line support for complaints, supplier development and validation, VAVE and sustainment engineering. What you'll do: Responsible for managing control systems, automation and electrical design product changes to the current product portfolio through their lifecycle; Working in close collaboration with team members and other departments such as R&D, Product Management, Quality and Operations as part of the new product development team where you provide early design input from a manufacturability perspective. Partner with internal and external automation vendors to provide continuous improvement of state-of-the-art automated product and processes. Part of cross functional teams to support projects at global level and lead on local level, and coordinate between PE, R&D, Operations and Quality teams. Focus on continuous improvement of products and processes. Who you are: Bachelor degree in Automation Engineering or relevant degree. 3 years relevant professional experience. Experience with electrical design. Experience with performing verification and validation testing. Experience with component selection based on requirements. It would be a plus if you also possess previous experience in: Experience with CE, UL, GAMP regulatory requirements. PLC programming - Siemens and/or Rockwell Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.