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Danaher
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  • Senior Manager, Regulatory Affairs  

    - High Wycombe
    This job is with Danaher, an inclusive employer and a member of myGwor... Read More
    This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Leica Biosystems, 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. At Leica Biosystems, we’re not just shaping the future of cancer diagnostics — we’re transforming lives. Our mission of “Advancing Cancer Diagnostics, Improving Lives” is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you’re not just taking a job; you’re becoming part of a passionate team that knows every moment matters when it comes to cancer. You’ll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you’ll be inspired each day to stretch, grow, and make an impact. Learn about the Danaher Business System which makes everything possible. The Senior Manager, Regulatory Affairs is responsible for developing and executing global regulatory strategies for high-complexity diagnostics including but not limited to IVDs, Companion Diagnostics and digital pathology in the clinical oncology space. This individual will lead cross-functional regulatory initiatives, partnering with internal teams and external stakeholders to enable successful global commercialization of innovative technologies (including but not limited to IDEs; Performance Study Applications; IVDR TF in EU and 510k and PMA in USA). This position reports to the Senior Director, Regulatory Affairs and is part of the Global Regulatory Affairs Team. In this role, you will have the opportunity to: Lead a team of Regulatory Affairs Professionals responsible for the development, authorship, and maintenance of global regulatory submissions (e.g., 510(k), PMA, EU IVDR Technical Files, STED) by defining requirements, standardizing processes, optimizing timelines, and adapting plans as needed. Collaborate globally and cross-functionally (e.g., Clinical Affairs, Business Development, QA, R&D, Program Management) to define and execute regulatory strategies for Leica Biosystems technologies in cancer diagnostics, IVD, and Companion Diagnostics markets. Provide regulatory input for program planning, including resource needs, budgets, and timelines, while aligning with external partners on study designs and submission strategies. Engage and negotiate with global regulatory agencies to achieve product clearance/approval, while staying current on evolving regulations, guidance, and competitive landscapes. Share regulatory expertise across Leica and Danaher sites, contribute to cross-functional initiatives, and apply Danaher Business System (DBS) tools to drive continuous improvement and measurable results. The essential requirements of the job include: Bachelor’s, Master’s, or PhD in a scientific or engineering discipline. In-depth working knowledge of FDA and EU regulatory requirements for IVD devices. Extensive progressive experience supporting new product development and sustaining high-complexity diagnostic products. Proven track record in developing and executing regulatory strategies and preparing global submissions for complex diagnostic products, including 510k and PMA submissions. Experience supporting clinical trials is a plus, along with strong understanding of regulatory requirements across international markets. Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel – list specifics 15% travel, overnight, within territory or locations It would be a plus if you also possess previous experience in: Applies deep regulatory expertise to the development and global commercialization of complex, high-risk products, balancing short-term problem-solving with long-term strategic outcomes and risk-benefit analysis. Leads effectively in matrixed and cross-cultural environments, driving timely decisions, issue resolution, and resource agility while setting high expectations and modeling accountability and integrity. Communicates complex and sensitive information clearly across diverse audiences; builds consensus, demonstrates strong writing and documentation skills, and uses sound judgment to influence and lead through change. Leica Biosystems, 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 www.danaher.com . Read Less
  • Global Strategic Account Manager  

    - Crawley
    This job is with Danaher, an inclusive employer and a member of myGwor... Read More
    This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. 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 Global Strategic Account Manager (GSAM) partners closely with Global Strategic Account Directors (GSADs) to translate account strategies into flawless execution. Acting as the operational right hand to the GSADs, this role ensures seamless delivery of customer-facing interactions—including Quarterly Business Reviews, Executive Relationship Meetings, Sales & Operations Planning forums, and global multi-product requests for quotation. By driving governance, orchestrating complex cross-functional initiatives, and ensuring a differentiated GSA customer experience across all touchpoints, the GSAM strengthens strategic partnerships and supports long-term growth. This role is deliberately designed as a development pathway toward future account leadership roles, building the strategic, governance, and executional capabilities required to progress into Global Strategic Account Director positions. T his position is part of the Global Strategic Accounts team, located on site. What you will do: Lead preparation and coordination of customer governance meetings with GSADs and internal stakeholders, including QBRs, ERMs, and S&OP forums. Manage and track global multi-product RFQs, ensuring timely, accurate, and competitive responses aligned with strategic account objectives. Coordinate and execute account initiatives defined by GSADs, ensuring deliverables, timelines, and responsibilities are clearly tracked. Drive cross-functional collaboration across regions and functions to deliver differentiated customer experiences and strategic outcomes. Monitor progress across multiple parallel initiatives, highlighting risks or issues and driving timely resolution. Support governance and reporting by preparing materials, consolidating updates, and ensuring alignment with account governance structures. Who you are: A collaborative, highly organized professional with 5+ years of experience in program, project, or portfolio management, ideally within the biotechnology, life sciences, or biopharmaceutical industry. Experienced in customer governance (QBRs, ERMs, S&OP) and driving execution that strengthens global strategic account partnerships. Proficient in program management methodologies (e.g., MSP, Agile, Six Sigma) and tools; adept at managing multiple priorities with strong attention to detail. Bachelor’s degree in Life Sciences, Business, or a related field. Travel Requirements: Ability to travel globally up to 15 % , including overnight travel. It would be a plus if you also possess: Experience working with large global customers in a commercial or program management capacity. Prior exposure to account management within a global, matrixed organization. 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 www.danaher.com . Read Less
  • Senior Regulatory Support Manager  

    - Portsmouth
    This job is with Danaher, an inclusive employer and a member of myGwor... Read More
    This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. 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. We’re looking for a Senior Regulatory Support Manage r to join Cytiva’s Customer Regulatory Support (CRS) team. As Regulatory Support Manager you are responsible for providing support to Product Managers, Regions and customers by providing quality documents and regulatory support in response to customers’ requests for quality, regulatory and technical-related information. As a member of the Customer Regulatory Support team, you will add value to bioprocess products and demonstrate a commitment to customer satisfaction. What you´ll do: Build and maintain knowledge and understanding of customers’ regulatory requirements related to the bioprocess business at a high level. Develop and update regulatory support documentation for products in customers’ regulated environments. Perform necessary investigations and prepare and deliver statements and certificates. Participate in creating and updating guidelines and steering documents. Act as regulatory support expert and discussion partner to R&D, QA, Product Management and other functions and regions. Participate in project teams as regulatory support expert. Respond efficiently and promptly to customers’ regulatory based issues, which will include necessary investigations, preparations and delivery of certificates, use of available internal and external databases and other relevant databases. File and maintain complete documentation of questions and answers in databases; specify, prepare, update and review regulatory support documentation, including RSF, VG, VSF, CCN, statements, certificates and other regulatory related documentation for new and existing products. The essential requirements of the job include: Bachelor of Science degree in Chemistry, Pharmacy or related field. 5-10 years of experience from relevant positions within Quality Assurance, Regulatory, or Product Management. Good understanding of GMP and knowledge of regulatory requirements in the bioprocess industry. Excellent communication skills and fluency in English, both written and spoken. It would be a plus if you also have: Experience of working in large matrix organizations. Fluency in the language of the country of employment. Experience in customer communication. 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 www.danaher.com . Read Less
  • This job is with Danaher, an inclusive employer and a member of myGwor... Read More
    This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Pall Corporation, 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. As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers solve their toughest challenges. Our products serve diverse, global customer needs across a wide range of applications to advance health, safety and environmentally responsible technologies. From airplane engines to hydraulic systems, scotch to smartphones, OLED screens to paper—everyday Pall is there, helping protect critical operating assets, improve product quality, minimize emissions and waste, and safeguard health. For the exponentially curious, Pall is a place where you can thrive and amplify your impact on the world. Find what drives you on a team with a more than 75-year history of discovery, determination, and innovation. Learn about the Danaher Business System which makes everything possible. Within the region and the Energy+ division, the Technical Inside Sales Engineer will provide technical and product expertise to sales representatives, resellers, and customers during the sales process. Additionally, they will support the commercial sales team through product recommendations and solution generation. This position reports to the Technical Solutions Manager and is part of the Western Europe Technical Solutions Team located in Portsmouth (UK) and will be an on-site role. In this role, you will have the opportunity to: Support the commercial sales team in developing and closing new business Understand client requirements and collaborate with the Sales team to establish key technical differentiators and use technical value proposition Working closely with other support departments including Pall Engineering, suppliers to ensure readiness of the quotation and costing solution and drive customer satisfaction. Provide Technical direction and supporting documentation to our sales force to resolve customer needs The essential job functions: Customer Relationships: Establish and maintain Sales, Key customer relationships, acting as a trusted technical advisor, reliable on commitments for design and costing delivery Value proposition: Understand the client RFQ and scope requirement and set up the Pall value proposition in coordination with sales Customized Solution : select the right technology, sizing and design to fit with the client’ specification, work closely with our suppliers, the sourcing, operation or Engineering to come-up with an optimise costing solution Technical Expertise: Provide technical support to customers, addressing clarification and concerns. Act as a trusted technical advisor, offering innovative and customized solutions. Drive Projects: Drive project progress for standard solutions in coordination with customer, suppliers and internal departments. The essential requirements of the job include: Bachelor’s degree minimum in Hydraulics, Fluid Mechanics or Mechanical Engineering 5 to 7 years’ experience on projects in Oil Hydraulic, Automotive, Power Generation, Nuclear markets Fluent in English Proficient in the use of Outlook, SAP, Sales Force, MS Office computer applications including Word, Excel, and Power Point Travel Requirements: Ability to travel occasionally within Europe (twice a year) It would be a plus if you also possess previous experience in: Experience in Technical support within industrial processes or in filtration Fluent in another European language Pall Corporation, 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 . #LI-Onsite#LI-VF1 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 www.danaher.com . Read Less
  • Field Applications Specialist  

    - London
    This job is with Danaher, an inclusive employer and a member of myGwor... Read More
    This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. 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 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. As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory’s 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 making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible. The Field Application Specialist is responsible for providing expert support and training on Beckman Coulter’s, Clinical IT and Automation, with oppurtunity to expand on our full solution. This role plays a critical part in driving customer adoption, optimizing laboratory workflows, and strengthening confidence in Beckman Coulter systems. By partnering closely with laboratory teams and internal colleagues, the Field Application Specialist contributes directly to improved patient care and enhances the organization’s reputation as a trusted leader in diagnostic solutions. This position reports to the Field Application Manager and is part of the Northern Region, encompassing, the United Kingdom, Ireland and the Netherlands. You will be located in the south of the United Kingdom, this position will be a hybrid role, visiting customer sites across the region with travel outside of the UK. In this role, you will have the opportunity to: Deliver expert application support for Beckman Coulter’s diagnostic solutions, ensuring customers achieve optimal use of their systems in line with laboratory and clinical needs. Provide on-site and remote training for laboratory staff, focusing on workflow optimization, troubleshooting, and best practices. Support product installations and implementations , working closely with Field Service Engineers, Project Managers, and other stakeholders to ensure seamless go-lives. Act as the primary technical contact for customers , addressing application-related issues, escalating to appropriate teams when necessary, and maintaining clear, proactive communication. Collaborate with sales and service teams to identify opportunities, support product demonstrations, and help drive customer satisfaction and retention. Collect and share customer feedback (Voice of the Customer, NPS surveys, direct interactions) to inform product improvements and service delivery. The essential requirements of the job include: Education : Bachelor’s degree in Information Technology, Biomedical Science, Biomedical Engineering, Life Sciences, or a related field (Master’s degree advantageous but not essential) and or experience in a IT, clinical laboratory, diagnostics, or medical device environment, Ideally with exposure to IT support, system implementation, or end-user training Technical Knowledge : Strong understanding of laboratory workflows, IT networking, Laboratory Information Management Systems, Middleware Platforms, and instrument connectivity, with practical troubleshooting skills. Customer Focus : Excellent communication and interpersonal skills, with the ability to train and support laboratory staff, resolve application issues, and build trusted customer relationships. Problem Solving : Demonstrated ability to analyse technical and workflow challenges, provide effective solutions, and escalate issues appropriately. Flexibility : Willingness to travel regularly to customer sites to deliver training, support installations, and provide applications expertise. Travel, Motor Vehicle Record & Physical/Environment Requirements: Driving License Ability to travel 80% It would be a plus if you also possess previous experience in: Previous experience in the healthcare or diagnostics industry , with exposure to implementing or supporting laboratory instrumentation and applications in customer environments. Experience contributing to complex projects , such as instrument installations, workflow optimizations, or cross-functional collaborations, with the ability to work both independently and as part of a team. Creative and innovative mindset , with the ability to “think outside the box” when addressing customer needs, workflow challenges, or technical problems. Beckman Coulter Diagnostics, 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 Beckman Coulter Diagnostics 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 Beckman Coulter Diagnostics 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 www.danaher.com . Read Less
  • European Service Administrator  

    - London
    This job is with Danaher, an inclusive employer and a member of myGwor... Read More
    This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Molecular Devices, 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. Join Molecular Devices and help drive scientific discovery for life science customers in academia, biotech, pharma, and government. Our automated and AI-enabled technology empowers researchers to tackle complex questions and gain deep insights, accelerating the development of safer, more effective therapeutics. As part of our team—rooted in collaboration, authenticity, and innovation—you’ll ultimately contribute to groundbreaking science that enhances lives globally and shapes a healthier future for all. Learn about the Danaher Business System which makes everything possible. The European Service Administrator is responsible for supporting the European Sales and Service teams by updating CRM records, producing quotations and invoices, processing service plan orders, and contributing to continuous improvement activities. This position reports to the European Service Admin Manager and is part of the Europe Service team located in Winnersh, UK and will be an on-site role. In this role, you will have the opportunity to: Update internal and external CRM records utilizing Molecular Devices ERP Systems. Create quotations and invoices for billable work. Work Order Creation for our Field Service Engineers Process Service Plans and Spare Part Orders. Participate in continuous improvement activities (including Daily Management). Perform ad hoc administrative tasks as needed. The essential requirements of the job include: Experience in a customer‑facing support role using ERP/CRM systems (Oracle / Salesforce / ServiceMax) preferred. Experienced working in a high-volume role updating internal and external CRM records and creating quotations and invoices for billable work. Strong communication skills to support varied internal and external customers. It would be a plus if you also possess previous experience in: Experience working in an international environment and matrix Organization (Europe/US). The job language is English, but an additional European language would be highly beneficial (i.e. German or French). Molecular Devices, 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 www.danaher.com . Read Less
  • This job is with Danaher, an inclusive employer and a member of myGwor... Read More
    This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. 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 Senior Finance Manager- Plant Controller , Ilfracombe will serve as the primary finance business partner for Operations and along with the Ilfracombe Site Leadership team will have Ownership and accountability for the financial results of the operations on site. This position reports to the Finance Director, Filtration Operations and is part of the Filtration Operations finance team. The position is located in Ilfracombe and will be an on-site role. What you will do: Be a trusted advisor and Business Partner for the Site Management team providing analysis and recommendations to ensure sound financial decision making and have the skillset to build a strong partnership with Operations team. Support Site Operations team in delivering annual cost reduction objectives (productivity, cost of quality/VAVE, PPV), capital request analysis and cost management while also overseeing cost accounting procedures and inventory control policies, ensuring accurate reporting and compliance whilst driving inventory reductions. Prepare accurate site budgets and forecasts for P&L, Inventory, Capex and Headcount. Prepare accurate and timely month end close Financial and Operational reporting to include; Manufacturing variances, Costs/Absorptions, Headcount, Inventory, Capex, Labor Utilization and detailed analysis of variances to forecast.. Demonstrate strong analytical skills with the ability to interpret complex financial data and provide actionable insights Closely monitor capital expenditure, ensuring controls and processes are adhered to, assessing for any financial risk or adjustments required, and ensuring that "assets under construction" are capitalized in a timely and accurate manner Support internal SOX audit and external audit requests and coordinate ad-hoc analytics based on Site and business needs. Who you are Bachelor’s degree in Accounting, Finance, or Business Administration with a minimum of 4 years’ experience in a business environment Advanced Excel proficiency is essential for success in this role Excellent analytical skills with a track record of using data to support decision‑making Cost accounting knowledge, emphasis on budgeting, forecasting, financial analysis, internal controls and familiarity with ERP systems (production modules a large benefit) is seen as advantage. Being a self-starter and proactive, structured with demonstrated ability to deliver results consistently. Application We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found. We look forward to seeing your application. 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 www.danaher.com . Read Less
  • IT Systems Engineer  

    - London
    This job is with Danaher, an inclusive employer and a member of myGwor... Read More
    This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Genedata, 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. The biopharmaceutical industry is undergoing a digitalization revolution, adopting data-driven R&D approaches to develop innovative therapies quicker. Genedata’s market-leading enterprise software is fueling this revolution, enabling leading biopharma, biotech, and CRDMO companies worldwide to automate processes and leverage biopharma R&D data analytics so they can find breakthrough therapies faster. Join this digital transformation and help scientists around the world accelerate the pace of biopharma R&D. Learn about the  Danaher Business System  which makes everything possible. We are looking for a qualified IT Systems Engineer to join our expanding operational services team supporting the deployment and maintenance of our highly innovative Biopharma Platform. Genedata’s Biopharma Platform revolutionizes the process of biopharma R&D and we therefore have quickly taken a global market leadership position with a rapidly growing client base. The IT Systems Engineer will be responsible for working with our pre-sales team consulting on the optimal design, implementation, and management of the Genedata cloud-based applications and how they interact with customer computing environments. This includes, but is not limited to, the implementation design of cloud architecture for Genedata SaaS applications, system automation, application support, system administration, solution configuration and associated integration with optimal data security. Furthermore, this interdisciplinary, multi-faceted position offers an exciting opportunity to assist our global biopharma customers with IT-related challenges that relate to the effective deployment of the Genedata Biopharma Platform, by understanding customer needs and providing technical solutions and designs as required. The position offers excellent career development opportunities in a growing company, and the chance to work as part of a strong international service team. This full-time position is remote working role. It requires flexible working hours to support global projects. Minimal travel might be required. In this role, you'll have the opportunity to: System design: Design, develop and manage robust, secure, scalable, highly available, and dynamic solutions for Genedata applications in the cloud Collaborate with the business teams to understand customer technical requirements and provide pre-sales support across the Genedata application portfolio Identify, create and propose technical solutions to meet customer needs Support customers: Attend customer meetings and explain technical architecture concepts to technical and non-technical audiences Design and configure and manage cloud-based deployments of Genedata products for customers Support and lead validation projects at customer sites and ensure system design has full compliance with regulatory, internal, and client requirements The essential requirements of the job include: 3+ years’ experience in system, enterprise, or cloud architecture roles, with strong expertise in Linux/Unix and Windows environments Proven ability to assess complex computing environments and produce clear system architecture diagrams to communicate technical concepts Hands-on experience with DevOps practices and effective collaboration in cross‑regional teams In-depth experience deploying applications in cloud environments , particularly AWS (certifications or accredited training are an advantage) Nice to have: Experience working with IT helpdesk or service management tools Genedata, 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. 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 www.danaher.com . Read Less
  • Process Operator  

    - London
    This job is with Danaher, an inclusive employer and a member of myGwor... Read More
    This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. 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: To manufacture, inspect, test and package product in accordance with quality standards and health and safety Ensure production targets are met in line with production priorities Close inspection of all product to ensure it meets the required quality specification and cosmetic standard Precise, delicate and repetitive work to make product, fixing of tubing and connectors on product/ Boxing Ensure the safe and efficient operation of machine, or work station, and surrounding area Take personal responsibility for continuous improvement & make recommendations accordingly. Play an active part in finding ways to reduce costs & continuously improve our processes. Play an active part in finding ways to improve production efficiency Who you are: Reliable Punctual Motivated Flexible Good team-player Literate Numerate Excellent attention to detail Willing to participate in Kaizen events and learn principles of Lean Manufacturing Prepared to work unsociable shift pattern Able to stand for 8 or 12 hour shift It would be a plus if you also possess previous experience in: Experience with machine operating or working in a clean room environment 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 www.danaher.com . Read Less
  • Senior Product Manager  

    - Cambridge
    This job is with Danaher, an inclusive employer and a member of myGwor... Read More
    This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Abcam, 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. Learn about the Danaher Business System which makes everything possible. The Senior Product Manager, Flow Cytometry is responsible for strategy execution with a clear focus on growth, innovation, and revenue generation for a franchise within the Abcam portfolio by infusing strategy and portfolio management expertise into collaborations with the broader Abcam organization including marketing, commercial, digital, manufacturing, and R&D. This position reports to the Director, Flow Cytometry Solutions and is part of the Product Management team located in either Cambridge, UK or Waltham, MA and will be an on-site role. In this role, you will have the opportunity to: Lead the execution of franchise-level product strategy across short-, mid-, and long-term horizons, ensuring alignment with the broader portfolio vision and business objectives Champion the product portfolio by proactively gathering and analyzing Voice of Customer (VOC) insights to clearly define customer needs and inform strategic direction Oversee market research, perform competitive analysis and develop business plans to drive product innovation Drive go-to-market success across all channels, including digital, sales enablement, pricing strategies, and promotional development Build strategic relationships with key opinion leaders (KOLs), external collaborators, and industry groups to gather market intelligence, and guide product development via closely partnering with technical product manager Define KPIs and success metrics for product performance, and use data to drive decisions and communicate impact to stakeholders Manage product life cycle, including product performance management, portfolio curation and pricing strategy through robust data analysis that drives insights and can be clearly communicated to senior leadership The essential requirements of the job include: PhD or equivalent experience in a life science or related field e.g., biology, biochemistry, chemistry 3+ years of experience in product/portfolio management in the Life Science industry Demonstrated ability to translate customer needs into product solutions Strong interpersonal skills with the ability to influence cross-functional teams and manage priorities within a matrixed organization Ability to travel up to 20%, domestically and internationally It would be a plus if you also possess previous experience in: Relevant advanced degree, e.g., Ph.D. in life science, MD, MBA Knowledge of the flow cytometry market Using advanced analysis / visualization tools, e.g., Tableau Working with a global team and supporting customers across varying global market environments 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 www.danaher.com . Read Less

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