The Territory Customer Support Engineer - Jodhpur for Beckman Coulter Diagnostics is responsible for Installing and maintaining instruments and systems in a laboratory environment, delivers basic operational training at installation, provide effective product and customer support. Ensures Preventive Maintenance planning (PM) & Modification (MOD s) planning are performed in timely manner, seeks timely support for difficult product issues avoiding unnecessary down time, performs timely reporting of his activities, maintains excellent customer relationship, specifically with his/her directly assigned accounts. Adheres to field service policies procedures and standards, maintain recommended spare parts for his product range, ensures appropriate spare parts stock, travelling within the territory. Available to travel in short notice. This position is part of the Service Team-North India located in Gurgaon and will be Fully Remote. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Service Team-North India and will report to the State Service Manager responsible for managing service professional handling the area of NCR. If you thrive in a Challenging, Passionate, instrumental, and competitive role and want to work to build a world-class Service provider and Healthcare organization read on. In this role, you will have the opportunity to: Grow along with a leading IVD segment organization Provide on-site support for our instruments which will lead to advancing healthcare and patient support, provide immediate support to achieve client delight. Ability to interact with our team of service professionals and other cross function which are very critical for the role. The essential requirements of the job include: 1. Diploma or Graduation- Electrical/Electronics/ Biomedical Engineering (Any subjects with electrical and electronics in curriculum) 2. Three + years on any type of basic experience on In-Vitro Diagnostics Equipment (Hematology, Chemistry, or Immunoassay) , Should have knowledge of Networking and Interface related issues, also good in MS -office, Teams, Networking. 3. Can logically resolve or troubleshoot in times of crisis and leverage expert help. It would be a plus if you also possess previous experience in: Can independently handle 1 or more product group (example Immunoassay Analyzer, Hematology Analyzer or Chemistry Analyzer) with timely expert support. Able to identify application vs. service issues and collaborates to resolve Ability to prioritize customer needs. Ability to coordinate and collaborate with other functions to achieve client delight. 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.
At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world s most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we re working at the pace of change on diagnostic tools that address the world s biggest health challenges, driven by knowing that behind every test there is a patient waiting. The Process Engineer is responsible for developing a strategy and executing plan to deliver continuous process performance improvements related to Safety, Quality, Delivery, and Cost of a manufacturing process or line. The Process Engineer will work with continuous improvement initiatives and be responsible for overall equipment/process performance and executing equipment/process validations, including efficiency tracking and problem solving. The Process Engineer will also leverage process knowledge to identify opportunities/ solutions to improve throughput capacity by reducing impact of constraints. The role will require close interaction with the global teams. This person will be the technical partner to the engineering/manufacturing team in US/Sweden/India throughout the life cycle of the equipment/process. This position is part of Cepheid s MII Bangalore Plant and will be located in Mahadeva Kodigehalli, Bangalore. In this role, you will have the opportunity to: Be the primary lead for defining and executing installation and validation processes for new or existing equipment and products in compliance with company standards, IVD regulations and GMP standards. Plan & execute documentation as per QMS requirements, including preparation, writing, and filing of validation plans, SOPs, protocols and reports. Apply knowledge of relevant continuous improvement tools and approaches to increase production up-time, minimize unplanned maintenance, minimize work in process inventories (WIP) or plant inventories, and implement cost reduction initiatives across equipment and labor. The essential qualifications/requirements of the job include: Bachelors or master s in biotechnology or related engineering fields with Minimum 2 years of experience in manufacturing, preferably in Medical Device/ IVD sectors. Strong background in equipment and product validation for medical device manufacturing. Understanding of mechanical design concepts and machinery: mixing processes, motors, pumps, vacuum, and hydraulics. Experience of working in a regulated work environment (ISO, GMP, Medical Device regulations)
Perform registration dossier for all the Life Science Products in all countries (except USA) Participate to gathering the technical documentation for new product development Maintain the adequacy with the regulation for technical documentation Product lifecycle management: Support product design changes, labeling updates, sustainment, and improvement activities from regulatory perspective. Assess regulatory impact, develop detailed action plan to drive regulatory compliance and ensure on time completion of identified actions. The essential requirements of the job include: A Bachelor s degree in areas of life sciences or engineering field with a minimum of 8 10 years experience in a regulated medical device/diagnostic industry (less years required with advanced degree). Professional designations are not required but training and certificates in quality or regulatory affairs would be a plus (e.g. CQM, CQE, CQA, RAC, CLIA, Six Sigma, Lean) Experience in supporting filing of pre-market regulatory submissions domestically (Q-Subs, 510ks) and internationally (IVDR; China; ROW Global Registrations). Knowledge of domestic and international quality systems and other standards such as, IVDD/IVDR, ISO 13485, ISO 9001 and other applicable standards and regulations. Experience with Software as a Medical Device (SAMD) and Software as an accessory to a device highly desirable. Required Competencies: Ability to adopt a systemic view of process improvement and to advise process improvement teams to reach goals. Quick adaptability to embrace company culture and flexibility to manage multiple projects at the same time. Ability to participate in meetings outside of regular business hours to support global business.
Design and develop high-density, multi-layer PCBs with analog/digital/mixed-signal circuits of Beckman Coulter Diagnostics new and on-market products Architect power management, signal conditioning, and microcontroller-based subsystems. Own hardware development from concept to release, including design verification and risk mitigation. Ensure designs meet IEC 60601, ISO 13485, and FDA Class I/II device requirements. Coordinate external testing (EMC, safety) and manage design updates based on test outcomes. The essential requirements of the job include: B.E./B. Tech and M.E./M. Tech in Electrical/Electronic Engineering. 3 years of experience in medical or industrial-grade PCB hardware development. Deep understanding of EMI/EMC standards, IEC/FDA medical device regulations. And come up with EMI EMC mitigation strategies. Proficient in PCB design tools (Altium, Or CAD, PADS) and simulation software. Experience in product lifecycle management, Execution of Design changes and documentation. It would be a plus if you also possess previous experience in: Experience in medical device design & development with advanced certification in Electrical CAD tools is a plus Experience in IVD instrumentation, such as clinical chemistry, immunoassay, hematology, urinalysis, molecular microbiology or flow cytometry systems is a plus Exposure to medical device design processes and quality systems. Exposure to BOM & PCB Manufacturing techniques and Strong PCB Vendor communication skills
Design and develop high-density, multi-layer PCBs with analog/digital/mixed-signal circuits of Beckman Coulter Diagnostics new and on-market products Architect power management, signal conditioning, and microcontroller-based subsystems. Own hardware development from concept to release, including design verification and risk mitigation. Ensure designs meet IEC 60601, ISO 13485, and FDA Class I/II device requirements. Coordinate external testing (EMC, safety) and manage design updates based on test outcomes. The essential requirements of the job include: B.E./B. Tech and M.E./M. Tech in Electrical/Electronic Engineering. 5 years of experience in medical or industrial-grade PCB hardware development. Deep understanding of EMI/EMC standards, IEC/FDA medical device regulations. And come up with EMI EMC mitigation strategies. Proficient in PCB design tools (Altium, Or CAD, PADS) and simulation software. Experience in product lifecycle management, Execution of Design changes and documentation. It would be a plus if you also possess previous experience in: Experience in medical device design & development with advanced certification in Electrical CAD tools is a plus Experience in IVD instrumentation, such as clinical chemistry, immunoassay, hematology, urinalysis, molecular microbiology or flow cytometry systems is a plus Exposure to medical device design processes and quality systems. Exposure to BOM & PCB Manufacturing techniques and Strong PCB Vendor communication skills.
Design and develop innovative mechanical solutions to improve performance, safety, reliability, throughput and cost-effectiveness (Knowledge of Should costing and estimation), in Design Change Project. Act as a change lead, managing the entire Design change process independently. Handle multiple projects with proper project planning and minimal guidance Conduct root cause analysis and implement corrective actions. Collaborate with cross function teams to resolve manufacturing and field issue, conduct feasibility studies, risk assessments, and design reviews and validate designs through analysis and testing. The essential requirements of the job include: Bachelor s degree in mechanical engineering or a related field with 5 years of experience in mechanical design principles, materials, manufacturing processes. Proficiency in SolidWorks CAD software and simulation tools. Create and maintain detailed engineering documentation, including CAD models, drawings, specifications and test plans. Knowledge of dFMEA/pFMEA, DFX, Tolerance Stack-up Analysis and GD&T Basic knowledge of metals and materials, its application knowledge on mechanical parts fabrication, Rapid prototyping and testing. It would be a plus if you also possess previous experience in: Experience with medical device regulations (FDA, ISO 13485, ISO 14971, IEC 60601) Experience in IVD instrumentation, such as clinical chemistry, immunoassay, hematology, urinalysis, molecular, microbiology or flow cytometry systems is a plus Advanced certification in CAD tools Familiarity with lean manufacturing and Six Sigma principles. Prior work experience in Electro-Mechanical products, Robotics and Automation
You will be a part of the Application team -South India and report to the Application Manager -South-1 responsible for Managing application professional handling the area of entire of South-1 region. If you thrive in a Challenging, Passionate, instrumental, and competitive role and want to work to build a world-class Service provider and Healthcare organization. In this role, you will have the opportunity to: Grow along with a leading IVD segment organization Provide onsite Application support for our instruments which will lead to advancing healthcare and patient supports Provide immediate support to achieve client delight The ability to interact with our team of service professionals and other cross function which are very critical for the role. The essential requirements of the job include: Education: Bachelor s degree in science or bachelor s degree in MLT Three+ years experience as a field application specialist in IVD industry or Medical Technologist with 5 years experience within a hospital-based laboratory Must be able to travel across South India Requires flexibility in working hours Along with good written and verbal communication skills Can logically resolve or troubleshoot in times of crisis and leverage expert help, must have good knowledge of computers including MS Office & Teams Must have good planning and customer relationship skills, Knowledge of laboratory workflow and information systems Can independently handle 1 or more product groups (example Immunoassay Analyzer, Hematology Analyzer or Chemistry Analyzer) with prompt expert support Able to identify application vs service issues and collaborates to resolve Ability to prioritize customer needs, Ability to coordinate and collaborate with other functions to achieve client deligh
Perform registration dossier for all the Life Science Products in all countries (except USA) Write the technical documentation for new product development Maintain the adequacy with the regulation for technical documentation Product lifecycle management: Support product design changes, labeling updates, sustainment, and improvement activities from regulatory perspective. Assess regulatory impact, develop detailed action plan to drive regulatory compliance and ensure on time completion of identified actions. The essential requirements of the job include: A Bachelor s degree in areas of life sciences or engineering field with a minimum of 12-15 years experience in a regulated medical device/diagnostic industry (less years required with advanced degree). Professional designations are not required but training and certificates in quality or regulatory affairs would be a plus (e.g. CQM, CQE, CQA, RAC, CLIA, Six Sigma, Lean) Experience in supporting filing of pre-market regulatory submissions domestically (Q-Subs, 510ks) and internationally (IVDR; China; ROW Global Registrations). Knowledge of domestic and international quality systems and other standards such as FDA QSR, IVDD/IVDR, INVIMA, ANMAT, ANVISA, COFEPRIS, ISO 13485, ISO 9001 and other applicable standards and regulations. Knowledge of design control process requirements and requirements for technical documentation for in vitro diagnostics and or medical devices. Experience with Software as a Medical Device (SAMD) and Software as an accessory to a device highly desirable. Required Competencies: Critical thinker able to address complex situations and issues. Manages changing conditions, processes, and approaches; leads organizations through change effectively. Ability to adopt a systemic view of process improvement and to advise process improvement teams to reach goals. Organized and thorough with a high level of initiative, self-motivation and energy. Quick adaptability to embrace company culture and flexibility to manage multiple projects at the same time. Ability to participate in meetings outside of regular business hours to support global business.
Responsible for the detailed technical clarification (technology selection, design testing etc.) on requested equipment, including to take on responsibility and ownership for the proposed equipment during project Technical elaboration and vendor management of detail design (including functional specification as a base for the process coding, defining and creation of hardware equipment (Siemens/Rockwell/Schneider Automation), instrumentation list, and cable lists etc.). Respect current good engineering practice and industrial standards applicable for the project and work in accordance with our established quality management system. Willingness for international and national travel to to support sites commissioning, E&C activities at customers and local vendors. Qualifications & Experience: B.E/B.Tech (Electrical or Mechanical or EEE or CS) with 8-10 yrs of experience. Proven experience of automation & controls engineering of equipment used in process industry for example beer production, wine or water industry Skills in HMI and PLC Programming on Siemens & AB Rockwell platforms, WinCC, Tia Portal, Simatic ManagerKnowledge and understanding of the current industry guidelines for designing, manufacturing, testing and documenting food and beverage process equipment. Ability to handle Engineering changes that may come up during the course of the project including all related information and communication / agreements / cost/time impacts. Knowledge and understanding of the current industry guidelines for designing, manufacturing, testing and documenting food and beverage process equipment. 50% Willingness for international and national travel to to support sites commissioning, E&C activities at customers and local vendors. This could be up to 50% out of the office workload! 20 % Responsible for the detailed technical clarification (technology selection, design testing etc.) on requested equipment, including to take on responsibility and ownership for the proposed equipment during project 20 %Technical elaboration and vendor management of detail design (including functional specification as a base for the process coding, defining and creation of hardware equipment (Siemens/Rockwell/Schneider Automation), instrumentation list, and cable lists etc.). 10 % Respect current good engineering practice and industrial standards applicable for the project and work in accordance with our established quality management system.
The Research Operations Manager, Customer & Market insights is the essential backbone of the team, enabling and enhancing team performance through efficiency, training and innovation while supporting the team in the journey of democratizing insight to drive a market orientation across Cytiva. The role is focused on customer research but will also encompass competitive intelligence and other insight areas as relevant. The job holder utilises their strong insight skills together with a meticulous focus on organisation and planning to ensure that the Customer & Market insights team are able to consistently deliver for the business. This position reports to the Senior Director, Customer & Market Insights and is part of the Marketing function. The role is located in Bangalore, India and will be an on-site role. At Cytiva, our vision is to advance future therapeutics from discovery to delivery. What you will do: Ways of Working: Identifying and delivering a program of initiatives to improve team ways of working including opportunities for standardization, the creation of templates, the introduction of new team and business processes and tools including for example AI/ML or other novel approaches. Communications Lead: Create and ensure delivery of a Cytiva business knowledge sharing calendar as well as the Customer & Market Insights team meeting and events calendar, coordinating with the Senior Managers to identify and deliver appropriate content. Training Lead: Create and ensure delivery of a functional (e.g. research techniques and methodologies) and business understanding training and development curriculum based on team audits and consultation with Senior Managers. Tools Management: Overseeing the tools and platforms that are central to efficient team operation, including analytical tools (e.g. Q) and dashboards, project planning tools and the knowledge management platform. Vendor Management: Managing vendors, identifying new vendors as required Metrics Management: Gather, synthesize and report key team performance metrics, including stakeholder satisfaction, knowledge platform utilization, newsletter readership as well as budget management. Who you are: Bachelor s Degree is essential, MBA or relevant graduate degree an preferred At least 5 years experience in customer insight, market research or a related field ideally within a research agency Proficient in quantitative and qualitative research with end-to-end experience i.e. from briefing to final reporting and delivery It would be a plus if you also possess previous experience in: Market research operations in either agency or client-side organizations Project management Secondary research and/or competitive Intelligence Providing on-the-job training, mentorship, and/or guidance to junior team members Creating and/or delivering insight learning and development courses/programs Implementing improvements to the insight lifecycle Evaluating AI for use in the insight lifecycle 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 .
The Trade Compliance Analyst II position plays a critical role in ensuring the company s trade compliance practices are conducted in accordance with the rules and regulatory requirements of Customs authorities and other applicable governmental agencies. The work this position performs to ensure our products qualify for key compliance programs is strategically critical to our success. It will support qualification activities across the full Diagnostics Platform. This position is part of the Global Logistics & Distribution organization and is based on-site at our office in Bangalore, India. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. If you are an experienced Trade Compliance professional that thrives in a dynamic role and wants to work towards building a world-class program read on. In this role, you will have the exciting opportunity to direct, assist with, and participate in, the following activities in support of our Trade Compliance Program: Analyze product components (bills of material) to determine country of origin. Work closely with engineering, sourcing, or product teams to gather technical data needed for trade analysis. Navigate internal systems to research product details and prepare documentation to support origin and trade compliance decisions. Help maintain accurate trade data and records for audits or government reporting. Lead continuous improvement projects around how we determine product origin or qualify goods for trade agreements. Maintain operational metrics and KPI s to track the overall health of the program (utilization, savings, etc.). The essential requirements of the job include: Bachelor s degree with 2+ years in trade compliance related discipline such as rules of origin, classification, export compliance, etc. Understanding of product structures (like bills of material) and how they relate to trade compliance or country of origin as well as knowledge of trade regulations, including Free Trade Agreements and export control concepts (e.g., Foreign Direct Product Rule). Understanding of the rules of origin interpretation and application (tariff shift, regional value content, De Minimis, etc.) Fluent in conversational and written English. Hands-on experience in data manipulation in MS Excel (fluency in pivot tables, v-lookups, etc.)
The Trade Compliance Analyst II position plays a critical role in ensuring the company s trade compliance practices are conducted in accordance with the rules and regulatory requirements of Customs authorities and other applicable governmental agencies. This role performs critical work to ensure our products are accurately classified for import and export, enabling compliant and efficient global trade. It will support classification activities across the full Diagnostics Platform. This position is part of the Global Logistics & Distribution organization and is based on-site at our office in Bangalore, India. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. If you are an experienced Trade Compliance professional that thrives in a dynamic role and wants to work towards building a world-class program read on. In this role, you will have the exciting opportunity to direct, assist with, and participate in, the following activities in support of our Trade Compliance Program: Assign Harmonized Tariff Schedule (HTS) and Export Control Classification Numbers (ECCNs) to products using available tools, guidance, and product data. Review product specifications and other technical information to support accurate classification decisions. Research classification resources (e.g., rulings, government guidance) to support decision-making. Collaborate with sourcing, engineering, and trade compliance teams to gather information and clarify product details. Maintain and update classification data in internal systems, ensuring records are complete and audit ready. Support process improvements and documentation efforts related to product classification. The essential requirements of the job include: Bachelor s degree with 2+ years in trade compliance with direct experience in customs classification assignment. Strong analytical and research skills Able to interpret technical data and apply rules or guidelines to determine correct classifications. Detail-oriented mindset Accuracy and consistency are key in managing classification data and documentation. Effective communication skills Comfortable asking questions and working with cross-functional partners to collect product information. Fluent in conversational and written English.
The Trade Compliance Analyst II position for Beckman Coulter Diagnostics plays a critical role in ensuring the company s trade compliance practices are conducted in accordance with the rules and regulatory requirements of Customs authorities and other applicable governmental agencies. This role performs critical work to ensure our products are accurately classified for import and export, enabling compliant and efficient global trade. This position is part of the Global Logistics & Distribution organization and is based on-site at our office in Bangalore, India. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. If you are an experienced Trade Compliance professional that thrives in a dynamic role and wants to work towards building a world-class program to help optimize Beckman Coulter supply chain while maintaining the highest standards of integrity and compliance read on. In this role, you will have the exciting opportunity to direct, assist with, and participate in, the following activities in support of our Trade Compliance Program: Assign Harmonized Tariff Schedule (HTS) and Export Control Classification Numbers (ECCNs) to products using available tools, guidance, and product data. Review product specifications and other technical information to support accurate classification decisions. Research classification resources (e.g., rulings, government guidance) to support decision-making. Collaborate with sourcing, engineering, and trade compliance teams to gather information and clarify product details. Maintain and update classification data in internal systems, ensuring records are complete and audit ready. Support process improvements and documentation efforts related to product classification. The essential requirements of the job include: Bachelor s degree with 2+ years in trade compliance with direct experience in customs classification assignment. Strong analytical and research skills Able to interpret technical data and apply rules or guidelines to determine correct classifications. Detail-oriented mindset Accuracy and consistency are key in managing classification data and documentation. Effective communication skills Comfortable asking questions and working with cross-functional partners to collect product information. Fluent in conversational and written English.
The Trade Compliance Analyst II position for Beckman Coulter Diagnostics plays a critical role in ensuring the company s trade compliance practices are conducted in accordance with the rules and regulatory requirements of Customs authorities and other applicable governmental agencies. The work this position performs to ensure our products qualify for key compliance programs is strategically critical to our success. This position is part of the Global Logistics & Distribution organization and is based on-site at our office in Bangalore, India. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. If you are an experienced Trade Compliance professional that thrives in a dynamic role and wants to work towards building a world-class program to help optimize Beckman Coulter supply chain while maintaining the highest standards of integrity and compliance read on. In this role, you will have the exciting opportunity to direct, assist with, and participate in, the following activities in support of our Trade Compliance Program: Analyze product components (bills of material) to determine country of origin, check if products qualify for Free Trade Agreements, and assess export rules like the Foreign Direct Product (FDP) Rule. Work closely with engineering, sourcing, or product teams to gather technical data needed for trade analysis. Navigate internal systems to research product details and prepare documentation to support origin and trade compliance decisions. Help maintain accurate trade data and records for audits or government reporting. Lead continuous improvement projects around how we determine product origin or qualify goods for trade agreements. Maintain operational metrics and KPI s to track the overall health of the program (utilization, savings, etc.). The essential requirements of the job include: Bachelor s degree with 2+ years in trade compliance related discipline such as rules of origin, classification, export compliance, etc. Understanding of product structures (like bills of material) and how they relate to trade compliance or country of origin as well as knowledge of trade regulations, including Free Trade Agreements and export control concepts (e.g., Foreign Direct Product Rule). Understanding of the rules of origin interpretation and application (tariff shift, regional value content, De Minimis, etc.) Fluent in conversational and written English. Hands-on experience in data manipulation in MS Excel (fluency in pivot tables, v-lookups, etc.)
The Account Manager, Bengaluru, Karnataka role is responsible for driving the primary and secondary revenue for Bengaluru, Mysuru and neighboring districts in Karnataka. This position is part of the Sales Function located based in Bengaluru, Karnataka and will be in a remote work set-up. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. You will be a part of the Sales function and report to the Zonal Sales Manager, South zone. Your core area of responsibility will be to successfully drive the hospital & Diagnostic Labs sale from introduction of new screening and diagnostic concepts through closure and implementation, working with medical professionals /clinicians/intensivists, diagnostic laboratory heads to identify needs, gain consensus, and close new assay and instrumentation business. If you thrive in a fast paced, target driven leadership, role and want to work towards building a world-class Commercial organization read on. In this role, you will have the opportunity to: Manage and grow business in existing and new accounts in assigned territory Expand menu utilization and assay maximization in existing accounts Negotiate and manage contracts Develop demand for and adoption of new assays and implement customer -specific action plans Work closely with Clinical Application Specialists to develop sales strategies Host and assist with product shows in association with Marketing team The essential requirements of the job include: 3-5 years of sales experience with a strong track record in Medical devices/Diagnostic equipment to hospitals /clinical laboratories. Bachelor s Degree with Science background / Diploma/Degree in Medical instrumentation is desirable Skilled in Microsoft Word, Excel, PowerPoint applications, using a CRM application such as Microsoft Dynamics or Salesforce.com
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. 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. The Sr. Design Engineer, Mechanical is responsible for product sustenance activities in Single use products including design feasibility and evaluation, change control management, customer case resolution, verification etc. This position reports to the Sr. Manager Engineering and is part of the Cytiva R&D center located in Bangalore and will be an on-site role . At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Design, develop, and release single-use consumables (components, assemblies, packaging, tooling, fixtures). Utilize CAD skills and assembly considerations to explore and optimize design solutions. Engage in all phases of product sustaining, including feasibility study, evaluation, documentation, supplier interfaces, manufacturing, and service collaboration. Develop and maintain project documentation (technical reports, testing protocols, risk analyses, design docs) within the QMS. Identify and execute proactive product quality improvement efforts. Follow QMS and Change Control processes to ensure quality and compliance. Use engineering judgment and creativity to continually improve processes and product outcomes. Who you are: Education: Bachelor s degree in Mechanical Experience: 3 - 5 years in mechanical engineering Skilled in meeting customer requirements and collaborating across departments. Proficient in CAD solid modeling (SolidWorks, CREO) and technical documentation. Familiar with GMP and regulatory requirements, ensuring accurate documentation and compliance. Previous engineering experience including design or analysis of Single-use consumables, molded components, BOM analysis Previous experience in sustaining engineering project teams for change management activities. It would be a plus if you also possess previous experience in: Engineering Change Management Consumable design and development CAD Modelling and Drawing BOM creation Technical review
The Account Embedded Sales Specialist is responsible for providing support to the assigned customer for the entire Cytiva workflow and ensuring compliant handling. This position reports to the Key Account Specialist Leader and is part of the Bioprocess Modality located in Pune and will be a remote role based in customer site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: SPOC at the respective customer site for all the BUs. First-line Application support at the site across BU; liaison with the Respective sales specialist to coordinate the second layer of support activities. Preliminary Investigator for all product complaints. Lead generation at the customer site. Presales/Post sales support for the Bioprocess product ranges. Customer warehouse, consumable stock coordination at the customer site. Who you are: Master s in Bioprocess Engineering or any stream of Biology. 3-5 Years of experience in Biomanufacturing domain. Strong perseverance and communication skills It would be a plus if you also possess previous experience in: Manufacturing scale up studies experience, Bioprocess modeling.
The Senior Customer Support Engineer for Beckman Coulter Diagnostics is responsible for delivering customer support in terms of technical service at Mumbai , Maharashtra. This position is part of the Service department located at Mumbai and will be indicated as a fully Remote position providing service support to our esteemed clients aligned with our vision of delivering healthcare to patients across the globe. You will be a part of the West Service Team and report to the State Service Manager Maharashtra region responsible for client support across the state. If you thrive in a fast-paced, competitive, collaborative, and high-performing role and want to work to build a world-class Service organization read on. In this role, you will have the opportunity to: 1. Install, maintaining the instruments and Providing Basic Operation Training during Installation to Provide effective product and customer support. 2. Ensures Preventive Maintenance planning (PM), MOD are performed in timely manner 3. Seeks timely support for difficult product issues avoiding unnecessary down time, Maintain recommended Spare Parts for all product Range and Maintain excellent customer relationship, specifically with his/her directly assigned accounts by adhering to field service policies procedures and standards. The essential requirements of the job include: Must be an Engineering Graduate with B.E./B.Tech. Degree Should have a minimum working experience of 3 to 5 years in the relevant field with exposure in customer services (Technical) in the IVD industry. Should have advance Technical Competency in one of the Product lines in IVD product. Should have adequate skills to consultatively help & support technical troubleshooting along with other functions. And able to drive corrective and preventive actions to improve service delivery based on customer feedback. It would be a plus if you also possess previous experience in: Technical field services of IVD products (hardware & SW) with advance Technical Skills in one product line in IVD Generating Service Revenue Usage of Customer Relationship Management (CRM) SW based for Call Handling & Closure in System
The Senior Customer Support Engineer for Beckman Coulter Diagnostics is responsible for delivering customer support in terms of technical service at Pune , Maharashtra. This position is part of the Service department located at Pune and will be indicated as a fully Remote position providing service support to our esteemed clients aligned with our vision of delivering healthcare to patients across the globe. You will be a part of the West Service Team and report to the State Service Manager Maharashtra region responsible for client support across the state. If you thrive in a fast-paced, competitive, collaborative, and high-performing role and want to work to build a world-class Service organization read on. In this role, you will have the opportunity to: 1. Install, maintaining the instruments and Providing Basic Operation Training during Installation to Provide effective product and customer support. 2. Ensures Preventive Maintenance planning (PM), MOD are performed in timely manner 3. Seeks timely support for difficult product issues avoiding unnecessary down time, Maintain recommended Spare Parts for all product Range and Maintain excellent customer relationship, specifically with his/her directly assigned accounts by adhering to field service policies procedures and standards. The essential requirements of the job include: Must be an Engineering Graduate with B.E./B.Tech. Degree Should have a minimum working experience of 3 to 5 years in the relevant field with exposure in customer services (Technical) in the IVD industry. Should have advance Technical Competency in one of the Product lines in IVD product. Should have adequate skills to consultatively help & support technical troubleshooting along with other functions. And able to drive corrective and preventive actions to improve service delivery based on customer feedback. It would be a plus if you also possess previous experience in: Technical field services of IVD products (hardware & SW) with advance Technical Skills in one product line in IVD Generating Service Revenue Usage of Customer Relationship Management (CRM) SW based for Call Handling & Closure in System
The Senior Customer Support Engineer for Beckman Coulter Diagnostics is responsible for delivering customer support in terms of technical service at Rajamundry, APT. This position is part of the Service department located at Hyderabad and will be indicated as a fully Remote position providing service support to our esteemed clients aligned with our vision of delivering healthcare to patients across the globe. You will be a part of the Service Team and report to the State Service Manager APT region responsible for client support across the state. If you thrive in a fast-paced, competitive, collaborative, and high-performing role and want to work to build a world-class Service organization read on. In this role, you will have the opportunity to: 1. Install, maintaining the instruments and Providing Basic Operation Training during Installation to Provide effective product and customer support. 2. Ensures Preventive Maintenance planning (PM), MOD are performed in timely manner 3. Seeks timely support for difficult product issues avoiding unnecessary down time, Maintain recommended Spare Parts for all product Range and Maintain excellent customer relationship, specifically with his/her directly assigned accounts by adhering to field service policies procedures and standards. The essential requirements of the job include: Must be an Engineering Graduate with B.E./B.Tech. Degree Should have a minimum working experience of 3 to 5 years in the relevant field with exposure in customer services (Technical) in the IVD industry. Should have advance Technical Competency in one of the Product lines in IVD product. Should have adequate skills to consultatively help & support technical troubleshooting along with other functions. And able to drive corrective and preventive actions to improve service delivery based on customer feedback. It would be a plus if you also possess previous experience in: Technical field services of IVD products (hardware & SW) with advance Technical Skills in one product line in IVD Generating Service Revenue Usage of Customer Relationship Management (CRM) SW based for Call Handling & Closure in System