147 Cytometry Jobs

Date: 9 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Discovery Services Job Description Designation: Associate Scientist/Senior associate scientist Job Location: Bangalore Department: Discovery Biology About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose To be a part of the Assay Biology group and support various assay development activities. Key Responsibilities To develop cell based assays- optimization and assay validation on different assay formats Biochemical, Enzyme based assay development Screening of the compounds- small and large molecules. Data analysis and report preparation Possess the knowledge and exposure to environment, health, and safety (EHS) practices Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Educational Qualification M.Sc/M.Tech in Biological Sciences Technical/functional Skills Expertise and in-depth knowledge of mammalian cell culture. Experience in conducting TR-FRET, HTRF, Fluorescence Intensity, Alpha screen, Radioactive assays and Luminesce based assay. Experience in ELISA and Luminex based assays for cytokine estimations Experience with human primary cells and tissue samples Experience with RT-PCR and Westerns would be desirable Experience in Flow cytometry and immune-phenotyping would be desirable Ability to analyse and present data using excel, ppt and statistical tools (Graph Pad Prism, Excel-fit) Willingness and flexibility to work in cross functional teams across technical domains Ability to plan and execute work and perform multiple activities in parallel. Experience M.Sc/M.Tech with 6 to 9 years of experience Behavioral Skills Good work ethics. Good interpersonal skills, and the ability to work effectively in a team environment. Ability to work with co‐workers professionally. General ability to thrive in a growing infrastructure and culture and also think out of box approach when troubleshooting and problem solving. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Date: 9 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Discovery Services Job Description Designation: Assay Biologist Job Location: Bangalore/Hyderabad Department: Discovery Biology About Syngene Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self. Compliance to Syngene’ s quality standards at all times. Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Purpose To be a part of the Assay Biology group and support various assay development activities. Key Responsibilities To develop cell based assays- optimization and assay validation on different assay formats Biochemical, Enzyme based assay development Screening of the compounds- small and large molecules. Data analysis and report preparation Possess the knowledge and exposure to environment, health, and safety (EHS) practices Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Educational Qualification M.Sc/M.Tech in Biological Sciences Technical/functional Skills Expertise and in-depth knowledge of mammalian cell culture. Experience in conducting TR-FRET, HTRF, Fluorescence Intensity, Alpha screen, Radioactive assays and Luminesce based assay. Experience in ELISA and Luminex based assays for cytokine estimations Experience with human primary cells and tissue samples Experience with RT-PCR and Westerns would be desirable Experience in Flow cytometry and immune-phenotyping would be desirable Ability to analyse and present data using excel, ppt and statistical tools (Graph Pad Prism, Excel-fit) Willingness and flexibility to work in cross functional teams across technical domains Ability to plan and execute work and perform multiple activities in parallel. Experience M.Sc/M.Tech with 9 to 12 years of experience Behavioral Skills Good work ethics. Good interpersonal skills, and the ability to work effectively in a team environment. Ability to work with co‐workers professionally. General ability to thrive in a growing infrastructure and culture and also think out of box approach when troubleshooting and problem solving. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Date: 9 Sept 2025 Location: Kolthur Shamirpet, Medchal, TG, IN, 500078 Custom Field 1: Discovery Services Job Description Designation: Assay Biologist Job Location: Hyderabad/Bangalore Department: Discovery Biology About Syngene Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self. Compliance to Syngene’ s quality standards at all times. Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Purpose To be a part of the Assay Biology group and support various assay development activities. Key Responsibilities To develop cell based assays- optimization and assay validation on different assay formats Biochemical, Enzyme based assay development Screening of the compounds- small and large molecules. Data analysis and report preparation Possess the knowledge and exposure to environment, health, and safety (EHS) practices Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Educational Qualification M.Sc/M.Tech in Biological Sciences Technical/functional Skills Expertise and in-depth knowledge of mammalian cell culture. Experience in conducting TR-FRET, HTRF, Fluorescence Intensity, Alpha screen, Radioactive assays and Luminesce based assay. Experience in ELISA and Luminex based assays for cytokine estimations Experience with human primary cells and tissue samples Experience with RT-PCR and Westerns would be desirable Experience in Flow cytometry and immune-phenotyping would be desirable Ability to analyse and present data using excel, ppt and statistical tools (Graph Pad Prism, Excel-fit) Willingness and flexibility to work in cross functional teams across technical domains Ability to plan and execute work and perform multiple activities in parallel. Experience M.Sc/M.Tech with 3 to 8 years of experience Behavioral Skills Good work ethics. Good interpersonal skills, and the ability to work effectively in a team environment. Ability to work with co‐workers professionally. General ability to thrive in a growing infrastructure and culture and also think out of box approach when troubleshooting and problem solving. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Date: 9 Sept 2025 Location: Kolthur Shamirpet, Medchal, TG, IN, 500078 Custom Field 1: Discovery Services Job Description Designation: Associate Scientist/Senior associate scientist Job Location: Hyderabad Department: Discovery Biology About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose To be a part of the Assay Biology group and support various assay development activities. Key Responsibilities To develop cell based assays- optimization and assay validation on different assay formats Biochemical, Enzyme based assay development Screening of the compounds- small and large molecules. Data analysis and report preparation Possess the knowledge and exposure to environment, health, and safety (EHS) practices Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Educational Qualification M.Sc/M.Tech in Biological Sciences Technical/functional Skills Expertise and in-depth knowledge of mammalian cell culture. Experience in conducting TR-FRET, HTRF, Fluorescence Intensity, Alpha screen, Radioactive assays and Luminesce based assay. Experience in ELISA and Luminex based assays for cytokine estimations Experience with human primary cells and tissue samples Experience with RT-PCR and Westerns would be desirable Experience in Flow cytometry and immune-phenotyping would be desirable Ability to analyse and present data using excel, ppt and statistical tools (Graph Pad Prism, Excel-fit) Willingness and flexibility to work in cross functional teams across technical domains Ability to plan and execute work and perform multiple activities in parallel. Experience M.Sc/M.Tech with 3 to 8 years of experience Behavioral Skills Good work ethics. Good interpersonal skills, and the ability to work effectively in a team environment. Ability to work with co‐workers professionally. General ability to thrive in a growing infrastructure and culture and also think out of box approach when troubleshooting and problem solving. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Date: 9 Sept 2025 Location: Kolthur Shamirpet, Medchal, TG, IN, 500078 Custom Field 1: Discovery Services Job Description Designation: Associate Scientist/Senior associate scientist Job Location: Hyderabad Department: Discovery Biology About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose To be a part of the Assay Biology group and support various assay development activities. Key Responsibilities To develop cell based assays- optimization and assay validation on different assay formats Biochemical, Enzyme based assay development Screening of the compounds- small and large molecules. Data analysis and report preparation Possess the knowledge and exposure to environment, health, and safety (EHS) practices Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Educational Qualification M.Sc/M.Tech in Biological Sciences Technical/functional Skills Expertise and in-depth knowledge of mammalian cell culture. Experience in conducting TR-FRET, HTRF, Fluorescence Intensity, Alpha screen, Radioactive assays and Luminesce based assay. Experience in ELISA and Luminex based assays for cytokine estimations Experience with human primary cells and tissue samples Experience with RT-PCR and Westerns would be desirable Experience in Flow cytometry and immune-phenotyping would be desirable Ability to analyse and present data using excel, ppt and statistical tools (Graph Pad Prism, Excel-fit) Willingness and flexibility to work in cross functional teams across technical domains Ability to plan and execute work and perform multiple activities in parallel. Experience M.Sc/M.Tech with 3 to 8 years of experience Behavioral Skills Good work ethics. Good interpersonal skills, and the ability to work effectively in a team environment. Ability to work with co‐workers professionally. General ability to thrive in a growing infrastructure and culture and also think out of box approach when troubleshooting and problem solving. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Beckman Coulter LS Beckman Coulter Life Sciences’ mission is to empower those seeking answers to life’s most important scientific and healthcare questions. With a legacy spanning 80+ years, we have long been a trusted partner to our customers, who are working to transform science and healthcare with the next groundbreaking discovery. As part of our team of more than 2,900 associates across 130 countries, you’ll help drive our vision of accelerating answers—and our commitment to excellence. Beckman Coulter Life Sciences 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. Position Summary and Overview: Responsible for managing the site's Non-conformance (NC) and deviation processes. This includes reviewing and approving NC records, containing non-conforming material, conducting trend analysis, managing related CAPAs, and driving root cause investigations. The role maintains compliant Quality Management System (QMS) procedures for NCs and supports internal and external audits and inspections. Essential Duties and Responsibilities: Reviews and approves all aspects of Non-conformance (NC) records, including initial accuracy, dispositions, investigations, impact assessments, categorization, closure, and due date extensions, ensuring all actions are accurately recorded as per the procedural requirements. Ensures appropriate physical segregation and labeling of nonconforming material in the designated quarantine area. Performs trend analysis on Non-conformances to identify improvement opportunities and manages the system for Corrective Actions (CAPAs) initiated through NCs. Participates in root cause investigations for Non-conformances and other quality issues and presents findings to management. Responsible for the overall handling and management of product-related non-conformances and planned deviations within the site. Maintains and monitors the Quality Management System, including site-specific and global Non-conformance procedures, ensuring full compliance with requirements, regulations, and standards. Supports audit and inspection activities, including preparation, liaison with auditors, and resolution of findings, and performs other related duties as required. Qualification and Experience: Minimum Requirements: Bachelors or master’s degree in biology, Engineering or related disciplines Minimum of 5-7 years related experience in quality assurance and/or regulatory affairs Knowledge of ISO 13485, GMP and GLP requirements would be advantageous Experience with handling non-conforming products and other Quality Management System processes. Demonstrated experience in flow cytometry is crucial and will be highly advantageous. Required Competencies: Exceptional communication skills (verbal/written/presentation/relationship building) with ability to work collaboratively with cross-functional project teams and regulators Ability to drive results, foster teamwork, handle pressure, and provide feedback. Must be able to demonstrate skills in root cause investigation and problem solving. Organized, detail-oriented with impeccable integrity. High level of initiative, self-motivation, and energy. 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.

About the Job: Reprosci Biosciences Private Limited is actively engaged in developing regenerative therapies in reproductive medicine, with a focus on autologous biologics such as PRP-derived exosomes. In collaboration with the Center for Translational Research in Reproductive Health, PSG Institute of Advanced Studies, we conduct cutting-edge research involving bioformulation, cell-based assays, exosome isolation and characterization, and in-vitro functional studies targeting endometrial regeneration. Our R&D aims to bridge lab-scale innovation and clinical translation, emphasizing personalized, non-hormonal fertility therapeutics. Ongoing activities include product optimization, preclinical validation, and preparation for regulatory submissions. About the Role: We are seeking a highly motivated and skilled Senior Research Scientist to join our team, driving innovation in regenerative medicine, stem cell therapy, and next-generation biotechnology platforms. The ideal candidate will lead research in cell culture, molecular biology, and advanced regenerative modalities, guiding a talented team toward impactful scientific and translational outcomes. What You’ll Do: Lead cell culture and molecular biology experiments, ensuring best practices in mammalian cell culture technologies and laboratory maintenance. Work with stable and transient transfections for recombinant protein/antibody expression across various mammalian cell lines (CHO, HEK, etc.). Design, execute, and troubleshoot complex cell culture, transfection, and cell line generation projects. Develop and perform a wide range of assays (cell-free, cell-based, cytotoxicity, biochemical, microscopy, flow cytometry, western blot, ELISA, high-throughput screening, etc.). Support experiments using molecular biology techniques, including DNA/RNA extraction, PCR, qPCR, gel electrophoresis, and related analysis. Supervise and mentor Research Assistants and Lab Technicians with clear weekly and monthly milestones. Prepare presentations, posters, study reports, government grant proposals, and manuscripts for publication. Manage lab operations, including ordering, inventory, and regulatory compliance. Explore and integrate futuristic areas including Exosomes, 3D Bioprinting, and advanced Stem Cell technologies into ongoing and upcoming projects. What We’re Looking For: PhD in Molecular Biology, Cell Biology, Biotechnology, Biochemistry, or a related field. Strong knowledge of biochemistry and molecular biology principles and methodologies. Proven experience with mammalian cell culture, molecular biology techniques, PCR, ELISA, SDS-PAGE, Western blot, enzyme assays, and chromatography. Demonstrated leadership, organizational, and multitasking skills with attention to detail and strong record-keeping practices. Excellent communication and teamwork skills. Why Join Us: At ReprOsci , you'll be part of a passionate team at the forefront of regenerative medicine, working to translate breakthrough science into life-changing therapies. We offer a collaborative, innovation-driven environment where your ideas matter, your expertise shapes next-generation solutions, and your work directly contributes to addressing unmet clinical needs in reproductive health. With access to cutting-edge technologies, strategic academic collaborations, and a culture that values both scientific rigor and creative problem-solving, this is a unique opportunity to grow your career while making a tangible impact on the future of fertility therapeutics.

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 Electrical Engineer I is responsible for designing, developing, troubleshooting modules for laboratory medical device new product development. The incumbent practices best design practices and follow quality processes defined during development. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In this role, you will have the opportunity to: 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 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.

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 Senior Systems Verification Engineer I for Beckman Coulter Diagnostics is responsible for designing, developing, troubleshooting Electro-Mechanical / Opto-Electrical System modules for laboratory medical device new product development. The incumbent practices best design practices and follow quality processes defined during development. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In This Role, You Will Have The Opportunity To Author, review, and execute system-level test protocols to validate design changes. Ensure test coverage for accuracy, performance, throughput, carryover, and linearity Etc. requirements. Analyze test data and generate statistically sound reports to support design verification and release decisions. Evaluate whether design changes meet existing system specifications/requirements and performance benchmarks and changes do not compromise product integrity or clinical outcomes. Participate in DFMEA reviews, identifying and testing for potential failure modes. Perform DFMEA test protocols to validate mitigations and assess risk impact. Develop and execute reliability test protocols, including accelerated life testing and environmental stress testing. Perform statistical analysis of reliability and performance data using tools such as Minitab, JMP, or Python/R. Interpret results to estimate product life, failure rates (MTBF = Mean Time Between Failures), and confidence intervals. The Essential Requirements Of The Job Include Bachelor’s or Master’s degree in Biomedical engineering, Electrical Engineering, Systems Engineering, or related field. 3+ years of experience in medical device V&V, preferably in diagnostics or imaging systems. Strong understanding of design control, risk management, and reliability engineering. Proficiency in statistical analysis and tools for data interpretation. Familiarity with DFMEA, ISO 14971, IEC 60601, and FDA QSR. Experience in setting up experiments using external sensors and data acquisition systems such as LabVIEW, NI DAQ, or similar platforms. Experience with requirement management tools (e.g., IBM DOORS, Jama) is a plus. Familiarity with regulatory and safety standards (IEC 62304, ISO 13485, FDA Class II). It would be a plus if you also possess previous experience in: Experience in medical device design & development is a plus Experience in IVD instrumentation, such as clinical chemistry, immunoassay, hematology, urinalysis, molecular, microbiology or flow cytometry systems is a plus Familiarity with lean manufacturing and Six Sigma principles 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.

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 Senior Electrical Engineer I is responsible for designing, developing, troubleshooting modules for laboratory medical device new product development. The incumbent practices best design practices and follow quality processes defined during development. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In This Role, You Will Have The Opportunity To 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. 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.

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 Life Sciences, 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 Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results. We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory. It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow. Learn about the Danaher Business System which makes everything possible. The Flow Cytometry Development Scientist is responsible for driving efforts to design, develop and transfer IVD assays to launch for use in Flow Cytometric applications. This position reports to the Manager, development science and is part of the R&D, development science department located in BDC, Bangalore and will be an on-site role. In This Role, You Will Have The Opportunity To Apply analytical skills and independent judgment to develop innovative, practical and consistent solutions to a wide range of complex problems. Use your experience in flow cytometry to perform Panel design, data analysis including gating strategies, interpretation of specimens and review of data quality. Strictly adhering to good laboratory and good documentation practices throughout the design and development cycle Perform data collection including specimen staining and preparation, acquisition Develop or build and QC the assay lots during the development cycle of feasibility through verification. Creating study plan and reports in alignment with requirements of applicable standards and regulatory requirements and ensures the studies are conducted in agreement with approved plan. The Essential Requirements Of The Job Include Advanced degree in Immunology/ Biotechnology/hematology, Life sciences, or related discipline, for example Bachelor’s degree in field with 7+ years’ experience OR Master’s degree in field with 5+ years’ experience OR Doctoral degree in field with 3+ years’ experience. A minimum of 4 years’ experience in clinical hematopathology and/or flow cytometry interpretation, especially in a Lymphoma &Leukemia lab Beckman Coulter Life Sciences, 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.

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Job Description – Business Analyst I Join Thermo Fisher Scientific and contribute to high-caliber software products that speed up scientific exploration and lab efficiency! Our collaborative setting nurtures imagination, analytical problem-solving, and improving human welfare. This is an outstanding opportunity to integrate biotech specialization with software product understanding. Position Title: Business Analyst I Purpose The Business Analyst I collaborate with product managers, customers, and engineering teams to grasp business needs and transform them into functional specifications. Acting as the customer's representative, this role ensures that user stories and features are clearly outlined, prioritized, and aligned with business objectives. Flawless opportunity for candidates keen on merging biotech proficiency with software product understanding, particularly those familiar with flow devices and scientific processes, to progress into product ownership. Roles & Responsibilities Work closely with product managers, senior product owners, and customers to collect and elaborate on business and functional requirements. Work closely with development/UX, engineering, and QA teams to ensure shared understanding of requirements and goals. Assist in managing and refining product backlogs, including writing user stories, acceptance criteria, and use cases. Participate in Agile ceremonies such as sprint planning, stand-ups, reviews, and retrospectives. Help translate product roadmaps into actionable tasks for development teams. Help define operational processes, particularly for laboratory and flow instrument applications (like flow cytometry, flow analyzers, or other relevant laboratory systems). Document and validate user workflows related to connected lab instruments and data-driven applications. Supervise progress, dependencies, and risks, advancing concerns to senior collaborators as necessary. Chip in to go-to-market activities, user enablement content, and release documentation. Promote Agile guidelines, Lean-Agile values, and collaborative team culture. Ensure adherence to QMS (ISO9001:2015) & ISMS (ISO 27001) standards and assist in audit procedures. Candidate Requirements Education Bachelor’s degree in Engineering, Computer Science, IT, Biotechnology, or a related field of study. Having a Master’s degree in Computer Science, Information Systems, or Biotechnology would be advantageous. Mandatory Skills, Knowledge, And Experience 2–4 years of overall experience, with at least 1 year in business analysis, software development, or product owner role. Familiarity with Agile frameworks (Scrum, SAFe, or Kanban). Experience documenting requirements, crafting user stories, and working with engineering teams. Proficiency in using flow instruments such as flow cytometry machines, flow analyzers, and other relevant lab apparatus, along with a solid grasp of laboratory protocols. Ability to convert business needs into detailed specifications for scientific software solutions. Basic technical knowledge of software development (Java, Angular, AWS, Jenkins, or similar technologies preferred). Strong analytical and problem-solving skills with attention to detail. Superb communication skills—ability to articulate sophisticated workflows to technical and non-technical audiences. High degree of organization, initiative, and accountability. Collaborative approach and skill in partnering with geographically scattered teams. Nice To Have Experience with Atlassian suite (JIRA, Confluence, Bitbucket, etc.). Exposure to SAFe or other scaled Agile environments. Completed certifications (e.g., CSM, CSPO, or equivalent). Experience defining or validating Non-Functional Requirements (performance, security, cost). Proficient in following QMS (ISO9001:2015) & ISMS (ISO 27001) guidelines. Prior experience in scientific data management, lab automation software, or connected instruments.

Work Schedule Standard Office Hours (40/wk) Environmental Conditions Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Title: Scientist II Job Location: Bangalore, India About Company: Thermo Fisher Scientific Inc. is the world leader in serving science, with revenues of more than $40 billion and approximately 125,000 employees globally. Our m ission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics, deliver medicines to market and increase laboratory productivity. About Team: Candidate will be working as part of Thermo Fisher Scientific Research and Development in the Cell Biology Applications Team (CBAT). The team contributes towards strengthening the company’s portfolio and enhancing its visibility amongst customers by showcasing relevant applications for new and existing products. We generate customer-facing resources in the form of application notes, white papers, protocols, as well as virtual training decks to provide guidance on the use of our products to improve the research experience of scientists. Role & Responsibilities Thermo Fisher Scientific is recruiting an R&D scientist who can foster innovation and improve customer experience through developing application workflows for cell culture consumables and instruments. Responsibilities: Design, plan, and carry out experiments for cell biology projects. Collaborate with product management and R&D teams to define requirements for demonstrating relevant applications for the corresponding product(s). Responsible for data integrity and accuracy. Deliver high quality results as per project schedule in support of product commercialization during early feasibility, development and validation phases. Prepare customer facing collaterals like application notes, technical guides, and training decks based on the internal R&D data generated. Train customers on diverse workflows and provide insights with troubleshooting. Adhere to environmental health and safety guidelines in lab. Skills And Proficiencies Should have extensive experience with mammalian cell culture, including primary and/or stem cells. Should have clear understanding of and hands-on experience with techniques like immunocytochemistry, flow cytometry, western blot, and qPCR. Experience in cell-based bioassays for recombinant proteins. Highly motivated, with strong problem-solving, rational troubleshooting, attention to detail, and independent decision-making skills. Excellent oral and written communication skills. Adaptability, and agility to work independently, and in collaboration on diverse projects, with good interpretation and reporting of data. Should be a teammate. Should have good presentation skills and ability to present data to cross-functional teams. Requirement: Should have a Master’s degree in Cell Biology/Biotechnology or related Life Science with 6+ years of research experience, or PhD with 3+ years of relevant experience. Demonstrated expertise in publishing research and technical writing. GLP or any other certification in laboratory practices and EHS will be considered a bonus. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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 Life Sciences, 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 Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results. We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory. It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow. Learn about the Danaher Business System which makes everything possible. We are currently seeking a Flow Application Specialist at Chennai, who will be responsible for high-quality onsite customer support and represent the face of the company to our customers. Responsible for providing Instrument and application training to Beckman customers on site as per the requirement. To support the Sales Team in identifying market opportunities and assisting in actualizing market potential. Positioning of products and technology through presentations, product demonstrations, workshops, seminars, etc., in alignment with company values, business objectives, and marketing strategy. In This Role, You Will Be Responsible For Application and Training Support: Provide Instrument and Applications training on Beckman coulter cell analysis range of products to ensure a high level of end-user satisfaction. Attend to resolve customer queries telephonically and over email and related applications and if necessary, planned visits to customers. Inclined to learn and improve technical knowledge and skills on existing and new Beckman Coulter products. Plan and organize training programs for Sales teams and the application team to raise and strengthen the technical bar and increase the capability of product knowledge. Marketing: Maintain active dialogue and interactions with key opinion leadership network in flow cytometry, immunology and cell biology. Sales support: Understanding the requirements of the customer’s experiment and provide appropriate technical and product solutions through discussions, presentations and/or product/application demonstrations to positively impact sales and increase productivity. Co-ordinate / support / lead awareness activities such as seminars, conferences, workshops etc in alignment with marketing team. Monitor your plan: Prepare and provide a monthly report to the supervisor on the training and marketing activities. Ensure timely submission of training and evaluation reports. Tracking of customer feedback on product quality and escalating product issues to the appropriate authority within the organization Activity: Work in coordination with sales, service, and other application associates towards achieving the business objectives. Support a culture of constructive feedback and continuous improvement within the organization. The Required Qualifications For The Job Include B. Tech/ B. Pharma/ B.Sc. MLT with 2 yrs experience or MSc. With 1 year of experience in flow Cytometry or Ph.D. with experience in flow Cytometry publications. Minimum 2 years on a Beckman or other analyzer flow Cytometry platform and Sorter experience will be preferable. Two or more flow cytometry-focused publications (preferrable). Good interpersonal skills with the ability to communicate effectively both internally and externally at all levels. IT literate, good knowledge of Microsoft Office products & confidence with other IT applications. Beckman Coulter Life Sciences, 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 Life Sciences 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 Life Sciences 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.

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 Life Sciences, 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 Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results. We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory. It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow. Learn about the Danaher Business System which makes everything possible. The Scientist – Innovation and Custom Design is responsible for supporting improvement, implementing and maintaining manufacturing methods, techniques, processes. Interacting with cross-functional teams and sales representatives. This position reports to the Team Lead – Innovation and Custom Design and is part of the Engineering team located in Bangalore and will be an on-site role. In This Role, You Will Have The Opportunity To Communicate with customers and sales representatives for alignment and locking of the design and manufacturing requirements. Preparing guiding and / or manufacturing documents for reagents, preparing test procedures and reports. Perform Dose-titrations and experiments in supporting investigations and analysis of the data. The Essential Requirements Of The Job Include Bachelors/Master's in Biochemistry/ Biotechnology with 5-8 years’ experience Strong experience in Multicolor Flow cytometry. Experience working on the Panel design. It would be a plus if you also possess previous experience in: Flow cytometry testing - Single color and multi color. Understanding of QMS elements like Non-Conformance, investigations, Customer feedback and Corrective action and preventive actions. Beckman Coulter Life Sciences, 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.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office – Business Analyst I Join Thermo Fisher Scientific and contribute to high-caliber software products that speed up scientific exploration and lab efficiency! Our collaborative setting nurtures imagination, analytical problem-solving, and improving human welfare. This is an outstanding opportunity to integrate biotech specialization with software product understanding. Position Title: Business Analyst I Purpose: The Business Analyst I collaborate with product managers, customers, and engineering teams to grasp business needs and transform them into functional specifications. Acting as the customer's representative, this role ensures that user stories and features are clearly outlined, prioritized, and aligned with business objectives. Flawless opportunity for candidates keen on merging biotech proficiency with software product understanding, particularly those familiar with flow devices and scientific processes, to progress into product ownership. Roles & Responsibilities: Work closely with product managers, senior product owners, and customers to collect and elaborate on business and functional requirements. Work closely with development/UX, engineering, and QA teams to ensure shared understanding of requirements and goals. Assist in managing and refining product backlogs, including writing user stories, acceptance criteria, and use cases. Participate in Agile ceremonies such as sprint planning, stand-ups, reviews, and retrospectives. Help translate product roadmaps into actionable tasks for development teams. Help define operational processes, particularly for laboratory and flow instrument applications (like flow cytometry, flow analyzers, or other relevant laboratory systems). Document and validate user workflows related to connected lab instruments and data-driven applications. Supervise progress, dependencies, and risks, advancing concerns to senior collaborators as necessary. Chip in to go-to-market activities, user enablement content, and release documentation. Promote Agile guidelines, Lean-Agile values, and collaborative team culture. Ensure adherence to QMS (ISO9001:2015) & ISMS (ISO 27001) standards and assist in audit procedures. Candidate Requirements Education: Bachelor’s degree in Engineering, Computer Science, IT, Biotechnology, or a related field of study. Having a Master’s degree in Computer Science, Information Systems, or Biotechnology would be advantageous. Mandatory Skills, Knowledge, and Experience: 2–4 years of overall experience, with at least 1 year in business analysis, software development, or product owner role. Familiarity with Agile frameworks (Scrum, SAFe, or Kanban). Experience documenting requirements, crafting user stories, and working with engineering teams. Proficiency in using flow instruments such as flow cytometry machines, flow analyzers, and other relevant lab apparatus, along with a solid grasp of laboratory protocols. Ability to convert business needs into detailed specifications for scientific software solutions. Basic technical knowledge of software development (Java, Angular, AWS, Jenkins, or similar technologies preferred). Strong analytical and problem-solving skills with attention to detail. Superb communication skills—ability to articulate sophisticated workflows to technical and non-technical audiences. High degree of organization, initiative, and accountability. Collaborative approach and skill in partnering with geographically scattered teams. Nice to Have: Experience with Atlassian suite (JIRA, Confluence, Bitbucket, etc.). Exposure to SAFe or other scaled Agile environments. Completed certifications (e.g., CSM, CSPO, or equivalent). Experience defining or validating Non-Functional Requirements (performance, security, cost). Proficient in following QMS (ISO9001:2015) & ISMS (ISO 27001) guidelines. Prior experience in scientific data management, lab automation software, or connected instruments.

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 Senior Mechanical Engineer I is responsible for the design and re-design of certain Hardware components and the development of new products, on-market products and support manufacturing activities. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In This Role, You Will Have The Opportunity To 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 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.

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 Electrical Engineer I is responsible for designing, developing, troubleshooting modules for laboratory medical device new product development. The incumbent practices best design practices and follow quality processes defined during development. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In This Role, You Will Have The Opportunity To 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 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.

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 Lead Electrical Engineer I is responsible for designing, developing, troubleshooting modules for laboratory medical device new product development. The incumbent practices best design practices and follow quality processes defined during development. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In this role, you will have the opportunity to: Lead design and validation of high-density, multi-layer PCBs with analog/digital/mixed-signal circuits. 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. 7+ 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, OrCAD, PADS) and simulation software. Experience in product lifecycle management and documentation for regulatory submissions with excellent troubleshooting, communication, and team leadership skills. 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 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.

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 Senior Mechanical Engineer I is responsible for the design and re-design of certain Hardware components and the development of new products, on-market products and support manufacturing activities. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In this role, you will have the opportunity to: 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 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.

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 Electrical Engineer I is responsible for designing, developing, troubleshooting modules for laboratory medical device new product development. The incumbent practices best design practices and follow quality processes defined during development. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In this role, you will have the opportunity to: 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 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.

The University of Hong Kong Apply now Ref.: 533055 Work type: Full-time Department: School of Public Health (22400) Categories: Research Staff Hong Kong Applications are invited for appointment as Research Assistant I/II (several posts) in the HKU-Pasteur Research Pole of the School of Public Health (Ref: 533055) to commence as soon as possible for a one-year temporary term contract, with the possibility of renewal subject to satisfactory performance and funding availability. Applicants should have a Bachelor’s degree or above in Biomedical Sciences, Science, or related disciplines. They should demonstrate a good command of written and spoken English, self-motivation, and a strong sense of responsibility. Experience with animal experiments and flow cytometry will be considered advantageous. The appointees will assist with research projects focused on T cell immune responses following respiratory virus infections and vaccinations. Specific responsibilities include conducting animal experiments, processing blood samples, managing inventory and consumable orders, and performing other duties as assigned by the Principal Investigator. Shortlisted applicants will be invited to attend an interview. A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits. The University only accepts online applications for the above posts. Applicants should apply online and upload an up-to-date CV. Review of applications will commence as soon as possible and continue until December 31, 2025 , or until the posts are filled, whichever is earlier. Advertised: Sep 4, 2025 (HK Time) Applications close: Dec 31, 2025 (HK Time) Back to search results Apply now Whatsapp Facebook LinkedIn Email App

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 Lead Mechanical Engineer is responsible for designing, developing, troubleshooting Beckman Coulter Diagnostics modules and applying life cycle management principles and upholding established design practices and quality processes throughout development. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In this role, you will have the opportunity to: Lead and manage sustaining engineering activities for existing electro-mechanical products, including root cause analysis, corrective actions, and continuous improvement initiatives. Drive innovation by designing and developing mechanical solutions to enhance performance, safety, reliability, and cost-effectiveness. Own and maintain the prototyping infrastructure with adherence to 5S standards. Oversee prototype development internally or through suppliers, and executing testing, verification, and validation. Ensure thorough documentation including CAD models, drawings, specifications, and test plans. Collaborate with global cross functional teams to resolve manufacturing and field issues. Provide technical support to stakeholders, mentor junior engineers, and manage multiple projects with minimal guidance. Adapt quickly to changes in project direction and ensure successful project execution through feasibility studies, risk assessments, and design reviews. The essential requirements of the job include: Bachelor’s degree in mechanical engineering or a related field with 7-10 years of experience. Strong knowledge of mechanical design principles, materials, manufacturing processes, Rapid Prototyping and Proficiency in SolidWorks CAD software and simulation tools. Strong knowledge on lean principles, 5S, Kaizen and Proto build workshop management. Hands-on experience in building mechanical parts and assemblies using tools and machines. Skilled in teardown analysis, reverse engineering, and selection of off-the-shelf Electro-mechanical components. Thorough knowledge of vendor and supplier management for prototype builds, including managing quality and delivery timelines. Familiar with import/export processes documentation between India and other countries. Knowledge of should-costing, estimation, and dFMEA/pFMEA, DFX, Tolerance Stack-up Analysis and GD&T. Create and maintain detailed engineering documentation, including CAD models, drawings, specifications, test plans. Experience with medical device regulations (FDA, ISO 13485, ISO 14971, IEC 60601) and Ensure compliance with industry standards, regulations, and company policies. It would be a plus if you also possess previous experience in: Medical device design & development or IVD instrumentation, such as clinical chemistry, immunoassay, hematology, urinalysis, molecular microbiology or flow cytometry systems is a plus Electro-Mechanical products, Robotics and Automation 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.

Date: 14 Aug 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Discovery Services Designation: Team Lead: Cell Line Engineering Job Location: Bangalore Department: Discovery Biology About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines: Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self. Compliance to Syngene’ s quality standards at all times. Job Purpose Looking for a candidate with experience in mammalian cell culture. The candidate will be a part of the Cell Engineering team working on generating stable cell lines to be used as tools or for production purposes. He or she will be in a fast-paced work environment that offers a great opportunity to learn and grow. Key Responsibilities Generation of stable cell lines and Kock out and Knock-In to be used as tools or for production purposes Characterization of cell lines using techniques like flow cytometry, western and ELISA blotting etc. Experiment design and planning, conducting experiments, analysing and communicating results with the team and the clients (Presentation and email communication) Documentation of data and inventory maintenance for all audit purposes. Aware of all the documentation and data integrity policies. Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Attend training on environment, health, and safety (EHS) measures imparted company Educational Qualification Ph.D in Lifesciences relevant to cell line and clone development 1-8+ years of post-PhD experience in relevant field of Cell and Molecular biology (Industrial experience is Plus) CRO experience with client facing role is plus Technical/functional Skills Experience with stable cell line generation is necessary Experience with generation of lentivirus and/or retrovirus is necessary Experience with genome editing (CRISPR-Cas9 or others) is a plus Experience with generation of reporter cell lines is a plus Experience with fundamental molecular biology techniques and flow cytometry Experience with cell banks preparation and inventory maintenance Excellent attention to details, diligent documentation and efficient communication skills (Verbal and Written) Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Attend training on environment, health, and safety (EHS) measures imparted company. Behavioural Skills Good work ethics. Good interpersonal skills, and the ability to work effectively in a team environment. Ability to work with co‐workers professionally. General ability to thrive in a growing infrastructure and culture and think out of box approach when troubleshooting and problem solving. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, ational origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Overview We are seeking a highly skilled and motivated Laboratory Manager to oversee our clinical and research laboratory operations. The ideal candidate will possess extensive experience in laboratory management, ensuring compliance with quality assurance standards and regulatory requirements. This role requires strong leadership skills, a deep understanding of laboratory procedures, and the ability to manage a team effectively. The Laboratory Manager will play a crucial role in maintaining high standards of laboratory practices while supporting clinical trials and research initiatives. Responsibilities Oversee daily laboratory operations, ensuring compliance with safety and quality standards. Manage specimen collection, processing, and analysis, including blood sampling and venipuncture. Supervise laboratory staff, providing training and guidance on laboratory techniques and procedures. Implement quality control measures to ensure the accuracy and reliability of test results. Coordinate data management processes, including data collection, documentation, and analysis. Develop and maintain document management systems for laboratory protocols and procedures. Ensure compliance with regulatory requirements related to clinical trials and laboratory practices. Collaborate with clinical teams to support research initiatives and provide technical expertise. Maintain knowledge of current trends in laboratory technology and methodologies. Requirements Bachelor’s degree in a relevant field; advanced degree preferred. Proven experience in a clinical or research laboratory setting, with hands-on experience in ELISA, RNA extraction, DNA isolation, PCR, flow cytometry, immunoassays, and other laboratory techniques. Strong background in quality assurance (QA/QC) and compliance management. Experience with document management systems and laboratory information management systems (LIMS). Excellent leadership skills with prior supervising experience in a laboratory environment. Knowledge of medical terminology, anatomy, physiology, and vital signs is essential. Strong analytical skills with the ability to manage schedules effectively. Familiarity with phlebotomy techniques and aseptic practices is preferred. Ability to work collaboratively within a team while managing multiple priorities effectively. Join us as we strive for excellence in laboratory services while contributing to impactful clinical research! Job Type: Full-time Pay: ₹20,973.17 - ₹50,591.34 per month Work Location: In person