28 Flow Cytometry Jobs

Nirali Cancer Hospital is looking for Consultant Nuclear Medicine Physician to join our dynamic team and embark on a rewarding career journey Undertake short-term or long-term projects to address a variety of issues and needs Meet with management or appropriate staff to understand their requirements Use interviews, surveys etc. to collect necessary data Conduct situational and data analysis to identify and understand a problem or issue Present and explain findings to appropriate executives Provide advice or suggestions for improvement according to objectives Formulate plans to implement recommendations and overcome objections Arrange for or provide training to people affected by change Evaluate the situation periodically and make adjustments when needed Replenish knowledge of industry, products and field

This senior level position is based in the Centre for Cancer Immunology at Southampton General Hospital, which is a newly constructed, dedicated research building resulting from a significant fund-raising campaign. The center is the first dedicated cancer immunology center in the UK, building on Southampton's 40-year history of pioneering immunology and cancer research. It spans activities from pioneering discovery science to applied research, preclinical modeling, and first-in-human clinical trials. You will work within the laboratory of Professors Sally Ward and Raimund Ober, contributing to an interdisciplinary research program focused on developing novel antibody-based therapeutics using protein engineering. The group's research is funded by major grants from organizations such as the Wellcome Trust and Cancer Research UK. You will oversee in vitro and in vivo cellular assays, with a strong background in analyzing the behavior of antibody or other protein-based therapeutics. In addition to leading research projects, you will play a supervisory role, responsible for guiding junior technicians and training laboratory members in immunological and in vivo techniques. The position requires teamwork and collaboration within the laboratory, spanning molecular and cellular analyses to studies in mouse models of disease. To be successful in this role, you should have scientific knowledge equivalent to a Ph.D. level, with 2-3 years of additional experience. Relevant academic qualifications, proven leadership skills, and good IT proficiency are essential. Professional development and career advancement opportunities are available, with support for pursuing them actively encouraged. As part of the Ward/Ober laboratory, this position is a key long-term role, initially limited to a two-year term based on current grant support. Non-UK/non-EU citizens are encouraged to apply. For more information, informal enquiries can be directed to Professor E. Sally Ward at e.s.ward@soton.ac.uk. The University of Southampton fosters an inclusive, respectful, and equal opportunity environment, where staff are encouraged to bring their whole selves to work. The university offers generous holiday allowances, university closure days, and supports flexible working approaches. If interested, please apply online by the closing date, quoting the job number. For assistance, contact Recruitment at +44(0)2380 592750 or recruitment@soton.ac.uk.,

JOB DESCRIPTION • Completes all aspects of leukemia-lymphoma immune pheno typing, MRD panels (Blood/ Bone marrow) including sample preparation, staining, acquisition, and data analysis using established protocols • Demonstrates knowledge and application of theory and clinical relevance of Flow Cytometry with the ability to identify abnormal cell populations, understands general immune pheno typic results, and knows how to proceed in variant situations • Recognize and take appropriate action in response to critical or unexpected results and communicate effectively with Pathologists • Assists with the development, optimization, and validation of new tests as requested by the Flow Supervisor • Performs all duties at a high level of competency and actively participates in problem solving using advanced level of decision-making skills • Demonstrates knowledge and application of computer systems used in Flow Cytometry analysis • Determines the acceptability of specimens for testing according to established guidelines • Accurately performs cell counts and make dilutions to ensure optimal staining • Prepares reagent stock, antibody cocktails, and working solutions • Monitors proper use and consumption of reagents, materials and consumables • Assists in cleaning and maintenance of lab equipment • Prepares stains on peripheral blood smears, bone marrow aspirates (Wright Stain, iron, enzyme cyto chemistry) as needed. MINIMUM REQUIREMENTS • Bachelor of Science Degree in Medical Technology, Clinical Laboratory Science, or Chemical/Physical/Biological Science with a minimum experience in Hematology, Immunology, or Flow Cytometry • MD/ DNB Pathology trained & routinely reporting on Leukemia/ Lymphoma/ MRD panels (Blood/ Bone marrow) • Minimum 2-3 years of experience • Ability to demonstrate initiative and a team-oriented mindset • Excellent organizational skills and attention to detail

• In vivo animal model development and screening of test compounds in disease models • Planning and execution of in vivo and ex vivo research experiments in preclinical models Required Candidate profile Dosing by different routes of administration and collection of body fluids and tissu Understanding of molecular biology techniques: Flow Cytometry, Western Blot, qPCR, IHC and ELISA

Role Skills & Competencies Strong conceptual and technical expertise in drug discovery with proven track record through clinical candidates nominations, IND filings, publications, patents and presentations at symposia. Therapeutic area experience in Oncology and target validation using CRISPR, PROTACS , RIPTACS, ADCs and payloads Technical experience in cell based mechanistic and functional assays and using automation for high throughput assays. Strong knowledge and hands on experience with CRISPR based approaches for knock out and knock in is a must. Excellent verbal/written communication skills; communicates in a clear, well-structured and professional manner with key stakeholders on a regular basis Experience in managing larger teams (>20 people) and/or departments (including management of resource and budget with the ability to work closely with support functions such as HR, finance, quality/regulatory and facilities) Ability to manage multiple discovery projects and responsibilities at the same time. Experience in managing project teams regarding quality, timelines and cost. Effectively applies and enables state-of-the-art technologies and best practices to improve operational efficiency. Excellent attention to experimental details, data quality, documentation with strong work ethics Acts as a subject matter expert and mentor, providing scientific expertise to the collaboration and across disciplines & responsibilities Preferred candidate profile - Mandatory to have - Assay Biology (Crispr gene editing, shRNA, lentiviral transductions, viability assays, proliferation assays, molecular biology, QPCR, Western blotting, Flow cytometry, Mammalian cell culture, 3D cell culture, experience in IPSC and organoids is a plus). PHD with 10+ years and exp in managing team Educational Qualification PhD in Cell Biology/Biochemistry/ Biotechnology with Post doctoral experience and >10 years of relevant industry (CRO, Pharma or Biotech) experience in Assay Biology and screening platforms. Proven track record preferably in a contract research environment would be desirable.

Role & Responsibilities: Leadership and Management: Provide strategic and professional leadership for the Hematopathology section, including team management, service development, and resource allocation. Diagnostic Services: Interpret hematological specimens, including blood smears and bone marrow smears, to diagnose a wide range of hematological disorders and ensure all reports are released well within the defined turnaround time. Specialized Testing: Utilize microscopy skills and specialized testing, such as flow cytometry, to ensure accurate reporting of hematological malignancy samples in conjunction with other departments like Cytogenetics, Molecular Diagnostics, and Histopathology, wherever required. Clinical Discussion: Engage in proactive and detailed case discussions with clinicians, especially for hematological malignancy samples, to support accurate diagnosis and better patient management. Quality Control: Ensure accurate testing, validation, and timely release of reports. Implement and monitor quality control measures for all tests and equipment. Collaboration and Communication: Collaborate with clinicians, other pathologists, and laboratory staff to ensure comprehensive patient care. Education and Training: Participate in teaching activities for residents, fellows, and medical students, and contribute to continuing education for the team. Research: May be involved in research related to hematological disorders, including developing new diagnostic methods. Service Development: Contribute to the development and improvement of the Hematopathology service, including implementing new technologies and optimizing workflows. Preferred Candidate Profile: Medical Degree (MD or DO) with specialization in Pathology; board certification in Hematopathology is typically required. • Extensive experience in Clinical Hematopathology, including work with bone marrow, lymph node, and flow cytometry analysis. • Strong analytical and problem-solving skills with the ability to interpret complex data and make accurate diagnoses. • Excellent communication and interpersonal skills to effectively collaborate with colleagues and healthcare professionals. • Proven leadership and management skills to lead and motivate a team, manage resources, and drive service improvements.

JOB DESCRIPTION Designation: Associate Scientist / Senior Associate Scientist Job Location: Bangalore Department: TM-TDDT 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 (1-2 Lines) We are seeking motivated master s level scientists (MS, MTech, MSc, etc) to join the Translational Medicine team at the Biocon Bristol Myers Squibb Research Center in Bangalore, India. Key responsibilities of this role are to serve as an execution arm for the preclinical support of asset programs through mechanism of action-based studies, differentiation from standard of care and competitive therapeutics, combination rationale, new indications (life cycle management), and patient selection strategies. S/He will work directly with translational scientists, disease leaders within translational medicine, and will also interact with thematic research centers in early development within the company. Key Responsibilities: Conduct preclinical/laboratory experiments on late stage BMS portfolio compounds to support annual goals and objectives for Translational Medicine (for internal /external, collaborations, compound specific plans etc). Responsible for delivering data in support of translational strategies including biomarkers, patient selection hypotheses, dose and schedule, combination strategies, resistance mechanisms and differentiation. Interfaces with TM scientists across departments to ensure seamless flow of information for assets which are entering the remit of translational medicine. Assists in designing experiments and delivering data for collaborative projects along with TM scientists. Maintains comprehensive records, communicates regularly and makes presentations within the department, as required. Reports experimental finding in written nonclinical pharmacology study reports, to support regulatory filings. Educational Qualification: Masters with at least 2 years of relevant work experience across immunology, oncology, heme-oncology focus areas. Industry experience is a plus. Multiple positions can range upto 6 years of experience. Technical/functional Skills: Cell culture, primary cell isolation, cell transfection and single cell cloning; including siRNA / CRISPR / TALEN or HDR workflows Gene expression methods including qRT-PCR and/or familiarity with RNA sequencing, epigenomic methods including methylation analysis, ChIP etc Protein analyses and immunoassays, and cell phenotyping analysis (e.g. ELISA, MSD, Luminex, TSA, CBA, flow cytometry). Design, setup and execution of autoimmune, solid tumor oncology or heme-oncology in vivo pharmacology models. Excellent verbal and written communication skills, familiarity with standard or relevant software platforms, and scientific qualities are expected. Competence in analysis and solving of problems, keeping track of overall goals. Maintain a good understanding of the methodological basis and biological significance of assays performed. Forecast potential issues regarding support of assays for current and long term projects. Devise strategic solutions to identified and potential hurdles/issues and efficiently and proactively troubleshoot technical and experimental problems. Experience: 2-6 years Behavioral Skills: A self-starter, who is/can become technically proficient in a diverse set of techniques and assays with a focus on quality and speed, and will meticulously follow internal SOPs Good basic lab skills required (pipetting, balances, etc.) Highly detailed and meticulous, high standards of data entering and QC Must be highly adaptive to changing timelines and goals Must be comfortable taking on complex tasks with minimal direct supervision An excellent multitasker with an ability to be level-headed in a fast-paced lab setting Team-oriented and comfortable working in a highly dynamic matrix environment across multiple locations Prior experience working with patient samples (i.e. FFPE tissue, Fresh Frozen tissue, blood) or working in a CLIA/GCLP/clinical environment is a plus Must be comfortable and able to work with animal (rodent) or human derived samples Equal Opportunity Employer: .

Prayoga Lifesciences Inc is looking for Field Application Specialist Cellular Science / Flow Cytometry to join our dynamic team and embark on a rewarding career journey. Provide technical support and training for cellular science and flow cytometry products. Conduct product demonstrations and presentations. Collaborate with sales and marketing teams to achieve targets. Troubleshoot and resolve product issues. Maintain up - to - date knowledge of cellular science and flow cytometry technologies.

JOB DESCRIPTION Designation: Associate Scientist / Senior Associate Scientist Job Location: Bangalore Department: TM-TDDT 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 (1-2 Lines) We are seeking motivated master s level scientists (MS, MTech, MSc, etc) to join the Translational Medicine team at the Biocon Bristol Myers Squibb Research Center in Bangalore, India. Key responsibilities of this role are to serve as an execution arm for the preclinical support of asset programs through mechanism of action-based studies, differentiation from standard of care and competitive therapeutics, combination rationale, new indications (life cycle management), and patient selection strategies. S/He will work directly with translational scientists, disease leaders within translational medicine, and will also interact with thematic research centers in early development within the company. Key Responsibilities: Conduct preclinical/laboratory experiments on late stage BMS portfolio compounds to support annual goals and objectives for Translational Medicine (for internal /external, collaborations, compound specific plans etc). Responsible for delivering data in support of translational strategies including biomarkers, patient selection hypotheses, dose and schedule, combination strategies, resistance mechanisms and differentiation. Interfaces with TM scientists across departments to ensure seamless flow of information for assets which are entering the remit of translational medicine. Assists in designing experiments and delivering data for collaborative projects along with TM scientists. Maintains comprehensive records, communicates regularly and makes presentations within the department, as required. Reports experimental finding in written nonclinical pharmacology study reports, to support regulatory filings. Educational Qualification: Masters with at least 2 years of relevant work experience across immunology, oncology, heme-oncology focus areas. Industry experience is a plus. Multiple positions can range upto 6 years of experience. Technical/functional Skills: Cell culture, primary cell isolation, cell transfection and single cell cloning; including siRNA / CRISPR / TALEN or HDR workflows Gene expression methods including qRT-PCR and/or familiarity with RNA sequencing, epigenomic methods including methylation analysis, ChIP etc Protein analyses and immunoassays, and cell phenotyping analysis (e. g. ELISA, MSD, Luminex, TSA, CBA, flow cytometry). Design, setup and execution of autoimmune, solid tumor oncology or heme-oncology in vivo pharmacology models. Excellent verbal and written communication skills, familiarity with standard or relevant software platforms, and scientific qualities are expected. Competence in analysis and solving of problems, keeping track of overall goals. Maintain a good understanding of the methodological basis and biological significance of assays performed. Forecast potential issues regarding support of assays for current and long term projects. Devise strategic solutions to identified and potential hurdles/issues and efficiently and proactively troubleshoot technical and experimental problems. Experience: 2-6 years Behavioral Skills: A self-starter, who is/can become technically proficient in a diverse set of techniques and assays with a focus on quality and speed, and will meticulously follow internal SOPs Good basic lab skills required (pipetting, balances, etc. ) Highly detailed and meticulous, high standards of data entering and QC Must be highly adaptive to changing timelines and goals Must be comfortable taking on complex tasks with minimal direct supervision An excellent multitasker with an ability to be level-headed in a fast-paced lab setting Team-oriented and comfortable working in a highly dynamic matrix environment across multiple locations Prior experience working with patient samples (i. e. FFPE tissue, Fresh Frozen tissue, blood) or working in a CLIA/GCLP/clinical environment is a plus Must be comfortable and able to work with animal (rodent) or human derived samples Equal Opportunity Employer: .

About the job Our Hubs are a crucial part of how we innovate, improving performance across Sanofi departments and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As a Senior Biomarker Biostatistician within our Statistics Team at Hyderabad , you will play a crucial role in developing and implementing different statistical and machine learning algorithms to solve complex problems and support our clinical biomarker data insights generation. You will work closely with cross-functional teams to ensure data is accessible, reliable, and optimized for analysis. Your expertise in omics data, machine learning and deep learning will be essential in driving our data initiatives forward. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people s lives. We re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? Main responsibilities: Provide high quality input regarding TM/Biomarker aspects into the design of the clinical study (including protocol development), the setup of the study to make sure biomarker data are adequately captured and collected to answer the study objectives and to support the planned statistical analyses under guidance of project biomarker statistical lead. Coordinate the activities of external partners and CROs for biomarker data generation, dataflow or biomarker statistical activities Perform pre-processing and normalization of biomarker data (e.g., RNAseq, scRNAseq, Olink, flow cytometry data etc.) Perform and/or coordinate with the programming team the production of the definitions, documentation and review of derived variables, as well as the quality control plan. Perform and/or coordinate with study programmer the production of biomarker statistical analyses. Review and examine statistical data distributions/properties. Oversee execution of the statistical analyses according to the SAP, prepare statistical methods & provide statistical insight into interpretation and discussion of results sections for the clinical study report (CSR) and/or publications to ensure the statistical integrity of the content according to internal standards and regulatory guidelines and in compliance with SOPs. Propose, prepare and perform exploratory biomarker data analyses, ad-hoc analyses as relevant for the study, project objectives or publication. About you Experience : 2+ years (Master) or 1+ years (PhD) of pharmaceutical or related industry experience Soft and technical skills : o Basic knowledge of pharmaceutical clinical development o Good knowledge and good understanding of key statistical concepts and techniques, in particular high-dimensional statistics o Good knowledge in handling complex biomarker data (e.g., RNAseq, scRNAseq, Olink, flow cytometry data etc.)), knowledge in pathway level and network analyses is a plus. o Able to work in departmental computing environment, do advanced statistical analyses using R&R-Shiny and possibly other languages (python, C++, ) o Demonstrated interpersonal and communication skills and able to work in cross functional and global team setting Education : Master s or Ph.D. in Data Science, Bioinformatics, Statistics, or a related field. Soft and technical skills :

Scope of TSM: Ensure achievement of sales objectives in line with the Company's mission. Control, organize and involve in direct sales activities for premium analytical, proteomics and flow cytometry brands through both strategic and planned activities. The role will involve 60-70% travel for territory coverage. Job Responsibilities: Cover the target customers with effective product promotion & achieve assigned sales target. Generate new business opportunities through effective territory and KOL management. Taking responsibility for accurate forecasting, maintain lead, and up to date opportunity information on CRM database. Remain up to date with technology, new projects, market development and competitors offering. AR management for smooth business operations. Qualification and Experience required: B.sc/B.Tech/M.Tech/M.Sc in Molecular Biology/Biotechnology/Life Sciences with minimum 4-5 years of sales experience. Good knowledge and previous working experience in Life Sciences and Analytical/Flow Cytometry-Proteomics market is mandatory. Capital Instruments Sales experience is preferred. Previous work experience in Biopharma and Pharmaceutical markets with good KOL connect is preferred.

R&D (Synthesis) -Agrochemical Industry-Saykha,Gujarat. Industry Engineering Engineering Design R&D Quality Qualification M.Sc Key Skills R&D Synthesis R&D R&D Chemist Research & Development Executive UPLC HPLC GC R & D Chemical Agro We are looking for a skilled professional with 4 to 10 years of experience in R&D synthesis to join our team. The ideal candidate will have a strong background in research and development, particularly in synthesis. Roles and Responsibility Develop and implement new methods for synthesizing complex molecules. Collaborate with cross-functional teams to design and optimize experiments. Conduct literature reviews to stay updated on the latest developments in R&D synthesis. Design and execute experiments to test hypotheses and validate results. Analyze data and interpret results to inform future experiments. Maintain accurate records of experiments, results, and procedures. Job Requirements Strong understanding of chemical principles and laboratory techniques. Experience with R&D software and equipment. Excellent problem-solving skills and attention to detail. Ability to work independently and as part of a team. Strong communication and interpersonal skills. Familiarity with safety protocols and regulations.

Industry Pharma R&D Biotech Qualification M.Sc Key Skills Green Field Projects UPLC R&D R&D Chemist R&D Synthesis Brownfield M.Sc Chemistry Pharma Research Chemist We are looking for a skilled R&D (Synthesis) Professional with 4 to 10 years of experience to join our team in the Employment Firms/Recruitment Services Firms industry. The ideal candidate will have a strong background in research and development, particularly in synthesis. Roles and Responsibility Develop and implement new methods for synthesizing complex molecules. Collaborate with cross-functional teams to design and optimize experiments. Conduct literature reviews and analyze data to identify trends and areas for improvement. Design and execute experiments to test hypotheses and validate results. Analyze and interpret data to draw meaningful conclusions. Stay up-to-date with industry developments and advancements in chemistry. Job Requirements Master's degree in Chemistry or related field. Minimum 4 years of experience in R&D, preferably in synthesis. Strong knowledge of chemical principles and laboratory techniques. Excellent analytical and problem-solving skills. Ability to work independently and as part of a team. Effective communication and interpersonal skills. Experience working with employment firms/recruitment services firms is preferred.

We have an urgent opening for one of the BIG MNC for Territory sales manager - Hyderabad / Bangalore Please Note: This will be ON site job only interested people anywhere from India who's willing to relocate can apply. We are currently seeking a Territory Sales Manager Biopharma who will be responsible for handling Biopharma Account Sales responsibilities of Karnataka and Tamilnadu region . The incumbent shall be responsible for growth and expansion of direct sales and profit margins within assigned accounts and/or territory/region on products or services. Establishes professional relationships with key personnel in customer accounts. Meets assigned targets for profitable sales volume and margin dollars. In this role, you will be responsible for: Reporting to Business Manager Biopharma Sales and Business Development: Actively promoting and selling flow cytometry, centrifugation and automation products to biopharma customers in the assigned territory. Relationship Management: Building and maintaining strong relationships with key customers, opinion leaders, and key stakeholders in Biopharma accounts in the assigned region. Providing excellent customer service and addressing customer queries and concerns. Product Demonstrations and Training: Conducting product demonstrations and training sessions for customers to showcase the features, benefits, and applications of BECLS portfolio of instruments and reagents. Sales Forecasting and Reporting: Monitoring and analyzing sales performance and market trends in the assigned territory. Generating accurate sales forecasts and reports to track progress and identify areas for improvement. Collaboration: Collaborating with cross-functional teams, including marketing, technical support, and customer service, to ensure seamless customer experience and successful implementation of sales strategies. The required qualifications for the job include: MSc/MTech/ in Biological Sciences /Biotechnology 10 years work experience in sales at Biopharma & Life sciences vendor companies Experience in Sales of equipment and consumables in Biopharma accounts Key Account Identification/New lead generation & Customer Presentations Competitive Market analysis & preparation of competitive documents. Interested candidates can revert with their updated resume on below mentioned email id or else can contact me on - 8850029601 pdhotre@allegisglobalsolutions.com

- Responsible for maintaining and improving the overall pre-analytical, analytical and postanalytical operations within the laboratory. - Responsible for the implementation of the Quality Management System and Quality Policy within the laboratory. - Accountable to ensure that sufficient resources are available to provide medical laboratory services, that meets the end requirements of the users. - Implementation of a safe laboratory environment in compliance with good practice and applicable requirements. - To ensure the provision of clinical advice with respect to the choice of examinations, use of the service and interpretation of examination results. - Selection and monitoring of referral laboratories and monitoring the quality of their service. - Addressing complaints, requests and suggestions from the staff/ users of laboratory service (s). - Designing and implementation of a contingency plan to ensure essential services are available during emergency situations. - Responsible for liaison with external parties such as certification bodies and consultants. - Authorized to issue, review and amend the Quality Manual. - Authorized to release patient reports and issue amended reports. - To handle patient & doctor queries for the report released ensuring they resolved smoothly Location-Bengaluru,Pune,Chennai,Coimbatore

#hiring . Know anyone who might be interested? "Bengaluru Location" Veeda Lifesciences is seeking a passionate "SPR Specialist". Experience Required: 3 to 6 Years Education Required: B pharma and M pharma Drop your CV to: mahendra.t3705@veedalifesciences.com Role & responsibilities Surface Plasmon Resonance (SPR) based studies for Drug substances and Drug products that include therapeutic peptides, therapeutic monoclonal antibodies and other therapeutic large molecules. Design and execute project experiments. Demonstrate acceptable technical/scientific skills. Adequate knowledge in various immobilization chemistries. Analyze and report the observations and conclusions. Provide rationale or hypothesis for the observations and conclusions. Work in a regulated environment and record laboratory data as per the SOPs, standards and ALCOA++ principles. Prepare or review SOPs with guidance, as required. Participate in routine lab related activities. Develop new SPR capabilities. Experience in any of the following assays will be an added advantage. Cell based flow cytometry assays Flow cytometry based immunophenotyping Flowcytometry or multiplex based cytokine analysis ADCC, ADCP and CDC assays

Additionally, industry experience in the above skills will be preferred. Responsibilities Designing and executing a multitude of in vitro experiments in cell biology/ mammalian cell culture and evaluation by fluorescence (confocal) imaging, flow cytometry, styding knockdown assays by RT qPCR and western blot, ELISA and other cell based assays Establishing and executing various mammalian cell-based viability and potency assays, using reporter cell lines, primary cells, or transformed mammalian cell lines Preparing solutions and culture media Maintenance of multiple cell lines Isolating cells, proteins, particles, or analytes from experimental tissues or cell cultures Collect, analyse and present experimental data Maintain clear and complete experiment records on a daily basis Drafting/ revising protocols and standard operating procedures (SOPs) Ability to work well within the team and communicate effectively Read relevant literature Support and foster a safe and efficient working environment within the Laboratory and ensure the safety of colleagues and visitors and adhere to all health and safety guidelines. Standard lab management and routine maintenance and troubleshooting of scientific equipment. Any other task as and when required by company Adherence to company policies and instructions Laboratory Management Support and foster a safe and efficient working environment within the Laboratory and ensure the safety of colleagues and visitors and adhere to all health and safety guidelines Identifying and sourcing equipment and consumables (ordering and stocking) necessary Routine maintenance and troubleshooting of scientific equipment Carry out administrative work associated with the program of research as necessary Performs any additional tasks or projects as required {Position title will be senior research associate during probation period of three months if you are a fresh PhD. After confirmation of probation, it will be Research Scientist I (RS 2)} Money Competitive compensation commensurate with the person s experience and qualifications. Qualification PhD in Biotechnology/ cell biology/ molecular biology/ biochemistry MSc/ MTech degree in biotechnology/ life science/ biochemistry/ biology with 4 - 5 years of strong expertise in cell biology/ western blot/ RT qPCR/ mammalian cell culture and fluorescence (confocal) imaging, flow cytometry, ELISA and other cell based assays. STRONG UNDERSTANDING and SKILLS in cell culture, fluorescence imaging and RTqPCR STRONG sense of RESPONSIBILITY, ETHICS, INTEGRITY and COMMITMENT to the project Experience Experience with molecular and cell biology techniques including mammalian cell (including stem cell and primary cells) culture, DNA and RNA isolation, RT-qPCR, various cell based assays, ELISA, flow cytometry, confocal microscopy and western blot is must Collaborative, openness, can do attitude, proactive, ownership mindset Result oriented, organized, delivering progress toward our mission Demonstrated respectful attitude towards organization structure, culture and values for maintaining peaceful and motivated environment Track record of strong problem solving and troubleshooting skills, organized, ability to prioritize responsibilities, and remain flexible with changing needs Must be motivated and able to work under strict deadlines Strong written and oral communication skills Proficiencies in MS Office and relevant software

Job Description Relevant biosimilar experience from reputed biosimilar companies with Experience of development of cell-based assays, ELISA and Experience working on flow cytometry-based assays (preferable). Capable of designing experiment with minimal supervision and having experience with development of functional bioassays to evaluate different mechanism of action. Experience of analyzing data using different software s like PLA (equivalence testing), GraphPad Prism, Minitab etc. Development of ELISAs and other characterization bioassays for biosimilars with application of novel technical concepts. Good understanding of assay kinetics and mode of action of receptor biology and Mabs Bioassay Method qualification/validation and transfer to Quality Control with good troubleshooting and documentation skills. Writing protocols and reports, participation in scientific discussions, ability to work in a team. Knowledge of ICH and other regulatory guidelines is preferred. Work Experience 2-5 years of experience Education Masters in Biotechnology or Biochemistry Post Graduation in Biochemistry or Biotechnology Competencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility

Hello Candidate, We are #hiring for Project Research Scientist-I (Non-Medical) ! Government Project Payroll company: - E Solutions Job role: - Project Research Scientist-I (Non-Medical) ! Essential Qualifications: 1st Class Post Graduate (PG) Degree, including the integrated PG Degree in Biotechnology/Life Sciences/Applied Biology/Life Sciences OR Second Class Post Graduate degree including the integrated PG degrees in Sciences with Ph.D. in Biotechnology/Life Sciences/Applied Biology Desired Qualification 1. Experience in Molecular Biology techniques and ELISA. 2. Experience in working with flow cytometry.. 3. Experience of working in Lab Diagnosis of IEI 4. Knowledge of project related documentation and maintenance of records 5. Knowledge of computer application and data management. 6. Candidate must be willing to travel between the collaborating centre for training/standardisation/work related to the project. Name of the Project: Understanding Immune defects in Pediatric non-cystic bronchiectasis and recurrent pneumonia cases: A multicentric study." Location:- Parel, Mumbai No. of Vacancy :- 01 Age Limit: The upper age limit is 35 years. If you are interested, Kindly share your updated CV on this Email I'd :- anchal.g@esolglobal.com

Technical/functional skills: 1. Development, performance and troubleshooting of cell-based assays development, qualification and sample analysis for therapeutic protein, monoclonal antibodies. 2. Development, performance and troubleshooting of SPR, ELISA and flow cytometry assays for monoclonal antibodies. 3. Preparation of technical documents. 4. Writing of SOP, Protocol and Reports. Key responsibilities : 1. Cell based assays development, qualification and sample analysis for therapeutic proteins, monoclonal antibodies. 2. To take charge of the equipment/instruments in the lab and ensure their proper functioning. 3. To support and maintain inventory of reagents & consumables required for general lab activities.

Bhagwan Mahaveer Cancer Hospital & Research Centre is looking for Senior Resident Radiation Oncology to join our dynamic team and embark on a rewarding career journey. Patient Care: Provide comprehensive medical care to patients under the supervision of attending physicians Perform physical examinations, diagnose medical conditions, develop treatment plans, and monitor patient progress Clinical Supervision: Supervise and provide guidance to junior residents, interns, and medical students in their clinical duties Assist in their training, evaluation, and professional development Hospital Rounds: Conduct regular hospital rounds to assess patients, review test results, and discuss treatment plans with the healthcare team Coordinate and communicate patient care plans with nurses, specialists, and other healthcare professionals Medical Procedures: Perform or assist in various medical procedures, such as venipuncture, wound care, suturing, and bedside procedures Ensure adherence to sterile techniques, safety protocols, and best practices Medical Documentation: Maintain accurate and up-to-date medical records, including patient history, physical examination findings, treatment plans, and progress notes Ensure compliance with legal and regulatory requirements Patient Education: Educate patients and their families about their medical conditions, treatment options, and preventive measures Provide counseling on lifestyle modifications, medication management, and post-discharge care instructions Interdisciplinary Collaboration: Collaborate with other healthcare professionals, including nurses, pharmacists, therapists, and social workers, to ensure coordinated and holistic patient care Participate in interdisciplinary team meetings and contribute to care planning Continuity of Care: Facilitate smooth transitions of care between inpatient and outpatient settings Coordinate follow-up appointments, referrals, and discharge planning to ensure continuity of care and optimal patient outcomes Medical Research and Education: Stay updated with the latest medical advancements, evidence-based practices, and clinical guidelines Engage in research activities, present at conferences, and contribute to medical education and scholarly activities Quality Improvement: Participate in quality improvement initiatives to enhance patient safety, clinical outcomes, and healthcare delivery Identify areas for improvement, implement evidence-based practices, and contribute to quality assurance programs Professional Development: Engage in continuing medical education (CME) activities, attend conferences, and pursue opportunities for professional growth Maintain licensure and board certification requirements

Responsible for developing the cell based assays and conduct routine screening. Expert knowledge/skill sets in cell culture, biochemical and cell based assays, animal tissue samples. Analytical techniques : Cell culture, ELISA, flow-cytometry, Confocal microscopy, animal Industry - Pharma / Biotech / Clinical Research Functional Area - RD, Pharmaceuticals, Biotechnology Role Category - Research Scientist Desired Profile PG - M.Sc - Bio-Chemistry, Microbiology, M.Tech - Bio-Chemistry / Bio- Technology.

Immunology innate immune mechanisms in disease pathogenesis Metabolomics, particularly in the context of aging and metabolic disorders Organoid-Based Cell and Developmental Biology Genomics Informatics Lipid Trafficking Department hosts state-of-the-art research facilities in genomics, mass spectrometry, drug screening, flow cytometry, Drosophila biology, protein expression and characterization, in vivo & in vitro biosafety laboratories and an advanced imaging facility. Additionally, they are home to two major research centers: the Center for Integrative and Translational Research, which support preclinical models of health and disease and the Center of Excellence in Epigenetics. These are further strengthened by university-wide initiatives such as the SNU-Dassault Systems Center that facilitates computational biology studies. Selected candidates will be expected to establish and maintain an independent, externally funded research program, actively engage in undergraduate and graduate teaching, and contribute to the development of interdisciplinary courses and initiatives in collaboration with other departments across the university. Qualification Faculty appointments are open at all levels from Assistant to Full Professor based on the candidate s qualifications, experience, and alignment with the department s strategic vision. Applicants must hold a Ph.D. in the Sciences and have completed a productive postdoctoral tenure that clearly demonstrates strong potential for an internationally recognized and impactful research career.

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 Technician 1 - Innovation and Custom Design is responsible for supporting improvement, implementing and maintaining manufacturing methods, techniques, processes. 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 on the design and manufacturing requirements. Preparing guiding documents for manufacturing 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 in Biochemistry/ Biotechnology with 1 or 2-years experience and/or Masters in Biochemistry/ Biotechnology with 0 - 2 years experience. Understanding of Flow cytometry It would be a plus if you also possess previous experience in: Flow cytometry testing - Single color and multi color

Establish, maintain, and scale mammalian cell lines including adherent and suspension cultures under sterile conditions.Perform routine cell-based assays such as viability, proliferation, cytotoxicity, reporter assays, and high-content imaging.