56 Elisa Jobs - Page 2

Title of project: Development of lateral flow based rapid immunochromatographic point-of-care assays for diagnosis of viral diseases of public health importance (Component B) Name of the Positions :- Project Technical Support III. No. of vacancy :- 01 Consolidated Salary :- 28,000/- + HRA Essential Qualification: - Three Years Graduate in relevnt subject /field + Three Years post qualification experience or Post Graduate in relevnt subject /field. Desirable :- 1. B.Sc./M.Sc. Microbiology / Biotechnology/Virology 2. Work experience in diagnostic laboratory/Cell Culture/ ELISA / PCR / sequencing. 3. Knowledge of computer application/report preparation. Age Limit :- 35 Interested Candidates can share their cv on this mail id anushka.y@esolglobal.com

The incumbent is responsible for selling to new channel partners/distributors and cross/up/repeat sales to existing channel partners/distributors. Maintain existing relationships with organizations distributing products, services and/or solutions. Deliver product demonstrations, sales bids and presentations to channel partners/distributors. Manage the relationship with the channel partners/distributors. What were looking for Education: Science Graduates or Postgraduates / MBA are preferred. Experience: Minimum of 8+ years of IVD sales experience required How you will thrive and create an impact Develops and executes territory plan to achieve revenue targets and control expenses. Works with channel partners where appropriate to drive specific opportunities. Establishes high-level customer and distributor relationship/intimacy by way of technical and business skills/competencies and situational fluency. Understands current customer processes and applications and communicates customer technology product requirements to internal stakeholders. Utilizes a variety of communication and engagement methodologies including quarterly business reviews, executive meetings and technical collaborations; ensures they meet the targeted number of face to face key account interactions per week. Demonstrates effective employee relationships built on trust, teamwork and accountability. Performs other duties as assigned with or without accommodation. Regards, Vimal Sharma Email ID: vimal.sharma@avantorsciences.com

Educational Qualifications:- First class Masters Degree in Life Science: specialization-Microbiology/Biotechnology Virology/Bioinformatics OR Second class Masters Degree in above subject with Ph.D. Desirable Qualifications:- Prior experience of working in disease diagnosis using molecular (PCR, RT-qPCR, DNA sequencing, sequence data analysis) and immunological assays (ELISA, Immunofluorescence, neutralization) and animal cell culture will be preferred. In addition, candidates with experience of patients clinical data collection, documentation and analysis using different softwares are desirable. Prior experience working in virology laboratory will be preferred. Position:- Project Scientist I

(1) In charge of independent territory with own set target. (2) Has to visit Diabetologists, KOLs , Hospital's ,Corporate OHC's, Labs, etc. (3) Handle HPLC systems, Urine Analyzers, Fully Automated Biochemistry Analyzers and Hematology Analyzers. 4) New business development & maintenance of existing accounts

Job Responsibilities: A) Project Management Undertake on-going referencing and literature reviews and provide strategic inputs to projects at all stages Evaluate methods under consideration by conducting literature survey (incl. regulatory guidelines, pharmacopeia guidelines, publicly available research, etc.) Identify initial cell-lines/ anti-body requirement based on method(s) identified Conduct lab experiments for bio-assay/ immuno-assay development and optimization Conduct lab experiments to qualify the method for reproducibility Prepare/provide inputs for the preparation of necessary documents like Method development report, Method qualification protocol and report. Method validation protocol and report, Standard Analytical Procedures (SAP), Method transfer protocol and report. Ensure tech-transfer by demonstrating process to plant operators (in lab premises) Observe process in plant and resolve any queries that may arise (post-transfer) B) Bio-assay/Impurity assay (HCP and HCDNA) /Binding ELISA assay/SPR assay/BET Method development, qualification and transfer Conduct regular analysis for non-GMP and non- release batches (not transferred to plant) - support other labs by stability testing samples provided by them Prepare and share detailed reports with the relevant labs upon completion of the tests Conduct Bioassay, HCP, HCDNA, Protein A ELISA, SPR, Binding assay and BET method development/qualification and routine analysis (C) Other tests and routine processes Conduct / guide RAs for conduct of regular analysis for non-GMP and non-release batches (not transferred to plant) - Support other labs by stability testing samples provided by them tests as requested. Prepare/review and share detailed reports with the relevant labs upon completion of the tests Conduct/ guide RAs for conduct of method development/qualification and routine analysis Review protocols and reports provided by CRO (based on expertise) Coordinate CRO with ADA assays, Antibody generation, purification and biotinylating activity for in-house HCP method. (D) Materials and equipment management Procure and maintain inventory of cell-lines/anti-bodies/ consumables/ equipment: Share details of requirements with purchase team Engage in technical discussions with vendors to identify and recommend suitable ones to lab head and Supply Chain Raise PR for purchase Oversee Check materials upon receipt and store them as per set-norms (freeze in case of cell-lines) Track and maintain inventory in order to control and manage short-falls and damage Maintain inventory-logs and intimate superiors in case of short-falls and damage Manage cell-culturing and sub-culturing process: Prepare cell-banks (by freezing cell-lines) for storage Passage cells (remove vials from these banks) as per testing need Calibrate select lab-equipment on regular basis to facilitate use Ensure scheduled and break-down maintenance by coordinating with vendors/ maintenance team ( E) Regulatory and compliance Accurately capture all lab experiments in raw- data and lab-notebooks (incl. electronic data- capture) in real-time on an on-going basis. Adhere to regulatory, SOPs and safety guidelines for all processes. Ensure timely closure of regulatory queries by conducting and documenting lab experiments. Ensure data integrity in all respects Compile and Review all project-related documents created during lab activity on a regular basis Prepare/ modify SOPs by gauging work ability of the processes/practices in timely manner (F ) Business (people & budgets) planning, continuity and improvement Conduct SOP and induction trainings for subordinates Provide timely and relevant inputs for the preparation of capex budget Identify and implement continuous improvement initiatives to enhance process efficiency Take initiative to provide time and inputs (based on expertise/interest) to other on-going projects (G) Learning and improvement Attend all mandatory trainings Take initiative to provide inputs (based on expertise/interest) to other on-going projects Take initiatives for self-development and update self on recent developments in own area of work Take initiative to train fresh RAs upon induction or guide them with select lab processes (basis expertise) (F) Quality Compliance Initiate change control for New instrument IQ/OQ/PQ/CSV of new instrument. GDP Compliance Compliance related to internal and external audits

1. Essential Qualifications:- (a) First Class Post Graduate Degree, including the integrated PG degrees in Microbiology / Veterinary Sciences/ Immunology/ Biotechnology with 3 years experience or PhD. (b) Second Class Post Graduate Degree, including the integrated PG degrees, with PhD in Microbiology/ Veterinary Sciences / Immunology / Biotechnology and 3 years experience 2. Desirables:- (a) Experience in laboratory animal experimentation (b) preclinical animal studies. (c) Experience in flow cytometry techniques (d) Immunophenotyping, ELISPOT. (e) Work experience in BSL-3 laboratories Position:- Research Scientist II [Non- Medical]

Role & responsibilities The Product & Revenue Growth Specialist plays a vital role in combining scientific product knowledge with customer engagement, distributor coordination, sales team collaboration, and revenue growth initiatives . Operating primarily from the corporate office with limited field travel (57 days per month) , this position focuses on enhancing customer relationships , driving market expansion , managing key accounts , and supporting distributors to increase product adoption and revenue generation . This role is part of Immunoshop’s Unified Sales Framework , ensuring a balance between scientific communication, lead conversion, account management, and data-driven revenue strategies . The ideal candidate will have a strong scientific background with a passion for engaging with Diagnostic Lab professionals, distributors, and internal teams to promote Immunoshop’s IVD products . Key Responsibilities: Scientific Customer Engagement – Engage with laboratory professionals and key stakeholders to deliver scientific insights and technical information about Immunoshop’s IVD products. – Conduct discussions emphasizing scientific advantages, product benefits, and comparative analysis to promote product adoption. – Provide scientific support during the sales process, addressing technical queries and customer concerns. Lead Management & Conversion: – Manage and monitor lead pipelines through CRM, ensuring timely follow-ups and effective conversion strategies. – Work on leads generated by the sales team and marketing initiatives , providing scientific validation and conversion support. – Collaborate closely with the sales team to prioritize high-potential leads and assist in closing deals. Account & Distributor Management: – Build and maintain strong relationships with key accounts and distributors to ensure customer satisfaction and business growth. – Identify upselling and cross-selling opportunities by understanding customer needs and product applications. – Coordinate with distributors to secure repeat orders and improve product reach in target markets. – Support distributors with scientific product knowledge to enhance customer interactions and sales effectiveness. Service Coordination & Customer Support: – Coordinate with SCM, customers, and distributors regarding order processing, payment follow-ups, and order status updates. – Collaborate with the service team to address product-related service issues, ensuring quick resolutions and customer satisfaction. – Act as a central point of contact between sales, service, and customers for seamless communication and issue resolution. Preferred candidate profile Perks and benefits

Install, calibrate, and maintain IVD instruments Diagnose and resolve technical issues promptly Train customers on equipment usage and care Maintain accurate service records and reports Adhere to safety standards and travel as required

Job Vacancy: Lab Technician (Protein Biochemist) Location: Hyderabad (CDFD, or AIC-CCMB) Type: Full-time Company: ANLISA Biotech Anticipated start-date: April-June 2025 Are you passionate about protein biochemistry and eager to make a significant impact in a dynamic startup environment? We are seeking a talented and motivated Lab Technician in Protein Biochemistry to join our startup team to pioneer an attomolar-ultrasensitive (single-cell-resolution) immunoassay technology for high-throughput detection of molecular biomarkers. If you have hands-on experience in protein purification and a strong foundation in protein biochemistry, wed love to hear from you! Key Responsibilities: Prepare and optimize buffers Handle sensitive proteins (SDS page, Bradford method, Dialyse) Prepare and autoclave bacterial media and buffers Maintain lab inventory and equipment. Document experimental results, prepare technical reports, and contribute to scientific patents/publications. Qualifications: MSc in Biochemistry (preferred) or BSc (with 5-10 years research/industry experience in protein purification). Hands-on experience with analytical techniques such as SDS-PAGE, ELISA and spectrofluorometry. Ability to work in a fast-paced, collaborative startup environment. Excellent lab-management, communication, and problem-solving skills. What We Offer: The opportunity to be part of an innovative team developing a revolutionary molecular detection and quantification technology. A collaborative and supportive work culture. Competitive salary and performance bonus. Employee stock options Professional growth and learning opportunities. If you are driven by scientific curiosity and eager to contribute to breakthrough discoveries, we invite you to apply. Join us in building a company that makes a difference in science and beyond! About ANLISA Biotech ANLISA Biotech is a startup company based in Hyderabad, pioneering a breakthrough immunoassay technology for high-throughput detection of macromolecular targets at ultralow concentrations. It has patented a unique biochemical invention based on the principles of nanothermodynamics of actin polymerization to detect and quantify molecular targets at ultralow concentrations that were hitherto impossible to analyse through conventional immunoassay approaches. To Apply: Please email Dr. Balendu Avvaru (balendu.avvaru@gmail.com) with CV and describe your previous experience as a lab technician

The Biotech Laboratory Specialist will ensure that all activities within the department align with current Good Manufacturing Practices (cGMP) and current Good Laboratory Practices (cGLP). This role is critical for managing and performing a range of laboratory techniques, including PCR, ELISA, Capillary Electrophoresis, Isoelectric Focusing, Western Blotting, and Flow Cytometry. The specialist will also be responsible for preparing and executing method validation protocols and reviewing routine analysis reports. Experience with Quality Management Systems (QMS), particularly LIMS and EQMS, is essential. Key Responsibilities: Laboratory Techniques: Perform Polymerase Chain Reaction (PCR) assays for molecular analysis. Conduct Enzyme-Linked Immunosorbent Assay (ELISA) tests for biochemical assays. Operate and maintain Capillary Electrophoresis and Isoelectric Focusing systems. Execute Western Blotting and Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE) techniques for protein analysis. Perform Flow Cytometry for cell analysis and sorting. Conduct other biochemical and molecular biology tests as required. Method Validation: Develop and prepare method validation protocols to meet regulatory and internal standards. Execute validation procedures in accordance with regulatory guidelines and company practices. Accurately document and report validation results in a timely and comprehensive manner. Report Review: Review routine analysis reports to ensure accuracy, compliance with quality standards, and adherence to regulatory requirements. Identify and investigate any discrepancies or deviations in data, ensuring proper corrective actions are taken. Quality Management Systems: Maintain and manage Laboratory Information Management Systems (LIMS) for effective sample tracking and data management. Support and contribute to the Electronic Quality Management Systems (EQMS) to enhance and maintain laboratory quality processes. Ensure compliance with internal quality standards and regulatory guidelines at all times. Experience & Qualifications: Experience: 4-5 years of hands-on laboratory experience in a biotech or pharmaceutical setting. Education: Masters degree in Biotechnology or a related field. Key Skills: Expertise in PCR, ELISA, Capillary Electrophoresis, Isoelectric Focusing, Western Blotting, SDS-PAGE, and Flow Cytometry. Strong understanding of method validation and documentation. Familiarity with LIMS and EQMS systems. Knowledge of cGMP and cGLP requirements. Excellent attention to detail and strong problem-solving abilities. Work Schedule: Flexibility to work in 1st , 2nd , and General shifts as required. Additional Requirements: A proactive approach to quality and compliance, with a commitment to improving lab efficiency and accuracy. Ability to handle multiple tasks and meet deadlines in a dynamic, fast-paced environment.

NiedlFree Technologies is a Biotech and Bio-Pharma formulations Company, located in Hyderabad, Telangana State, India. Looking for scientists with minimum qualifications of Ph.D, M.Sc or M.Tech having not less than 2 years hands-on experience in protein chemistry, formulations and nano-technology, cell culture, analytical techniques etc.

trong sales and support experience with knowledge of IVD Diagnostics Product Segment only as mentioned above. Candidates must have work experience in IVD Diagnostics, Immunoassays and Molecular industry only. Required Candidate profile 3 -5 years in IVD Diagnostic Industry Sales of ELISA, RIA, HEMATOLOGY, IFA, HPLC, LC/MS & Molecular. Analytical, Autoimmunity, Microbiology, Endocrinology. implementing sales and support strategies,

Role & Responsibilities Role: To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, and cell biology methods. Responsibilities: Meticulous experimental planning and execution to meet program goals. Timely record keeping of results into data sheets and laboratory note-books. Regular mining of literature and keeping oneself up to date with developments in field of antibody development, protein engineering and molecular biology. Timely compilation and presentation of data in written and oral formats. Active participation in team meetings. Active participation in organizing common workspace and tracking common use reagents Attention to detail and adherence to schedules. Candidate Requirement: Education & Experience levels: Applicants should have Masters with 0-4 years experience or a PhD in a life sciences field (submitted within the last one year) with a strong focus on biotechnology, biochemistry, molecular biology or immunology. Nature of experience: Thorough in biochemical and immunoassay workflows such as recombinant protein expression and purification, ELISA, SDS-PAGE, Western blotting, IF, IHC Proficient in molecular biology workflows such as high-throughput molecular cloning, plasmid vector construction, PCRs, Restriction digestion, Ligation, Transformation, Mini and maxi preps, sequencing. Practical experience in designing and execution of flow cytometry experiments is desirable. Ability to provide technical trouble shooting to resolve scientific problems. Proficient in software or platforms for molecular biology and sequence analysis, MS Office and statistical software such as GraphPad Prism. Theoretical or practical experience in antibody development platforms is desirable. Project or work experience in support of relevant skills such as publications, project reports or thesis work. Proficient in MS Office applications such as Word, Powerpoint, Excel and possess a strong statistical knowledge and familiarity with statistical software such as Prism.

Position - Lab Technician Location - Bhiwandi (Near Mankorli Flyover) Qualification Required- DMLT/ BSc MLT Experience- 1- 5 years Role & responsibilities To perform assigned analytical testing procedures in an accurate, precise, and timely manner in the assigned lab. To perform routine and non-routine activities pertaining to laboratory testing and reporting and maintaining external and Internal Quality control Maintain required records and documentation. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result. Analyze specimens using approved testing procedures as per SOP's, review and release test results. Adhere to the laboratory's quality control policies, instrument and procedural calibrations and follow safety guidelines as per established organization protocols. Interested Candidates can share their resume at kbplhr@krishgen.com

Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : Amazon Web Services (AWS), agile development methodologie, Java RIA, JQuery JSON XML, HTML5, CSS3 Good to have skills : Java Enterprise Edition Minimum 7.5 year(s) of experience is required Educational Qualification : Must have minimum 15 years of full time education Summary :As an Application Lead for Packaged Application Development, you will be responsible for designing, building, and configuring applications using Amazon Web Services (AWS) and Java Enterprise Edition. Your typical day will involve leading the effort to deliver high-quality applications, acting as the primary point of contact for the project team, and ensuring timely delivery of project milestones. Roles & Responsibilities: Lead the effort to design, build, and configure applications using AWS and Java Enterprise Edition. Act as the primary point of contact for the project team, ensuring timely delivery of project milestones. Collaborate with cross-functional teams to ensure the successful delivery of high-quality applications. Provide technical guidance and mentorship to team members, ensuring adherence to best practices and standards. Professional & Technical Skills: Must To Have Skills:Proficiency in Amazon Web Services (AWS). Good To Have Skills:Java Enterprise Edition. Strong understanding of software engineering principles and best practices. Experience in designing, building, and configuring applications using AWS. Experience in leading the effort to deliver high-quality applications. Excellent communication and collaboration skills. Additional Information: The candidate should have a minimum of 7.5 years of experience in Amazon Web Services (AWS). The ideal candidate will possess a strong educational background in computer science or a related field, along with a proven track record of delivering impactful solutions. This position is based at our Pune office. N/A

Experience in sales in preferably criticals care/respiratory hospital Understanding of the Molecular Diagnostic & Point of Care market in India Maintain relationship with customer, identifying opportunity for growth Analyze market trend & competition

Maintenance, stimulations and assays using animal cell lines Establishment of mouse bone marrow-derived MSC cultures Gene cloning and generation of knock out cell lines Performing qRT-PCR, ELISA, Western blotting etc. Data analysis, data compilation and manuscript writing. Experience Proficiency in molecular biology and immunology techniques Hands-on training in gene cloning Experience in animal cell culture

Applications are invited from eligible candidates for the Junior Research Fellow (JRF) position in the research project entitled Studies on Therapeutic Aspects of Nucleic Acid Aptamer-grafted-RGD Receptor Targeted Theranostic Chitosan-PLGA Nanoparticles for Brain Cancer Diagnosis and Treatment funded by the Science and Engineering Research Board (SERB), Department of Science and Technology, Government of India, New Delhi Advertisement Apply Now

Name of the Post - Project Technical Support-III No. of Vacancy - 01 (One) Emoluments- Rs-20000/ + HRA, as admissible Essential Qualification:- 12th in Science + Diploma (MLT/DMLT/) + Five Year Experience in relevant subject / field Desirable Qualification :- Experience in handling and testing clinical samplesinvolving techniques such as ELISA and qPCR & knowledge of computer application and data management. Candidates with hands-on experience in molecular biology techniques shall be preferred. One- year previous work experience in research related to medical sciences in a reputed institute . Age Limit :- The upper age limit fs 30 years. Location:- CRMCH, Chandrapur Scope of Work :- Project Technical Support will be involved in the collection of samples from hospitals and field camps, processing of the blood sample, washing of laboratory materials, maintaining reagents record, indenting chemicals, preparation of regents, tabulating haematological and biochemical reports etc, Performing basic tests like CBC, Retic count, peripheralblood smear, microscopic examination.

Name of the Post - Project Technical Support-III No. of Vacancy - 02 (Two) Emoluments- Rs.28000/- + HRA, as admissible Essential Qualification:- BSC in MLT/ Biotechnology/ Biochemistry /Molecular Biology from a recognized university/field + Three Years' experience or PG in relevant subject /field. Desirable Qualification :- Experience in handling and testing clinical samples involving techniques such as ELISA and qPCR & knowledge of computer application and data management. Candidates with hands-on experience in molecular biology techniques shall be preferred. One-year previous work experience in research Age Limit :- The upper age limit is 35 years. Location:- CRMCH, Chandrapur Scope of Work :- Project Technical Support will be involved in the collection of samples from hospitals and field camps, processing of the blood sample, washing or laboratory materials, preparation of regents, tabulating Haematological and biochemical reports etc., Performing basic tests like CBC, Retic count, peripheral blood smear, microscopic examination PCR, DNS sequencing. Interested candidates can share their cv on this mail id anchal.g@esolglobal.com

Install, calibrate, and maintain IVD instruments Diagnose and resolve technical issues promptly Train customers on equipment usage and care Maintain accurate service records and reports Adhere to safety standards and travel as required

Install, calibrate, and maintain IVD instruments Diagnose and resolve technical issues promptly Train customers on equipment usage and care Maintain accurate service records and reports Adhere to safety standards and travel as required

Install, calibrate, and maintain IVD instruments Diagnose and resolve technical issues promptly Train customers on equipment usage and care Maintain accurate service records and reports Adhere to safety standards and travel as required

Role & responsibilities Design, develop, and optimize ELISA assays of drug or other targets in complex biological matrices using Immunologic, Chromatographic or other methods. Align with the concepts of drug molecule and endogenous biomarker bioanalysis in support of pharmacokinetics, Pharmacodynamics and other purposes. Perform ELISA-based analysis on biological samples and interpret results. Ensure accuracy, precision, and reproducibility of assay results in accordance with established protocols and standard operating procedures (SOPs). Troubleshoot, validate, and optimize assays to improve sensitivity, specificity, and throughput. Work closely along with team members to understand their requirements, provide technical support, and deliver high-quality data in a timely manner. Prepare and maintain accurate laboratory records, including experimental design, methodologies, data analysis, and reports. Adhere to all safety guidelines and regulatory compliance requirements (e.g., GLP, GCP). Stay up to date with current trends in immunoassay technologies and applications. Education: A Bachelors or Masters degree in Immunology, Biochemistry, Molecular Biology, or a related field. A Ph.D. is a plus. Experience: Minimum of 5 years of hands-on experience in ELISA assay development and execution in a laboratory setting, preferably in a CRO or similar industry. Experience in performing various types of ELISA, including sandwich, competitive, and indirect assays. Knowledge of other immunoassay techniques (e.g., Western blot, flow cytometry) is a plus. Skills: Strong understanding of immunology and biochemistry principles. Proficiency in laboratory techniques, instrumentation, and data analysis. Experience with data management software and laboratory information management systems (LIMS). Strong problem-solving and troubleshooting skills. Excellent attention to detail and organizational skills. Ability to work effectively both independently and as part of a team. Excellent written and verbal communication skills. Preferred Skills: Familiarity with regulatory guidelines (e.g., GLP, GMP). Experience in assay validation, qualification, and report writing. Prior experience in CRO or contract research environments is highly desirable. Preferred candidate profile: can send updated resume to email: hr@qpsbioserve.com.

Dear Candidate, WE ARE HIRING Department: - Production- DS Designation: - Dy Manager / Manager Qualification: - Preferably Post Graduation in Science Experience: - 15+ Years Age: - Between 35- 40Years Mandatory: - Should come in all shifts, including Night shifts Role: Shift-in-charge for entire DS floor Job Description: > Strong Functional knowledge of DS Biologics (Chromatography and related purification experience protein/ Insulin handling experience preferable). Capable of handling large teams as we have around 45 members in each shift, around 50% of contractual staff. Strong administration / team management capabilities to streamline GMP across the floor. Monitoring the efficiency of employee performance on the job. > Coordinating with other departments to ensure that production runs smoothly Ensuring that all safety regulations are followed in the production area. Managing all aspects of production, including hiring workers, ordering supplies, maintaining production schedules, and overseeing equipment maintenance. Reviewing production schedules and work orders to ensure that production goals are being met in handling QMS activities. for more details please reach out Venkat -9381915043 or please share your CV to venkateswara.k@talent21.in