132 Elisa Jobs

As a Sales Executive at Anand Brothers, you will be an integral part of our team serving the diagnostic industry with a dedication to quality and reliability since 1978. Your role will involve working with various technology platforms such as ELISA, RIA, IFA, HPLC, and Molecular. With a diverse portfolio of over 1700 products from international companies, you will have the opportunity to engage with customers, provide technical support, explain products, handle inquiries, and manage customer relationships. Your responsibilities will also include maintaining records and contributing to sales strategies to drive revenue growth. To excel in this position, you should possess strong customer engagement, communication, and relationship management skills. Technical knowledge in diagnostic platforms and products will be essential, along with proficiency in sales strategies, record-keeping, and data management. Problem-solving and technical support capabilities are key attributes that will contribute to your success in this role. Prior experience in the diagnostic or healthcare industry is advantageous, and a bachelor's degree in a relevant field will be beneficial. Join us in our mission to deliver exceptional service to the diagnostic industry and be a part of a dynamic team that values innovation, excellence, and customer satisfaction. If you are passionate about sales, support, and driving growth in a challenging yet rewarding environment, we welcome you to apply for the Sales Executive position at Anand Brothers.,

You will be joining our team as a Deputy Manager/Manager, Analytical method transfer, responsible for delivering developed analytical assays from R&D scale to GMP-compliant commercial quality control labs. Your role will involve overseeing projects related to analytical method transfer, collaborating with cross-functional teams, and ensuring technology transfer and assays qualification activities are conducted in compliance with GLP and GMP standards. The ideal candidate will possess expertise in cGMP, regulatory requirements, technical troubleshooting, method transfer, method validation, technology transfer, and laboratory techniques to support routine testing and release of research and cGMP grade materials. You will be directly involved in drafting technology transfer documents, risk assessments, process FMEA, method validation protocols, facility fit assessments, and other related activities necessary for the release and testing of microbial and mammalian fermentation-based products. You should have familiarity with analytical assays such as HPLC, GC, SDS-PAGE, agarose gel electrophoresis, densitometry, dd-PCR, RT-PCR, ELISA, UV-Visible spectrophotometry, western-Blot, as well as microbiological techniques like BET, BioBioburdend Sterility testing. Additionally, the position may entail assisting in cell bank testing and release under cGMP regulations and coordinating with third-party collaborators for external testing as needed. Your responsibilities will also include authoring and reviewing research studies, compiling experimental data, and contributing to protocols, study reports, and publications with minimal supervision. You will work as part of the method transfer and method validation team, ensuring timely and successful completion of process transfers while addressing any unexpected technical challenges. We are looking for individuals who are enthusiastic, highly motivated, and capable of multitasking. The role requires working collaboratively within a team environment and independently across various aspects of projects related to microbial-derived products.,

As a Cell Biologist at MS Clinical, a leading research organization dedicated to advancing the understanding and treatment of multiple sclerosis (MS), you will play a crucial role in managing various aspects of cell biology research related to multiple sclerosis. Your responsibilities will include performing cellular and molecular biology experiments, designing and troubleshooting experiments, utilizing laboratory techniques such as immunofluorescence and flow cytometry, analyzing experimental data, and collaborating with multidisciplinary teams. You will be expected to maintain accurate records of experiments, stay current with advancements in cell biology and multiple sclerosis research, contribute to the development of research protocols and scientific publications, and integrate cell biology findings into broader research projects. The ideal candidate will have a Bachelor's or Master's degree in Cell Biology, Molecular Biology, Biochemistry, or a related field, along with 5+ years of hands-on experience in cell biology research. Proficiency in cell culture techniques, strong analytical and problem-solving skills, excellent written and verbal communication skills, and the ability to work effectively in a collaborative team environment are essential for this role. Experience with molecular biology techniques and familiarity with laboratory safety protocols are desirable qualifications. In return, MS Clinical offers a competitive salary, comprehensive benefits package, opportunities for professional development and career advancement, and a supportive work environment that values diversity and innovation.,

Graduate from recognized universities. (B Tech CSE/IT not eligible). Freshers and experienced candidates from 2.5 to 4 years are eligible Preferred candidates with Claims/Claims Adjudication Experience with BPO sector/ domain are preferrable Possess strong Problem solving skills, analytical knowledge and communication skills- both written and verbal. Collaborative, high-energy and diligent work ethics to be displayed at all times. Strong ability to multi-task and support different functions based on business requirements. Complete tasks according to the established standards with limited instruction and supervision. Should possess team-based working style coupled with the zeal to expand the learning horizon and be open to new learning. Willingness to work in shifts in different time zones. Professional attitude and projection of professional company image. Ability to work under pressure esp. during Peak seasons. Stay aligned to the Company's Mission, Vision & Values.

Responsibilities: * Conduct biochemistry, biotech, biomedical tests with IVD equipment * Prepare samples for ELISA assays and RT-PCR analysis * Ensure quality control through documentation and QA processes

Responsibilities: * Conduct lab tests using Hematology, Microbiology, Molecular Biology techniques with expertise in RT-PCR, Serology, ELISA. * Prepare samples for analysis and record results accurately. Annual bonus Provident fund

Key Responsibilities: Analytical Method Development & Validation Develop and validate robust HPLC methods for characterization and quantification of biological products (e.g., monoclonal antibodies, recombinant proteins). Perform method optimization, robustness studies, and transfer protocols as per ICH guidelines. Routine & Stability Testing Conduct analysis of in-process, release, and stability samples using: HPLC/UPLC Capillary and Gel Electrophoresis UV spectrophotometric methods Host Cell DNA quantification (e.g., qPCR-based methods) HCP ELISA and other immunoassays Instrument Operation & Maintenance Perform routine maintenance, calibration, and troubleshooting of analytical instruments including HPLC, electrophoresis systems, spectrophotometers, and ELISA readers. Ensure timely qualification and performance verification of instruments. Documentation & Compliance Prepare and review SOPs, STPs, protocols, reports, and analytical records in compliance with regulatory requirements. Maintain accurate and complete documentation in laboratory notebooks and electronic systems. Quality & Regulatory Compliance Participate in internal and external audits, and support regulatory submissions with analytical data. Cross-functional Collaboration Work closely with R&D, Quality Control, and Regulatory Affairs teams to support product development and lifecycle management. Provide technical support during investigations, deviations, and CAPAs. Training & Development Train junior analysts and new team members on analytical techniques and laboratory practices. Stay updated with advancements in analytical technologies and regulatory expectations. Qualifications & Experience: M.Sc. / M.Tech / M.Pharm in Biotechnology, Biochemistry, or related life sciences discipline. 4 8 years of relevant experience in analytical development or QC of biopharmaceuticals. Hands-on experience with HPLC method development and ELISA based techniques. Familiarity with regulatory guidelines (ICH, FDA, EMA) and quality systems. Key Skills: Strong analytical and problem-solving skills Attention to detail and data integrity Excellent documentation and communication abilities Proficiency in software tools like Empower, Chromeleon, SoftMax Pro, etc. Ability to manage multiple projects and meet deadlines

Exp in seafood industry is must Exp in shrimp/fish/cephalopods Exp in Antibiotic -Elisa and Microbiology test is must Eia Approved Technologist an added advantage Exp in Eia, Haccp and Audit work and documentation Candidate from Sea food industry Required Candidate profile Candidate from Sea food industry Candidate from Food Lab testing with experience in Antibiotic(elisa) and Microbiology can apply Experience in shrimp testing an added advantage call 044-26284700/01

To take charge as Technical and Administrative head of Lab. You shall look after the various technical aspects of the laboratory, such as timely calibration of the various instruments installed, running of the controls to ensure accurate results of the samples tested, daily maintenance of the machines for which the concerned engineer is to be contacted on need basis. You shall strictly monitor Quality control of all tests conducted. Ensure accurate testing, validation, timely release of reports, and efficient inventory control. Providing guidance to the Technicians and other staff members of Lab. Keeping the cost of operation of the lab, under budgeted limits. Please share your resume at ritu.jakhar@lalpathlabs.com

Role & responsibilities Preparation of SOP, STP and Protocols as per requirement. Perform the Instrument calibration/ verification as per SOP. Involving in analytical method validation /verification and technology transfer activity. Handling of equipment the UV Spectrophotometer, SDS PAGE, RT-PCR, ELISA. Implementing all documentation as per GMP, cGLP & WHO GMP guidelines. Follow the established procedures and policies of the company Pertaining to EHS management system. Preferred candidate profile Execution of biochemical analysis like total protein Content, mycoplasma testing and DNA content etc., Perform cell culture analysis and virus titration performing micro biological tests such as micro bio identification, micro biological testing of material/intermediate products, Sterility testing, BET, mycoplasma and mycobacterial testing Performing Environmental monitoring Perfuming water testing (bio Chemical & Microbiology) Job Location: Kadi, Gujarat ( Bus facilities are available)

The Research Scientist position involves conducting a variety of in vitro assays such as cell culture, FACS, ELISA, and data documentation. Your responsibilities will include preparing compound dilutions, maintaining cell lines, isolating PBMCs, seeding cells for treatment, performing FACS staining, ELISA, and Western Blot. Additionally, you will be responsible for data analysis, understanding and adhering to SOPs for instruments and procedures, maintaining calibration schedules, raising change controls for SOPs, reviewing lab notebooks, managing reagents and consumables, scheduling instrument calibration and maintenance, and facilitating communication among project stakeholders. To qualify for this role, you should hold an MSc degree in Pharmacology, Biotechnology, or Life Sciences and have at least 2 years of experience in the pharmaceutical industry. The ideal candidate will possess functional competencies such as innovative thinking, meticulous documentation skills, punctuality in project documentation, and a passion for learning new techniques and assays. If you are looking to contribute your expertise in in vitro assays and data documentation within a pharmaceutical research setting, we encourage you to apply for this Research Scientist position.,

By joining Bio-Techne, you will become part of a company with a strong and positive mission to support cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, along with all its brands, offers tools to researchers worldwide to further the treatment and prevention of diseases. This is an exciting opportunity for a motivated and dynamic individual to join the fast-paced global Life Sciences organization of Bio-Techne, with the position based in India. As an Application Manager/Specialist, your responsibilities will include providing scientific expertise, application support, and training to customers and channel partners. You will collaborate with the commercial team in pre-sales and post-sales customer support activities, effectively resolving customer escalations. Acting as a trusted expert, you will enhance customer satisfaction and loyalty, contributing to the success of the Bio-Techne Protein Simple business in the Indian sub-continent region. In the role of Application Manager/Specialist, some of your key responsibilities will include: - Performing product demonstrations and Proof of Concepts (POC) experiments - Conducting seminars, conferences, and workshops for various audiences - Supporting technical training for Sales Representatives and channel partners - Developing technical selling strategies in collaboration with Sales Representatives - Monitoring market dynamics and implementing strategies for market proficiency - Participating in marketing activities such as roadshows, tradeshows, and workshops to promote Bio-Techne products - Providing post-sales support including customer training and troubleshooting assistance - Coordinating cross-functional engagements for urgent responses - Assisting customers with experimental design and setup guidance Education and Experience requirements: - PhD/MSc./M. Tech in Biotechnology or Biochemistry - Minimum 5-10 years of laboratory or related technical experience - Experience in Analytical method development, Proteins, Monoclonal Antibody analysis - Previous experience in support or training-related roles preferred - Knowledge of Cell culture, Immunoassays, Proteins, Antibodies - Hands-on experience with Flow cytometry, PCR, and Bioassays preferred Key Skills and Abilities: - Strong communication and presentation skills - Effective teamwork abilities - Problem-solving aptitude - Self-motivated and proactive approach - Ability to manage multiple priorities - Fluent in English, additional language skills are a plus - Willingness to travel locally up to 50% of the time - Proficient in computer and internet usage Bio-Techne offers competitive wages, extensive benefits, retirement programs, and opportunities for career development and advancement. The company fosters an empowering and innovative culture where employees are valued and encouraged to contribute new ideas. To protect the interests of all, Bio-Techne does not accept unsolicited resumes from any source other than candidate applications. Unsolicited resumes will be considered Bio-Techne property.,

As an enthusiastic individual with a background in Biotechnology, Biochemistry, or Immunology, you have an exciting opportunity to join Amity University Uttar Pradesh, Noida at the Amity Centre for Translational Research (ACTR) as a Project Technical Support - III. In this role, you will be part of a project focused on restoring adaptive immunity of foamy macrophages against Mycobacterium tuberculosis infection by Sphingosine -1 Phosphate in an experimental model system, sponsored by the Indian Council of Medical Research (ICMR). Key Details: - Position: Project Technical Support III - Number of Posts: 01 - Duration: 1 year & 5 months - Fellowship/Monthly Compensation: Rs.28,000/- + 27% HRA Qualifications & Experience: - Minimum M.Sc. in Biotechnology, Biochemistry, or Immunology with a minimum of 60% from a recognized University - Preference for candidates with NET/GATE qualification - Experience in working with mammalian cell culture, ELISA, and molecular biology techniques Additional Information: - Age Limit: 35 years - Interested candidates meeting the qualifications are encouraged to send their detailed CV within 07 days of the advertisement via email to hprakash@amity.edu with cc to sushils@amity.edu. Please mention "Project Technical Support III - ACTR" in the subject line. - No TA/DA will be provided for attending the interview. If you are passionate about translational research and eager to contribute to a project aimed at combating tuberculosis infection, we look forward to receiving your application.,

What We Want You To Do Analyze and manage the NGS / Nanopore data using relevant pipelines. Develop customized pipelines and workflows and tweak current pipeline filters for NGS and Nanopor analysis Help in developing and executing various data management strategies Identify the databases, tools, catalogs, and their reliability in future and help the research team in data collection strategies. Interpret genetic sequence variations identified through the pipelines Check quality and accuracy of the data Work in conjunction with team members to ensure consistent result generation Work in conjunction with wet lab and tech teams to ensure smooth operations and development work Troubleshoot issues related to data analysis tools and software Review literature for new technologies in the field of Bioinformatics Write grants and papers in the company Creating documentation and maintaining it What Are We Looking In You PhD in Genetics/Genomics or related fields or 8+ years of experience in the field of human genomics/genetics Experience with building bioinformatics pipelines for various kinds of NGS data Assisting in drafting and completing manuscripts for publication Experience with handling various different databases and tools Perform statistical analysis on the datasets Comfortable working on Linux OS system Ability to read, interpret and curate scientific literature Excellent communication skills (oral and written) and attention to detail Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow, instructions, complete deadlines, and comply with company policies Experience of 1-2yrs+ in Python & experience of 3-5 yrs in Bash scripting Experience with pipeline orchestration tools (Nextflow or Snakemake) will be a bonus

What we want you to do Work with diagnostic lab partners for smooth functioning of infectious disease test Work with partners to ensure timely upgrades to the test are done Liaison with partners for technical support as needed Document activities What are we looking in you MSc in Microbiology or Biotechnology Experience in DNA Extraction & RT PCR Ability to quickly prioritize and execute tasks Good oral and written communication skills. Strong analytical skills and attention to detail Strong documentation skills Compulsory rotation shift (i.e day shift, mid shift, night shift) 6 days working with rotational week off What you will gain Exposure of working with one of the leading companies in genomics Experience in working with advanced sequencing technology in diagnostic industry i.e NGS, WGS, Nanopore, and Illumina Gain skills in troubleshooting during sequencing. Skills: ngs,troubleshooting,biotechnology,documentation,data management,organizational skills,excel,rna isolation,data entry,dna extraction,analytical skills,record-keeping,rtpcr,communication skills,powerpoint,word,microsoft office,documentation skills,rt pcr

What We Want You To Do Analyze and manage the NGS / Nanopore data using relevant pipelines. Develop customized pipelines and workflows and tweak current pipeline filters for NGS and Nanopor analysis Help in developing and executing various data management strategies Identify the databases, tools, catalogs, and their reliability in future and help the research team in data collection strategies. Interpret genetic sequence variations identified through the pipelines Check quality and accuracy of the data Work in conjunction with team members to ensure consistent result generation Work in conjunction with wet lab and tech teams to ensure smooth operations and development work Troubleshoot issues related to data analysis tools and software Review literature for new technologies in the field of Bioinformatics Write grants and papers in the company Creating documentation and maintaining it What Are We Looking In You PhD in Genetics/Genomics or related fields or 8+ years of experience in the field of human genomics/genetics Experience with building bioinformatics pipelines for various kinds of NGS data Assisting in drafting and completing manuscripts for publication Experience with handling various different databases and tools Perform statistical analysis on the datasets Comfortable working on Linux OS system Ability to read, interpret and curate scientific literature Excellent communication skills (oral and written) and attention to detail Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow, instructions, complete deadlines, and comply with company policies Experience of 1-2yrs+ in Python & experience of 3-5 yrs in Bash scripting Experience with pipeline orchestration tools (Nextflow or Snakemake) will be a bonus

Achieve sales targets & expand market share for IVD products. Develop and manage relationships with hospitals,diagnostic labs & channel partners Coordinate with application specialists & service teams Mointor market trends & provide strategic inputs.

Role & responsibilities Biological (Therapeutical Protein) sample analysis by HPLC, UV, pH meter, Osmometer, ELISA and SDS-PAGE methods. Calibration of instruments and equipment as per the SOP. Responsible for analysis of in-process, finished products and stability samples. Raw material sampling and outsourcing activity. Preparation of certificate of analysis. Preparation of standard operating procedures, specifications, Protocols and standard testing procedures Operation of High Performance Liquid chromatography, UV spectrophotometer, Osmometer, pH Meter, gel power pack, Plate reader and stability chambers. Initiation of QMS events like lab event, Deviation, OOS, CAPA and Change controls Daily Maintenance of QC laboratory as per GMP requirement. Supervision of AMC and CMC activities for all instruments in the QC. Work in Shifts Preferred candidate profile

Responsible for Sales of IVD Diagnostic Products. Product Segment Focus: ELISA, RIA, Hematology, IFA, HPLC, LC/MS, Molecular Diagnostics, Analytical, Autoimmunity, Microbiology, Endocrinology

At ArshBio, a competitive package and a professionally stimulating work environment are provided to team members, where standards are consistently redefined. This is an opportunity to work with cutting edge technology, lead, and be part of a highly vibrant and result-oriented work culture. We are currently hiring for the position of Diagnostics Service Manager at our new facility in Pitampura, DELHI. The remuneration offered is as per industry standards, based on the candidate's experience and ability. Interested candidates are requested to write to careers@arshbiotech.com along with a copy of their resume. The ideal candidate should have a Bachelors's degree in any of the Life Sciences and at least 1 year of experience working in a laboratory setting. Proficiency in performing commonly used immunological techniques such as ELISA, ELISPOT, Flow Cytometry, RDTs, etc., is required. Desirable qualifications include a PG Diploma or Masters in any of the Life Sciences and experience working in a Diagnostics setting.,

Role & responsibilities Responsible for analysis and documentation of in-process, finished products and stability samples. Handling of QMS, Preparations of Protocols and analytical documents. Preferred candidate profile Biological (Therapeutical Protein) sample Plate based analysis such as ELISA techniques (HCP, HCD, Protein A leachates), PCR, RT-PCR and SDS-PAGE methods. Bioassay analysis for finished products and stability samples by using Gen5 and PLA software. Maintenance of cell lines, Cell culture media and Revival of cell lines. Responsible for analysis of in-process, finished products and stability samples. Preparation of certificate of analysis. Preparation of standard operating procedures, specifications, Protocols and standard testing procedures Operation of UV spectrophotometer, pH Meter, gel power pack, Plate reader and RT-PCR. Initiation of QMS events like lab event, Deviation, OOS, CAPA and Change controls Daily Maintenance of QC laboratory as per GMP requirement. Supervision of AMC and CMC activities for all instruments in the QC. Calibration of instruments and equipment as per the SOP. Work in Shifts

You will be joining USP's Global Biologics department as a Sr. Scientist - I (RSS-Review), where you will play a crucial role in supporting the development of USP documentary standards and reference standards for biological products. In this hands-on, non-supervisory position, you will be responsible for ensuring the accuracy, clarity, and compliance of scientific documents, managing the reference standard stability program, and driving continuous process improvements. Your primary responsibilities will include performing technical and quality reviews of documents, developing and reviewing SOPs and training materials, assisting in investigations of quality-related issues, and collaborating with internal stakeholders to develop new standards for analytical analysis of biological products. You will also be involved in maintaining the reference standard stability program, reviewing testing data, preparing stability trend reports, and updating databases to document laboratory data and program determinations. To succeed in this role, you must have a PhD degree in Biochemistry/Biology/Pharmacy or a related field with 7 to 10 years of experience, or a Master's degree with 11 to 13 years of experience. You should have demonstrated expertise in technical review of analytical documents in Quality Assurance and hands-on experience with analytical techniques for characterizing biological products. Strong communication skills, both written and verbal, along with the ability to work collaboratively with internal and external stakeholders, are essential for this position. Additionally, knowledge of USP products and services, experience in the pharmaceutical or biotechnology industry, and the ability to work effectively in a fast-paced environment are desired preferences. While there are no supervisory responsibilities associated with this role, you will be expected to take ownership of your work, ensure timely delivery of tasks, and maintain the highest quality standards. USP is committed to providing comprehensive benefits to protect the well-being of you and your family, including paid time off, healthcare options, and retirement savings. By joining USP, you will contribute to the organization's mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs.,

Experience the power of DNA Eurofins Genomics is part of Eurofins Scientific Group, an international provider of genomic services established around the core business lines of next generation sequencing, custom DNA sequencing, oligonucleotides, siRNA and gene synthesis. The company's main mission is focused on customer convenience and high quality services in industrial scale for the life science industries and academic research institutions around the world. Eurofins Genomics India corporate office is located in Bangalore with a 14000 sq.ft. with a state-of-the-art infrastructure having more than sixty highly qualified, trained and skilled scientific resources, production facility, data analysis par excellence expertise and quality of products and services. Our NGS projects are being delivered using advanced Illumina NextSeq500 platform, HiSeq2500, MiSeq, PacBio sequel with high performance computational infrastructure. Eurofins Genomics India's expertise and experience in the field of genomics has helped us to gain a solid reputation as a provider of high quality DNA/RNA oligonucleotides, NGS, Gene synthesis and Sequencing services to the top life science industries, research Institutes and academic research institutions across India and covering more than 6000 customers. The laboratory and production facility has established profound know-how and proprietary protocols to cover a broad range of applications. Our production facility is ISO 90012015 certified, which ensures you get the highest quality of products and services. Eurofins Genomics India's prime goal is to provide its customers with high-quality services, accurate results in fast turnaround time. We make our best effort to exceed our customer's expectations and help them in achieving their research goals in a cost-effective and quick way. With over 30,000 staff in over 375 laboratories across 41 countries, Eurofins Scientific is the world leader in food, environment, genomics and pharmaceutical products testing. It is also one of the global market leaders in agroscience, genomics, discovery pharmacology, and central laboratory services. In addition, Eurofins is one of the key emerging players in specialty Clinical Diagnostic testing in Europe and the USA. -Should have experience in NGS data analysis, such as WGS, RNASeq, Small RNA, Metagenome (16S, ITS, Whole metagenome), QTLseq, Exome, etc. -Should also have good programming skills in python, PHP,J Query, MySql. -Implement and execute data processing workflows and automate the pipelines. -Manage project timelines and deliverables. -Develop NGS pipeline for analysis and interpretation of NGS data Qualifications MSc or M.Tech/PhD in bioinformatics Additional Information Monday to Friday workings

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs Gain a technical understanding of the techniques in which review is being performed Use MS Windows applications such as EXCEL, Word, Access, Outlook email Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Master"™s degree in a science-related field with 0-2 years of experience in Bio/Pharmaceutical Chemistry drug product/substance testing with knowledge of regulatory requirements. Theoretical / Practical experience with analytical techniques such as Ligand binding assays, ELISA, RIA, etc. Knowledge of USP/EP compendia, and laboratory software applications such as LIMS, Electronic Notebook is preferred..

Planning and executing assay-runs for cell based assays and ELISA as part of Method Development and Method Qualification studies Analysis of the data using parallel line analysis and equivalence testing Writing protocols and reports for Method development and Method qualification studies Maintenance of the cell lines, preparation of cell banks Review of raw data and data recording sheets and to ensure good documentation practices. Planning of day-to-day activities independently. Trouble shooting of the issues (if any) aroused during execution of assay-run. Involving in documents preparation for SOP, STP, MOA.