23 Western Blotting Jobs

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.,

As a Gene Cloning Expression Studies Specialist in the microbial biosimilar projects, your primary responsibilities will include handling tasks such as screening, transformation, plasmid fusion, and more for projects like Teriparatide, Somatotropin, and upcoming projects. You will actively participate in executing experiments, plan, delegate, and supervise day-to-day activities to ensure successful execution of experiments. It is crucial for you to take full ownership of the quality of data generated while adhering to quality system norms. Additionally, you will be responsible for daily reviewing of ongoing experimental data and supporting GLs/SMEs in experiment design by providing data in appropriate formats. Your role will also involve tasks such as preparation of media, feeds, and buffers ensuring they are error-free and sterile through filtration or autoclaving. Proficiency in filtration techniques is required, and sterile operation while handling feeds and media is essential. You will also need to ensure the availability and calibration of equipment and instruments, promptly informing the respective InCharge/Supervisor in case of breakdowns for necessary troubleshooting. Furthermore, your responsibilities will extend to handling protein expression techniques like SDS page run, Western blotting, and Elisa techniques, as well as supporting the upstream and downstream processes of biosimilar projects. Generating daily work reports and reporting to the manager, collaborating with other teams, and coordinating effectively without conflicts are key aspects of your role. In addition to the primary responsibilities, ensuring the availability of chemicals, glassware, materials, and consumables through stock maintenance is part of your secondary responsibilities. You will be responsible for arranging required chemicals, materials, and consumables within specified timelines using PR creation tools to maintain workflow efficiency. Regularly checking email communications, seeking clarification from supervisors/seniors when needed, and fostering a positive team environment are also crucial elements of your role. For this position, candidates are expected to possess knowledge of bioprocess technology, recombinant technology in biosimilars, and upstream and downstream processes of biosimilars. The ideal candidate should hold an M.Sc./M.Tech in Biotechnology/Life Science with 4-6 years of experience or a Ph.D. in Biotechnology/Life Science with 0-2 years of experience.,

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.

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.,

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

As a Research Technician in the research group of Dr. Emre Sayan at the School of Cancer Sciences, University of Southampton, you will play a crucial role in supporting research activities focused on drug discovery and testing to combat metastatic liver, pancreatic, and neuroendocrine cancers. Your responsibilities will involve utilizing both common and cutting-edge techniques to test the activity of new small molecules in established cancer cell lines and animal models. Techniques such as flow cytometry, western blotting, and immuno-fluorescence will be predominantly utilized along with various molecular biology, biochemistry, and cell biology methods. Additionally, you will contribute to the development of single gene inducible or stable-inducible gene knock-down cell line models. In this role, you will receive comprehensive hands-on training in all relevant techniques essential for the project. This position not only provides a strong foundational experience for individuals considering a transition to the industry but also supports continuous scientific growth. It is expected that you will acquire a home office personal license within the first 6 months of your appointment. This position is offered on an 80% full-time basis and is fixed-term until December 31st, 2026 initially, with potential opportunities for extension and progression to full-time employment. To excel in this role, you should possess an undergraduate and/or graduate degree in Genetics, Biochemistry, Molecular Biology, or a related field, demonstrating a genuine interest in cancer biology and drug discovery. Strong organizational skills, the ability to work independently while effectively collaborating within a team, and experience supervising undergraduate and MSc. students are essential qualities. Your enthusiasm, curiosity, self-motivation, and eagerness to learn and implement new methodologies will be key to your success. Prior experience with apoptosis assays, viability assays, cell culture, and molecular biology techniques is advantageous. Please note that this role requires participation in animal experiments, for which you will receive the necessary training to obtain a home office license. For further details and to apply for this exciting opportunity, please refer to the provided job number and submit your application online by the specified deadline of 11.59 pm GMT. For any assistance during the application process, feel free to contact Recruitment at +44(0)2380 592750 or via email at recruitment@soton.ac.uk. We look forward to receiving your application and welcoming you to our dynamic research team dedicated to advancing cancer research and drug discovery.,

Production: Execute production batches, ensure GMP, manage documentation QA: Ensure cGMP, Issuance and retrievals and manage records. QC: Analyze biopharma samples & maintain Documentation R&D: Prepare stocks and buffers, extract proteins & analyze.

We are seeking Technical Sales Specialists to join our field sales team. It involves promoting and selling life sciences research consumables and benchtop instruments to clients such as medical colleges, universities, and research institutions.

Role & responsibilities To own YBL Vision, Values and Mission. Responsible for using antibody phage display platform for discovering antibodies with diagnostics and therapeutic application. Reformat recombinant antibodies into other isotypes, species and conformations like bi-specific, tri/tetravalent. R&D scale expression and purification of antibodies, their bio-physical characterization and application specific validation. Efficiently analyze, record and report data; experience with electronic notebook will be an added advantage Prepare presentations, project reports and present in weekly and/or monthly group meetings. Actively participate in non-technical activities required for smooth functioning of the department. Preferred candidate profile M.Sc/ M.Tech in life sciences (Biotechnology, Biochemistry etc.) with 2-5 years of relevant experience. Experienced in Basic molecular and protein biology techniques like DNA manipulation and analysis, plasmid extraction, cloning, PCR; Protein Estimation Methods, SDS PAGE, Western Blotting, ELISA etc. Microbial (bacteria / yeast) expression and small scale purification of recombinant proteins Candidates with experience in bacteriophage M13 based antibody phage display techniques will be preferred. Experience of Data Science/QBD approach will be an added advantage. Well acquainted with MS Office (MS Word, Excel, and PowerPoint).

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the Anusandhan National Research Foundation (ANRF) Prime Minister Early Career Research Grant (PMECRG) project in the Center for Nanobiotechnology (CNBT), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : “ Preparation of chiral magnetic nanomaterials for enantiomer dependent nanotherapeutics against drug resistant Melanoma ”. Qualification : M.Sc. Chemistry, B. Tech Biotechnology, Nanotechnology, Material Science, Chemical Engineering with a GATE score or Or M. Tech in Biotechnology, Nanotechnology, Material Science or allied branch. Or M.Pharm with GPAT or equivalent examination. Desirable Skills : Prior experience in nanomaterial synthesis, in vitro cell culture studies will be given preference Stipend : Rs. 37,000 + 10 % HRA, per month , stipend will be as per Institute norms. No. of Vacancies : 01 Posts Age Limit (if any) : Not exceeding 30 years i.e. Age must be from 18 to 30 years Sponsoring Agency : ANRF, NEW DELHI. Duration : 12 Months Principal Investigator : Dr. Pranav, Assi stant Professor (Sr), Center for Nanobiotechnology, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Send your complete CV along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before ( 31/07/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

PathnSitu Biotechnologies is a leading biotech company located in Nacharam, Hyderabad, with additional offices in California, USA and Hyderabad, India. The Hyderabad office boasts a state-of-the-art facility and lab, adhering to ISO 9001:2008, ISO13485:2003, and USFDA certifications. The company strictly follows USFDA and GMP, GDP, and GLP regulations. PathnSitu has established partnerships with labs in the US and is actively engaged in the production of Rabbit/Mouse monoclonal antibodies. The Hyderabad facility plays a crucial role in raw material validation, concentration determination, rigorous quality control, and the final manufacturing of diagnostic kits. We are currently seeking candidates to join the following departments: - R&D and QC - Manufacturing - QA - Marketing Candidates will be selected through an interview process, with promising individuals potentially considered for future opportunities within the company. Skills required for the roles include proficiency in: - ELISA - Western Blotting - Cell Culture - SDS PAGE - PCR - Protein Estimation - Protein Purification Qualification Requirement: Candidates should hold a Bachelor's degree in Biotechnology, Biochemistry, Microbiology, or any life science discipline, along with a strong command of English in both written and spoken forms. This is a full-time position with a morning shift schedule.,

Job Description: We are looking for a dynamic and detail-oriented professional with hands-on experience in upstream processing for biologics, biosimilars, and monoclonal antibodies (mAbs) to join our R&D team. The ideal candidate will work in a fast-paced, innovation-driven environment and contribute significantly to upstream bioprocess development activities. Key Responsibilities: Work in a vibrant R&D setup focused on analytical research for mAbs/biosimilars/biologics. Operate bioreactors (1L, 10L and above) with strict adherence to sterile practices, ensuring zero contamination and batch failures. Prepare media, feeds, and buffers with precision, ensuring sterile conditions via filtration and/or autoclaving. Handle various filtration techniques and sterile transfer of media and feeds. Perform Cleaning-In-Place (CIP) and Sterilization-In-Place (SIP) of bioreactors and ensure equipment is ready for use at any time. Ensure timely calibration, maintenance, and troubleshooting of instruments and equipment to avoid workflow interruptions. Learn and handle gel electrophoresis techniques, aiming for accurate and reproducible results. Perform cleaning and sterilization of lab glassware and materials using autoclave and dry heat methods. Learn and execute protein expression analysis techniques such as SDS-PAGE, Western blotting, and ELISA. Understand both upstream and downstream processes and support cross-functional activities accordingly. Maintain sufficient stock of chemicals, glassware, consumables, and other lab essentials to ensure uninterrupted workflow. Raise material requisitions as needed and ensure timely procurement to avoid delays. Prepare daily work reports and submit documentation to the reporting manager as required. Collaborate effectively with internal teams (e.g., STBI, Purchase, IT, HR) to meet project goals without conflict.

You have an exciting opportunity to join the research team at Sir Ganga Ram Hospital. We are seeking research students with a solid background in cell culture, cell biology, molecular biology assays, and experience handling patient samples in a healthcare environment. Your responsibilities will include culturing and maintaining various cell lines and primary cells derived from patient samples. You will be conducting molecular biology assays such as PCR, Western blotting, ELISA, and cell-based assays. Handling and processing patient samples for research purposes will be an essential part of your role, ensuring compliance with ethical and regulatory guidelines. Additionally, you will assist in data collection, analysis, interpretation, and contribute to the writing of research papers and presentations. To excel in this role, you should have expertise in cell culture and maintenance of cell lines and patient-derived primary cells. Proficiency in molecular biology assays like PCR, Western blot, and ELISA is essential. Prior experience working with patient samples in a healthcare or clinical research setting is preferred. A good understanding of healthcare and regulatory standards, including ethical approvals and patient confidentiality, is crucial. Strong analytical, communication, and teamwork skills are required, along with a background in life sciences (MSc or higher preferred). If you are interested in this opportunity or need more information, please contact Evanka Madan at evanka.madan@sgrh.com. To apply, kindly send your resume and a cover letter outlining your research experience and expertise to evanka.madan@sgrh.com as soon as possible.,

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.

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Applications are invited for the post of one Junior Research Fellow (JRF) for the Anusandhan National Research Foundation (ANRF) -Prime Minister Early Career Research Grant Scheme project in the Centre for Biomaterials, Cellular and Molecular Theranostics (CBCMT), at Vellore Institute of Technology (VIT), Title of the Project : Unveiling and Reprogramming the Cellular Package Mechanism of Tumor Extracellular Vesicles to Combat Cancer Metastasis. File : (ANRF/ECRG/2024/006012/LS). Qualification : M.Sc., /M. Tech., (Biomedical Science, Biotechnology, Biochemistry and Nanotechnology) with a minimum of 55% marks. Preference will be given for students with NET and/or GATE qualifications. Desirable (if any) : Candidates with research experience in cell culture, molecular biology and nanomedicine Stipend : For NET/GATE Qu For NET/GATE Qualified candidates: Rs. 37,000/- + 10% HRA per month for the first two years and Rs. 42,000/- + 10% HRA per month for the third year. For other Candidates: Institutional norms will be applicable. Sponsoring Agency : Anusandhan National Research Foundation (ANRF) -Prime Minister Early Career Research Grant Scheme, Government of India No. of Positions : 1 Duration : 3 Years Principal Investigator Dr. Arunkumar Pitchaimani, Ph.D., Assistant Professor & Ramalingaswami Fellow, Centre for Biomaterials, Cellular and MolecularTheranostics (CBCMT), Vellore Institute of Technology (VIT), Vellore - 632 014, Tamil Nadu, India. Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo, etc. on or before (04/07/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing in the interview. Shortlisted candidates will be called for an interview at a later date, which will be intimated by email. The selected candidate will be expected to join at the earliest.

About Intas Recruitment Fraud Disclaimer: Intas Pharmaceuticals does not request or accept any fees during recruitment If someone asks for payment on our behalf, it is a scam Please report the incident to the local police or cybercrime unit Your trust and safety are important to us, Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world, Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare, At Intas, our success is fundamentally built on the strength of our people Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence This approach ensures that every employee plays a meaningful role in driving both the companys growth and advancements in global healthcare, Job Title: Associate Scientist BDL Job Requisitions No : 13803 Job Description Purpose of Job To perform techniques as per a defined procedure and document the same for a given project under technical supervision, Skill Required Cell-Based Assays Understanding of assay setup, endpoint analysis, and result interpretation, ELISA (Enzyme-Linked Immunosorbent Assay) Strong proficiency in plate-based immunoassays, SDS-PAGE & Western Blotting Experience in protein separation and immunodetection techniques, SPR (Surface Plasmon Resonance) Exposure to or working knowledge of biomolecular interaction analysis, Analytical Instrument Handling Competence in using and maintaining relevant laboratory instruments, Data Compilation & Statistical Analysis Ability to compile raw data and interpret results using Excel or statistical tools, SOP Writing & Technical Documentation Experience in writing/revising technical documents and reports, Roles and Responsibilites Execution of the technique (Cell based assay, ELISA, SDS-PAGE, Western Blot, SPR) as per the defined procedure and documentation of the same, Training on system compliance and documentation Data compilation of sample analysis and method development and qualification experiments, Response to DQA observations related to data verification, Preparation of SOPs, Any other responsibility assigned by supervisor, To follow ?Good Documentation Practices and Data Integrityrequirements during any GxP Operation and recording at site, To take responsibility that application of Data Integrity requirements and potential consequences for not following it are understood and followed, To review in the perspective of compliance to Data Integrity requirements while reviewing any GxP data (Records, Reports) specific to Job description, To ensure that, In case of any event of potential data breach, it shall be handled through SOP on ?Handling of Potential Data Integrity Observation, Qualification Required MSC/MTECH Biotechnology Relevant Skills / Industry Experience Relevant professional / Educational background Any Other Requirements (If Any) Compensation / Reward Location: Biotech, Ahmedabad, GJ, IN, 382213 Travel: 0% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape, Date: 26 May 2025

Conduct Biochemical Assays Standardize and perform a range of biochemical assays including antioxidant and enzymatic/non-enzymatic tests like DPPH, ORAC, lipid peroxidation, and enzyme inhibition assays. Perform Immunoassays – Carry out immunological techniques such as ELISA for qualitative and quantitative analysis. Execute Analytical Techniques – Perform specialized assays including gluten estimation and Franz diffusion tests for compound permeation studies. Support Molecular Biology Work – Assist in molecular biology experiments like RT-PCR, western blotting, PAGE, and staining techniques. Cell Culture Handling – Maintain and handle cell lines, and conduct various cell-based assays. Data Analysis & Reporting – Process experimental results, analyze data, and prepare documentation in compliance with quality standards. Laboratory Compliance – Ensure all lab activities align with NABL or other regulatory guidelines, including proper documentation. Equipment Maintenance – Perform daily equipment checks, verifications, and intermediate calibrations to ensure optimal functioning.

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.

Candidate should have experience in Molecular Biology techniques PCRs, Plasmid Isolation, Site directed Mutagenesis, Gene synthesis and Cloning techniques Protein expression in bacterial and Mammalian cells Industry - Pharma / Biotech Functional Area - Medical, Healthcare, RD, Pharmaceuticals, Biotechnology Role Category - Molecular Biology. Desired Profile PG - M.Sc - Bio-Chemistry, Microbiology, M.Tech - Bio-Chemistry/Bio- Technology

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.

Screening of phytocompounds by cell culture, Western blotting, RNA experiments. Assist in preparing manuscripts for international publication; will be given authorship on papers. Will work in state-of-the-art labs, MSC in Life science & biotechnology

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.