81 Cell Culture Jobs - Page 2

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.,

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF-PM-ECRG Funded Project in the School of Bio Sciences and Technology (SBST), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : miR146a-loaded exosomes in suckerin patch for targeted diabetic wound healing via IRAK1 suppression Qualification : Essential qualification: M. Tech / M. Sc in Biotechnology/ Biochemistry Preferred qualification: The candidates must have qualified GATE (with currently valid score)/CSIR-UGC NET including lectureship (Assistant Professorship) or 2 years of research experience and publications relevant to the proposed project title The selection and administration of the research fellow will be as per terms and conditions laid down by ANRF. Mandatory Skills : Candidates having knowledge in exosome isolation, extraction, purification, rDNA technology, protein expression & purification, cell culture techniques and animal handling. Stipend : Rs. 37,000/- per month plus HRA as per rule. No. of Vacancies : 01 Age Limit (if any) : Not exceeding 27 years i.e. Age must be from 18 to 27 years Sponsoring Agency : ANRF (Prime Minister Early Career Research Grant), Ministry of Science & Technology, Government of India. Duration : 3 years (36 Months) Principal Investigator : Dr. Kanagavel Deepankumar, Associate Professor -Grade I, Department of Biotechnology, School of Bio Sciences & Technology, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Applicants must apply online at http://careers.vit.ac.in by 15/07/2025 and email a single PDF containing the CV, statement of purpose detailing the motivation for working in the research project, essential certificates and a passport-size photograph to Dr. for the ANRF project JRF . No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview, later which will be intimated through email. The selected candidate will be expected to join at the earliest.

Job Title- Executive/ Sr Executive - Viral Vector Production Role & Responsibilities :- -Execute routine LVV batch manufacturing under GMP conditions. - Perform cell thawing, expansion, transfection, and harvest in adherent systems. - Maintain aseptic conditions during all upstream processes. - Document batch manufacturing steps in BMRs accurately and on time. - Prepare and filter buffers/media for production use. - Support equipment cleaning, calibration, and area readiness. - Collaborate with QA/QC for sampling, deviation documentation, and investigations. - Participate in process improvement initiatives. Mammalian cell culture handling (HEK293T or similar) - Adherent culture in flasks, cell factories, or multilayer vessels - Aseptic operations in cleanroom environments (Grade B/C) - Batch-wise documentation and compliance with GMP - Execution of cell thawing, expansion, transfect ion, and harvest - Buffer/media preparation and sterile filtration - Understanding of deviations, change controls, and process improvements - Coordination with QA/QC for in-process checks Biosafety Cabinets (Class II) - CO Incubators - Roller bottles / Cell factories / Multilayer vessels - Small-to-large scale Bioreactors (for adherent systems) - Peristaltic pumps - pH/conductivity meters - Microscopes

We are seeking an experienced professional to join our Biotech Production Department in India. The ideal candidate will have a strong background in biotech production processes and will be responsible for overseeing and optimizing production operations. Responsibilities Oversee the production processes in the Biotech department ensuring compliance with industry standards. Assist in the scale-up of bioprocesses from laboratory to production scale. Conduct routine maintenance and troubleshooting of bioprocess equipment. Collaborate with cross-functional teams to ensure timely and efficient production schedules. Ensure adherence to safety and quality protocols throughout the production process. Skills and Qualifications Bachelor's degree in Biotechnology, Bioengineering, or related field. 3-6 years of experience in biotech production or a related area. Strong understanding of bioprocessing techniques and equipment. Familiarity with regulatory guidelines and Good Manufacturing Practices (GMP). Excellent problem-solving skills and attention to detail. Ability to work effectively in a team-oriented environment and communicate clearly.

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.

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF-PM-ECRG Funded Project in the School of Bio Sciences and Technology (SBST), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : “miR146a-loaded exosomes in suckerin patch for targeted diabetic wound healing via IRAK1 suppression” Qualification : Essential qualification: M. Tech / M. Sc in Biotechnology/ Biochemistry Preferred qualification: The candidates must have qualified GATE (with currently valid score)/CSIR-UGC NET including lectureship (Assistant Professorship) or 2 years of research experience and publications relevant to the proposed project title The selection and administration of the research fellow will be as per terms and conditions laid down by ANRF. Mandatory Skills : Candidates having knowledge in exosome isolation, extraction, purification, rDNA technology, protein expression & purification, cell culture techniques and animal handling. Stipend : Rs. 37,000/- per month plus HRA as per rule. No. of Vacancies : 01 Age Limit (if any) : Not exceeding 27 years i.e. Age must be from 18 to 27 years Sponsoring Agency : ANRF (Prime Minister Early Career Research Grant), Ministry of Science & Technology, Government of India. Duration : 3 years (36 Months) Principal Investigator : Dr. Kanagavel Deepankumar, Associate Professor –Grade I, Department of Biotechnology, School of Bio Sciences & Technology, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Applicants must apply online at http://careers.vit.ac.in by 15/07/2025 and email a single PDF containing the CV, statement of purpose detailing the motivation for working in the research project, essential certificates and a passport-size photograph to Dr. Kanagavel Deepankumar ( deepankumar.k@vit.ac.in ) with the subject line: “Application for the ANRF project JRF”. No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview, later which will be intimated through email. The selected candidate will be expected to join at the earliest.

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF Funded Project in the School of Biosciences and Technology (SBST), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : Development and evaluation of Ape1 degrading peptide to sensitize genotoxic drug resistance tumor cells for apoptosis . Qualification : MSc/MTech in Biology/Biotechnology related- subjects with two years of experience. Mandatory Skills : Candidates having good knowledge in field of cancer and practical experience in animal cell culture and Western blot analysis Stipend : Rs. 37,000/- + HRA per month No. of Vacancies : 01 Posts Age Limit : 24 to 30 years Sponsoring Agency : ANRF Duration : 12 Months Principal Investigator : Dr. M. Anbalagan, Professor, School of Biosciences and Technology, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience and latest passport size photo etc. on or before ( 01/06/2025) 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.

Applications are invited for the Post of Project Technical Support-III for the ICMR Funded Project in the School of Bio Sciences and Technology (SBST), at Vellore Institute of Technology (VIT), ( IIRP-2023-3019 dated 04-04-2025) Title of the Project : Preparation and Evaluation of Wound Dressing Material and Topical Ointment Using Magnetosome Conjugated Lemon Grass Extract (MLGE) Qualification : First Class Post-Graduate (PG) Degrees (M.Tech., M.Sc.,) degrees in Biotechnology /Botany /Microbiology or equivalent Describe if any Candidates having knowledge and hands-on experience in the area of animal work/herbal formulations / nanoformualtions / cell culture work will be preferred. Publication records relevant to the field. Fluent in English, both written and spoken. Stipend : Rs. 28,000/- + 10% HRA of Rs. 2800/- Total Rs. 30,800/- per month Sponsoring Agency : ICMR Duration : 11 Months or till the completion of project Principal Investigator : Dr. K. Suthindhiran , Professor, Department of Biomedical Sciences, School of Bio Sciences and Technology Vellore Institute of Technology (VIT), Vellore - 632 014, Tamil Nadu. Co-Principal Investigator : Dr. M. A. Jayasri, Associate Professor, Department of Biomedical Sciences, School of Bio Sciences and Technology Vellore Institute of Technology (VIT), Vellore - 632 014, Tamil Nadu. 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 ( 16/04/2025) 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.

Are you a medical graduate or post-graduate with a passion for research If the clinical challenges excite you and you are eager to delve into new knowledge about health and diseases, including the discovery of rare diseases, then this Ph.D. opportunity might be the perfect fit for you. The Clinical Research Training Programme (CRTP) for rare diseases is designed to equip physicians with the necessary skills to navigate the complex landscape of rare genetic diseases. These diseases often lack effective treatments and impose a heavy burden on patients and their families. By participating in this program, you will have the chance to earn a Ph.D. degree upon completion and become a multi-domain expert capable of bridging the gap between patient care and cutting-edge research in the field of rare genetic diseases. Eligible candidates include post-graduates and graduates in Medical or Dental Sciences with qualifications such as DM, MCh, MD, MS, MBBS, or their equivalents. This program is a collaborative effort between Manipal Academy of Higher Education, Manipal, Institute of Bioinformatics, Bengaluru, and Dr. Reddys Institute of Life Sciences, Hyderabad. It is supported by funding from the DBT Wellcome Trust India Alliance. The program spans 3-4 years and offers comprehensive training in basic science research for physicians. You will gain hands-on experience in various research techniques such as handling samples, sequencing, data analysis, molecular biology, cell culture, animal models, systems biology, and exposure to drug development in both clinical and laboratory settings. The first year of training will take place at MAHE, Manipal, followed by training at MAHE or other participating institutions, with opportunities for international training with collaborators abroad. Mentorship will be provided by approved Ph.D. guides from MAHE, Institute of Bioinformatics, and Dr. Reddys Institute of Life Sciences. Additionally, students will have the chance to learn from international collaborators at renowned institutions around the world. Each candidate will receive a budget of Rs. 50,00,000 to cover salaries, research expenses, and travel. There are six fellowships available, and successful candidates may have the opportunity for permanent positions at the host institution upon completion of the program. To apply, interested candidates can submit their CV and a statement of interest explaining their passion for research and the program to jobs.research@manipal.edu. Join us on this exciting journey to explore the world of rare diseases and make a meaningful impact on healthcare and research!,

The Center for Advanced Neurological Research at KS Hegde Medical Academy, a constituent college of NITTE (Deemed-to-be University) in Mangalore, Karnataka, is looking for a Scientist Grade 1. The research center, led by Professor Lekha Pandit, a renowned clinician researcher, focuses on autoimmune central nervous system disorders. Professor Pandit has patented two diagnostic live cell based assays for antibody mediated CNS demyelinating disorders. The current research at the center includes molecular biomarkers, microbial influences on CNS demyelinating disorders, and animal models of disease. This position offers the opportunity to enhance research abilities, translate clinical findings to basic science research, and collaborate on international studies. Candidates with expertise in microbiology/molecular biology, particularly in cell culture and flow cytometry, with a minimum of one year postdoc experience in India/Abroad and a proven track record of research publications are preferred. The ideal candidate should possess strong research skills and a commitment to teamwork in a disciplined environment. The salary for this position is as per norms. The qualification required is M.Sc and Ph.D. Interested and eligible candidates are invited to apply by sending their CV to lekhapandit@nitte.edu.in by October 31st, 2024.,

Role & responsibilities Responsible for cell revival, subculture, cell counting of MRC-5 cells. Preparation of MCB/WCB. Experience in Preparation of media and in process buffers in media mixing vessels. Experience in handling Roller bottles, Cell stacks, TCFs. Experience in working in GMP conditions / production department of viral vaccines. Preparation of SOP, BMR’s, Protocols related to cell culture / virus culture. Experience in virus infection, virus harvesting procedures. Experience in working with Chicken embryo fibroblast cells, pooling of embryos, seeding of RB’s . Preparation of Media, in process solutions using preparation vessels. Preferred candidate profile Candidate should have experience in Cell Culture vaccine 6 days work from office based at Ahmedabad

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.,

Adhiparasakthi Dental College And Hospital is looking for Cell Culture - Lab Technician to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes. Apply subject expertise to support operations, planning, and decision-making. Utilize tools, analytics, or platforms relevant to the job domain. Ensure compliance with policies while improving efficiency and outcomes.

Position: Research Associate (RA) for Gene Editing Project Overview: Human stem cell differentiation technology enables the generation of any cell or tissue in the body, leveraging human-origin cells for their easy accessibility and scalability. Recent advances in gene editing, particularly CRISPR-Cas technology, are revolutionizing the generation of human pluripotent stem cell-based experimental platforms to model "disease in a dish." In this role, you will advance research on neurological diseases by utilizing CRISPR/Cas technology to introduce disease-causing mutations in human pluripotent stem cell (iPSC) lines. Additionally, you will develop gene-targeting strategies for direct pluripotent stem cell differentiation into enriched cultures of neurons, astrocytes, and oligodendrocytes, using inducible gene expression systems (optogenetic and chemical methods) (Sheta etal. ,2023;Teixeira etal. ,2023). Furthermore, you will be involved in generating isogenic (gene-corrected controls) pluripotent stem cell lines against patient pluripotent stem cell lines (Banerjee etal. ,2023). The candidate will play an integral role in projects related to development, optimization of new gene editing tools. Collectively, candidates should have an expertise and interest in CRISPR-Cas technology for generating cellular models recapitulating neurological diseases. Essential Requirements: Educational Background: MSc/PhD in a relevant field, with around 3-5 years of experience in gene editing and molecular biology Genome Editing Expertise: Demonstrated proficiency in creating knock-out/knock-in lines utilizing CRISPR/Cas technology. The ideal candidate should have a publication record that showcases their expertise in gene editing. In-depth knowledge of the latest advancements in gene editing technologies is essential for this role. Technical Proficiency: Skilled in using genome browsers, DNA analysis software, and CRISPR/Cas related on/off target specificity analysis, primer design, designing guides, molecular cloning Cellular Characterization Techniques: Proficient in immunofluorescence staining, FACS analysis, and PCR Team Collaboration: Demonstrated ability to contribute effectively to a team with a collaborative and flexible approach Project Management: Strong independent work ethic with excellent project planning, time-keeping, organizational, and online record-keeping skills in electronic lab-books Health and Safety: Understanding of health and safety requirements related to genetic engineering of cell lines Professional Development: Commitment to continued professional development. Communication Skills: Excellent oral and written communication skills, capable of conveying complex information through power point presentation Interpersonal Skills: Strong interpersonal skills to influence and deliver results Desired additional qualifications: iPSC Experience: Experience in gene-editing of pluripotent stem cells or mammalian cell lines to generate stable lines Neurobiology basics: Understanding of the functions of brain cells and their relevance to neurological diseases Knowledge on Sequencing: Familiarity with Sanger sequencing. Viral Vector Generation: Experience in generating viral vectors for labelling cells, regulating gene expression, and manipulating cell physiology CRISPR screening Relevant references Banerjee, P. et al. (2023) Cell-autonomous immune dysfunction driven by disrupted autophagy in C9orf72-ALS iPSC-derived microglia contributes to neurodegeneration., Science Advances , 9(16), p. eabq0651. doi:10.1126/sciadv.abq0651. Sheta, R. et al. (2023) Optimized protocol for the generation of functional human induced-pluripotent-stem-cell-derived dopaminergic neurons.,” STAR Protocols , 4(3), p. 102486. doi:10.1016/j.xpro.2023.102486. Teixeira, M. et al. (2023) “Optogenetic-mediated induction and monitoring of -synuclein aggregation in cellular models of Parkinson’s disease.,” STAR Protocols, 4(4), p. 102738. doi:10.1016/j.xpro.2023.102738.

Job Description Candidate should have sound knowledge about upstream process development (Cell culture and Fermentation). Hands on experience of shake flask studies including sample analysis and documentation. Experience in handling and operation of cell culture and microbial related experiments in bioreactor including sample analysis and documentation. Aseptic handling of seed inoculum and its maintenance Independently handle media and feed preparation for conducting studies. Should be able to trouble shoot in case of any deviation from process/parameter. Good documentation practice. Should be able to perform cell culture (IPQC) analysis. Preparation of SOP, Support for Equipment qualification, Calibration pertaining to Upstream process as per laid down procedures Ensure quality compliance in Biotechnology Upstream laboratory as per Quality standards requirements

JOB DESCRIPTION Designation: Associate Scientist / Senior Associate Scientist Job Location: Bangalore Department: TM-TDDT About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose (1-2 Lines) We are seeking motivated master s level scientists (MS, MTech, MSc, etc) to join the Translational Medicine team at the Biocon Bristol Myers Squibb Research Center in Bangalore, India. Key responsibilities of this role are to serve as an execution arm for the preclinical support of asset programs through mechanism of action-based studies, differentiation from standard of care and competitive therapeutics, combination rationale, new indications (life cycle management), and patient selection strategies. S/He will work directly with translational scientists, disease leaders within translational medicine, and will also interact with thematic research centers in early development within the company. Key Responsibilities: Conduct preclinical/laboratory experiments on late stage BMS portfolio compounds to support annual goals and objectives for Translational Medicine (for internal /external, collaborations, compound specific plans etc). Responsible for delivering data in support of translational strategies including biomarkers, patient selection hypotheses, dose and schedule, combination strategies, resistance mechanisms and differentiation. Interfaces with TM scientists across departments to ensure seamless flow of information for assets which are entering the remit of translational medicine. Assists in designing experiments and delivering data for collaborative projects along with TM scientists. Maintains comprehensive records, communicates regularly and makes presentations within the department, as required. Reports experimental finding in written nonclinical pharmacology study reports, to support regulatory filings. Educational Qualification: Masters with at least 2 years of relevant work experience across immunology, oncology, heme-oncology focus areas. Industry experience is a plus. Multiple positions can range upto 6 years of experience. Technical/functional Skills: Cell culture, primary cell isolation, cell transfection and single cell cloning; including siRNA / CRISPR / TALEN or HDR workflows Gene expression methods including qRT-PCR and/or familiarity with RNA sequencing, epigenomic methods including methylation analysis, ChIP etc Protein analyses and immunoassays, and cell phenotyping analysis (e.g. ELISA, MSD, Luminex, TSA, CBA, flow cytometry). Design, setup and execution of autoimmune, solid tumor oncology or heme-oncology in vivo pharmacology models. Excellent verbal and written communication skills, familiarity with standard or relevant software platforms, and scientific qualities are expected. Competence in analysis and solving of problems, keeping track of overall goals. Maintain a good understanding of the methodological basis and biological significance of assays performed. Forecast potential issues regarding support of assays for current and long term projects. Devise strategic solutions to identified and potential hurdles/issues and efficiently and proactively troubleshoot technical and experimental problems. Experience: 2-6 years Behavioral Skills: A self-starter, who is/can become technically proficient in a diverse set of techniques and assays with a focus on quality and speed, and will meticulously follow internal SOPs Good basic lab skills required (pipetting, balances, etc.) Highly detailed and meticulous, high standards of data entering and QC Must be highly adaptive to changing timelines and goals Must be comfortable taking on complex tasks with minimal direct supervision An excellent multitasker with an ability to be level-headed in a fast-paced lab setting Team-oriented and comfortable working in a highly dynamic matrix environment across multiple locations Prior experience working with patient samples (i.e. FFPE tissue, Fresh Frozen tissue, blood) or working in a CLIA/GCLP/clinical environment is a plus Must be comfortable and able to work with animal (rodent) or human derived samples Equal Opportunity Employer: .

Research Associate, Cell Culture and Bioassays About Mynvax Mynvax is a clinical-stage vaccine biotechnology company headquartered in Bangalore, India, developing novel, recombinant, and thermostable vaccines against respiratory viral infections, including influenza and RSV. With a pipeline of promising candidates and multiple ongoing collaborations, Mynvax offers a unique opportunity to work at the cutting edge of vaccine development. Role Maintain and passage mammalian cell lines under sterile conditions. Support in vitro bioassays such as ELISA, virus neutralization assays, and cytopathic effect-based assays. Perform RNA isolation, cDNA synthesis, and qPCR for viral load estimation. Assist in the preparation and handling of BSL-2 viruses under appropriate biosafety protocols. Process animal sera or tissue samples for immunological analysis. Maintain laboratory notebooks and electronic records with high attention to detail. Assist with assay optimization, reagent preparation, and documentation for preclinical studies. Ensure compliance with biosafety and quality standards during laboratory operations. Required Qualifications M.Sc. or M. Tech in biotechnology, microbiology, immunology, or related life science fields. 0-3 years of hands-on laboratory experience in academic or industrial settings. Familiarity with mammalian cell culture, ELISA, and virus-based neutralization assays. Knowledge of BSL-2 biosafety practices and handling of infectious materials. Good understanding of basic laboratory techniques and experimental design. Desirable Skills Experience with in vivo sample collection or processing from preclinical models. Exposure to data analysis tools and statistical interpretation of assay results. Prior work in a regulated or GLP/GMP-compliant environment. What Mynvax offers: A dynamic research environment with exposure to cutting-edge vaccine development. Training and mentorship in immunology, virology, and preclinical research. Collaborative environment with growth opportunities and skill development. Competitive salary and full-time employment benefits.

JOB DESCRIPTION Designation: Associate Scientist / Senior Associate Scientist Job Location: Bangalore Department: TM-TDDT About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose (1-2 Lines) We are seeking motivated master s level scientists (MS, MTech, MSc, etc) to join the Translational Medicine team at the Biocon Bristol Myers Squibb Research Center in Bangalore, India. Key responsibilities of this role are to serve as an execution arm for the preclinical support of asset programs through mechanism of action-based studies, differentiation from standard of care and competitive therapeutics, combination rationale, new indications (life cycle management), and patient selection strategies. S/He will work directly with translational scientists, disease leaders within translational medicine, and will also interact with thematic research centers in early development within the company. Key Responsibilities: Conduct preclinical/laboratory experiments on late stage BMS portfolio compounds to support annual goals and objectives for Translational Medicine (for internal /external, collaborations, compound specific plans etc). Responsible for delivering data in support of translational strategies including biomarkers, patient selection hypotheses, dose and schedule, combination strategies, resistance mechanisms and differentiation. Interfaces with TM scientists across departments to ensure seamless flow of information for assets which are entering the remit of translational medicine. Assists in designing experiments and delivering data for collaborative projects along with TM scientists. Maintains comprehensive records, communicates regularly and makes presentations within the department, as required. Reports experimental finding in written nonclinical pharmacology study reports, to support regulatory filings. Educational Qualification: Masters with at least 2 years of relevant work experience across immunology, oncology, heme-oncology focus areas. Industry experience is a plus. Multiple positions can range upto 6 years of experience. Technical/functional Skills: Cell culture, primary cell isolation, cell transfection and single cell cloning; including siRNA / CRISPR / TALEN or HDR workflows Gene expression methods including qRT-PCR and/or familiarity with RNA sequencing, epigenomic methods including methylation analysis, ChIP etc Protein analyses and immunoassays, and cell phenotyping analysis (e. g. ELISA, MSD, Luminex, TSA, CBA, flow cytometry). Design, setup and execution of autoimmune, solid tumor oncology or heme-oncology in vivo pharmacology models. Excellent verbal and written communication skills, familiarity with standard or relevant software platforms, and scientific qualities are expected. Competence in analysis and solving of problems, keeping track of overall goals. Maintain a good understanding of the methodological basis and biological significance of assays performed. Forecast potential issues regarding support of assays for current and long term projects. Devise strategic solutions to identified and potential hurdles/issues and efficiently and proactively troubleshoot technical and experimental problems. Experience: 2-6 years Behavioral Skills: A self-starter, who is/can become technically proficient in a diverse set of techniques and assays with a focus on quality and speed, and will meticulously follow internal SOPs Good basic lab skills required (pipetting, balances, etc. ) Highly detailed and meticulous, high standards of data entering and QC Must be highly adaptive to changing timelines and goals Must be comfortable taking on complex tasks with minimal direct supervision An excellent multitasker with an ability to be level-headed in a fast-paced lab setting Team-oriented and comfortable working in a highly dynamic matrix environment across multiple locations Prior experience working with patient samples (i. e. FFPE tissue, Fresh Frozen tissue, blood) or working in a CLIA/GCLP/clinical environment is a plus Must be comfortable and able to work with animal (rodent) or human derived samples Equal Opportunity Employer: .

Role & responsibilities Recombinant vector and clone development Cell line development Clone screening & clone evaluation Cell banking and maintenance Handling of cell cultures up to 5L (SF) and AMBR Cell line engineering: Crispr/Cas KI/KO of Mammalian cell lines Experiment performing, monitoring and reporting Data analysis and presentation Implementation/Execution of the safety norms. SOP preparation, LNB (lab note book) writing and maintenance. Lab management Report preparation Literature study Preferred candidate profile Knowledge of Molecular-biology/Microbiology. Knowledge of cell culture. Knowledge of ICH and other regulatory guidelines w.r.t recombinant production cell line development

Company Location: Kelambakkam Candidates Should have - Bachelors in Lifesciences degree Lifecell is giving carrier beginnings to so many youths. So far, 230 candidates have happily placed in 3 months. https://maps.app.goo.gl/YghwtdA7uQw3r9Dt9 Address: No: 26, Kelambakkam - Vandalur Rd, Main Rd, Keelakottiyur, Tamil Nadu 600127. (Opp to VIT) Join the group for all entry level Job updates https://chat.whatsapp.com/EvNybnEJDx48OkplyeEhTS Share this with your friends. If they are in need of immediate opportunities Food is provided Transportation provided (Terms and conditions applied) There will be rotational shifts which include night shift too.

Research Scientist- Biologics @chennai Full Time Qualifications: PhD or MSc in Lifesciences/Biotechnology or related field At least 5-10 years experience in Cell and Tissue manufacturing, including GMP environment. Demonstrated experience in an research and development/manufacturing role is highly required Must Have - Lyophiliser Work Experience Key Responsibilities: Responsible for new product development, scale up of successful R&D batches & transfer of technology to commercial batches Implementation of new product development process. Answering regulatory related queries within lead time Review regular basis stability studies protocol and reports Document preparation (PDR, MFR,PV,Stability) for regulatory dossiers Developing the quality of product with cost effectiveness Training the formulators for literature study before development & conduct patent search Achieving development target of sample product for registration of export samples as well as domestic samples Checking all Project In Process Data, COA & Log books of all project members. Fulfil requirement of MFR, BMR & Tech Transfer Products. Reducing development costs & product cost Resolve trouble shooting in production during scale up and commercial batches Customized sampling for different customer Review process validation and analytical validation protocols and reports Providing information for vendor management approval system Leading the entire department Competencies Required: Aseptic processing techniques. GMP working knowledge. Human tissue and cell handling techniques. Closed loop operations. Cell expansion techniques. Process equipment handling like Biosafety cabinets,Lyophilizer, filling etc. For Faster Response Apply Here - https://forms.gle/bdnTopW6fEA4WFLW8

Role & responsibilities Vaccine Manufacturing (Cell Culture) Responsible for cell revival, subculture, cell counting of MRC-5 cells. Preparation of MCB/WCB. Experience in handling Roller bottles, Cell stacks, TCFs. Quality Control (Bacterial/Viral) Candidate should have good knowledge of Product testing techniques like : Biochemical, Chromatography, Electrophoresis, Immuno assay, Cell culture & Molecular techniques. Experience in handling HPLC, Dionex, UV-Spectrophotometer, Multimode plate reader and ELISA. Shall be well versed with Biochemical assays (Protein, O-acetyl) immuno-chemical assays and electrophoresis, Education: - Post-Graduate M.Sc. in Biochemistry, Biotechnology, Microbiology, Lifesciences. Experience: - 1-6 years of hands-on experience in relevant field, preferred Vaccine/Biotech background.

Role & responsibilities Cell Culture & Production Support: Perform aseptic handling and maintenance of cell cultures (e.g., Vero, BHK or other cell lines) in adherent and/or suspension formats. Prepare and sterilize culture media, buffers, and reagents as per batch requirements and SOPs. Monitor and record cell growth parameters, viability, and morphology. Scale-up cell cultures for downstream processing or viral seed production. Facility & Environmental Monitoring: Conduct routine facility checks including temperature, humidity, pressure differentials, and cleanroom conditions. Coordinate and ensure compliance with environmental monitoring schedules (viable/non-viable particles, surface, and air sampling). Assist in maintaining facility readiness and hygiene per cGMP standards. Documentation & Quality Compliance: Prepare and review SOPs, batch manufacturing records (BMRs), logbooks, and calibration/maintenance records. Maintain data integrity and compliance with Good Documentation Practices (GDP). Participate in internal and external audits, ensuring timely closure of CAPAs. Quality Management System (QMS): Support implementation and maintenance of QMS elements: deviations, change controls, CAPA, risk assessments, and document control. Participate in training programs related to QMS and GMP compliance. Working knowledge of QMS software/tools is an added advantage. Desired Skills: Proficiency in aseptic techniques and cleanroom operations. Strong understanding of GMP, GLP, GDP, and ISO standards. Good written and verbal communication skills. Job Location: Kadi, Gujarat ( Bus facility available from Ahmedabad, Kalol & Kadi)

BUILD CAREER WITH CHIRON ! WALK IN INTERVIEW On 29 June 2025, Sunday TIME: 10:00 AM to 2:00 PM MANUFACTURING Qualification: M.Sc / B.Sc (Micro, Biotech, Virology, Biochemical) / B.Tech / Diploma/ BE Experience 0 5 Years Production: Drug substance Qualification: M.Sc / B.Sc (Micro, Virology, Biochemical) / B.Tech / Diploma Sterile aseptic operation Autoclave /DHS operation Automated CIP/SIP operation Cell culture Aseptic operation Zonal Centrifuge operation Facility commissioning QMS/ Deviation/ Change control/ CAPA/ Investigation of deviation

We're looking for a highly skilled and motivated Scientist/Research Associate with hands-on experience in mammalian and/or microbial cell culture and molecular biology . You'll play a crucial role in our therapeutic protein expression and purification efforts. Key Responsibilities: Hands-on work experience in mammalian cell culture and/or microbial cell culture . Expertise in therapeutic protein expression and purification using E. coli / yeast expression systems. Well-versed with molecular biology techniques , including: Molecular cloning Primer designing Expression vector generation Characterization and related molecular biology techniques. Experience in the generation of CHO-based stable monoclonal cell lines for mAb/therapeutic protein production. Preferred experience includes: Single-cell cloning Fed-batch studies Cell bank preparation (RCB, MCB, WCB, EPCB) and characterization.