80 Cell Culture Jobs

You will be responsible for Vaccine Manufacturing (Cell Culture), including tasks such as cell revival, subculture, and cell counting of MRC-5 cells. You will also be involved in the preparation of MCB/WCB and handling Roller bottles, Cell stacks, and TCFs. Experience in virus infection, virus harvesting procedures, and working with Chicken embryo fibroblast cells will be required. In the Quality Control department, you will be expected to perform various biochemical techniques, chromatography techniques, electrophoresis techniques, and immunoassay techniques. Your responsibilities will also include cell culture techniques, molecular techniques, analytical method validation (AMV), and analytical method development and transfer quality control (QC). Knowledge of cGMP, cGLP, and QMS will be essential for this role.,

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.,

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. 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 virus infection, virus harvesting procedures. Experience in working with Chicken embryo fibroblast cells, pooling of embryos, seeding of RB’s . Quality Control Analyst Biochemical techniques, Chromatography techniques, Electrophoresis techniques, Immuno assay techniques Cell culture techniques, Molecular techniques Analytical method validation (AMV), Analytical Method Development and Transfer Quality control (QC), cGMP, cGLP and QMS. Drug Product (Filling-Officer/Executive/Sr. Executive/Operator) Experienced in handling of O-RABS, Operation of Vial washing/Filling/Lyophilizers/Autoclave/Process vessels.

As a Research Scientist1 DMPK at the Foundation for Neglected Disease Research in Bengaluru, you will play a crucial role in supporting drug discovery and development projects by performing and analyzing in vitro and in vivo DMPK studies. Your responsibilities will include planning, designing, and executing DMPK experiments, maintaining laboratory instruments, and preparing protocols. Additionally, you will be tasked with writing reports, communicating with the project team, and presenting DMPK data during project meetings. Your technical skills will be put to the test as you set up and conduct physiochemical assays, in vitro DMPK assays, and bioanalytical methods. Your experience in analyzing in-vivo pharmacokinetic samples and familiarity with sample processing techniques will be invaluable. Proficiency in handling LC-MS/MS for quantitative analysis, protocol preparation, and report writing is essential for this role. Moreover, your additional experience in animal handling, conducting PK studies, and working with cell lines such as Caco-2 will be advantageous. Knowledge of interpreting pharmacokinetic data using Phoenix WinNonlin and operating in a GLP or GLP-like environment will also be beneficial. Basic skills required for this position include working independently with enthusiasm, strong decision-making and problem-solving abilities, effective collaboration across multidisciplinary functions, and knowledge of drug discovery and development processes. Excellent oral, written, and interpersonal communication skills in English, along with proficiency in computer applications, are essential for success in this role. To be considered for this position, you must be an Indian citizen with an M.Pharm, MS (Pharm), or PhD qualification and possess 2 to 5 years of industry experience. The salary offered will be commensurate with your experience. If you meet the qualifications and are excited about this opportunity, please submit your resume to hr@fndr.in with the subject line "Application for Research Scientist 1 DMPK," including your notice period, current location, and current and expected CTC in the body of the email. We look forward to receiving your application.,

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.,

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

Roles & Responsibilities: Supervision and Management: Oversees all diagnostic work in the cytogenetics lab, including personnel management, quality assurance, and project management. Technical Expertise: Possesses a strong understanding of cytogenetics, including cell culture, chromosome analysis (karyotyping), FISH, and microarray analysis. Result Interpretation and Reporting: Analyses and interprets cytogenetic results, prepares reports, collaborates with other healthcare professionals and releases reports well within defined turn around time. Quality Assurance: Implements and maintains quality control procedures and ensures adherence to regulatory compliance standards. Training and Development: Trains and supervises laboratory staff in cytogenetic procedures and safety protocols. Clinical Governance: Participates in laboratory quality assurance and clinical governance processes, including internal audits and service improvements. Communication and Collaboration: Effectively communicates complex information to colleagues and other healthcare professionals. Troubleshooting: Possesses specialized training and experience in troubleshooting cytogenetic issues. Strategic Planning: Contributes to the strategic planning and operational management of the cytogenetics laboratory section. Staying Current: Remains up-to-date with advancements in cytogenetics and related fields. Sample Handling: Oversees the handling and processing of patient samples for cytogenetic analysis. Equipment and Software: Utilizes advanced laboratory equipment and software for the evaluation of genetic disorders. Adherence to Protocols: Ensures that all procedures are performed according to established protocols and guidelines. Preferred candidate profile A degree with specialization or experience in Genetics and Cytogenetics or Molecular Cytogenetics. National registration with specialization/experience in Genetics and Cytogenetics or Molecular Cytogenetics. Strong analytical and problem-solving skills. Excellent verbal and written communication skills. Ability to work independently and as part of a team. Experience in a clinical laboratory setting. Familiarity with relevant software and bioinformatics tools. Commitment to ongoing professional development

Department: Cell Biology Location: R&D, Thane KRAs: Handling and Maintenance of Cell Lines Execution of in vitro bioassays such as ELISA & Cell Based assays Preparation of SOPs, Reports with documentation practices Maintenance of consumables inventory and & timely procurement of reagents. Roles and Responsibilities: Revival & culturing of cell lines Subculturing of cell lines Cryopreservation of cell lines Execution of in vitro bioassays

At Umami Bioworks, we are a leading bioplatform for the development and production ofsustainable planetary biosolutions. Through the synthesis of machine learning, multi- omics biomarkers, and digital twins, UMAMI has established market-leading capability for discovery and development of cultivated bioproducts that can seamlessly transition to manufacturing with UMAMI s modular, automated, plug-and-play production solution By partnering with market leaders as their biomanufacturing solution provider, UMAMI is democratizing access to sustainable blue bioeconomy solutions that address a wide range of global challenges. Umami Bioworks is looking to hire an inquisitive, innovative, and independent Research Associate for either Cell Line and Media Development to join our R&D Team in Bangalore, India with hands-on experience in animal cell culture and media formulation to support the development of scalable, serum-free cell culture platforms for marine species. This role involves the isolation, characterization, and optimization of cell lines from fish and crustaceans, as well as the formulation and screening of food-grade, cost-effective culture media to support proliferation and differentiation. You ll work directly with senior technical leadership and cross-functional teams to meet scientific and commercial milestones. Responsibilities: Develop, characterize and optimize cell lines derived from fish and crustacean species Primary cell isolation & suspension adaptation Plan and execute experiments to evaluate cell growth, viability, and differentiation potential towards muscle or fat cells etc. Optimize protocols for cell lines characterization Sourcing of animals of various developmental stages for cell line isolations Design and execute experiments using high-throughput screening approaches to identify optimal media compositions. Formulate and produce novel, food-grade, serum-free media formulations for cell proliferation and differentiation. Collaborate with external vendors, suppliers, and internal teams to source raw materials and animal tissue samples. Prepare reports and technical presentations in coordination with senior scientists for internal and external updates. Core competencies: Minimum 2 years of experience in cell line development, preferably in aquatic species Proficient in animal cell culture techniques, including primary cells, stem cells, suspension culture, and primary cell culture Experience working with high-throughput screening in multi-well plate formats for molecular biology or cell biology applications. Familiarity with statistical analysis tools and DoE methodologies for data interpretation and process optimization. Strong experimental design skills and attention to detail in documentation and data analysis. Experience Master in Biology/Life Science, or related field with more than 2 years of relevant industry experience Bachelor in Biology/Life Science, or related field with more than 5 years of relevant industry experience

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

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 Title: ADME Scientist Job Location: Bangalore/Hyderabad Department: Discovery Biology 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 Support the ADME team by planning and conducting the metabolic stability, Single point inhibition, reversible CYPIC50 inhibition and TDI-IC50 shift assays using Human liver microsomes with highest quality Time management and multi-tasking skills to meet the demand of high-volume wave 1 ADME assays to complete multiple projects within timelines. Contemporaneous recording of lab activities and experiments performed, practices high level of house keeping Adhere to all safety rules and maintains safe workplace. Predominantly laboratory-based job Key Responsibilities: Extensive experience in planning metabolic stability, CYP inhibition assays Design and execute in-vitro Single point inhibition, reversible CYPIC50 inhibition and TDI-IC50 shift assay with human liver microsomes. Seamless coordination with BA-DMPK group to design in-vitro CYP inhibition studies. Preparation of SOPs and EOPs. Reporting of executed studies without any noncompliance. Reporting of study results clearly in the cross functional scientific meetings. Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Ensure environment, health, and safety (EHS) measures are imparted via training and adhered within the team. Educational Qualification: A M Pharm. in any pharmaceutical science or M Sc. in biological science. Technical/functional Skills: Comprehensive understanding of in vitro ADME assays and technical expertise in trouble shooting the assays In depth understanding of biochemical and aspects of enzyme kinetics is highly desirable related to the metabolism Good, demonstrated knowledge in software such as Microsoft excel and Graph pad prism Demonstrated cross functional leadership capabilities Experience with automation is desirable Experience: A M Pharm. in pharmaceutical sciences or M SC in biological science with nine or more years of Industrial experience in DMPK/ADME research. Behavioral Skills: Demonstrate ability to be a team player. Commitment to deliver the study reports within the agreed timelines Adaptability to changes in the dynamic lab environment Communicate confidently with colleagues and collaborators in the meetings and presentation of study reports and evidence of publications in the PEER reviewed Journals Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

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.,

Are you passionate about Life Sciences and ready to take the next step in your sales career Join us in shaping the future of biotech research! We are looking for a highly motivated Account Manager to drive growth and build lasting customer relationships in Chennai and surrounding regions. If you have a strong background in Life Sciences and a flair for consultative selling, this role is for you! Role: Account Manager - Bioresearch Location: Chennai Industry: Biotechnology / Life Sciences / Biomedical Experience: 5+ years in sales/customer-facing roles within Life Sciences Key Responsibilities: - Manage existing accounts and develop new opportunities in genomics, cell biology, and cell culture. - Understand customer needs and propose suitable scientific solutions. - Collaborate with researchers, KOLs, and internal teams. - Drive sales growth and exceed targets. - Represent the company at scientific events and conferences. Qualifications: - Bachelors or Masters in Life Sciences, Biotechnology, Biochemistry, or related field. - Strong understanding of scientific concepts and customer-centric selling. - Experience in handling instruments like multimode readers, cell counters, and lab automation systems is a plus. - Excellent communication and relationship-building skills. - Willingness to travel within the region. Apply Now or tag someone who would be a great fit! Send your updated resume to ganapathidas.v@spincotech.com,

Responsibilities: Experience in sales and Applications operations Proficient laboratory skills Bachelor's degree in Life Sciences, Biotechnology 0-2 years of experience in application sales Must be prepared to travel south and north Indian Cities

Lead Cell & Molecular Biology department. Design and execute recombinant antigen generation in E.Coli, Insect and mammalian cells for diagnostic kits. Generate monoclonal antibodies against antigens by Hybridoma / Phage display methods. Making recombinant antibodies Isolate genes from Hybridoma and expressing them in Mammalian cells. Preferred candidate profile Handson experience in Recombinant proteins and Monoclonal Antibody generation. Expertise in Molecular Biology, Cell culture and Purification. Knowledge about diagnostics assays CLIA, Rapid and ELISA would be an added advantage.

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.

Design and execute experiments related to the formulation development of oral solid dosage forms using HME techniques. Operate and maintain HME equipment including twin-screw extruders, feeders, and associated downstream processing units (milling, compaction, etc.). Conduct pre-formulation studies, including excipient compatibility and thermal analysis (DSC, TGA). Perform process optimization and scale-up studies for HME-based formulations. Prepare solid dispersions, amorphous systems, and evaluate physical and chemical stability. Perform solid-state characterization using tools such as XRPD, FTIR, Raman spectroscopy, and microscopy.

1) Preparationof Analytical method validation Protocols and reports for the relatedsubstances and Assay by HPLC and residual solvents by GC 2) Preparation of Analytical methodvalidation Protocols and reports for the Identification analysis by HPLC,GC andparticle size analyzer and performing the analytical method validations for theIdentification, content and purity analysis by HPLC,GC and Particle sizeanalyzer. 3) Performing the Analytical methodvalidations by HPLC and GC. 4) R esponsible to follow and ensure strict compliance to GLP practices in the laboratory to meet the organizational goal which in line with procedural references. 5) Maintenance of log books and Calibration records as per procedural references. 6) Preparation of Analytical method validation Protocols and report for the Elemental Impurities analysis by ICP-MS and Perform the analytical method validations for elemental impurities by ICP-MS.

Role & responsibilities Working on unit operations related to upstream processing during DS Manufacturing. GMP Documentation related to DS manufacturing. Preparation of documents like SOPs, MMDs and QMS related documents like change control, deviation, CAPA, Risk assessment. Preparation and maintenance of virus stocks. Coordination with cross-functional team. Involvement during regulatory audit preparation. Preferred candidate profile Must have experience in Biopharma

Egg Handling Pre-incubation Egg Candling Allantoic Fluids/Embryo Harvesting Inactivation Aseptic Handling and Sampling cGMP Practices Documentation

Fermenter handling & operation for production Fermenter media preparation & dispensing to fermenter Handled segments of products like nutraceuticals/probiotics/recombinant proteins

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.,