129 Cell Culture Jobs - Page 5

Applications are invited for the Post of Junior Research Fellow (JRF) for the ANRF-SERB funded Core Research Grant (CRG)Projectin theSchool of Chemical Engineering (SCHEME),atVellore Institute of Technology (VIT), Vellore (Sanction order dated 01 August 2024) Title of the Project Design and Characterization of Novel Hydrodynamic Cavitation Reactor for Wastewater Treatment Qualification M. Tech / M.E in Chemical/Environmental Engineering, or a related engineering field with one or two years of experience in water and wastewater treatment is desirable. Describe if any Candidates having knowledge inconducting lab/pilot scale experiments in wastewater treatment will be given preference.

Applications are invited for the Post of Junior Research Fellow (JRF) for the ANRF-SERB funded Core Research Grant (CRG)Projectin theSchool of Chemical Engineering (SCHEME),atVellore Institute of Technology (VIT), Vellore (Sanction order dated 01 August 2024) Title of the Project Design and Characterization of Novel Hydrodynamic Cavitation Reactor for Wastewater Treatment Qualification M. Tech / M.E in Chemical/Environmental Engineering, or a related engineering field with one or two years of experience in water and wastewater treatment is desirable. Describe if any Candidates having knowledge inconducting lab/pilot scale experiments in wastewater treatment will be given preference.

FULL TIME Educational Qualification BTech/MTech/MSc Experience Minimum of 15 Years of Experience in Cell Culture Upstream Process Job Description To lead Upstream team in Drug Substance Manufacturing Department. To provide guidance and train the sub ordinates. To Ensure cGMP principles are followed by team members. Responsible to Prepare / review protocols, reports, Batch Manufacturing Records, Standard Operating Procedures and Qualification Documents. To comply with National and International quality and regulatory standards and always be ready for all kinds of internal and external audits.

Key Responsibilities: Execute routine downstream operations including chromatography (affinity, ion exchange, HIC), filtration techniques (TFF, UF, DF, NF), buffer preparation, and formulation of mammalian cell culture-derived products. Maintain accurate documentation including batch records, deviation reports, SOPs & other QMS elements. Support scale-up and tech transfer from lab to pilot/production scale. Ensure strict compliance with cGMP and safety protocols. Collaborate with QA/QC, maintenance, and engineering teams for smooth operations. Troubleshoot process deviations and contribute to root cause analysis and CAPA implementation.

PrimeGen Healthcare Laboratories Private Limited is looking for Jr. Biochemist to join our dynamic team and embark on a rewarding career journey. Research : Conduct laboratory experiments and studies to investigate biochemical processes, including metabolism, cellular signaling, and genetic expression. Analysis : Analyze and interpret data from experiments, using various techniques such as spectroscopy, chromatography, and molecular biology methods. Hypothesis Testing : Develop and test hypotheses to understand the molecular and chemical basis of biological phenomena. Publication : Prepare and publish research findings in scientific journals, contributing to the advancement of knowledge in the field. Teaching and Education : Educate and mentor students and junior researchers in biochemistry, often in an academic or research institution. Collaboration : Collaborate with other scientists, researchers, and interdisciplinary teams to address complex biological questions. Instrumentation : Use and maintain laboratory equipment and instruments to carry out experiments effectively.

Qualification: MSc / B.Tech (Chemical) / B.Pharm with MBA or PG Diploma in Supply Chain Management Experience & Skills (Essential): 35 years of experience in Opex procurement, preferably in Pharmaceutical R&D, CRO, Discovery Research, or CRAMS industry In-depth knowledge of procurement cycle and CRO/R&D-related activities Hands-on experience in procurement of: Lab chemicals, consumables, glassware, chromatography columns MRO items (engineering, maintenance, spares) Biologics-specific materials (mandatory) Experience in managing long-term contracts: ARC, AMC, O&M Exposure to equipment services procurement Strong data management and reporting skills (MIS, PPTs, Excel) Proficient in computer applications and ERP systems Excellent communication skills for coordination with international suppliers and internal stakeholders Proactive, quality-focused, and problem-solving mindset Job Responsibilities Ensure timely procurement and delivery of chemicals, Opex materials, and services Follow SOPs and procurement policies diligently Handle estimate requests, obtain competitive quotations, and prepare comparative statements Coordinate with scientific teams for indent processing and approvals Create and circulate POs; ensure supplier acknowledgment Liaise with logistics for timely delivery and documentation Coordinate with scientific teams for material receipt and issue resolution Ensure timely supplier payments in coordination with finance Identify and onboard new vendors; negotiate for cost-effective procurement Submit MIS reports regularly Support new business projects and vendor consolidation Manage consolidated and open orders efficiently

Role & responsibilities Responsible for performing and overseeing ELISA (Enzyme-Linked Immunosorbent Assay) testing, ensuring high standards of accuracy, quality control, and efficiency in laboratory operations. This role involves leading a team of technicians, optimizing assay protocols, managing lab inventories, and analyzing data. Deliver GLP and non-GLP ELISA/LBA, MSD ECL, and Luminex Multiplex Analysis for Pharmacokinetic (PK), Toxicology (Tox), Biomarker, Bioavailability (BA), Biosimilar, Immunogenicity, and other bioanalytical studies. Complete Method Development or Method Transfer of customized, robust, and highly sensitive Chromatographic Assay using necessary sample preparation Develop, validate, and optimize ELISA protocols and procedures to improve lab performance and efficiency. Conduct and supervise ELISA testing for various research, diagnostic, and quality control purposes. Analyze data generated from ELISA experiments, including quantification of analytes and assessing assay performance. Analyze and interpret test results, ensuring proper documentation and reporting of data. Well versed in Operation and Calibration of ELISA Instrument with advancements in ELISA technology and laboratory best practices. Manage Incidents, deviation and investigations of ELISA results with documentation. Prepare and review of SOPs, work instructions, method development and method validation protocols and reports. Ensure compliance with safety and quality standards, including SOPs (Standard Operating Procedures) and regulatory requirements. Client management, including acting as company representative to help existing and potential clients, and serving as operational lead in client visits, facility and pre-qualification audits. Supervise junior and senior scientific staff, including evaluating performance and ensuring that all bioanalytical service activities are performed in a safe manner and according to SOPs and GLP regulations. Train, mentor, and provide technical support to junior lab staff and technicians. Work with cross-functional teams to support ongoing research or clinical studies. Preferred candidate profile Bachelor's or Master's degree in Biology, Biochemistry, Biotechnology, or a related field (PhD preferred). Minimum of 8-10 years of experience working with ELISA assays, including advanced experience in assay development and troubleshooting. Ph.D. plus 8 years relevant industry experience or 6 years CRO experience Master's Degree plus 13 years relevant industry experience or 9 years CRO experience Bachelor's Degree plus 14 years relevant industry experience or 12 years CRO experience Interested and suitable applicants can mail their updated CV to hr@qpsbioserve.com

Greetings from Kashiv Biosciences!!! We are looking for Upstream Process Specialist for our Biosimilar manufacturing facility based out of Ahmedabad. Following are the Roles and Responsibilities Roles & Responsibilities Responsible for Upstream Process for Microbial Cell culture and Mammalian Cell culture. Should have exposure on various F ermentation techniques. Qualification and validation of equipment. Exposure to Perfusion process and technique is must. Candidate Details The candidate should have worked in Biosimilars Upstream production(Microbial/ Mammalian Culture) Exposure to Regulatory Audit is Must. Should be aware of QMS Documentation. The candidate should have good communication skills. Interested candidates Please share the resumes at my manan.hathi@Kashivindia.com

WALK-IN INTERVIEW FOR EXPERIENCED PROFESSIONALS Job Location: Hyderabad Experience: 2 to 10 Years Qualification: ITI / Diploma / B.Sc / B.Pharmacy / M.Sc Designations: Operator Sr. Operator Jr. Executive Executive Sr. Executive Openings in the Following Areas: 1. Drug Substance (Bioprocess) Roles & Responsibilities: Upstream Process: Cell Culture Fermentation Autoclave Operation Downstream Process: Virus Culture Centrifugation Tangential Flow Filtration (TFF) Purification Chromatography 2. Drug Product (Formulation & Filling) Roles & Responsibilities: Formulation Activities Filling (Vials, BFS, PFS) Operating Equipment in: Closed RABS (C-RABS) Open RABS (O-RABS) Isolators Sealing and Capping Vial Washing & Autoclaving 3. Packing & Visual Inspection Roles & Responsibilities: Primary and Secondary Packing Operations Handling Track and Trace Systems Operating Labeling and Cartonator machine Documentation & SAP Entries Visual Inspection of Vials & Pre-Filled Syringes (PFS) Note: Candidates with relevant experience in regulatory and compliance environments (USFDA, EU GMP, etc.) will be preferred. Please bring: Updated resume, latest salary slips, passport-size photo, and original certificates.

Job Description: This role is to generate revenue from Commercial organizations and government accounts in and around Karnataka, through selling Stratasys 3D Printers and Handheld 3D Scanners/CAD/CAM/CAE software. Hardware sales covering salesperson whole of Karnataka based out of Bangalore Requirements: Enthusiastic and passionate candidates with experience in selling 3D Printers (FDM, Polyjet, SLS, SLA, DMLS etc) or any 3D Scanners, CAD/CAM/CAE software will be an ideal fit. Preference will also be given to candidates who has experience in selling metrology equipment s and any testing equipment s to Research and development department in an organization. Candidate having sales track record in selling to Large commercial organizations, academic, research institutions SME enterprises, Education Institutions shall be preferred. Yr. of Exp. (Yrs): 3years 9years Required Qualifications: BE Mechanical is preferred or any graduate

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF-SERB funded Core Research Grant (CRG) Project in the School of Chemical Engineering (SCHEME), at Vellore Institute of Technology (VIT), Vellore (Sanction order dated 01 August 2024) Title of the Project : “ Design and Characterization of Novel Hydrodynamic Cavitation Reactor for Wastewater Treatment” Qualification : M. Tech / M.E in Chemical/Environmental Engineering, or a related engineering field with one or two years of experience in water and wastewater treatment is desirable. Describe if any : Candidates having knowledge in conducting lab/pilot scale experiments in wastewater treatment will be given preference. Stipend : Rs. 37,000/- per month + HRA (As per Institute norms). Sponsoring Agency : Science and Engineering Research Board Duration : 3 Years Principal Investigator : Dr. K.Sivagami, Assoicate Professor, School of Chemical Engineering, 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 (27 /05/2025) 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 later which will be intimated by email. The selected candidate will be expected to join at the earliest.

Position Overview:This position involves in optimizing and scale-up fermentation-based processes for nutraceutical manufacturing.Essential Duties and Responsibilities:Prepare media according to established protocolsCalibration of data loggers and handling instruments used in the upstream processesUtilize your knowledge of fermentation principles to improve microbial cultures and optimize fermentation Knowledge of seed transfer into fermentation vessels5. Prepare detailed technical reports, batch records, and other documentation in compliance with regulatory guidelines and company procedures - upstreamCollaborate effectively with cross-functional teams Knowledge of downstream processing techniques and purification of microbial products

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description When you re part of the team at Thermo Fisher Scientific, you ll do important work. Surrounded by collaborative colleagues, you ll have the support and opportunities that only a global leader can give you. Our respected, growing organization has an outstanding strategy for the near term and beyond. Take your place on our strong team, and help us make significant contributions to the world. Location/Division Specific Information This position is based in Mumbai, Pune, or Ahmedabad, within our Bioproduction Division. Our team drives innovation in Cell Culture and Cell Therapy, ensuring that we deliver world-class solutions to our customers. Discover Impactful Work: Join us to make a significant impact on the biopharmaceutical industry! As a Field Application Scientist, you will play a crucial role in advancing research and development, helping to bring new therapies to market. A day in the Life: Lead technical discussions on product specifications, applications, and protocol optimizations. Provide field-based technical support and troubleshooting to customers. Conduct seminars and training programs for both internal teams and external customers. Keys to Success: Your ability to collaborate effectively with sales teams and customers will be key to your success. Your expertise in Cell Culture and Cell Therapy, coupled with your proactive approach to problem-solving, will ensure perfect execution of projects. Education Postgraduate or equivalent experience in Biotechnology or PhD or equivalent experience in Biotechnology, Biosciences. Experience 8-10 years of proven experience in the Bioprocess Industry. Experience in handling cell lines, process optimization, and CQA modulation. Knowledge, Skills, Abilities Proficient in cell culture, maintenance, and propagation. Hands-on experience in cell cloning and selection. Strong presentation skills and the ability to present at customer sites and conferences. Physical Requirements / Work Environment This role requires regular travel to customer sites and participation in various seminars and training sessions. You must be able to handle laboratory equipment and work in a dynamic, fast-paced environment. Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Tasks Planning and maintenance of laboratory records, perform routine Cell culture maintenance, Microbiology preparations,Documentation and other allied works and statistical analysis of data Requirements Maximum Age: 28 yrs as on 01.05.2025 Stipend : Rs.13,500 for First Year, Rs 15,000/- for Second Year & Rs.18,000/- for Third Year respectively Qualification: Essential :MSc. (Biotechnology) with 60% mark No. of Positions: 1 Posting Location : Thiruvananthapuram Period of Training : Three Years General Conditions: 1. Before applying, candidates should ensure that they fulfil all the eligibility criteria mentioned in the advertisement. 2. All information submitted in the application will be verified with original documents at the time of the interview. If any information provided by the candidate is found to be false or incorrect or not in conformity with the eligibility criteria, then his/her candidature is liable to be rejected/cancelled at any stage of the recruitment process. 3. Only Indian Nationals are eligible to apply. 4. SC/ST/OBC/PwD candidates will be eligible for relaxation as per Government of India directives. 5. The crucial date for determining the age limit shall be same as the cut of date for calculating Qualification & Post Qualification Experience of the candidates. 6. HLL reserves the right to cancel, restrict, or modify the selection process, or to not fill any or all of the posts notified, at its discretion. The number of vacancies may also be increased or decreased based on organizational requirements. 7. Candidates working in Government, Semi-Government Organizations, Public Sector Undertakings, or Autonomous Bodies must provide a No Objection Certificate (NOC) at the time of the interview. 8. The decision of Management regarding selection will be final. 9. Canvassing in any form will be a disqualification Contract Type Training & Development Scheme For more details and to apply ONLINE please visit www.lifecarehll.com/careers

Role & responsibilities : The candidate should also possess practical experience in the following techniques: Bacterial characterization Maintenance of bacterial cultures Phenotypic and genotypic characterization Antimicrobial susceptibility testing using disc diffusion and broth dilution methods Time-kill curve studies Fractional Inhibitory Concentration (FIC) studies Bioburden analysis in biological samples

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.

" Jubilant Biosys is looking for Research Associate II - DMPK Qualification : M Pharm Experience : 3-5 Years Responsibilities : Understand the broader ADME requirements of various projects Interact with other cross functional teams (internal and external) and contribute to the progression of the compounds in the project Design tailor made ADME protocols for biochemical and cell based assays (Caco-2, MDCK etc) In charge of Cell culture lab and cell bank maintenance Collate the obtained results and prepare presentations for internal and external meetings Contribute to the design of the critical path for various projects Method validations and analytical trouble shooting; Data generation, compilation, report preparation; Lab note book, record keeping; SOP writing Prepare regular project updates and share with DMPK team management. Guide people/team on planning and execution of work and SOP writing Potential for assisting in high throughput assay conduct Conduct assays and sample preparations following established procedures to support drug discovery programs of the clients. Operate LC-MS for compound tuning, method development, and sample analysis. Assist development of new assays to help improve service capabilities. Assist troubleshooting of the issues/problems arisen from the assays and execute solutions for problem solving. Train other scientists in running established assays. ",

To carry out routine Lab activities. To carry out assigned Lab experiments. To prepare documents as per requirements. Good knowledge of biological science. Good skills of MS Office for documents preparations.

Roles & Responsibility: Perform method development, method validation and study sample analysis under supervision of Project Manager (s). Passaging of cells as well as performing cell based assays while maintaining aseptic conditions in cell culture laboratory. Perform ELISA & other Ligand Binding Assay according to study protocol guidelines and/or SOPs Processing of specimens to support the clinical studies. Preparation of required reagents and solvents. Preparation of SOP(s) and work instruction. Following GLP, GDP, GCLP & other good practices. Desirable candidate: MSc BioTech/ Biochemistry/ Microbiology or BTech Biotech fresher. 0-1 year of relevant experience will be preferable. Sound knowledge on Immunology. Good communication skills, analytical skills and team coordination.

experience in cell culture Strong exposure to In-Process Quality check in Cell biology & Quality Management Systems Knowledge of GMP guidelines and documentation practices cell culture, cell sorting, cell.manufactiring

Greetings from Kashiv Biosciences!!! We are looking for Upstream Process Specialist for our Biosimilar manufacturing facility based out of Ahmedabad. Following are the Roles and Responsibilities Roles & Responsibilities Responsible for Upstream Process for Mammalian Cell culture. Should have exposure on various Fermentation techniques and Single use Bio reactors. Qualification and validation of equipment. Exposure to Perfusion process and technique is must. Candidate Details The candidate should have worked in Biosimilars Upstream production (Mammalian Culture) for atleast 10 Years and exposure to Perfusion technology is must Exposure to Regulatory Audit is Must. Should be aware of QMS Documentation. The candidate should have good communication skills. Interested candidates Please share the resumes at my manan.hathi@Kashivindia.com

Applications are invited for the Post of Senior Research Fellow ( SRF ) for the Centre for High Technology, Ministry of Petroleum and Natural Gas f unded Project in the School of Chemical Engineering (SCHEME), at Vellore Institute of Technology (VIT), Vellore (CHT project MoA dated 06-10-2023 between VITV, IITM and other partner industries) Title of the Project : “ Catalytic Pyrolysis of Multilayer Plastic Waste (MLP) to Value Added Products – A Circular Economy Approach ”. Qualification : M. Tech / M.E in Chemical/Mechanical engineering, or a related engineering field with one or two years of experience in fuel processing techniques in lab/pilot scale plants. Describe if any : Candidates having knowledge in conducting lab/pilot scale pyrolysis experiments and fuel processing techniques will be given preference. Stipend : Rs. 35,000/- per month , stipend will be as per Institute norms. Sponsoring Agency : CHT, Ministry of Petroleum and Natural Gas. Duration : 2 Years Principal Investigator : Dr. K.Sivagami, Associate Professor, School of Chemical Engineering, 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 (1 5/08/2025) 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 later which will be intimated by email. The selected candidate will be expected to join at the earliest.

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.

PRINCIPAL DUTIES AND RESPONSIBILITES: Note: These statements reflect the general description of the position and are not intended to be an all-inclusive list of tasks to which the employee may be assigned. I STUDY RELATED ACTIVITIES: A. Centrifuges, freeze specimens as required. B. Performs aliquots of samples for ELISA & other Ligand Binding Assay & Perform study sample analysis and validation batches. C. Performs ELISA & other Ligand Binding Assay according to study protocol guidelines and/or SOPs. D. Completes documentation as required by protocol and/or SOP. E. Operates Microplate Reader, Microplate Washer and troubleshoots problems and performs minor repairs. F. Prepares required reagents and solvents. G. Under direction of the project manager, performs method development, method validation and study sample analysis experiments. H. Safety Implement a safe laboratory environment in compliance with good practice and applicable regulations. II GENERAL LAB DUTIES: A. Prepares required reagents and solvents. B. Under direction of the project manager, may perform some method development. III ADMINISTRATIVE DUTIES: A. Conforms to training schedule for own position and maintains awareness of SOP content, according to company requirements.

Position: Pre-Clinical Designation: Research Associate Job Location: Dholka, Gujarat 1. Study Sample Analysis- Clinical studies 2. Method Development and Method Validation - Preparation of STP And MVP 3. Coordinate with QA & QC department for timely completion of Projects reports 4. Preparation of SOP and method development and method validation documents 5. Maintaining GLP & ensure 100% compliance