129 Cell Culture Jobs

About Immuneel Immuneel Therapeutics Private Limited is a pioneering start-up company leading the charge in cell therapy and personalized immunotherapy for patients in India. For more details, please refer www.immuneel.com We Pursue, with Purpose, to serve our Patients (3 Ps) by Connecting within, Collaborating globally and Creating (3 Cs) solutions. Our flexible, diverse, and vibrant team is bringing together best practices and innovations in the field of cell and gene therapy. Working at Immuneel promises the excitement of an agile startup on a critical mission. Proudly Indian in solutioning, yet global in outlook, we are keen to collaborate. We value diversity including in experience and perspectives. We value work-life balance and believe that having fun on the job is integral to achieving the right results. We pride ourselves on providing an open environment and our mission resonates with humanity everywhere. At Work, we are: Passionate in driving patient outcomes: We are passionately committed to doing the RIGHT thing to achieve the best outcomes for our patients through innovation, agility and performance orientation. We put the impact on the patient above all else. Responsible and accountable: We demonstrate ownership and accountability for our actions. We make timely and well-informed decisions, learning from our performance. Transparent, honest, and supportive in how we work together: We insist on integrity and respect for the individual. We demand excellence. Our performance management is focused on excellence through timely and constructive feed-forward. Inclusive and flexible: We are full of life and embrace all opportunities to collaborate and work together. We are excited about the collective knowledge and expertise that we share. Being and thinking different is valued. Immuneel prides itself as an organization that is keeping pace with best practices in organization design. Our role-based organization incorporates global trends in human capital that promote focus on work and greater nimbleness. Our role-based structure allows you to be cherished by the work you do and bring value to your work rather than designations, our organization is simplified into a flat, non-hierarchical, millennial, organization where you may fully inherit the role you play in the organization and are recognized by the accountability you take and the work you deliver. Immuneels employees are integral to our quest to develop and deliver high quality engineered cell therapies in India. We believe that our culture provides an environment for employees to excel and find purpose. The strength of our team is every bit as important as our cutting-edge technology and we invest in clear compensation and comprehensive benefits for our employees. People for us, are not resources, but our capital. If you are a talented professional, an out-of-box thinker with a zeal to help change, and passionate about healthcare, we invite you to join us and be a part of a historic initiative in India. Interested to be a part of the next revolution in cancer treatment Send your resume to [HIDDEN TEXT] 1. Role Title: Trainee - Research & Development (Viral Vector) 2. Department/Function: Research and Development 3. Reporting Structure: Reports to: Viral Vector Direct Reports: NA 4. Role Summary: Immuneel is looking for an intern to support the upstream and downstream process development for viral vectors and associated analytics. The said candidate must have a strong understanding of cell culture, filtration, molecular biology and cell biology. Key deliverables will be to support Viral Vector Scientists to drive projects and programs through process development culminating in global IND applications. Knowledge on process development, analytical method development and single use technologies is an added advantage. 5. Key Responsibilities: Execution of studies for Viral Vector process and analytical method development under the guidance of Scientists. Experience in Biologics with brief exposure to Viral Vector acceptable Scientific support for upstream and downstream process development/improvement for suspension & adherent based Viral Vector platforms, with an intent of making cost-affordable process. Ordering of reagents, consumables, inventory management. Preparation, cross-functional review and training of the SOPs/EOPs/Work Instructions and other documents required for quality management system requirement. Compilation and recording of data in process records (hard copy or digital) and preparation of technical reports. Coordination with Application Scientists and Engineers for technical trouble shooting of Process Development facilities and associated utilities. 6. Primary Objectives: Support process development and analytical testing for viral vectors Associated documentation Support technology transfer of upstream process as a part of technology transfer of the viral vector manufacturing process 7. Competencies Required: Technical Competencies: Understanding of process development Understanding of Bioprocess technology Experience in Handling HEK293 T cells, Cell Banking and Scaleup Sterile Practices and Handling Soft Skills: Project planning Data presentation Collaboration Team Player Willingness to Learn Challenge 8. Qualifications: B.Tech or M.Tech (Science) 9. Working Conditions: Role Type: Full Time and Onsite Work Hours: 9:00 AM to 6:00 PM for the General Shift and 2:00 PM to 11:00 PM for the Post-Noon Shift (on a rotational basis). There will be two days off each week, which may not necessarily fall on a Saturday or Sunday. Travel Requirements: No Trainee Tenure: The traineeship period is for a duration of 11 months. Base Location: Immuneel Therapeutics Private Limited, 8th Floor, Mazumdar Shaw Medical Center, Narayana Health City, Bommasandra Industrial Area, Bangalore - 560099 Show more Show less

As a Biosimilar Process Development Scientist, your role involves strategizing the process development using CHO & other mammalian cell lines for non-infringing Upstream processes. You will be responsible for understanding cell lines, cell culture, and bioreactor processes for biotherapeutic proteins development in India and other regulated countries. Your key responsibilities include: - Planning and executing experiments for process development at shake flask and bioreactor stages - Formulating media & feed, verifying components" roles, and utilizing spent media analysis for process improvement - Designing and conducting process characterizations for upstream development - Scale up & scale down operations at various bioreactor scales - Analyzing scientific research data using statistical software to interpret trends and patterns - Leading a team for day-to-day cell culture works and coordinating with other groups for project completion - Overseeing work performance at production plants or manufacturing units - Supporting commercialization activities such as tech transfer, process validation studies, and troubleshooting Your qualifications should include being well-versed in the latest upstream-related instruments, cell culture, and bioreactor processes. You should be a team player, exhibit good documentation practices, demonstrate scientific acumen, and possess clear communication skills in English. Additionally, you should have a good working knowledge of MS Office, statistical software, and analytical tools. Ideally, you hold a PhD or post-doc degree with bioprocess cell culture experience from abroad. You are expected to engage in scientific discussions, be a constant learner, and deliver targeted outcomes efficiently.,

Diagnose and treat cancer patients, providing personalized treatment plans including chemotherapy, radiation, and immunotherapy. Conduct research and stay updated on the latest advancements in oncology treatments. Collaborate with a team of surgeons, radiologists, and pathologists to ensure comprehensive patient care. Must have an MD/MS/M.Ch degree with extensive experience in medical oncology. Experience in clinical trials and cancer research publications is a plus.Keywordsmedical oncology,clinical trials,cancer research,mdt,chemotherapy,radiology,diagnosis,patient care,biochemistry,general medicine,biotechnology,internal medicine,dnb,clinical research,immunology,molecular biology,nursing,pharmacovigilance,Oncology*Mandatory Key Skillsmedical oncology,clinical trials,cancer research,mdt,chemotherapy,radiology,diagnosis,patient care,biochemistry,general medicine,biotechnology,internal medicine,dnb,clinical research,immunology,molecular biology,nursing,pharmacovigilance,Oncology*

Diagnose and treat cancer patients, providing personalized treatment plans including chemotherapy, radiation, and immunotherapy. Conduct research and stay updated on the latest advancements in oncology treatments. Collaborate with a team of surgeons, radiologists, and pathologists to ensure comprehensive patient care. Must have an MD/MS/M.Ch degree with extensive experience in medical oncology. Experience in clinical trials and cancer research publications is a plus. Mandatory Key Skills clinical trials,cancer research,oncology,mdt,chemotherapy,radiology,patient care,biochemistry,general medicine,biotechnology,internal medicine,clinical research,immunology,molecular biology,nursing,pharmacovigilance,medical oncology*

Role Overview: Immuneel is seeking an intern for the position of Trainee - Research & Development (Viral Vector) to assist in the upstream and downstream process development for viral vectors and associated analytics. The ideal candidate should possess a strong understanding of cell culture, filtration, molecular biology, and cell biology. The primary responsibilities include supporting Viral Vector Scientists in driving projects and programs through process development towards global IND applications, with knowledge in process development, analytical method development, and single-use technologies being beneficial. Key Responsibilities: - Execute studies for Viral Vector process and analytical method development under the guidance of Scientists, with experience in Biologics and brief exposure to Viral Vector being acceptable - Provide scientific support for upstream and downstream process development/improvement for suspension & adherent based Viral Vector platforms to create cost-affordable processes - Manage ordering of reagents, consumables, and inventory, along with the preparation, review, and training of SOPs/EOPs/Work Instructions and other quality management system documents - Compile and record data in process records and prepare technical reports, while coordinating with Application Scientists and Engineers for technical troubleshooting of Process Development facilities and utilities Primary Objectives: - Support process development and analytical testing for viral vectors - Documentation and technology transfer of the upstream process as part of the viral vector manufacturing process technology transfer Qualifications: - B.Tech or M.Tech (Science) Working Conditions: - Role Type: Full Time and Onsite - Work Hours: General Shift (9:00 AM to 6:00 PM) and Post-Noon Shift (2:00 PM to 11:00 PM on a rotational basis) with two days off each week - Travel Requirements: No - Trainee Tenure: 11 months - Base Location: Immuneel Therapeutics Private Limited, Bangalore (Note: Additional details about the company were not explicitly mentioned in the provided job description.),

As a candidate for this role, you will be responsible for the following key responsibilities: - Thorough knowledge of HPLC based analysis of recombinant proteins including RP-HPLC, SE-HPLC, and glycan analysis. - Independently design method development of proteins, qualification, transfer following ICH/USP/EP/IP guidelines. This includes writing and reviewing protocols, transfer plans, and reports. - Carry out day-to-day analytical work and collaborate with the Cell culture and downstream teams in Biotech R&D. - Set up product-related test/release specifications and analytical protocols for Biotech products. - Design in-house/outsource methods for Physico-chemical characterization of biological products. - Coordinate with QC for the smooth implementation of new methods. - Maintain equipment logs and documentation in the lab. - Monitor and maintain stability of various products in Biotech. - Prepare lab-related documents, regulatory submission documents, and provide QC support (SOP, STP, COA, MOA, Specification). - Interpret data and write reports in support of regulatory submissions. - Review analytical data for in-process & stability related activities. Qualifications required for this role: - Strong knowledge of HPLC based analysis of recombinant proteins. - Experience in method development, qualification, and transfer following ICH/USP/EP/IP guidelines. - Good understanding of analytical work in a Biotech R&D setting. - Ability to design analytical protocols for Biotech products. - Knowledge of Physico-chemical characterization of biological products. - Proficiency in interpreting data and writing reports for regulatory submissions.,

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

Description We are seeking a dedicated and dynamic Assistant Professor of Biotechnology to join our academic team. The ideal candidate will have a strong background in biotechnology research and education, with a passion for mentoring students and advancing the field through innovative research. Responsibilities Deliver high-quality lectures and engage students in biotechnology-related subjects. Conduct and supervise research projects in biotechnology. Collaborate with faculty members on interdisciplinary research initiatives. Guide and mentor undergraduate and postgraduate students in their research endeavors. Participate in academic committees and contribute to curriculum development. Skills and Qualifications Ph.D. in Biotechnology or a related field from a recognized university. Strong understanding of molecular biology, genetic engineering, and bioprocessing. Experience with laboratory techniques. Demonstrated ability to conduct independent research and publish results. Excellent communication and presentation skills. Strong organizational and time-management skills.

As a Senior Scientist specializing in Process Modeling and Hybrid Modelling within the Manufacturing Intelligence (MI) team of Pfizer's Global Technology & Engineering (GT&E), your role will involve the development and implementation of advanced analytics solutions such as AI/ML, soft sensor, advanced process control, and process condition monitoring in support of manufacturing operations at Pfizer Global Supply (PGS). **Responsibilities:** - Make technical contributions to high-impact projects requiring expertise in data analytics, advanced modeling, and optimization. - Identify valuable opportunities for applying Advanced Analytics, Advanced Process Control (APC), Artificial Intelligence (AI), Machine Learning (ML), and Industrial Internet of Things (IIoT) in manufacturing settings. - Develop mathematical and machine learning models and assist in the GMP implementation of analytics solutions. - Utilize engineering principles and modeling tools to improve process understanding and enable real-time process monitoring and control. - Collaborate with cross-functional teams, communicate progress effectively to management, and drive project advancement. **Basic Qualifications:** - Preferably a B. Tech in computer science. - Must possess expert-level knowledge in Python; familiarity with R, Matlab, or JavaScript is a plus. - Proficiency in performing data engineering on large, real-world datasets. - Demonstrated experience in applying data science and machine learning methodologies to drive insights and decision-making. - Ability to work collaboratively in diverse teams and communicate effectively with technical and non-technical stakeholders. - Knowledge of Biopharmaceutical Manufacturing processes and experience in technical storytelling. **Preferred Qualifications:** - Expertise in first principles such as thermodynamics, reaction modeling, and hybrid modeling. - Experience with Interpretable Machine Learning or Explainable AI and familiarity with Shapley values. - Proficiency in cloud-based development environments like AWS SageMaker and data warehouses like Snowflake or Redshift. - Understanding of feedback control algorithms, real-time communication protocols, and industrial automation platforms. - Experience in data visualization tools like Streamlit, Plotly, or Spotfire. - Knowledge of Cell Culture, Fermentation, and Vaccines Conjugation. This role offers a flexible work location assignment, including the option to work remotely. Pfizer is an equal opportunity employer, adhering to all applicable equal employment opportunity legislation across jurisdictions.,

Inviting Science Graduates ONLY with Biology Candidates from Vadodara (Gujarat) only eligible to apply as this is work from office 5 days a week offering 20K for freshers and 25K for exp candidates Must onbaord within 7 days

As a Scientific Officer in the Molecular Biology department at Gene to Protein, a division of Biotech Desk Pvt. Ltd., you will be an integral part of our fast-growing biotech company. Your role will involve designing, executing, and analyzing molecular biology experiments to contribute to projects in drug discovery, diagnostics, and genetic research. By generating high-quality data, you will ensure scientific excellence and play a crucial role in advancing life sciences research. Your key responsibilities will include designing, planning, and executing experiments in molecular biology and cell culture. You will be involved in nucleic acid extraction (DNA/RNA), quality control, and quantification processes. Furthermore, you will conduct PCR, qRT-PCR, digital PCR, and cloning techniques such as restriction, Gibson, and Golden Gate. Additionally, you will be responsible for constructing and purifying plasmids, performing protein expression and analysis using methods like Western Blot and ELISA. Your role will also involve analyzing, interpreting, and presenting experimental results to project teams, troubleshooting experiments, optimizing protocols, and ensuring reproducibility. It is essential to maintain equipment, uphold lab safety standards, and comply with regulations. Staying updated with scientific advancements will be crucial to enhancing project outcomes. To qualify for this position, you should hold an M.Sc. in Biotechnology, Molecular Biology, Biochemistry, or a related field. A minimum of 2-3 years of hands-on research experience in academia or industry is required. Proficiency in core molecular biology techniques such as PCR, cloning, and electrophoresis is essential. Strong problem-solving skills, analytical abilities, and excellent documentation skills are highly valued. Effective communication skills and the ability to work both independently and collaboratively are key attributes for this role. In return, we offer a competitive salary and benefits package along with professional growth and career development opportunities. You will have exposure to cutting-edge biotech research and applications, providing a stimulating environment for your career growth. To apply for the position of Scientific Officer in Molecular Biology at Gene to Protein, please send your CV and a cover letter highlighting your relevant experience to volety.biotechdesk@gmail.com with the subject line: Application for Scientific Officer [Your Name]. Join our dynamic team and be part of our mission to advance life sciences research through innovative solutions.,

BUILD CAREER WITH CHIRON ! WALK IN INTERVIEW On 13 Sep 2025, Saturday TIME: 09:00 AM to 2:00 PM Fresher's & Experienced (0 6 Years) Production: Drug substance (* Shift applicable) 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 Qualification requirement: M.Sc/B.Sc (Life Science) , B.Pharm/M.Pharm , Diploma / ITI Benefits PF, ESIC, Transportation/Local Allowance, Canteen Facility, GMC Venue CHIRON BEHRING: Plot No. 3502, GIDC Estate, Ankleshwar, Gujarat 393002

Job Title: Upstream Process Development Scientist Job Location: Bangalore We're looking for an Upstream Process Development Scientist with 2-5 years of experience to join our team. In this role, you'll be crucial in developing and optimizing upstream processes for the production of large molecules, including monoclonal antibodies (mAbs) and biosimilars. If you have a strong background in handling CHO cells and experience with cutting-edge bioreactor systems, we encourage you to apply! Responsibilities: Design, execute, and analyze experiments for the development and optimization of upstream cell culture processes, focusing on CHO cell lines. Work with large molecules, including monoclonal antibodies (mAbs) and biosimilars, throughout the process development lifecycle. Operate and troubleshoot various bioreactor systems, including AMBR250, Single-Use Bioreactors (SUBs), and 10L reactors. Optimize cell culture media, feeding strategies, and process parameters to maximize yield and product quality. Analyze process data, interpret results, and present findings to the team. Contribute to the transfer of developed processes to manufacturing. Maintain detailed and accurate documentation of all experimental work. Stay current with industry trends and advancements in upstream process development. Qualifications: Master's in Chemical Engineering, Biotechnology, Bioengineering, or a related scientific discipline. 3-6 years of hands-on experience in upstream process development within the biopharmaceutical industry. Demonstrated expertise in handling and culturing CHO cells. Proven experience with large molecule production, specifically monoclonal antibodies (mAbs) and biosimilars. Hands-on experience operating and troubleshooting AMBR250, Single-Use Bioreactors (SUBs), and 10L reactors. Strong understanding of cell culture principles, bioreactor operations, and process scale-up. Excellent data analysis, troubleshooting, and problem-solving skills. Ability to work independently and collaboratively in a fast-paced environment. Strong written and verbal communication skills. Bonus Points if You Have: Experience with Design of Experiments (DoE) software and statistical analysis. Knowledge of GMP principles and regulatory guidelines

Dr. Reddys is looking for Manufacturing Scientists or senior scientists specialized in cell therapy (CAR-T) programs to join their Manufacturing facility team. As a Manufacturing Scientist, you will collaborate with Research and Product Development teams to support GMP Manufacturing operations, Technology transfer, quality assessments, and process validation of the CAR-T process for various Cell therapy programs. Your responsibilities will include designing and executing experiments to develop robust manufacturing processes for cell therapy products, leading and training a team of cell process scientists/engineers, managing T-cell culture and differentiation, documenting experimental procedures and results, supporting the development of SOPs and batch records, and reviewing production batch records for deviations and investigations. You will also be responsible for communicating progress, identifying critical issues affecting supply and timelines, collaborating within departmental teams, contributing to deliverables, serving as a technical subject matter expert for technology transfers, and aligning with leadership to develop a strategic roadmap on continuous medium optimization. To qualify for this role, you should have a PhD/MSc/BSc in biotechnology, biology, immunology, Cell Biology, or a related life-science discipline, along with 5-12 years of industry experience in Cell and gene therapy, biologics manufacturing, or product development functions. Experience in aseptic processing, cell culture, automated equipment, T-cell culture processes, GMP requirements, and DOE is required. Strong organizational, communication, and decision-making skills are essential to succeed in this role. If you are a dynamic individual who can work in a fast-paced environment, collaborate effectively with teams, and drive successful outcomes in manufacturing processes, this position offers an exciting opportunity to contribute to cutting-edge cell therapy programs at Dr. Reddys.,

As an intern at our company, you will have the opportunity to contribute to various laboratory experiments in fields such as biochemistry, immunology, molecular biology, and cell culture. Your day-to-day responsibilities will include assisting senior scientists in tasks related to documentation, research, quality management, and data analysis. Our company is an exclusive genetics and molecular diagnostics company that specializes in high-end diagnostic tests for medical specialties like pediatrics, gynecology, IVF, and oncology. Founded by a renowned scientist and supported by a team of experienced professionals, we provide a dynamic and open work environment that fosters learning and growth for individuals across all domains. Join us at Labassure - Agile and be a part of a team dedicated to making a difference in the field of molecular diagnostics.,

Job Title: Area Manager Sales and Marketing (Genomics & Molecular Biology) Location: New Delhi, India Experience: 2-5 yrs Company: CellSeq Solutions LLP Company Description CellSeq Solutions LLP is a leading Life Science company with a vision to become the world's top organization in our field. Located in the vibrant heart of Delhi, India, CellSeq Solutions specializes in genomics, providing access to clinical and phenotypic information that offers deep insights at the genetic and molecular levels. Our innovative work supports groundbreaking research in various Life Sciences. Job Description: We are seeking a dynamic and result-oriented Area Manager – Sales and Marketing (Genomics & Molecular Biology), with hands-on experience in genetic, molecular biology, and genomics-based products . The ideal candidate will have strong connections or prior working experience with key institutions like Delhi University, IP University, Jamia Hamdard , or similar research and medical organizations. Key Responsibilities: Drive sales and marketing of genomic, molecular biology, and life science products in assigned territory. Identify and develop new business opportunities in hospitals, research institutes, diagnostics labs, and biotech companies. Engage and build relationships with researchers, clinicians, lab heads, and procurement departments. Demonstrate technical knowledge and product value to potential clients through presentations, seminars, and field visits. Manage pre-sales inquiries, post-sales support, and customer satisfaction. Work closely with internal product, logistics, and support teams to ensure timely delivery and service. Maintain accurate records of customer interactions, sales activities, and forecasts using CRM tools. Support marketing initiatives including LinkedIn campaigns, webinars, and scientific events. CellSeq Solutions LLP. Required Skills & Qualifications: B.Sc./M.Sc. in Biotechnology, Genetics, Molecular Biology, or related life science disciplines 2–5 years of proven sales experience in genomics, PCR kits, sequencing reagents, or related molecular biology tools Strong understanding of research workflows and procurement processes in institutions like Delhi University, IP University, Jamia Hamdard , etc. Excellent communication, negotiation, and interpersonal skills Willingness to travel and meet customers on field regularly Knowledge of government e-marketplace (GeM) sales will be an added advantage Preferred Candidate Profile: Prior experience selling to or working at Delhi University, IP University, NICPR, Apollo & Fortis Hospital, Jamia Millia Islamia, Jamia Hamdard University or similar institutions Established client base or network within major hospitals/research institutions in North India Technical understanding of genomics platforms (qPCR, NGS, microarray, etc.) Send your resume at “ ritesh@cellseq.in”

Job Profile: 1. Lead, manage, coordinate and orchestrate operations including business and R&D operations (in multiple locations), laboratory operations and provide smooth horizontal integration of different operational verticals. 2. Manage dynamic needs of R&D and product development teams, laboratory logistics and laboratory procurement. 3. Manage and meet the timelines for project deliverables across the organization and along with external stakeholders. 4. Lead and co-ordinate requirements for regulatory compliance and various audits. 5. Lead stakeholder management, especially with external partners, government, hospitals, industry and other organizations. 6. Coordinate with CROs and specialized service providers. 7. Manage and oversight good laboratory practices (GLP) and ensure R&D labs (laboratory, cell culture rooms) adhere to excellent laboratory standards. 8. Manage workflows in laboratory including coordinating workflows of R&D among different sites and vendors. 9. Manage supply chain for various consumables, including clinical-grade materials. 10. Manage operational, laboratory budgets and laboratory meetings, documentation of information, laboratory and business reports, writing technical reports. 11. Identify new business opportunities and partners and cultivate strong relationships with new clients and nurture existing client relationship. 12. Assist with drafting business plans, business pitches, presentations, reference materials, and other documents as required. 13. Identify and represent Pandorum in business and scientific networking platforms. 14. Manage and assist in administration related activities of the company. 15. Train and manage employees assigned to work under supervision. 16. Undertake work related business travel from time to time as required. 17. Additional duties as necessary and assigned by the Cofounders from time to time. Work Location: Electronic City, Bangalore Required Skills / Experience: PhD in Life Science or related discipline with 8 to 12 years of experience in R&D management, product development, lab operations, procurement, inventory and vendor management. Scientific writing (grants/articles) and Import/export experience are desirable. The role holder would report directly to the cofounders of Pandorum and a team of four employees from the Operations team would report to this role holder.

Roles and Responsibility Conduct neurological tests and examinations to diagnose and treat patients with neurological disorders. Operate and maintain specialized equipment used in neurology procedures. Collaborate with healthcare professionals to develop treatment plans for patients. Monitor patient vital signs and respond to emergencies during testing. Maintain accurate records of test results and patient information. Participate in ongoing education and training to stay updated on the latest techniques and technologies in neurology. Job Requirements Diploma or degree in a relevant field, such as neuroscience or medical technology. Possess strong knowledge of neurology procedures and protocols. Demonstrate excellent communication and interpersonal skills. Ability to work effectively in a team environment and prioritize tasks. Familiarity with laboratory safety protocols and quality control measures is essential.

Roles and Responsibility Conduct neurological tests and examinations to diagnose and treat patients with neurological disorders. Operate and maintain specialized equipment used in neurology procedures. Collaborate with healthcare professionals to develop treatment plans for patients. Monitor patient vital signs and respond to emergencies during testing. Maintain accurate records of test results and patient information. Participate in ongoing education and training to stay updated on the latest techniques and technologies in neurology. Job Requirements Diploma or degree in a relevant field, such as neuroscience or medical technology. Minimum 4 years of experience working in a neurology setting, preferably in a clinical research or pharmaceutical industry. Possess strong knowledge of neurology procedures and protocols. Demonstrate excellent communication and interpersonal skills. Ability to work effectively in a team environment and prioritize tasks. Familiarity with laboratory safety protocols and quality control measures is essential. For more information, please contact us at 6882422.

Role & responsibilities Manufacturing of cell line/cell culture based AG for FG Cell culture operations, including inoculation and observatory monolayer work Compilation of all commercial batch data and BMR filling RM/PM issuance, sterilization, and monitoring of all supportive data Maintaining procell-related modules, areas, and utility fixed assets Receiving NPD from R&D and scaling up for commercialization Areas, equipment validation, and maintenance Cell bank passage history maintenance and reconciliation Preferred candidate profile Throughout knowledge of cell line/primary culture Propagation of cell line & maintenance Aseptic handling Sound knowledge of QMS Sound knowledge of cGMP, GDP

Immuneel Therapeutics Private Limited is a pioneering start-up company leading the charge in cell therapy and personalized immunotherapy for patients in India. We Pursue, with Purpose, to serve our Patients by Connecting within, Collaborating globally and Creating solutions. Our flexible, diverse, and vibrant team is bringing together best practices and innovations in the field of cell and gene therapy. Working at Immuneel promises the excitement of an agile startup on a critical mission. Proudly Indian in solutioning, yet global in outlook, we value diversity including in experience and perspectives. We believe in work-life balance and consider having fun on the job integral to achieving the right results. At Work, we are passionate in driving patient outcomes, responsible and accountable, transparent, honest, and supportive in how we work together, inclusive and flexible. Immuneel prides itself as an organization that is keeping pace with best practices in organization design. Our role-based organization promotes focus on work and greater nimbleness. Our employees are integral to our quest to develop and deliver high-quality engineered cell therapies. We invest in clear compensation and comprehensive benefits for our employees. If you are a talented professional, an out-of-box thinker with a zeal to help change, and passionate about healthcare, we invite you to join us and be a part of a historic initiative in India. Role Title: Scientist - Research & Development Department/Function: Research & Development (Innovation) Reporting Structure: - Reports to: Innovation - Direct Reports: None Role Summary: Immuneel is looking for a Scientist for Research & Development (Innovation). The candidate must have a strong understanding of various processes like design, Immunology/Molecular Biology. Key deliverables will be to drive projects and programs innovation-related research and development activities or work cross-functionally to build and progress Immuneel's cell and gene therapy product pipeline. Key Responsibilities: - Independently design, plan and personally conduct Immunology/Molecular Biology-based studies in vitro - Think innovatively and design studies accordingly - Interact cross-functionally to fulfill all job responsibilities - Contribute to projects as part of the R&D matrix - Stay updated on published literature related to areas of interest - Evaluation of new technologies for experimental goals - Present posters/talks, publish research articles, and patents - Industry standard Documentation: Experimental records, Protocols & Reports. Support XOP generation and closure of change controls, CAPA etc. where required - Ordering of reagents, consumables & inventory management - Equipment management: Support purchase & maintenance of equipment and associated documentation, co-ordination with FAO, QA for same Primary Objectives: - Perform innovation-related research and development activities - Generate data and documentation for patent filings - Generate data and documentation for regulatory filings - Contribute to projects as part of the R&D matrix Competencies Required: Technical Competencies: - Mammalian cell culture - Basic immunological assay development - ELISA-based techniques - Flow-cytometry - Molecular biology - Genome engineering including CRISPR Soft Skills: - Innovative thinking - Independent, passionate, self-motivated, and proactive - Hardworking - Adaptable - Focused, organized, and detailed-oriented - Good communication skills - Collaborative team player IT Skills: Powerpoint, Excel, Word Qualifications: - Masters with a minimum of 3 years of relevant experience or a Ph.D with a minimum of 2 years post-doctoral experience - Established track record in form of publications and/or patents Working Conditions: - Role Type: Full Time and Onsite - Work Hours: 9:00 AM to 6:00 PM for the General Shift and 2:00 PM to 11:00 PM for the Post-Noon Shift (on a rotational basis). Two days off each week - Travel Requirements: Yes (only when required; < 1%) - Base Location: Immuneel Therapeutics Private Limited, 8th Floor, Mazumdar Shaw Medical Center, Narayana Health City, Bommasandra Industrial Area, Bangalore - 560099,

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.

Garuda3D is a leading in-house manufacturer of affordable 3D printers in India, specializing in FFF & SSE (Food & Bio) 3D printing technology. With over 8.3 years of experience, our team of professionals produces a wide variety of large format 3D printers that cater to both professional and industrial applications. We are now developing Bio3d printers. For that, we're seeking a highly motivated Biomedical Engineering Intern to join our team! We're looking for a talented and enthusiastic Biomedical Engineering Intern to contribute to our bio 3D printing project. As an intern, you will have the opportunity to work on exciting Bio 3d printing projects, collaborate with our team, and gain hands-on experience in bio 3D printing. Roles and Responsibilities: - Research and understand Bio 3D printing technologies, materials, and applications - Assist in designing and developing Bio 3D printing experiments - Conduct literature reviews and analyze data related to Bio 3D printing - Assist in writing proposals and reports - Collaborate with our team to achieve project goals and objectives - Develop and present project updates and findings to the team Requirements: - A degree in Biomedical Engineering, Bioengineering, Biotechnology, Pharmaceutical, or related field - Strong understanding of Bio 3D printing principles, materials, and applications - Knowledge in Tissue Engineering and Cell culture - Knowledge in Bio fabrication and Bio mechanics - Experience in Biomimetics This is a paid Internship with a stipend between Rs.10000 - Rs.12000 Internship duration is 6 months,

Design and perform efficacy and safety studies of herbal and plant-based formulations using standard pharmacological models. Conduct bioassays, toxicity tests, and mechanism of action studies using in vitro and/or in vivo techniques. Analyze and interpret pharmacodynamic and pharmacokinetic data. Prepare technical reports, research papers, and regulatory documentation as needed. Assist in developing protocols for standardization and quality control of herbal products. Preferably 1- 2 years of experience in pharmacological evaluation of herbal formulations, plant-based extracts, or natural products. Familiarity with in vitro/in vivo testing methods and pharmacological screening protocols for herbal compounds. Candidates with knowledge of Ayurvedic formulations, traditional medicine, or toxicological studies will be given preference. Proficiency in pharmacological testing equipment and techniques (e.g., ELISA, HPLC, GC-MS, cell culture, animal studies). Sound understanding of herbal pharmacology, phytochemistry, and drug development pipelines. Strong analytical and critical thinking skills. Good scientific writing and documentation skills.

As a Probationer-HO Staff in the VTC Mfg - BVP department, you will be responsible for bacterial vaccine manufacturing processes including both drug substance upstream and downstream operations. In the upstream process, you will be involved in activities such as seed germination, fermenter operations, harvest, centrifugation, process performance qualification, and cleaning validation. It is crucial to work in compliance with cGMP facility standards and be prepared for regulatory audits. This role offers an opportunity to gain insights and experience in manufacturing bacterial toxoid vaccines like Typhoid, Tetanus, Diphtheria, Pertussis, and more. Similarly, in the drug substance downstream operations, your responsibilities will include downstream purification activities such as cell lysis, homogenization, TFF, chromatography, centrifugation, sterile filtration, process performance qualification, and cleaning validation. Adherence to cGMP facility requirements and readiness for regulatory audits are essential. This position also provides a chance to delve into bacterial toxoid vaccine manufacturing and purification processes for vaccines like Hepatitis, Tetanus, Diphtheria, Pertussis, among others. Furthermore, within the LVP department, your tasks will involve cell revival, subculture, cell counting, preparation of cell culture media and in-process buffers, handling of TCFs, as well as the creation of SOPs and documentation related to cell culture. This role requires meticulous attention to detail and a strong focus on maintaining quality standards throughout the manufacturing processes.,