20 Qpcr Jobs

Company Description Genient Technologies is a specialized Genomics & Molecular Diagnostics company committed to advancing healthcare through cutting-edge technologies. Our expertise encompasses in-vitro diagnostics, life science research, and genomics discovery. We offer innovative solutions to empower healthcare providers and researchers in improving patient care and outcomes. Our mission focuses on enhancing healthcare effectiveness through strategic technology integration, driving advancements in personalized medicine, diagnostics, and scientific discovery. Role Description This is a full-time, on-site role for a General Manager: Clinical Genomics Solutions, located in Noida. The General Manager will oversee the development and implementation of clinical genomics solutions including NGS infectious disease panels, Oncology, Genetic testing, NIPT and Multiplex PCR. Responsibilities include managing sales activities , project timelines, coordinating with cross-functional teams, ensuring compliance with regulatory standards, developing strategic partnerships, and driving product innovation. The role requires effective leadership and communication to achieve organizational goals and enhance operational efficiency. Qualifications Sales experience in genomics, molecular diagnostics, and life science research, NGS and QPCR based expression studies and HRM. Project management and strategic planning skills Leadership and team management experience Knowledge of regulatory compliance in the healthcare sector Strong communication and interpersonal skills Ability to develop and manage strategic partnerships Experience in product innovation and development Master's degree in Life Sciences, Biotechnology, or related field; advanced degree preferred Show more Show less

Environmental PCR Laboratory Technician Key Responsibilities PCR Experimentation Prepare PCR reactions, including DNA/RNA extraction and template preparation. Execute PCR assays, gel electrophoresis, and quantitative PCR (qPCR) experiments. Accurately document experimental procedures and results. Equipment Operation and Maintenance Operate and maintain PCR instruments, thermocyclers, and related equipment. Perform routine calibration and troubleshooting of laboratory equipment. Ensure that equipment and work areas are clean and organized. Sample Management Handle and process biological samples, including sample preparation and storage. Maintain sample inventory and tracking records. Assist in sample accessioning and labeling. Quality Control Implement quality control measures to ensure the reliability and accuracy of PCR results. Participate in proficiency testing and validation studies. Report any anomalies or deviations promptly. Collaboration Collaborate with researchers and laboratory staff on various molecular biology projects. Assist in the analysis and interpretation of PCR data. Communicate effectively within the team and contribute to a collaborative research environment. Laboratory Safety Adhere to laboratory safety protocols and practices. Handle hazardous materials and chemicals in a safe and responsible manner. Maintain awareness of safety guidelines and promote a culture of safety. Qualifications Bachelor's degree in molecular biology, genetics, or a related field. Previous experience in a molecular biology or PCR laboratory is preferred. Proficiency in PCR techniques, primer design, and experimental setup. Familiarity with laboratory equipment and instrumentation. Strong attention to detail and record-keeping skills. Effective communication and teamwork abilities. Commitment to laboratory safety and adherence to protocols. Willingness to learn and adapt to new techniques and technologies. Proficient in English Good written and verbal communication Experience with Microsoft office tools (Excel / Word) Ability to work in teams Ability to work under pressure Customer oriented attitude Ready to travel at short notice and conduct med-term abroad assignments Good organizational skills This PCR Laboratory Technician role offers an exciting opportunity to work in a dynamic research environment and contribute to the advancement of molecular biology research. If you are a dedicated and detail-oriented individual with a passion for scientific discovery, we encourage you to apply for this position. This is a new role with therefore a new challenge and a great opportunity to work in a truly international environment and in a highly-motivated and friendly team. Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Schedule: Night shift Rotational shift Experience: PCR Laboratory Technician: 4 years (Required) Language: Excellent English (Required) Work Location: In person

Maintain theoretical and practical knowledge of molecular biology methods including NGS sequencing, qPCR, SNP Genotyping, mRNA Seq, and digital PCR across a variety of specialty applications Provide high quality sales support, engaging with customers to provide technical discussion, seminars, and demonstrations Provide multi-faceted customer support including on-site and in-house training, email and phone inquiries, applications discussion, planning and troubleshooting, and data analysis Collaborate with in-house teams to provide customer feedback and enhance future products the training program Provide challenging opportunities for personal and professional growth Provide a unique, exciting, and highly engaging team culture aimed at integration of corporate and field based colleagues … working as one for all Host excellent team and company-wide events multiple times a year Assist sales and support in pre-sales functions working with customers to enable analysis based on experimental design and application Documents and processes all service and customer account related reports, updates, and communicates in a timely and professional manner Contribute to presales activities by providing technical presentations on the features and benefits of POROS and CaptureSelect products Job Types: Full-time, Permanent, Fresher Pay: ₹18,455.00 - ₹28,755.00 per month Benefits: Provident Fund Shift: Day shift Evening shift Fixed shift Work Days: Monday to Friday Work Location: In person

University: French National Research Institute for Agriculture, Food, and the Environment (INRAE) Country: France Deadline: June 13, 2025 The French National Research Institute for Agriculture, Food, and the Environment (INRAE) invites applications for a postdoctoral position in synthetic biology and microbiology, as part of the TARGET Project at the UMR INRAE BFP unit in Villenave d’Ornon, France. This interdisciplinary research initiative aims to advance the cultivation of noncultivable bacteria, focusing on the plant-pathogenic Flavescence Dorée phytoplasma, and integrates approaches from microbiology, culturomics, genetic engineering, systems biology, and computational modeling. Requirements PhD in microbiology, metabolomics, systems biology, molecular biology, biochemistry, or a related discipline Experience with transcriptomics and/or LC-MS-based metabolomics Knowledge of metabolic modeling or biochemical pathway analysis is advantageous Background in microbiology, molecular biology, or bioinformatics Desirable skills include RT-qPCR, metabolic imaging, or protein expression/purification Strong analytical, organizational, and communication skills, with a collaborative approach Role And Responsibilities Develop and validate methods to distinguish phytoplasma metabolic responses from those of host organisms using transcriptomics and metabolomics Conduct targeted and untargeted metabolomics (LC-MS) to identify metabolites in infected and healthy host tissues Utilize metabolic imaging techniques (e.g., MALDI, DESI-MS) to map metabolite distributions Integrate multi-omics data to infer host-pathogen metabolic interactions Support metabolic modeling and culture medium formulation Perform biochemical analyses such as RT-qPCR, enzyme characterization, and protein expression Collaborate with bioinformaticians and contribute to scientific publications and presentations Benefits Gross monthly salary between €3,135 and €4,544, depending on experience and profile Up to 30 days of annual leave plus 15 days of reduced working time (full-time) Parenting support, skills development opportunities, social support, and leisure benefits Access to sports, cultural activities, and collective catering Application Procedure Interested candidates should submit a detailed CV, cover letter outlining research interests and motivation, and contact details for two references to Dr. Pierre Pétriacq (pierre.petriacq@inrae.fr) and Dr. Bessem Chouaia (bessem.chouaia@inrae.fr). Applications will be reviewed on a rolling basis until the position is filled. For further inquiries, please contact the supervisors at the provided email addresses. Start Date: October 1, 2025 Contract Duration: 23 months (with possible renewal for an additional 24 months) Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: phdfinder.com/register Show more Show less

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. Immuneel’s 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 careers@immuneel.com 1. Role Title: Scientist - Research & Development 2. Department/Function: Research & Development (Innovation) 3. Reporting Structure: Reports to: Innovation Direct Reports: None 4. Role Summary: Immuneel is looking for a Scientist for Research & Development (Innovation). The said 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 5. Key Responsibilities: Independently design, plan and personally conduct Immunology/Molecular Biology-based studies in vitro Think innovatively and design studies accordingly Interact cross-functionally, as necessary, to fulfill all job responsibilities Contribute to one or more projects as part of the R&D matrix Stay updated on published literature related to areas of interest for the company’s therapeutic objectives, besides general awareness on research publications Evaluation of new technologies that could be used to achieve experimental goals or company’s therapeutic objectives. 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. 6. Primary Objectives: Perform innovation-related research and development activities or work cross-functionally to build and progress Immuneel’s cell and gene therapy product pipeline To generate data and documentation for patent filings To generate data and documentation for regulatory filings To contribute to one or more projects as part of the R&D matrix 7. Competencies Required: Technical Competencies : Mammalian cell culture (with primary cells and cell lines) Basic immunological assay development ELISA-based techniques Flow-cytometry Molecular biology (cloning, qPCR etc) 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 8. Qualifications: 1. Masters with a minimum of 3 years of relevant experience or a Ph.D with a minimum of 2 years post-doctoral experience 2. Established track record in form of publications and/or patents 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: 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 Show more Show less

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities. Brief Job Overview This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent work collaboratively in the reference standard/ARM development program within the Global Biologics department. The incumbent will participate in the development of replacement and new reference standards /ARM in support of USP’s mission and core business. The incumbent will also focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in timely manner. How will YOU create impact here at USP? In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments. The Sr. Scientist -I (RSS) Has The Following Responsibilities Roles and Responsibilities Maintain smooth collaboration and works closely with key stakeholders across the globe to develop reference standards for biotechnology pharmaceutical products including proteins, peptides, heparins, antibiotics, and advanced therapies. Works to draft protocols, reports and address scientific and technical queries from internal and external stakeholders in timely manner pertaining to reference standards/ARMs Oversees and facilitates the development of standards and solutions to address analytical challenges associated with biological medicines. Supports day to day operations of the Stability (CSU) program covering the USP Biologics RS catalog inventory. Reviews RS testing history and drafts test protocols for collaborative studies and CSU studies and submits to labs based on designated testing requirements and schedules. Liaisons and Assists laboratories to ensure collaborative testing/CSU testing is completed accurately and in timely manner. Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use. Compiles current and historical Stability testing data assessment and prepare stability trend reports. Maintains and updates various databases documenting laboratory data and program determinations on suitability and Stability interval updates. Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Quality Assurance and Reference Standard Evaluation with investigation of unexpected stability testing results Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps. Prepare, present and discuss regular work updates with Team Lead and other team members Reviews protocols and/or reports of other Scientists as assigned by manager. Who is USP Looking For? Preferred Qualifications The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc. Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development. Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays. Excellent technical writing, presentation and oral communication skills are required. Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders. Sr. Scientist I Ph.D. degree in Biochemistry, Analytical Chemistry or Biological Sciences . Minimum of 7 to 10 years of post-educational work experience in recombinant therapeutic proteins, peptides and carbohydrates. in Biochemistry, or Biological Sciences with minimum of 11 to 13 years of commensurate industrial experience. Additional Desired Preferences Knowledge of USP products and services is highly desirable. Operates collaboratively at all levels of the organization in a highly technical environment. Must be able to work in a fast-paced environment and respond to shifting priorities. Well-developed interpersonal, negotiation, conflict-resolution and listening skills. Must possess the ability to multi-task and to work effectively with a team. Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality. Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred. Supervisory Responsibilities No Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time Show more Show less

Job Title: Research Scientist – Molecular Biology Location : Varanasi, Uttar Pradesh (Inside BHU Campus, On-Site) Job Type : Full-time Joining Type: Immediate About Us: Technoculture Research Pvt. Ltd. is a leading research and development company focused on innovative solutions in biotechnology, engineering, and software development. We specialise in bio-instrumentation research, pharmacogenomics-based drug testing, and precise diagnosis of infectious diseases. Our technology-driven approach ensures cutting-edge advancements in healthcare and enterprise solutions. Job Description: We are seeking a highly skilled and motivated Research Scientist with a Ph.D. in Molecular Biology and a solid background in cell culture techniques. The ideal candidate should have extensive hands-on experience in molecular biology methods and strong proficiency in designing and conducting independent experimental research. This role offers a unique opportunity to work in a collaborative and innovation-driven environment within the prestigious BHU campus. Responsibilities: Design and execute experiments in molecular biology with a focus on gene expression, genetic modification, and cell signalling pathways. Should be able to design vectors and primers for downstream processes. Perform advanced cell culture techniques including maintenance, transfection, and viability assays in mammalian cell lines. Apply core molecular biology techniques such as DNA/RNA isolation, PCR, qPCR, Western blotting, and cloning. Should be able to create stable cell lines using transfection and transduction. Analyse experimental data, troubleshoot protocols, and optimise methods to improve outcomes. Maintain accurate documentation of experiments, results, and methodologies. Present research findings to internal teams and contribute to publication and patent efforts. Adhere to safety protocols, standard operating procedures, and quality control standards. Qualifications: Ph.D. in Molecular Biology or a closely related discipline. Strong expertise in cell culture techniques and mammalian cell handling. Demonstrated experience in molecular biology techniques including PCR, qPCR, Western blotting, plasmid preparation, cloning, transfection, transduction, and electroporation. Ability to work independently on experimental design and data interpretation. Preferred Qualifications: Postdoctoral or industry research experience in cell and molecular biology. Exposure to RNA-based technologies or translational biology. Familiarity with microscopy and flow cytometry is an advantage. Basic understanding of bioinformatics tools for gene and protein analysis. Skills: Excellent analytical, problem-solving, and troubleshooting skills. Strong documentation and communication abilities (written and verbal). Well-organised and detail-oriented with good time management. Ability to work in a fast-paced, team-oriented environment. Personal Attributes: Passionate about scientific innovation and research excellence. Self-driven, proactive, and committed to continuous learning. Capable of taking initiative and working with minimal supervision. Collaborative mindset with the ability to work across diverse scientific disciplines. Show more Show less

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 start-up 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. Immuneel’s 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 careers@immuneel.com 1. Role Title: Specialist - Quality Control (Molecular Biology) 2. Department/Function: Quality Control 3. Reporting Structure: Reports to: Quality Direct Reports: 2-3 4. Role Summary: The primary responsibility will be hands-on wet lab analysis and managing the molecular biology team. The candidate focusses on development, qualification, and validation of molecular biology /genomics assays to test samples and generate quality control reports. Candidate is required to carry out molecular biology workflows and qPCR/ddPCR-based assays to support various tests under safety test panel required for Quality Control and Release/ Testing of Cell Therapy products. The candidate will also coordinate the sample management activities of QC. 5. Key Responsibilities: Perform hands-on experiments, validation, quality checks and guide the team. Serve as subject matter expert for the genomics, analytical & molecular biology-based QC assay requirements relevant to product safety, function, purity, identity, and other relevant parameters. Design assays/experiments, verify, qualify, and validate assays as per requirements within the target timeline. Maintain/compile/archive records, process logs, asset logs, soft copy of QA approved data, ATRs and lab notebooks. 6. Primary Objectives: Reconciliation of samples received, used for assays, remaining samples. To coordinate between QC and QA team for issuance of ATRs for each batch, distribution of ATRs to QC team, collection of ATRs after analysis from QC team, verification of ATRs for its completeness, submission to HOD, QA personnel, and HOD for signatures (as required) and filling of batch data tracker. Preparation of Certificate of analysis from QC in coordination with QA. Supervise and manage function specific inventory, material supply and equipment upkeep along with personnel responsible for this activity. The management of QC molecular biology team with instrument & consumable suppliers/vendors, engineers etc. to complete installation, qualification, calibration, PM, AMC etc. on time. 7. Competencies Required: Technical Competencies: Expertise in molecular Biology and biotechnology Industrial experience in molecular biology Managerial experience of a team Analytical ability Should have handled Quality Management Systems and audits before Soft Skills: Good communication skills Presentation skills Collaborative Assertive Decisive (Manages) stress (Handles) Ambiguity Problem Solver Strategic Thinker 8. Qualifications: MSc or Ph.D. in Molecular Biology or Biotechnology Industrial Experience in Biopharmaceutical Sector or cell and gene therapy Experience in GMP or GLP environment or laboratories with aseptic sample handling/processing facilities 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 and 0% travel Base Location: Immuneel Therapeutics Private Limited, 8th Floor, Mazumdar Shaw Medical Center, Narayana Health City, Bommasandra Industrial Area, Bangalore - 560099 Show more Show less

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities. Brief Job Overview This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent work collaboratively in the reference standard/ARM development program within the Global Biologics department. The incumbent will participate in the development of replacement and new reference standards /ARM in support of USP’s mission and core business. The incumbent will also focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in timely manner. How will YOU create impact here at USP? In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments. The Sr. Scientist -I (RSS) Has The Following Responsibilities Roles and Responsibilities Maintain smooth collaboration and works closely with key stakeholders across the globe to develop reference standards for biotechnology pharmaceutical products including proteins, peptides, heparins, antibiotics, and advanced therapies. Works to draft protocols, reports and address scientific and technical queries from internal and external stakeholders in timely manner pertaining to reference standards/ARMs Oversees and facilitates the development of standards and solutions to address analytical challenges associated with biological medicines. Supports day to day operations of the Stability (CSU) program covering the USP Biologics RS catalog inventory. Reviews RS testing history and drafts test protocols for collaborative studies and CSU studies and submits to labs based on designated testing requirements and schedules. Liaisons and Assists laboratories to ensure collaborative testing/CSU testing is completed accurately and in timely manner. Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use. Compiles current and historical Stability testing data assessment and prepare stability trend reports. Maintains and updates various databases documenting laboratory data and program determinations on suitability and Stability interval updates. Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Quality Assurance and Reference Standard Evaluation with investigation of unexpected stability testing results Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps. Prepare, present and discuss regular work updates with Team Lead and other team members Reviews protocols and/or reports of other Scientists as assigned by manager. Who is USP Looking For? Preferred Qualifications The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc. Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development. Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays. Excellent technical writing, presentation and oral communication skills are required. Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders. Sr. Scientist I Ph.D. degree in Biochemistry, Analytical Chemistry or Biological Sciences . Minimum of 7 to 10 years of post-educational work experience in recombinant therapeutic proteins, peptides and carbohydrates. in Biochemistry, or Biological Sciences with minimum of 11 to 13 years of commensurate industrial experience. Additional Desired Preferences Knowledge of USP products and services is highly desirable. Operates collaboratively at all levels of the organization in a highly technical environment. Must be able to work in a fast-paced environment and respond to shifting priorities. Well-developed interpersonal, negotiation, conflict-resolution and listening skills. Must possess the ability to multi-task and to work effectively with a team. Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality. Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred. Supervisory Responsibilities No Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time Show more Show less

Company Description Lab on a chip & Biosensors Group of Prof. Sandeep K. Jha at Centre for Biomedical Engineering, IT Delhi is one of the forefront research team in India which works on microfluidics, point-of-care biosensors and embedded systems for clinical applications. Details at www.sandeepjha.com Indian Institute of Technology (IT) Delhi is a National Centre of Excellence for training, research, and development in science, engineering, and technology in India Established in 1961, I1T Delhi has graduated over 50,000 individuals, including more than 5500 with a Ph.D. degree. In 2018, IIT Delhi was granted the special status of Institution of Eminence by the Govt. of India, providing greater autonomy in hiring and collaborations Role Description This is a full-time on-site role for a Molecular Biologist cum Biochemist in Lab on a chip & Biosensors Group of Prof. Sandeep K. Jha at Centre for Biomedical Engineering, IIT Delhi. The role involves conducting laboratory experiments, utilizing techniques in molecular biology, PCR, pathogen culture and genome analysis, enzymology such as optimizing new mastermix compositions and primer and probe designing. In subsequent stages, the Candidate has to deploy these assays into microfluidic devices or paper fluidic kits to develop a clinical diagnostic product. The candidate should also have hands on expertise to run PCR machine, should be able to Culture microorganism and should have handled clinical Validation in atleast one project. These skillsets are required beforehand as learning Curve will be steep as project duration shall be Only 1.5 years. Candidates demonstrating this full potential Can be enrolled for Ph.D. program at the Centre as a Career reward after Successful Completion of project. Qualifications Laboratory Skills and Microbiology expertise Must have handled qPCR and RT-PCR with melt curve analysis Proficiency in Enzymology, Biosensors Uv-Vis based kinetic assays Strong background in Biology, Biochemistry, Biotechnology & Molecular Biology Excellent analytical and problem-solving skills Effective communication and collaboration abilities Detail-oriented with a passion for scientific research Master in Molecular Biology, Biochemistry, or related field Pay scale shall be commensurate with experience level It shall be a six days work week and difficulty level of job as you can imagine commensurate to India's top academic Institute. Therefore matching above skill sets utmost to apply for this challenging and career rewarding job Note Interested candidates having already completed or pursuing Ph.D. or those not interested in pursuing Ph.D. must not apply. We are seeking candidates who could continue as Ph.D. scholar. This post is a prelude for future research scholar in my lab who would get a headstart of 1-1.5 years before enrolment to Ph.D. program. Show more Show less

Field Application Scientist – Molecular Diagnostics Location: Bengaluru Travel: Up to 50% Experience: 1–3 years Industry: Biotechnology / Molecular Diagnostics About the Company Our client is a fast-growing Indian biotech company dedicated to building automation-friendly kits and instruments for rapid and reliable molecular diagnostics. With a strong focus on innovation and product development, they are now expanding their R&D team to strengthen their presence in the diagnostics space. Role Overview We are seeking a Field Application Scientist – Molecular Diagnostics for our client, someone who can seamlessly blend hands-on assay development with customer-facing field responsibilities. The ideal candidate will contribute to R&D efforts while also representing the company at customer sites for product validation, demonstrations, and technical support. Key Responsibilities Develop and optimize assays for DNA/RNA extraction and PCR/qPCR/RT-PCR applications. Conduct experiments on a range of clinical and biological samples (blood, swabs, tissue, etc.). Collaborate with internal teams (production, QA, marketing) to support product scale-up and launch. Maintain accurate experimental records and prepare clear technical documentation. Ensure compliance with GLP and ISO 13485 guidelines during lab and field operations. Travel (~50%) to customer and partner sites for training, demonstrations, and troubleshooting. Provide technical insights from the field to support continuous product improvement. Candidate Profile B.Sc. or M.Sc. in Molecular Biology, Biotechnology, or a related discipline. 1–3 years of hands-on experience in a molecular diagnostics or life sciences laboratory. Proficiency in nucleic acid extraction and PCR/qPCR techniques. Familiarity with automated liquid handling systems is preferred. Exposure to NGS workflows (e.g., Illumina, Oxford Nanopore) is an added advantage. Strong analytical and problem-solving skills; attention to detail. Excellent interpersonal and communication abilities. Willingness and ability to travel frequently for field assignments. Show more Show less

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Organization Overview At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana, USA. Our 39,000 employees worldwide work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. The Product Research and Development (PRD) organization strives to develop and deliver quality medicines to patients. The portfolio consists of development and commercialization of insulins, small molecules, monoclonal antibodies, novel therapeutic proteins, peptides, oligonucleotide therapies and gene therapy systems. This organization is a multidisciplinary group that works collaboratively with therapeutic business units and manufacturing to deliver the incredibly exciting Lilly clinical portfolio to patients around the world. The Lilly Capability Centre India (LCCI) located in Bengaluru India is a strategic investment made by Lilly to attract top talent from the vibrant academic and professional environment in India and deploy them to develop and enable critical capabilities for Lilly. The LCCI group in India houses a PRD team that works closely with the PRD team in Indianapolis in enabling the delivery of Lilly’s portfolio. Responsibilities And Skillsets The individual will be part of a multi-disciplinary team in synthetic molecule design and development (SMDD) and Bioproduct Research and Development (BRD) Analytical organizations that are critical teams within PRD. The individual works as a contributor on one or more project teams working on small or large molecules. Perform activities to evaluate the stability of a variety of active pharmaceutical ingredients (API) and dosage forms to support clinical trials, development and support of pediatric, line extension and commercial products in the Lilly portfolio. Assisting the activities like testing, evaluation and release/disposition of raw materials and excipients. The individual has experience in developing/executing analytical methods for oral and/or parenteral products. Knowledge on compendial method requirements and procedures related to raw material, drug substance and drug products. Supporting the activities such as testing, evaluating release and stability data and has technical skills in several critical areas of an analytical including troubleshooting, Method development, execution, qualification/verification, validation, method transfer to manufacturing sites and third-party testing laboratories. The individual has experience in handling various analytical techniques such as such as HPLC, GC, CE-SDS, SEC, ELISA, qPCR, DSC, Bioassay, Karl Fischer, UV, LC-MS, Dissolution, Disintegration, X-ray diffraction, etc. The individual has experience in working on analytical methods with at least 1 of following molecules and systems, Antibodies/bifunctional/ fusion proteins/ proteins Peptides/oligonucleotides/other genetic medicines Small molecules/other synthetic molecules Raw materials and packaging material testing Other Key Responsibilities Thorough understanding and adheres to all relevant job-related policies, including business, compliance, regulatory (cGMPs), quality, environmental, and safety expectations. Proactively communicates with other scientists and management. Assumes ownership and showcases accountability by effectively managing project deliverables. Develop, establish and maintain strong professional relationships with partners / internal and external customer and key stakeholders across geographical locations. Authoring of regulatory documents, following good documentation practice (e.g., Empower, NuGenesis, Signals (eLN)) and demonstrates proficiency in data integrity review, analysis, reporting and trending. Author and track the implementation of change controls. Use scientific expertise to conduct the laboratory investigations, addressing OOT/OOS/aberrant data, root cause analysis and CAPA implementation. Support inspection readiness activities including internal and external audits as needed. Skills in Power BI, Python and database tools Educational Requirements MS with 1-5 years of experience or BS with 3-5 years of experience in analytical department of a pharmaceutical organization developing API or DP for clinical or commercial use. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. #WeAreLilly Show more Show less

Establish, maintain, and scale mammalian cell lines including adherent and suspension cultures under sterile conditions.Perform routine cell-based assays such as viability, proliferation, cytotoxicity, reporter assays, and high-content imaging.

Job Summary: We are seeking a highly motivated and skilled Virology and Vaccine Development Scientist to join our team in the development of novel vaccines and antiviral strategies. The ideal candidate will have a strong background in virology, immunology, and molecular biology, with hands-on experience in pathogen research, vaccine design, and preclinical testing. Key Responsibilities: Conduct research on viral pathogens, including virus isolation, propagation, and characterization. Design and evaluate vaccine candidates (e.g., live-attenuated, inactivated, subunit, mRNA, or viral vector platforms). Perform in vitro and in vivo studies to assess immunogenicity and efficacy of vaccine candidates. Develop and optimize assays such as ELISA, PRNT, qPCR, Western blot, and neutralization tests. Collaborate with cross-functional teams including bioinformatics, regulatory affairs, and clinical development. Prepare research protocols, maintain lab records, and ensure compliance with biosafety and ethical standards. Analyze data and present findings in internal meetings, scientific conferences, and peer-reviewed journals. Stay updated on emerging viral threats and advancements in vaccine technologies. Qualifications: Education: PhD in Virology, Microbiology, Immunology, Molecular Biology, or a related field. Postdoctoral experience preferred (for senior roles). Skills and Experience: Proven experience in virological techniques and molecular cloning. Hands-on experience in vaccine development or antiviral drug screening. Familiarity with animal models of viral infection (e.g., mice, ferrets, non-human primates). Knowledge of regulatory requirements for preclinical and clinical vaccine development (e.g., FDA, EMA). Strong data analysis and problem-solving skills. Excellent communication and teamwork abilities. Preferred Qualifications: Experience with BSL-2/BSL-3 laboratory environments. Experience with mRNA, viral vector, or adjuvant formulations. Familiarity with high-throughput screening or computational vaccine design. Work Environment: Lab-based with potential exposure to biohazardous materials. May require flexible hours to support project timelines. If interested share profiles on - srexec-hr@symbiosis.ac.in Show more Show less

About Avam: Avam is an innovative biotechnology leader delivering cutting-edge solutions in molecular and microbiology technologies. Our products bridge scientific breakthroughs and real-world applications, serving a diverse customer base across research institutions, healthcare providers, pharmaceutical companies, and industrial laboratories globally. Position Overview: We are seeking an experienced and knowledgeable Product Specialist with expertise in molecular biology and/or microbiology techniques to join our dynamic team. This unique hybrid role combines deep product knowledge and technical communication skills, as you will engage directly with product support and customer training, while also drafting clear, accurate, and user-friendly technical documentation. Responsibilities: Provide specialized product support, training, and technical expertise to internal teams and external customers. Draft, maintain, and refine product technical documentation, including user manuals, application notes, protocols, technical datasheets, and troubleshooting guides. Collaborate closely with R&D, Quality Assurance, Regulatory Affairs, and Marketing teams to accurately translate product knowledge into effective documentation. Conduct technical demonstrations and webinars to educate customers and support sales efforts. Act as a primary resource for addressing technical questions, product applications, and resolving customer inquiries efficiently and effectively. Ensure accuracy, compliance, and consistency across all technical documentation, adhering to industry and regulatory standards. Qualifications: Bachelor’s or Master’s degree in Molecular Biology, Microbiology, Biotechnology, Life Sciences, or a related field. Demonstrated hands-on experience with molecular biology or microbiology laboratory techniques (PCR, qPCR, nucleic acid extraction, microbial culture methods, etc.). Proven experience in technical documentation, scientific writing, or related roles, preferably within biotechnology or life sciences sectors. Exceptional written and verbal communication skills, capable of translating complex scientific concepts into clear documentation. Fluent in English with strong English writing skills. Strong interpersonal skills, with experience in customer support or training roles being highly advantageous. Proficiency with documentation software and content management systems. Highly organized, detail-oriented, and capable of managing multiple tasks simultaneously. Benefits: Competitive salary and comprehensive benefits package. Opportunities for professional growth and career advancement. Collaborative and inclusive work environment. Flexible work arrangements. Why Avam? Contribute directly to innovative biotechnology solutions with global impact. Collaborative, supportive work environment that fosters professional growth and development. Competitive compensation package and benefits. Show more Show less

About Intas Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world, Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare, At Intas, our success is fundamentally built on the strength of our people Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence This approach ensures that every employee plays a meaningful role in driving both the companys growth and advancements in global healthcare, Job Title: Research Scientist Gene Therapy Job Requisitions No : 13325 Job Description Skill Required Candidate must have thorough understanding of cell and molecular biology along with several analytical techniques such as Flow Cytometry, PCR/qPCR, ELISA, etc Hands on experience in multicolor flow cytometry is indispensable for this position, Candidate should have good hands-on experience with aseptic handling, microbial and mammalian cell culture techniques, Candidate should have understanding of good documentation practices, preparation of SOPs, analytical reports, etc Understanding of regulatory guidelines with respect to analytical assay development and qualification will be an added advantage, Purpose of Job An experienced candidate (m-sc /m-tech in Biotechnology/biochemistry or other biological sciences with 5 to 6 years of relevant industry experience or Ph D fresher or with ~1 year of experience) for Cell and Gene Therapy Department, Cell Therapy Analytical Group at Intas Pharmaceuticals (Biopharma Division), Ahmedabad, Gujarat, India, Roles and Responsibilites Develop analytical methods (Flow Cytometry, qPCR, ELISA, Cell based assay (e-g In vitro cytotoxicity assay),) for Cell and Gene Therapy based products, Qualify analytical methods as per the regulatory guidelines, Provide support for analysis of in-process, DS and DP samples, Documentation in LNB, preparation of SOPs, Analytical Reports, etc Participate in method transfers to QC labs, AMC and CMC of instruments/equipment in analytical development lab, inventory management, etc Qualification Required Sc Competencies Intas Action Oriented Intas Customer Focus Intas Dealing with Ambiguity Intas Problem Solving Intas Time Management Relevant Skills / Industry Experience Flowcytometry, PCR/qPCR, ELISA, Cell based assay, etc Relevant professional / Educational background Sc Any Other Requirements (If Any) None Compensation / Reward As per HR policy Location: Ahmedabad, GJ, IN, 382213 Travel: 0% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape, Date: 11 Apr 2025

We are seeking a motivated Biotechnology Associate to join our Product Development and Field Support Team . This role involves hands-on work in kit preparation, ELISA, electrophoresis, DNA/protein extraction, troubleshooting , and client interactions across India. You will contribute to developing high-quality biotech kits while providing on-site technical support to clients. Key Responsibilities1. Laboratory Work & Kit Development Prepare and optimize biotechnology kits (e.g., DNA/RNA extraction, protein purification). Design and perform ELISA assays , gel electrophoresis (SDS-PAGE, agarose) , Cell culture and chromatography . Conduct quality control (QC) tests on reagents and kits. Troubleshoot technical issues in sample processing, extraction, and assay workflows . 2. Field Support & Client Management Travel to client sites (labs, hospitals, research centers) across India for product demonstrations, training, and troubleshooting . Build and maintain strong relationships with academic, clinical, and industrial clients . Gather customer feedback to improve product design and usability. 3. Documentation & Compliance Maintain detailed records of experimental protocols, QC data, and client reports . Ensure compliance with ISO or other regulatory standards (if applicable). 4. Cross-Functional Collaboration Work with R&D, manufacturing, and sales teams to refine product workflows. Attend scientific conferences, exhibitions, and networking events to promote products. Qualifications & SkillsEssential: Bachelor’s/Master’s degree in Biotechnology, Biochemistry, Molecular Biology, or related field . Hands-on experience with: DNA/RNA extraction (e.g., column-based, magnetic bead kits). ELISA (indirect, sandwich, competitive). Cell Culture Electrophoresis (agarose, SDS-PAGE). Protein purification (TFF, affinity chromatography). Strong analytical and troubleshooting skills . Willingness to travel up to 40% (client visits across India). Preferred: Familiarity with PCR, qPCR, or NGS workflows . Experience in IVD kit development (diagnostics). Knowledge of regulatory standards (ISO 13485, GMP). Fluency in English + regional Indian languages (Hindi, Tamil, etc.). Work Place: IIDC KOSI KOTWAN, NABIPUR Mathura, Uttar Pradesh, 281403 Job Types: Full-time, Permanent Pay: ₹9,154.29 - ₹22,928.79 per month Schedule: Fixed shift Monday to Friday Morning shift Ability to commute/relocate: Mathura, UP: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Minimum Salary Expectation: Work Location: Hybrid remote in Mathura, UP

Role & responsibilities : Extraction of nucleic acid from virus, bacteria and human samples. Designing of primers and probes for conventional PCR, qPCR and LAMP. Standardization, optimization & production of molecular assays (PCR/qPCR/LAMP/Crispr). Calibration, verification and validation of developed assay. Development of controls, standards and secondary reference material. Troubleshooting and application support to the customers for developed assay. Development of protocol, procedure, SOP, IFU, work instructions related to the developed product. Preparation of documents for regulatory approvals of developed assay. To ensure smooth tech transfers and to establish good manufacturing practices and quality checks. Preferred candidate profile Expertise in RTPCR assay development

Job Description: Molecular Biologist Position Overview: We are seeking a highly motivated Molecular Biologist to conduct research and experiments related to DNA, RNA, and protein functions. The ideal candidate will have expertise in molecular biology techniques, genetic analysis, and laboratory research, contributing to advancements in biotechnology, healthcare, and pharmaceuticals. Key Responsibilities: • Design and perform molecular biology experiments, including PCR, qPCR, cloning, gene expression analysis, and sequencing. • Extract, purify, and analyze DNA, RNA, and proteins from biological samples. • Conduct cell culture experiments, including transfection and gene editing ( CRISPR). • Utilize advanced molecular biology techniques such as Western blotting, ELISA, and immuno histochemistry. • Develop and optimize protocols for genetic and molecular assays. • Analyze experimental data, interpret results, and prepare technical reports. • Maintain laboratory equipment, ensure compliance with safety regulations, and document procedures. • Collaborate with interdisciplinary teams, including bioinformaticians, microbiologists, and clinical researchers. • Stay updated with the latest advancements in molecular biology and biotechnology. Required Skills & Qualifications: • Bachelors/ Master’s in Molecular Biology, Genetics, Biotechnology, Biochemistry, or a related field. • Hands-on experience with molecular biology techniques and laboratory research. • Strong knowledge of genetic engineering, genomics, and proteomics. • Familiarity with bioinformatics tools for DNA/RNA sequencing analysis. • Proficiency in data analysis and visualization using software like GraphPad Prism, R, or Python. • Excellent problem-solving, critical thinking, and communication skills.

Name of the Post - Project Technical Support-III No. of Vacancy - 01 (One) Emoluments- Rs-20000/ + HRA, as admissible Essential Qualification:- 12th in Science + Diploma (MLT/DMLT/) + Five Year Experience in relevant subject / field Desirable Qualification :- Experience in handling and testing clinical samplesinvolving techniques such as ELISA and qPCR & knowledge of computer application and data management. Candidates with hands-on experience in molecular biology techniques shall be preferred. One- year previous work experience in research related to medical sciences in a reputed institute . Age Limit :- The upper age limit fs 30 years. Location:- CRMCH, Chandrapur Scope of Work :- Project Technical Support will be involved in the collection of samples from hospitals and field camps, processing of the blood sample, washing of laboratory materials, maintaining reagents record, indenting chemicals, preparation of regents, tabulating haematological and biochemical reports etc, Performing basic tests like CBC, Retic count, peripheralblood smear, microscopic examination.