317 Serology Jobs

We are looking for a detail-oriented Lab Technician to assist in routine laboratory tasks, sample preparation, testing, and data. Perform basic lab tests and experiments Prepare and process samples Maintain lab equipment test results accurate

Excellent opportunity as "LAB ATTENDANT" from a well reputed & established CBSE affiliated school located near South City-II, Gurgaon. Position: Lab Attendant [for Bio & Phy Labs] [School experience is mandatory] Prepare and set up laboratory equipment and materials required for Lab experiments as instructed by the faculty. - Assist students during laboratory sessions, providing guidance and clarifying procedural instructions to ensure accurate and safe experiment execution. - Maintain a clean, organized, and safe laboratory environment, including proper storage and disposal of chemicals and hazardous materials. - Calibrate and maintain laboratory equipment, ensuring they are in optimal working condition for use. - Assist in the development and improvement of laboratory protocols and procedures, incorporating industry best practices. - Collaborate with the faculty to design and implement new experiments or modify existing ones to enhance student learning outcomes.

We are looking for a skilled Technician in Biochemistry to join our team at Vijaya Diagnostic Centre Limited. The ideal candidate will have 6-10 years of experience in the field. Roles and Responsibility Conduct biochemistry tests and analyze results with high accuracy and attention to detail. Operate and maintain laboratory equipment, including calibration and troubleshooting. Develop and implement new methods and procedures to improve test efficiency and quality. Collaborate with other technicians and staff to achieve departmental goals. Maintain accurate records of test results and patient information. Participate in quality control and quality assurance activities to ensure compliance with industry standards. Job Requirements Strong knowledge of biochemistry principles and practices. Experience with laboratory equipment operation and maintenance. Excellent analytical and problem-solving skills. Ability to work effectively in a team environment. Good communication and interpersonal skills. Familiarity with laboratory safety protocols and procedures.

Date: 9 Sept 2025 Location: IN Custom Field 1: Discovery Services Job Description Designation: Head Quality Review, Job Location: Semicon Park, Bengaluru Reporting to: Operating Unit Head, T&CR Company Overview Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene’s 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA. Role Summary The Head of Quality Control Review has a pivotal role within the Clinical Development Operating Unit, responsible for supporting operating teams and enhancing the quality standards across all departments. Clinical development OU operates in BA/BE studies, patient clinical trials, central clinical lab to support clinical research, small and large molecule bioanalytical lab. The primary purpose of this role is to ensure that the OU consistently meets or exceeds regulatory and internal quality benchmarks. This is achieved by owning and driving the quality metrics, leading process/SOP improvements, and ensuring the OU is anytime audit ready. Key Result Areas Support operating teams and QA in tracking Quality Metrics: support Operating teams to sustain comprehensive quality metrics that assess performance and compliance across all divisions, ensuring that the organization adheres to internal and regulatory standards. Enhance SOPs and Processes: Lead initiatives to refine standard operating procedures (SOPs) and workflows, enhancing operational efficiency and regulatory compliance in close collaboration with operating teams. Support QA and operating teams in Regulatory Audits: Support the organization through various audits and inspections, including internal, customer-based, and regulatory audits, ensuring all activities comply with applicable laws and standards. Collaboration and Error Minimization: Work closely with section heads and the Quality Assurance (QA) team to identify and reduce errors, fostering a culture of continuous improvement and compliance. Manage Quality Control Issues: Collaborate with operational teams to address, escalate, and resolve quality control issues, assisting in the development and implementation of corrective action plans. Audit Preparedness: Maintain a state of "anytime audit readiness" by implementing robust quality control systems and conducting regular internal reviews. Support operating teams to drive Continuous Improvement: Support operating teams with their efforts in process simplification, and other quality improvement initiatives, aiming to achieve and sustain world-class standards in both leading and lagging indicators of Quality KPIs. Role-specific BA/BE: Section Quality Control Plan Execution: Develop and oversee the implementation of the Quality Control Review Plan (QC) for each study, ensuring meticulous execution and adherence to standards. Monitoring and Oversight: Monitor protocol compliance and documentation, conduct clinical study conduct reviews, and ensure the integrity of study processes through a robust quality control plan execution.. Quality Control Processes Definition: Establish Quality Control Review processes to: Manage the review and approval of draft source documents, ensuring alignment with the protocol, HPU SOPs, ICH GCP (E6), and other relevant regulatory guidelines. Verify screening charts for accuracy of Inclusion/Exclusion criteria, informed consent form (ICF) documentation processes, and Investigator/Sub-investigator review activities. Ensure comprehensive review of all source documents against quality control standards as outlined in the QC Plan. Conduct reviews of study day records to confirm data completeness, consistency with protocol requirements, and adherence to good documentation practices and ALCOA+ principles. Documentation and Compliance: Ensure that the Quality Control Review process is thoroughly documented, with all QC observations and protocol deviations addressed and resolved in a timely manner before data entry. Verification and Reporting: Lead the Quality Control Review team in verifying source data against electronic Case Report Forms as stipulated in the QC Plan. Communicate any issues or deviations in protocol to clients, the Principal Investigator (PI), and the VP & OU Head of Clinical Development. Client and Team Interaction: Meet regularly with clients to discuss protocol adherence, address any deviations, and report on consistent QC observations. Resolution Deadlines: Establish and enforce deadlines for resolving queries, ensuring prompt compliance. Regulatory Documentation Review: Oversee the QC review of the Regulatory/TMF Binder at the conclusion of the study, ensuring readiness for archiving. Error Analysis and Liaison Duties: Analyze the nature and cause of errors to identify areas for improvement within departmental processes and systems. Serve as a liaison between staff and management to discuss error trends and areas of concern. Bioanalytical Laboratory operations Section activities Data Integrity and Review: Conduct comprehensive checks on method development, validation, sample analysis, concentration data, and database locks to ensure data integrity across all studies. Document Review for Compliance: Scrutinize all study documents to confirm readiness for Quality Assurance Unit (QAU) review, adhering to planned timelines for each review process. Collaborative Problem Solving: Engage directly with the study director to discuss observations, propose solutions, and reach consensus on Corrective and Preventive Actions (CAPA). Audit Support: Provide robust support during all QAU, sponsor, and regulatory audits, ensuring all practices meet required standards. Facility Oversight: Perform routine facility inspections to maintain the facility’s condition and ensure that all related documentation is up to date. Quality Control of Laboratory Practices: Regularly review laboratory logbooks and check the calibration and validation status of equipment to maintain operational standards. Data Trend Analysis: Analyze Quality Control observations monthly to support the Head of Department (HoD) in driving quality transformation initiatives. Drive sustainable quality improvement in lab operations: Spearhead the Quality Circle initiative, providing weekly updates to the HoD on progress and outcomes. Work closely with technical teams to drive sustainable quality improvement in all lab operation. Resource Allocation: Efficiently allocate staff for study reviews to ensure optimal team performance and study coverage. Standard Operating Procedures Support: Assist in the development and revision of Standard Operating Procedures (SOPs), participating actively in their preparation. Efficient Data Review: Manage the simultaneous review of multiple studies’ data, ensuring an efficient and effective process Central laboratory section activities Comprehensive Quality Checks: Oversee Pre-Analytical, Analytical, and Post-Analytical activities, ensuring all procedures adhere to the established Quality Control Standard Operating Procedures (QC SOP). Data Entry Verification: Ensure that all manually transcribed data is accurately captured and corresponds with the respective worksheets, guaranteeing data integrity. Logbook Management: Maintain strict control over logbook entries to ensure all records are legible and properly managed within the Clinical Laboratory (CLAB). Ensure that logbooks are maintained and controlled according to laboratory standards. Quality Control Data Review: Conduct daily reviews of Quality Control data across multiple disciplines, including Clinical Biochemistry, Hematology, Serology, Coagulation, and Clinical Pathology, to ensure consistency and accuracy. Non-Conformance (NC) Logbook Implementation: Manage the Non-Conformance logbook, identifying areas for improvement and implementing necessary changes to enhance laboratory processes. Instrument Maintenance and Calibration: Maintain rigorous follow-up of instrument preventive maintenance schedules and calibration records, ensuring all equipment operates according to industry standards and regulatory requirements. Clinical trials, data management, statistics, and pharmacy section activities Internal System Reviews: Conduct internal reviews of the Clinical Trial Management department and Syngene Clinical Supply Unit (SCSU) to ensure compliance with Standard Operating Procedures, Good Clinical Practice, and regulatory requirements in line with the Quality Management Plan. SOP and Training Review Coordination: Oversee the review of Standard Operating Procedures (SOPs) and assess the need for updates in training binders, ensuring all documentation supports current practices and regulatory standards. Quality Issue Reporting: Promptly inform the Department Head or designated representative about significant quality issues. Ensure reporting aligns with established operating procedures or work instructions, with a focus on patient safety, regulatory compliance, and data integrity. Syngene Clinical Supply Unit Quality Checks: Perform comprehensive quality checks within the Syngene Clinical Supply Unit as part of the Clinical Trial Management oversight to uphold system integrity. Database and Code Quality Control: Execute quality control checks on databases and associated programs or codes as specified in the Quality Control plan to maintain accuracy and functionality As a Syngene Leader Champion effective Environment, Occupational Health, Safety, and Sustainability (EHSS) practices for the company, and oversee compliance with those practices within the IDD team. Play an active leadership role in monitoring and verifying safety performance through GEMBA walks and other safety-led activities. Foster a corporate culture that promotes an environment, occupational health, safety and sustainability (EHSS) mindset as well as the highest standards of quality, integrity and compliance. Put people at the heart of Syngene’s success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning, and talent retention as a priority. Education and Experience Education M. Pharm, MSc – Post graduate degree in life sciences, Minimum required. PhD will be added advantage. Industry Experience At least 15 years’ experience in working in GxP and compliance environment. Deep understanding of process and compliance in GxP environment. Experience and exposure to GCP and GLP areas is critical experience criteria. People Leadership Experience At least 7 years’ experience in leading teams directly and working with cross functional teams in a metrics organization. International Exposure And Experience Not required, but desirable if any. Other Competencies Required For The Role Excellent people skills with extensive experience in leading change, and a proven ability to instill a culture of collaboration. Keen interest in scientific innovation in a commercial setting. Strong customer and service delivery mindset with a proven track record in delivering business growth. High degree of results orientation with a track record of growth and delivering against targets. Well networked and strong industry knowledge. Confident and well-practiced language and interpersonal skills Impeccable ethics and integrity along with an exposure to a multi-cultural work environment. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities. Pls visit us at https://syngeneintl.com/ to know more about us and what we do.

Job Summary: The Senior Lab Technician plays a critical role in ensuring the smooth functioning of the diagnostic laboratory by performing advanced clinical tests, supervising junior staff, ensuring compliance with NABL and other quality standards, and maintaining lab equipment. The role demands accuracy, efficiency, and leadership in supporting clinical decision-making and patient care. Key Responsibilities Technical & Diagnostic Perform diagnostic tests in hematology, clinical pathology, microbiology, serology, and biochemistry. Validate and interpret results before releasing reports. Collect, label, process, and store patient samples as per SOPs. Maintain accurate test records and documentation. Supervision & Training Supervise junior technicians, assistants, and trainees. Provide training on new equipment and safety protocols. Ensure compliance with SOPs, biosafety, and infection control. Quality & Compliance Adhere to NABL, ISO 15189, ICMR, and regulatory standards. Conduct internal audits and corrective actions. Participate in EQAS and proficiency testing. Equipment & Inventory Operate, calibrate, and troubleshoot analyzers, centrifuges, and microscopes. Schedule preventive maintenance. Monitor stock of reagents, consumables, and chemicals. Coordination & Reporting Communicate with pathologists/clinicians on critical cases. Manage data in the Laboratory Information System (LIS). Assist in reports, audits, and accreditation documentation. Qualifications Required: DMLT / B.Sc. in Medical Laboratory Technology. Preferred: M.Sc. in MLT or specialized diploma. 4–6 years’ experience in a diagnostic lab (NABL lab experience preferred). strong knowledge of lab equipment, LIS, quality control & safety. Certifications (added advantage): NABL Internal Auditor Training Biomedical Waste Management EQAS participation Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Health insurance Paid time off Provident Fund Ability to commute/relocate: Lucknow, Uttar Pradesh: Reliably commute or planning to relocate before starting work (Required) Application Question(s): Are you an immediate joiner? Do you have license? Experience: diagnostic laboratory : 4 years (Required) Location: Lucknow, Uttar Pradesh (Required) Work Location: In person

Supervise day-to-day laboratory operations across all sections (Microbiology, Histopathology, Biochemistry, Hematology, Serology, etc.). Ensure accurate, reliable, and timely test results by monitoring workflow and quality. Oversee the preparation, processing, and analysis of clinical samples in all specialties. Implement and maintain Quality Assurance (QA) and Quality Control (QC) programs as per NABL/NABH guidelines. Ensure compliance with statutory, ethical, and regulatory requirements in all laboratory practices. Train, mentor, and guide laboratory technicians and junior staff to maintain high professional standards. Coordinate with pathologists, clinicians, and other departments to support patient care. Oversee preventive maintenance, calibration, and validation of all laboratory equipment. Manage procurement, inventory, and usage of laboratory reagents, consumables, and supplies. Prepare, review, and approve SOPs (Standard Operating Procedures) for laboratory practices. Conduct regular audits, troubleshoot technical issues, and ensure continuous process improvement. Support R&D, validation, and implementation of new laboratory tests and technologies. Ensure strict adherence to biosafety, infection control, and patient data confidentiality protocols. Prepare periodic reports and MIS for management review. Qualifications & Requirements M.Sc. in Medical Laboratory Technology / Microbiology / Biochemistry / Life Sciences (Ph.D. preferred). 8–12 years of experience in a diagnostic laboratory / hospital lab, with strong exposure to microbiology, histopathology, and biochemistry. Prior experience in a managerial or supervisory role in a NABL/NABH accredited laboratory preferred. Excellent technical knowledge of laboratory procedures, instrumentation, and quality management systems. Strong leadership, team management, and problem-solving skills. Proficiency in laboratory software (LIS) and MS Office applications. Key Competencies Leadership & People Development Diagnostic Accuracy & Technical Expertise Quality Management & Compliance Strategic Planning & Process Optimization Strong Communication & Collaboration Skills Job Type: Full-time Work Location: In person

Job Summary: The Senior Lab Technician plays a critical role in ensuring the smooth functioning of the diagnostic laboratory by performing advanced clinical tests, supervising junior staff, ensuring compliance with NABL and other quality standards, and maintaining lab equipment. The role demands accuracy, efficiency, and leadership in supporting clinical decision-making and patient care. Key Responsibilities Technical & Diagnostic Perform diagnostic tests in hematology, clinical pathology, microbiology, serology, and biochemistry. Validate and interpret results before releasing reports. Collect, label, process, and store patient samples as per SOPs. Maintain accurate test records and documentation. Supervision & Training Supervise junior technicians, assistants, and trainees. Provide training on new equipment and safety protocols. Ensure compliance with SOPs, biosafety, and infection control. Quality & Compliance Adhere to NABL, ISO 15189, ICMR, and regulatory standards. Conduct internal audits and corrective actions. Participate in EQAS and proficiency testing. Equipment & Inventory Operate, calibrate, and troubleshoot analyzers, centrifuges, and microscopes. Schedule preventive maintenance. Monitor stock of reagents, consumables, and chemicals. Coordination & Reporting Communicate with pathologists/clinicians on critical cases. Manage data in the Laboratory Information System (LIS). Assist in reports, audits, and accreditation documentation. Qualifications Required: DMLT / B.Sc. in Medical Laboratory Technology. Preferred: M.Sc. in MLT or specialized diploma. 4–6 years’ experience in a diagnostic lab (NABL lab experience preferred). strong knowledge of lab equipment, LIS, quality control & safety. Certifications (added advantage): NABL Internal Auditor Training Biomedical Waste Management EQAS participation Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Health insurance Paid time off Provident Fund Ability to commute/relocate: Lucknow, Uttar Pradesh: Reliably commute or planning to relocate before starting work (Required) Application Question(s): Are you an immediate joiner? Do you have license? Experience: diagnostic laboratory : 4 years (Required) Location: Lucknow, Uttar Pradesh (Required) Work Location: In person

khushboofeed.com is looking for Lab Technician Feed Mill to join our dynamic team and embark on a rewarding career journey Assist with testing and calibrating lab equipment in preparation for specific tasksAnalyze retrieved data and prepare reports for laboratory management Experience in data collection and interpretation as well as the storage and retrieval of samples in a laboratory setting Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Medcare Hospitals Medical Centres is looking for Technician to join our dynamic team and embark on a rewarding career journey We are seeking a highly skilled and detail-oriented Laboratory Technician to join our team at Aster Laboratory As a Laboratory Technician, you will play a crucial role in performing various laboratory tests and procedures to support accurate diagnoses and patient care Your responsibilities will include conducting tests, maintaining laboratory equipment, documenting results, and ensuring compliance with safety and quality standards Responsibilities:Perform a variety of laboratory tests and procedures, including but not limited to, sample processing, specimen handling, and analysis of biological samples Prepare and maintain laboratory equipment, instruments, and supplies necessary for testing and experiments Adhere to standard operating procedures (SOPs) and safety protocols to ensure accurate and reliable test results Collect, label, and process specimens according to established protocols and maintain accurate records of sample information Conduct routine quality control checks to ensure accuracy and precision of test results Operate and maintain laboratory instruments, such as microscopes, centrifuges, spectrophotometers, and automated analyzers Analyze and interpret test results, and document findings accurately and promptly Collaborate with laboratory team members and healthcare professionals to ensure efficient workflow and timely delivery of test results Follow proper waste disposal procedures and maintain a clean and organized laboratory environment Stay updated on advancements in laboratory techniques, technologies, and best practices through continuous learning and professional development Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before

Company Description Agappe Diagnostics Ltd. is a leading company in the Indian diagnostics industry with significant domestic and international presence. The company offers a comprehensive range of Reagents and Equipment, including Biochemistry Kits, Serology Kits, and Hematology Reagents. Certified with ISO 9001-2008 and ISO 13485:2003, Agappe Diagnostics also adheres to GMP standards and has an FDA-approved manufacturing facility. Agappe Diagnostics' vision is to become a premier global in-vitro diagnostic corporation, and its mission is to continuously improve products and services with a world-class R&D program. Role Description This is a full-time on-site role for a Salesperson based in Indore. The Salesperson will be responsible for generating leads, developing client relationships, achieving sales targets, and providing after-sales support. Daily tasks will include conducting market research, meeting with potential and existing clients, preparing sales presentations, and maintaining sales records. The Salesperson will also need to stay updated on industry trends and competitor activities. Qualifications Experience in sales, lead generation, and client relationship management Knowledge of diagnostic products such as Biochemistry Kits and Hematology Reagents Excellent communication, presentation, and negotiation skills Strong analytical skills and ability to conduct market research Bachelor's degree in Marketing, Business Administration or a related field is preferred Proficiency in using CRM software and MS Office Suite Ability to work independently and as part of a team Willingness to travel as required

Role & responsibilities Collect and label biological samples (e.g., blood, urine, swabs) as per standard protocols. Prepare culture media, reagents, and slides for analysis Monitor and maintain stock of microbiology consumables (media, reagents, slides, etc.). Preferred candidate profile Looking for a nearby candidate for a Lab Technician role (preferably based in or around Nagpur). Minimum 1.5 years of experience required in the Microbiology or Serology department.

Role & responsibilities Handling Haematology, Biochemistry & immunology, Cytopathology, Histopathology Planning & Implementing of internal quality control measures, external quality control measures & proficiency tests with the laboratory manager. By using microscopes and other testing tools pathologist analyse samples of blood, urine, tissue, and other bodily specimens and run tests. Responsible for the smooth functioning of respective sections by ensuring effective rostering of the laboratory staff Approving/Authentication of Patient reports Implement safe laboratory environment in compliance with good practice and applicable regulations To ensure implementation and monitoring of standards and performance and quality improvement Training technical staff about scientific validity and clinical significance of the tests offered in the section Daily review of reports, managing the workload and ensuring that they meet TAT. Interacting with customers (referring clinicians and patients) to discuss and clarify results of clinical reports, and also measure for continual improvement of services provided. Daily IQC shows no violation of the documented policy and procedure The technical personnel posted during this period shall be well trained and of proven competence to apply IQC rules The regular authorized personnel shall go through the records on the next working day and issues a final report after verifying that the results of these tests showed no trend and that the IQC was valid. The records of these shall be available till the next assessment Preparation of SOPs where necessary Ensure recording of equipment's preventive/breakdown maintenance details Observation of punctuality and discipline in the department In case of emergency/major problem, inform the patient/customer's doctor or give provisional report it needed Ensure delivery of report in time. Help in selection and evaluation of suppliers Analysis of non-conformities and initiation of corrective actions. Disposition of non-conforming results/reports Controls further processing until any conditions likely to cause non-conformities are rectified. Ensure proper housekeeping and administration in the department Ensure recording of equipment's preventive/breakdown maintenance details (if needed) Wastes Management Supervise the working of technical and non-technical personnel. Looking for abnormalities in samples that evidence disease and conveying this information to the relevant medical practitioner. Using checklists, medical software, and retesting to get thorough and precise results. Suggesting potential treatment options. Writing pathology reports detailing specimens tested, results of tests, and the final diagnosis. Undertaking research to improve identification and testing methods and finding innovative ways to treat disease. Staying up to date with developments in the fields of pathology and medical practice. Preferred candidate profile Your duties will include analyzing bodily fluids and tissue samples to study, diagnose, and treat disease. You will work in various medical settings and carry-out research and patient tests in order to assist fellow medical professionals in their diagnoses. MD/DNB Pathology/ DM Hematopathology required Bachelors degree in biology, physical sciences, or a related field. 3 to 5 years internship and residency training, specializing in pathology. Should be holding a valid and active medical license registered in Delhi. Experience using lab testing equipment, such as microscopes and flow cytometers. Exceptional analytical and research skills. Strong oral and written communication skills. Works well independently and has strong laboratory and research skills. Demonstrates strong critical-thinking, problem-solving, and project management skills. Knows how to use common pathology laboratory management software and equipment Interested Candidate Share your Resume on - 9871235736

Job Summary: We are seeking a dedicated Laboratory Technician to support our construction team with material testing, quality control, and laboratory analysis. As a Laboratory Technician, you will be responsible for performing tests on construction materials (such as soil, concrete, asphalt, and aggregates) to ensure they meet the required specifications and standards. You will work closely with engineers, project managers, and site teams to ensure the quality and safety of construction materials used on site. Key Responsibilities: Material Testing & Analysis: Perform routine and specialized tests on construction materials, including concrete, asphalt, soil, and aggregates. Conduct tests according to standard procedures and report results accurately. Ensure that all materials are tested in compliance with local building codes, safety standards, and project specifications. Quality Control & Assurance: Assist in the development and implementation of quality control procedures and protocols for materials testing. Monitor and ensure the consistent quality of materials used in construction, providing feedback to project teams on findings. Conduct regular inspections of lab equipment, ensuring it is maintained and calibrated to meet industry standards. Sample Collection & Preparation: Collect material samples from construction sites, suppliers, and storage areas as required. Prepare and process samples for testing, including mixing, conditioning, or molding materials as necessary. Data Management & Reporting: Record and document test results, making sure they are accurate, clear, and consistent with project specifications. Prepare detailed reports on test results, including findings, recommendations, and deviations from standards. Communicate test results and findings to engineers, site managers, and other project stakeholders. Safety & Compliance: Ensure that all laboratory and field testing activities are carried out in accordance with health and safety regulations. Maintain a clean, organized, and safe laboratory environment. Follow and enforce proper waste disposal practices for hazardous materials used in testing. Collaboration & Communication: Work closely with project managers, engineers, and other team members to ensure that construction materials meet the necessary quality standards. Provide technical assistance in material selection, testing, and problem-solving when required. Qualifications: Education: A diploma or associate's degree in Civil Engineering, Construction Materials Technology, or a related field. Additional certifications or training in laboratory testing or quality control is a plus. Experience: 1-3 years of experience in a laboratory or quality control role, ideally within the construction or civil engineering industry. Familiarity with material testing procedures for concrete, soil, asphalt, and aggregates. Skills: Basic knowledge of construction materials and their testing methods. Proficiency in using laboratory equipment and tools such as compression testing machines, sieves, and moisture meters. Ability to follow standardized testing procedures and maintain accurate records. Familiarity with construction standards and industry regulations (e.g., ASTM, AASHTO). Soft Skills: Strong attention to detail and analytical skills. Good communication skills to report findings to engineers and other team members. Ability to work independently and manage time effectively. Strong organizational and problem-solving skills. Mandatory Key Skills construction,software testing,construction material,sample collection,biochemistry,dmlt,pathology,serology,clinical pathology,hematology,microbiology,haematology,mlt,phlebotomy,histopathology,equipment*,material testing*,soil*,lab*,quality control*

 To execute the routine work in the laboratory, including documentation (as instructed), processing and conducting tests/ analysis.  Preparation of reagents wherever required  Maintenance of all equipment as per the manufacturer’s instructions.  Informing seniors of critical / alert results as and when observed  Monitoring status of all critical inputs (purchased supplies) strictly as per norms.  Participating in all training programs arranged by the lab management.  Executing any other task assigned by the top management from time to time.  Ensuring that all test results are generated as per the specified turnaround time or time committed to customer.  Conducting in-house equipment maintenance as per schedule and keep them in up to date working conditions.  Following quality control plan including control run/ calibration of test parameters and take timely corrective actions for nonconforming testing work, where needed.  Ensuring the Bio-Medical waste disposal is done as per the guidelines.  Ensuring proper housekeeping and following safety and precautions guidelines.  Ensuring the reports are saved in line to the results received on the equipment. Job Types: Full-time, Permanent Pay: From ₹20,000.00 per month Benefits: Health insurance Provident Fund Ability to commute/relocate: Paschim Vihar, Delhi, Delhi: Reliably commute or planning to relocate before starting work (Required) Experience: Lab Technician: 3 years (Required) Work Location: In person

Job Summary: The Senior Lab Technician plays a critical role in ensuring the smooth functioning of the diagnostic laboratory by performing advanced clinical tests, supervising junior staff, ensuring compliance with NABL and other quality standards, and maintaining lab equipment. The role demands accuracy, efficiency, and leadership in supporting clinical decision-making and patient care. Key Responsibilities Technical & Diagnostic Perform diagnostic tests in hematology, clinical pathology, microbiology, serology, and biochemistry. Validate and interpret results before releasing reports. Collect, label, process, and store patient samples as per SOPs. Maintain accurate test records and documentation. Supervision & Training Supervise junior technicians, assistants, and trainees. Provide training on new equipment and safety protocols. Ensure compliance with SOPs, biosafety, and infection control. Quality & Compliance Adhere to NABL, ISO 15189, ICMR, and regulatory standards. Conduct internal audits and corrective actions. Participate in EQAS and proficiency testing. Equipment & Inventory Operate, calibrate, and troubleshoot analyzers, centrifuges, and microscopes. Schedule preventive maintenance. Monitor stock of reagents, consumables, and chemicals. Coordination & Reporting Communicate with pathologists/clinicians on critical cases. Manage data in the Laboratory Information System (LIS). Assist in reports, audits, and accreditation documentation. Qualifications Required: DMLT / B.Sc. in Medical Laboratory Technology. Preferred: M.Sc. in MLT or specialized diploma. 4–6 years’ experience in a diagnostic lab (NABL lab experience preferred). strong knowledge of lab equipment, LIS, quality control & safety. Certifications (added advantage): NABL Internal Auditor Training Biomedical Waste Management EQAS participation Job Type: Full-time Pay: ₹11,238.81 - ₹25,000.00 per month Benefits: Health insurance Paid time off Provident Fund Ability to commute/relocate: Gauriganj, Uttar Pradesh: Reliably commute or planning to relocate before starting work (Preferred) Experience: diagnostic laboratory : 4 years (Required) Location: Gauriganj, Uttar Pradesh (Preferred) Work Location: In person

 To execute the routine work in the laboratory, including documentation (as instructed), processing and conducting tests/ analysis.  Preparation of reagents wherever required  Maintenance of all equipment as per the manufacturer’s instructions.  Informing seniors of critical / alert results as and when observed  Monitoring status of all critical inputs (purchased supplies) strictly as per norms.  Participating in all training programs arranged by the lab management.  Executing any other task assigned by the top management from time to time.  Ensuring that all test results are generated as per the specified turnaround time or time committed to customer.  Conducting in-house equipment maintenance as per schedule and keep them in up to date working conditions.  Following quality control plan including control run/ calibration of test parameters and take timely corrective actions for nonconforming testing work, where needed.  Ensuring the Bio-Medical waste disposal is done as per the guidelines.  Ensuring proper housekeeping and following safety and precautions guidelines.  Ensuring the reports are saved in line to the results received on the equipment. Job Types: Full-time, Permanent Pay: From ₹20,000.00 per month Benefits: Health insurance Provident Fund Ability to commute/relocate: Paschim Vihar, Delhi, Delhi: Reliably commute or planning to relocate before starting work (Required) Experience: Lab Technician: 3 years (Required) Work Location: In person

Job Summary: The Senior Lab Technician plays a critical role in ensuring the smooth functioning of the diagnostic laboratory by performing advanced clinical tests, supervising junior staff, ensuring compliance with NABL and other quality standards, and maintaining lab equipment. The role demands accuracy, efficiency, and leadership in supporting clinical decision-making and patient care. Key Responsibilities Technical & Diagnostic Perform diagnostic tests in hematology, clinical pathology, microbiology, serology, and biochemistry. Validate and interpret results before releasing reports. Collect, label, process, and store patient samples as per SOPs. Maintain accurate test records and documentation. Supervision & Training Supervise junior technicians, assistants, and trainees. Provide training on new equipment and safety protocols. Ensure compliance with SOPs, biosafety, and infection control. Quality & Compliance Adhere to NABL, ISO 15189, ICMR, and regulatory standards. Conduct internal audits and corrective actions. Participate in EQAS and proficiency testing. Equipment & Inventory Operate, calibrate, and troubleshoot analyzers, centrifuges, and microscopes. Schedule preventive maintenance. Monitor stock of reagents, consumables, and chemicals. Coordination & Reporting Communicate with pathologists/clinicians on critical cases. Manage data in the Laboratory Information System (LIS). Assist in reports, audits, and accreditation documentation. Qualifications Required: DMLT / B.Sc. in Medical Laboratory Technology. Preferred: M.Sc. in MLT or specialized diploma. 4–6 years’ experience in a diagnostic lab (NABL lab experience preferred). strong knowledge of lab equipment, LIS, quality control & safety. Certifications (added advantage): NABL Internal Auditor Training Biomedical Waste Management EQAS participation Job Type: Full-time Pay: ₹11,238.81 - ₹25,000.00 per month Benefits: Health insurance Paid time off Provident Fund Ability to commute/relocate: Gauriganj, Uttar Pradesh: Reliably commute or planning to relocate before starting work (Preferred) Experience: diagnostic laboratory : 4 years (Required) Location: Gauriganj, Uttar Pradesh (Preferred) Work Location: In person

Looking for an Jr. Lab Technician skilled in Biochemistry & Hematology. Must be proficient in diagnostic procedures, QC protocols & lab documentation. Required Candidate profile Educational Requirement : B.Sc MLT / (DMLT) Diploma in Medical Laboratory Technology Interested Candidates Drop CVs to HR Himani WhatsApp: +91 73079 60780 Mail: hr@accurislabs.com

Join Our Medical Team at Lifenity Health Limited Parel, Kamala Mills Were hiring passionate and qualified professionals for part-time and full-time roles in our advanced diagnostic center. If you're committed to excellence in healthcare, wed love to meet you. Position Overview Role : MD Pathologist Type : Part-Time (Evening Shift) or Full-Time (Morning Shift) Location : Parel, Kamala Mills Openings : 2 Preferred Candidate : Male Evening Shift : 4 hours from 05:30 PM Onwards Morning Shift : 8.5 hours starting from 7:00 AM onwards Key Responsibilities: Lead diagnostic operations in Haematology, Biochemistry, Clinical Pathology, and Serology Validate test reports and uphold quality assurance standards Train lab staff and monitor turnaround times Collaborate with clinicians and ensure ethical lab practices Desired Candidate Profile: MBBS with specialization in Pathology 2+ years of experience in clinical pathology or related fields Strong command of biochemistry, hematology, serology , and lab procedures NABL certification or equivalent accreditation preferred

Jomb Vacancy: Lab Manager Company: MedEnnove8 Pvt Ltd Location: Kochi Experience: Minimum 3 years Employment Type: Full-time About MedEnnove8 Pvt Ltd: MedEnnove8 Pvt Ltd is a leading diagnostic and healthcare services provider dedicated to delivering accurate, reliable, and timely laboratory testing solutions. With a strong focus on innovation, patient care, and scientific excellence, we specialize in advanced testing protocols across Biochemistry, Serology, Immunology, and Hematology. Our commitment to improving healthcare outcomes is backed by state-of-the-art laboratory facilities, a team of expert professionals, and a customer-centric approach. We continuously strive to set new benchmarks in diagnostic services while ensuring precision and integrity in all our operations. Job Description: We are seeking a highly motivated and experienced Lab Manager to oversee and manage the day-to-day laboratory activities. The ideal candidate should have a minimum of 3 years of experience in laboratory operations and must be capable of handling all aspects of lab management, ensuring the highest standards of quality and compliance. Key Responsibilities: ✅ Oversee and manage laboratory operations in Biochemistry, Serology, Immunology, and Hematology ✅ Supervise lab staff, ensure proper training, and monitor performance ✅ Ensure adherence to safety, quality control, and regulatory guidelines ✅ Handle sample processing, testing protocols, and report verification ✅ Maintain equipment calibration, documentation, and lab maintenance ✅ Collaborate with cross-functional teams and coordinate with clinicians and healthcare providers ✅ Implement process improvements to enhance efficiency and accuracy ✅ Address technical issues and troubleshoot equipment malfunctions Requirements: ✔ Minimum 3 years of laboratory management experience ✔ Strong knowledge in Biochemistry, Serology, Immunology, and Hematology testing ✔ Excellent organizational, communication, and leadership skills ✔ Ability to work under pressure and ensure accuracy in testing ✔ Familiarity with laboratory information systems and documentation standards ✔ Commitment to patient care, confidentiality, and ethical practices Why Join Us? Work with a progressive, patient-focused healthcare organization Access to cutting-edge laboratory technology and tools Opportunity for professional growth and skill development Supportive and collaborative work environment Competitive salary and benefits Apply Now! If you are passionate about laboratory sciences and eager to lead a team committed to healthcare excellence, we want to hear from you! Send your resume to vinod.kuriakose@ennove8.com For inquiries, contact: 7594999880 MedEnnove8 Pvt Ltd – Advancing Diagnostics, Enabling Better Health Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Cell phone reimbursement Work Location: In person

About Company Founded in 2011, ReNew, is one of the largest renewable energy companies globally, with a leadership position in India. Listed on Nasdaq under the ticker RNW, ReNew develops, builds, owns, and operates utility-scale wind energy projects, utility-scale solar energy projects, utility-scale firm power projects, and distributed solar energy projects. In addition to being a major independent power producer in India, ReNew is evolving to become an end-to-end decarbonization partner providing solutions in a just and inclusive manner in the areas of clean energy, green hydrogen, value-added energy offerings through digitalisation, storage, and carbon markets that increasingly are integral to addressing climate change. With a total capacity of more than 13.4 GW (including projects in pipeline), ReNew’s solar and wind energy projects are spread across 150+ sites, with a presence spanning 18 states in India, contributing to 1.9 % of India’s power capacity. Consequently, this has helped to avoid 0.5% of India’s total carbon emissions and 1.1% India’s total power sector emissions. In the over 10 years of its operation, ReNew has generated almost 1.3 lakh jobs, directly and indirectly. ReNew has achieved market leadership in the Indian renewable energy industry against the backdrop of the Government of India’s policies to promote growth of this sector. ReNew’s current group of stockholders contains several marquee investors including CPP Investments, Abu Dhabi Investment Authority, Goldman Sachs, GEF SACEF and JERA. Its mission is to play a pivotal role in meeting India’s growing energy needs in an efficient, sustainable, and socially responsible manner. ReNew stands committed to providing clean, safe, affordable, and sustainable energy for all and has been at the forefront of leading climate action in India. Job Description Job Description POSITION TITLE AM – Module Quality (PV Module) BUSINESS/DEPARTMENT Quality-Solar JOB PURPOSE Assuring quality of PV Modules LINKAGES & REPORTING RELATIONSHIPS Reporting To: Head Solar Quality PRINICIPAL ACCOUNTABILITIES (a) Assuring Quality of PV Modules. (b) Planning and carrying out Module inspections at Module factories in India and outside India. (c) Planning third party lab testing as per IEC. (d) Preparation of Module QAP. (e) Review of QAPs and daily inspection reports. QUALIFICATIONS REQUIRED (a) B.Tech/Diploma in Electrical/ Electronics. WORK EXPERIENCE REQUIRED 5 to 10 years SPECIFIC SKILLS REQUIRED (a) Thorough knowledge about PV Module quality & Cell parameters. Good knowledge about PV module manufacturing. (b) Hands on experience of PV Module acceptance criteria and Reliability testing. In depth knowledge about BOM used in Modules and its selection critical parameters. (c) Knowledge about statistical sampling plans. (d) Experience of Calibration of Sun simulators and preparation of calibration Masters. (e) Experience in Third party lab testing of Modules. (f) Knowledge and understanding of IEC standards and MNRE requirements. (g) Skill of doing assessment and factory audits of Module Plants. SPECIFIC CHARACTERISTICS REQUIRED (a) Good at Auditing. (b) Good in managing 3rd party inspection agencies. (c) Good written and verbal communication. LOCATION Gurgaon TRAVELLING 70%

Role & responsibilities The Scientific Officer performs his/her duties diligently and methodically to analyze specimens allotted to him / her. Segregation of Samples Raising query in case of the problem sample Monitoring Performance of the equipment Observing all laboratory safety precautions in the handling of clinical specimens and running of tests. Identifying Errors Ensuring proper maintenance of equipment Ensuring equipment quality control Ensuring adequacy in onboard supplies Performing checks during sample testing to monitor performance Identifying problems in results as per re- check criteria/linearity Escalating identified issues to designated supervisor Timely Reporting of Sample Tests as per TAT Recording results of samples tested Handling inter department queries Preferred candidate profile Immeadiate joiner

Mission: The mission of the position Consultant Pathologist is to provide qualitative pathology services, contribute to accurate diagnostic interpretations, and ensure the highest level of patient care. The person in this role will play a vital role in supporting the business commitment to delivering accurate and timely results, maintaining quality standards, and fostering a culture of excellence in diagnostics. Key Responsibilities: Diagnostic Operations: Perform and interpret diagnostic tests, including cytopathology, hematopathology, biochemistry, immunohistochemistry, and microbiology. Analyze and evaluate laboratory data, including tissue samples, blood smears, body fluids, and molecular analyses to provide accurate diagnoses. Collaborate with other healthcare professionals, including clinicians to provide comprehensive diagnostic reports and contribute to patient management. Quality Assurance and Compliance: Ensure compliance with NABL standards, laboratory policies, and procedures to maintain the highest level of quality and patient safety. Participate in quality control activities, proficiency testing, and external quality assurance programs to monitor and improve laboratory performance. Contribute to the development and implementation of quality improvement initiatives to enhance the efficiency and accuracy of pathology services. Consultation and Collaboration: Provide expert consultation to referring physicians, hospitals, and healthcare providers to assist in patient management decisions. Collaborate with other pathologists and laboratory staff to discuss complex cases, share knowledge, and contribute to the continuous professional development of the team. Actively participate in interdisciplinary meetings, and research activities to enhance diagnostic capabilities and contribute to laboratory advancements. Training and Education: Mentor and supervise laboratory staff in the principles and practices of diagnostics. Conduct educational sessions, seminars, and workshops to enhance the understanding of pathology concepts and promote professional growth within the organization. Stay updated with the latest advancements in pathology through continuous learning, attending conferences, and engaging in professional societies. Documentation and Reporting: Prepare accurate and detailed diagnostic reports, incorporating clinical and laboratory findings, in a timely manner. Maintain comprehensive patient records, including specimen information, test results, and interpretations, following NABL guidelines and regulations. Assist in the development and implementation of standardized reporting templates and guidelines to ensure consistent and meaningful pathology reports. ** This job description provides a general outline of responsibilities and qualifications and is not exhaustive. The role may be required to perform additional duties as necessary for the smooth functioning of the business. Requirements: Medical degree (MBBS) with specialization in Pathology (MD/DNB) from a recognized institution. Valid state medical license and registration to practice pathology. Significant experience in diagnostic pathology and proficiency in performing and interpreting complex laboratory tests and techniques. Strong knowledge of NABL regulatory and accreditation requirements related to pathology services. Excellent communication and interpersonal skills to collaborate effectively with healthcare professionals and patients. Ability to work independently, handle multiple priorities, and meet deadlines in a fast-paced environment. Commitment to quality, accuracy, and continuous professional development Compensation and Benefits: We offer a competitive salary package commensurate with experience, along with comprehensive benefits and opportunities for professional growth and development.

CIITM is looking for Lab Technician to join our dynamic team and embark on a rewarding career journey Assist with testing and calibrating lab equipment in preparation for specific tasks Analyze retrieved data and prepare reports for laboratory management Experience in data collection and interpretation as well as the storage and retrieval of samples in a laboratory setting.

 To execute the routine work in the laboratory, including documentation (as instructed), processing and conducting tests/ analysis.  Maintenance of all equipment as per the manufacturer’s instructions.  Perform daily, weekly and monthly maintenance.  Report the values within the TAT.  To handle the queries.  Reconstituting the quality controls and calibrators as per the instructions.  Processing the quality controls as per the quality plan.  Calibrate the assay as per the requirement of the machine. Education & Qualifications: B.Sc. in Medical Laboratory Technology . DMLT (Diploma in Medical Laboratory Technology) . Experience: Minimum 2-4 years of hands-on experience in Elisa (Serology Department). Experience in a Serology Department in a diagnostic laboratory. Familiarity with quality control procedures and laboratory information systems (LIS) is a plus Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Health insurance Provident Fund Experience: Serology Department .: 3 years (Preferred) Work Location: In person