165 Spectrophotometer Jobs - Page 2

Date: 14 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Dedicated Centre Job Description Job Title: Executive or Senior Executive Job Location: Bangalore Job Grade: Level 9 (9-I or 9-II) About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene’ s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose Of The Role The candidate shall be responsible for method development, validation, and stability testing drug substance/drug product. The candidate shall be willing to work in shifts. Hands on experience with complex injectables is an added advantage. Role Accountabilities Must have strong hands-on experience in development and validation of Assay & related substances methods for drug substance/drug product. Must have experience in handling HPLC, UPLC (Empower-3 software), GC, UV Visible spectrophotometer balances, Potentiometer, and stability chambers Shall have experience on Good documentation/laboratory practices such as ALCOA+ Experience in calibration and qualification of HPLC, UPLC, GC, and other QC laboratory instruments Shall prepare and review the raw data sheets, instrument operating procedures, and standard operating procedures Shall have good experience in handling of QMS (such as incidents, Out of Specifications, Deviations, and Change control) Shall be responsible for procurement and inventory maintenance of Pharmacopeial Standards/Chemicals/Reagents/Consumables/Spares etc., required for the projects Shall adhere to the procedure of GxP/Safety and as per the procedure defined in the internal standard operation procedure Shall operate the MS office (word, excel, ppt), outlook, and other essential tools required for routine activity Good communication and e-mail writing skills are required since the candidate needs to communicate to client/external users situated overseas Experience in developing and validating SEC, CGE methods is an added advantage especially for monoclonal antibodies (mAb) Behavioral Skills Good Interpersonal skills Self-time management Good Team player Polite/Good Communication skills Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Accountabilities as a Syngene Leader (only for Leadership Hires) Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. 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 our 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. Specific requirements for this role Experience 3-6 years Skills And Capabilities Hands-on HPLC, UPLC/UHPLC, CG, UV-Visible spectrophotometer, Potentiometer, and QC other analytical instruments Good documentation/laboratory practices such as ALCOA+ Particle size determination, Zeta potential and particulate matter analysis techniques is an added advantage Experience in developing and validating SEC, CGE methods for mAbs is an added advantage Able to follow work instructions and perform the tasks under the supervision of the Team leader Preparation and Maintenance of all the documents Good knowledge of MS-office (word, excel, ppt) Education M. Pharm /M. Sc with 3-6 years' experience in R&D under GMP environment (QC)

Job Description Qualification: M. Sc/B. Pharma. Experience: Analyst in physical activity like Handling of UV visible spectrophotometer, Karl Fischer, Water content determination, Particle Size determination, Titration. and having knowledge of LIMS. Having knowledge about cGMP and good laboratory practices. Language: Having a good command over English Language Qualifications Qualification: M.Sc / B.Pharm Experience 4 years or more. Skills Analytical testing expertise and evaluation skills - Mastery Handling of simple analytical Instruments and Interpretation of Resulting Data - Mastery Handling of sophisticated analytical Instruments and Interpretation of Resulting Data - Master Quality Control & Compliance - Advanced Documentation & Data Integrity - Advanced Troubleshooting & Problem-Solving - Mastery LIMS Operation & Data Management - Advance Good Manufacturing Practices (GMP) & Good Laboratory Practices (GLP) Knowledge - Advanced

Key Responsibilities:  Perform chemical analysis of bulk and finished products (mainly Tablets).  Conduct weight variation tests during in-process and final stages.  Assist in stability studies using Dissolution & Disintegration apparatus.  Operate and calibrate UV-Spectrophotometer, Dissolution, and Disintegration test machines.  Maintain log books, SOPs, and ensure regulatory documentation.  Prepare bulk and finished product reports. Ideal Candidate:  B.Sc. / M.Sc. in Chemistry or related field.  Keen interest in pharmaceutical quality control.  Strong documentation habits and attention to detail.  Willing to learn and grow in a GMP-regulated environment. Job Type: Full-time Pay: From ₹12,000.00 per month Work Location: In person

Lab chemist required at pio manihari, sonipat for a spices company Qualification- Any graduate Exp- min 2 yrs Salary- upto 25k Timing - 9.30 to 7 pm

Job description Job Title: Analyst – Air/Water Location: Mohali Experience: Fresher Department: Environment Laboratory Employment Type: Full-Time About the Role: We are looking for an experienced and detail-oriented Analyst to join our Environment Laboratory team. The candidate must have prior experience in a NABL accredited lab with hands-on expertise in Air and Water analysis. Key Responsibilities: Conduct sampling and analysis of ambient air, stack emissions, drinking water, groundwater, and wastewater as per standard methods (e.g., APHA, BIS, CPCB guidelines). Operate and maintain laboratory instruments such as Spectrophotometer, BOD Incubator, COD Digester, pH Meter, and other relevant equipment. Ensure accuracy and reliability of test results with adherence to SOPs and quality protocols. Maintain proper documentation and records as per NABL ISO/IEC 17025 standards. Assist in calibration and validation of laboratory instruments. Follow safety practices and contribute to laboratory cleanliness and compliance. Coordinate with field staff for sample collection and support external audits/inspections. Desired Candidate Profile: B.Sc. / M.Sc. in Environmental Science, Chemistry, or related field 1–3 years of experience in Air/Water testing in a NABL accredited laboratory Familiarity with NABL documentation and audit requirements Proficiency in operating laboratory instruments Strong attention to detail and quality Good communication and teamwork skills Job Type: Full-time Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Cell phone reimbursement Health insurance Leave encashment Provident Fund Schedule: Day shift Application Question(s): Have you completed Master's of Chemistry? Education: Master's (Preferred) Work Location: In person

Key Responsibilities: Sampling & Testing of Raw Materials (RMs), In-Process Materials (IPMs), and Finished Goods (FGs) – powders, tablets, capsules, and liquids. Conduct macronutrient analysis: Protein (e.g., Kjeldahl/Dumas method) Fat (e.g., Soxhlet extraction or gravimetric methods) Carbohydrate (by calculation or direct testing as applicable) Perform routine physicochemical tests (e.g., pH, moisture, ash, bulk density, viscosity, disintegration, dissolution, assay). Conduct instrumental analysis using UV-Vis Spectrophotometer, HPLC, FTIR, etc. Ensure method validation and calibration of lab instruments as per SOP. Carry out stability testing and shelf-life estimation of finished products. Prepare and maintain all QC documentation: COAs, logbooks, analytical records, raw data, and reports. Ensure compliance with GMP, GLP, and FSSAI, AYUSH, or WHO regulatory standards. Support regulatory audits, including documentation and sample analysis. Coordinate with QA, Production, and R&D for timely release and troubleshooting. Skills & Competencies: Strong practical knowledge of Protein, Fat & Carbohydrate testing Experience with analytical instruments and wet chemistry methods Sound understanding of nutraceutical testing protocols and regulatory norms Proficient in documentation and compliance Computer literacy (MS Excel, Word, any LIMS software) Ability to work independently and in a collaborative environment Preferred Candidates: Experience in testing food or nutraceutical products Exposure to regulatory inspections (FSSAI, USFDA, WHO-GMP, etc.) Candidates residing near Mohali preferred Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Health insurance Schedule: Day shift Supplemental Pay: Overtime pay Ability to commute/relocate: Mohali, Punjab: Reliably commute or planning to relocate before starting work (Required) Application Question(s): Willing to work with R& D Department? (If Required) Education: Bachelor's (Required) Experience: Food Technology, Chemistry, Microbiology: 2 years (Required) QC within the nutraceutical, pharmaceutical: 2 years (Required) Shift availability: Day Shift (Required) Work Location: In person

Key Responsibilities: Sampling & Testing of Raw Materials (RMs), In-Process Materials (IPMs), and Finished Goods (FGs) – powders, tablets, capsules, and liquids. Conduct macronutrient analysis: Protein (e.g., Kjeldahl/Dumas method) Fat (e.g., Soxhlet extraction or gravimetric methods) Carbohydrate (by calculation or direct testing as applicable) Perform routine physicochemical tests (e.g., pH, moisture, ash, bulk density, viscosity, disintegration, dissolution, assay). Conduct instrumental analysis using UV-Vis Spectrophotometer, HPLC, FTIR, etc. Ensure method validation and calibration of lab instruments as per SOP. Carry out stability testing and shelf-life estimation of finished products. Prepare and maintain all QC documentation: COAs, logbooks, analytical records, raw data, and reports. Ensure compliance with GMP, GLP, and FSSAI, AYUSH, or WHO regulatory standards. Support regulatory audits, including documentation and sample analysis. Coordinate with QA, Production, and R&D for timely release and troubleshooting. Skills & Competencies: Strong practical knowledge of Protein, Fat & Carbohydrate testing Experience with analytical instruments and wet chemistry methods Sound understanding of nutraceutical testing protocols and regulatory norms Proficient in documentation and compliance Computer literacy (MS Excel, Word, any LIMS software) Ability to work independently and in a collaborative environment Preferred Candidates: Experience in testing food or nutraceutical products Exposure to regulatory inspections (FSSAI, USFDA, WHO-GMP, etc.) Candidates residing near Mohali preferred Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Health insurance Schedule: Day shift Supplemental Pay: Overtime pay Ability to commute/relocate: Mohali, Punjab: Reliably commute or planning to relocate before starting work (Required) Application Question(s): Willing to work with R& D Department? (If Required) Education: Bachelor's (Required) Experience: Food Technology, Chemistry, Microbiology: 2 years (Required) QC within the nutraceutical, pharmaceutical: 2 years (Required) Shift availability: Day Shift (Required) Work Location: In person

Job Summary: The QC Lab Chemist is responsible for conducting routine testing and analysis of water and packaging materials to ensure all products meet BIS, FSSAI, and internal quality standards. The chemist ensures compliance with regulatory norms and supports continuous improvement in product quality. Key Responsibilities: Sampling & Analysis Collect samples of raw water, RO water, treated water, rinsed water, and packaged product from various plant locations as per sampling plan. Perform physical, chemical, and microbiological analysis as per BIS 14543, FSSAI, and company standards. Test parameters include pH, TDS, Turbidity, Conductivity, Hardness, Alkalinity, Chlorides, Sulphates, Nitrates, Fluorides, Metals, Pesticides, and Microbial load (TPC, Yeast & Mold, Coliform, etc). Documentation Maintain daily laboratory records, test reports, calibration logs, and sample registers. Ensure traceability of all records for audits and compliance. Process Control Monitor online and offline water parameters, provide feedback to production for corrective actions. Conduct periodic line audits (rinsing, filling, capping, packaging). Calibration & Maintenance Calibrate and maintain all laboratory instruments (pH meter, TDS meter, Turbidity meter, Spectrophotometer, Incubator, Autoclave, etc). Ensure timely AMC and troubleshooting of laboratory equipment. Raw & Packaging Material Testing Test preforms, caps, bottles, labels, and packing materials for compliance to standards. Perform sensory and migration tests if required. Regulatory & Compliance Prepare and maintain all documentation required for BIS, FSSAI, and other regulatory inspections. Participate in internal and external audits. Reporting & Communication Report non-conformities and deviations immediately to the QC Manager. Prepare daily/weekly QC reports for management review. Hygiene & Safety Follow Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and plant safety norms. Ensure proper disposal of laboratory waste. Continuous Improvement Suggest and implement improvements in lab processes and product quality. Participate in trainings and skill-upgradation programs. Key Skills & Competencies: Knowledge of BIS 14543, FSSAI, and ISO standards for packaged drinking water Sound understanding of water chemistry and microbiology Hands-on with laboratory instruments & analytical methods Meticulous documentation and record-keeping Analytical thinking, troubleshooting skills, and attention to detail Good communication and teamwork Educational Qualification: B.Sc./M.Sc. in Chemistry, Microbiology, or equivalent (preferably with food/water testing experience) Experience: 0–3 years in QC lab, preferably in bottled water/beverage/food industry Work Environment: Laboratory & plant floor, regular interaction with production and QA teams, 3-shift rotation may be required.

Key Responsibilities:Conduct physical and chemical testing of raw oil, refined oil, and final tray oil products. Perform routine analysis such as viscosity, density, acid value, moisture content, FFA (Free Fatty Acids), and other parameters. Calibrate and operate lab instruments such as GC (Gas Chromatograph), pH meter, Karl Fischer, Spectrophotometer, etc. Maintain proper documentation of test results and report deviations to the Quality Manager. Collect and retain production samples as per standard operating procedures (SOPs). Ensure all lab work complies with ISO, FSSAI, BIS, or other applicable standards. Maintain cleanliness and safety of lab equipment and environment. Assist in validation, shelf-life studies, and R&D trials for new oil formulations. Communicate with the production team to suggest corrections or improvements in process quality. Conduct inspections of packaging materials like tray seals, oils filled, and batch labelling. Participate in audits, internal reviews, and continual improvement activities.

· MISSION Environmental Monitoring & Analysis and maintain documents. MAIN ACCOUNTABILITIES * Candidate must have sound knowledge in the analysis of Ambient Air, Stack, Noise monitoring, Meteorological monitoring, Soil & Sludge, Waste water, Drinking water. * Faced WBPCB & NABL audits. * Knowledge in handling Equipments like UV VIS Spectrophotometer, PM10, PM2.5, Flue Gas analyser, BOD, COD etc. * Knowledge in ISO / IEC 17025 : 2017 documentation. * Independently perform all physical, Chemical analysis of Ambient air, Stack gases, Noise monitoring, Soil, Sludge, Waster Water, Drinking Water. * Knowledge about Quality control process and documentation. Job Type: Full-time Pay: ₹20,000.00 - ₹40,000.00 per month Benefits: Commuter assistance Schedule: Morning shift Supplemental Pay: Performance bonus Work Location: In person

Job Summary: We are looking for a dedicated and detail-oriented Biochemist to join our research and development team. The ideal candidate will be responsible for conducting experiments, analyzing biological processes, and contributing to the development of new products, drugs, or diagnostic tools. The role requires strong analytical skills, laboratory expertise, and a passion for scientific discovery. Key Responsibilities: Conduct biochemical experiments and analyze the chemical composition of living organisms. Study the effects of substances such as drugs, hormones, and nutrients on biological systems. Develop and validate laboratory tests, procedures, and protocols. Operate and maintain laboratory equipment such as spectrophotometers, chromatography instruments, and electrophoresis systems. Record and interpret experimental results and present findings in reports or research papers. Collaborate with cross-functional teams including microbiologists, pharmacologists, and clinical researchers. Assist in the development of pharmaceutical compounds, diagnostic tools, or biotechnological products. Ensure compliance with safety standards, regulatory guidelines, and ethical practices in laboratory settings.

Job Summary: We are looking for a dedicated and detail-oriented Biochemist to join our research and development team. The ideal candidate will be responsible for conducting experiments, analyzing biological processes, and contributing to the development of new products, drugs, or diagnostic tools. The role requires strong analytical skills, laboratory expertise, and a passion for scientific discovery. Key Responsibilities: Conduct biochemical experiments and analyze the chemical composition of living organisms. Study the effects of substances such as drugs, hormones, and nutrients on biological systems. Develop and validate laboratory tests, procedures, and protocols. Operate and maintain laboratory equipment such as spectrophotometers, chromatography instruments, and electrophoresis systems. Record and interpret experimental results and present findings in reports or research papers. Collaborate with cross-functional teams including microbiologists, pharmacologists, and clinical researchers. Assist in the development of pharmaceutical compounds, diagnostic tools, or biotechnological products. Ensure compliance with safety standards, regulatory guidelines, and ethical practices in laboratory settings.

Job Summary: We are looking for a dedicated and detail-oriented Biochemist to join our research and development team. The ideal candidate will be responsible for conducting experiments, analyzing biological processes, and contributing to the development of new products, drugs, or diagnostic tools. The role requires strong analytical skills, laboratory expertise, and a passion for scientific discovery. Key Responsibilities: Conduct biochemical experiments and analyze the chemical composition of living organisms. Study the effects of substances such as drugs, hormones, and nutrients on biological systems. Develop and validate laboratory tests, procedures, and protocols. Operate and maintain laboratory equipment such as spectrophotometers, chromatography instruments, and electrophoresis systems. Record and interpret experimental results and present findings in reports or research papers. Collaborate with cross-functional teams including microbiologists, pharmacologists, and clinical researchers. Assist in the development of pharmaceutical compounds, diagnostic tools, or biotechnological products. Ensure compliance with safety standards, regulatory guidelines, and ethical practices in laboratory settings.

Job Summary: We are looking for a dedicated and detail-oriented Biochemist to join our research and development team. The ideal candidate will be responsible for conducting experiments, analyzing biological processes, and contributing to the development of new products, drugs, or diagnostic tools. The role requires strong analytical skills, laboratory expertise, and a passion for scientific discovery. Key Responsibilities: Conduct biochemical experiments and analyze the chemical composition of living organisms. Study the effects of substances such as drugs, hormones, and nutrients on biological systems. Develop and validate laboratory tests, procedures, and protocols. Operate and maintain laboratory equipment such as spectrophotometers, chromatography instruments, and electrophoresis systems. Record and interpret experimental results and present findings in reports or research papers. Collaborate with cross-functional teams including microbiologists, pharmacologists, and clinical researchers. Assist in the development of pharmaceutical compounds, diagnostic tools, or biotechnological products. Ensure compliance with safety standards, regulatory guidelines, and ethical practices in laboratory settings.

Job Summary: We are looking for a dedicated and detail-oriented Biochemist to join our research and development team. The ideal candidate will be responsible for conducting experiments, analyzing biological processes, and contributing to the development of new products, drugs, or diagnostic tools. The role requires strong analytical skills, laboratory expertise, and a passion for scientific discovery. Key Responsibilities: Conduct biochemical experiments and analyze the chemical composition of living organisms. Study the effects of substances such as drugs, hormones, and nutrients on biological systems. Develop and validate laboratory tests, procedures, and protocols. Operate and maintain laboratory equipment such as spectrophotometers, chromatography instruments, and electrophoresis systems. Record and interpret experimental results and present findings in reports or research papers. Collaborate with cross-functional teams including microbiologists, pharmacologists, and clinical researchers. Assist in the development of pharmaceutical compounds, diagnostic tools, or biotechnological products. Ensure compliance with safety standards, regulatory guidelines, and ethical practices in laboratory settings.

Job Summary: We are looking for a dedicated and detail-oriented Biochemist to join our research and development team. The ideal candidate will be responsible for conducting experiments, analyzing biological processes, and contributing to the development of new products, drugs, or diagnostic tools. The role requires strong analytical skills, laboratory expertise, and a passion for scientific discovery. Key Responsibilities: Conduct biochemical experiments and analyze the chemical composition of living organisms. Study the effects of substances such as drugs, hormones, and nutrients on biological systems. Develop and validate laboratory tests, procedures, and protocols. Operate and maintain laboratory equipment such as spectrophotometers, chromatography instruments, and electrophoresis systems. Record and interpret experimental results and present findings in reports or research papers. Collaborate with cross-functional teams including microbiologists, pharmacologists, and clinical researchers. Assist in the development of pharmaceutical compounds, diagnostic tools, or biotechnological products. Ensure compliance with safety standards, regulatory guidelines, and ethical practices in laboratory settings.

Job Summary: We are looking for a dedicated and detail-oriented Biochemist to join our research and development team. The ideal candidate will be responsible for conducting experiments, analyzing biological processes, and contributing to the development of new products, drugs, or diagnostic tools. The role requires strong analytical skills, laboratory expertise, and a passion for scientific discovery. Key Responsibilities: Conduct biochemical experiments and analyze the chemical composition of living organisms. Study the effects of substances such as drugs, hormones, and nutrients on biological systems. Develop and validate laboratory tests, procedures, and protocols. Operate and maintain laboratory equipment such as spectrophotometers, chromatography instruments, and electrophoresis systems. Record and interpret experimental results and present findings in reports or research papers. Collaborate with cross-functional teams including microbiologists, pharmacologists, and clinical researchers. Assist in the development of pharmaceutical compounds, diagnostic tools, or biotechnological products. Ensure compliance with safety standards, regulatory guidelines, and ethical practices in laboratory settings.

Job Summary: We are looking for a dedicated and detail-oriented Biochemist to join our research and development team. The ideal candidate will be responsible for conducting experiments, analyzing biological processes, and contributing to the development of new products, drugs, or diagnostic tools. The role requires strong analytical skills, laboratory expertise, and a passion for scientific discovery. Key Responsibilities: Conduct biochemical experiments and analyze the chemical composition of living organisms. Study the effects of substances such as drugs, hormones, and nutrients on biological systems. Develop and validate laboratory tests, procedures, and protocols. Operate and maintain laboratory equipment such as spectrophotometers, chromatography instruments, and electrophoresis systems. Record and interpret experimental results and present findings in reports or research papers. Collaborate with cross-functional teams including microbiologists, pharmacologists, and clinical researchers. Assist in the development of pharmaceutical compounds, diagnostic tools, or biotechnological products. Ensure compliance with safety standards, regulatory guidelines, and ethical practices in laboratory settings.

Position Title: Executive – Quality Control Qualification And Experience M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job Overview Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

Responsible for sampling (Raw material, packaging materials, in process and final product samples) as per quality plan on regular basis Assist in testing /documentation and release of incoming materials (Raw materials, finished goods and packing materials) and final product by confirming specifications Assist to completion of all assigned analysis/task in stipulated time without any error Responsible for spectrophotometric analysis and biochemical analysis (qualitative, quantitative, and titrimetric analysis) Should be able to handle equipment’s (Spectrophotometer, moisture analyzer, pH meter, conductivity meter) for QC testing Responsible for maintain and storage of samples in proper manner in sample cell Responsible for filing of result data of RM/FG/PM in proper manner Responsible for update and maintain the sampling record on regular basis without any error Follow all standard and timeline for all QC activities Follow GLP and safety protocol during laboratory work Assist in preparation and maintenance the all required documents for compliances of ISO 22000 /Koshar/Halal/FSSAI certification Fair understanding of ISO 9001, ISO 22000, FSSAI, Lab safety & GLP management Maintain safe work environment by following standards & procedures and complying with legal regulations Update Job knowledge by participating in educational opportunities, reading technical publications, & watching industry videos etc. Accomplish organization mission by completing related tasks as needed Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹38,359.40 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Experience: Sampling: 1 year (Required) Documentation: 1 year (Required) Spectrophotometer analysis: 1 year (Required) GLP & GMP: 1 year (Required) ISO 20000: 1 year (Required) FSSAI: 1 year (Required) Work Location: In person

Key Responsibilities Comply with the implemented Quality Management System as per ISO/IEC 17025:2017 , meeting the requirements of regulatory agencies and accreditation bodies (e.g., NABL, CPCB). Maintain confidentiality of laboratory data and uphold impartiality throughout your tenure with the organization. Ensure laboratory safety , data integrity , and adherence to Good Documentation Practices (GDP) and Good Laboratory Practices (GLP) . Manage procurement and inventory of chemicals, glassware, Certified Reference Materials (CRMs) , and other critical consumables for analysis of various water types (drinking water, ground water, surface water, industrial water, irrigation water, packaged drinking water, and packaged natural mineral water). Conduct routine and internal calibration as well as maintenance of analytical instruments used in water analysis. Perform sample preparation and chemical analysis of water parameters in accordance with relevant national/international test methods. Participate in Proficiency Testing (PT) and Inter-Laboratory Comparisons (ILC) for chemical analysis of water samples. Accurately record and enter test results into LIMS software within prescribed Turnaround Time (TAT) . Maintain log books , equipment records , and other day-to-day documentation as per QMS guidelines. Assist and participate in NABL, CPCB, or other regulatory audits related to chemical analysis of water. Perform any other task/activity assigned by management on an as-needed basis. Required Qualifications & Skills Education: B.Sc. / M.Sc. in Chemistry, Environmental Science, or related discipline. Experience: Minimum 1–3 years in an environmental or water testing laboratory. Sound knowledge of ISO/IEC 17025:2017 , NABL documentation , and regulatory compliance. Hands-on experience with analytical instruments (e.g., Spectrophotometer, pH meter, TDS meter, etc.). Familiarity with LIMS software and standard chemical testing procedures. Strong attention to detail, organization, and documentation skills. Good communication and team collaboration skills. Job Type: Full-time Pay: ₹18,000.00 - ₹28,000.00 per month Benefits: Cell phone reimbursement Health insurance Leave encashment Provident Fund Schedule: Day shift Ability to commute/relocate: Mohali, Punjab: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Do you have experience of working in NABL accredited LAB? Experience: total work: 2 years (Preferred) Work Location: In person

Job Title: STP Operator (Male Candidates Only – Immediate Joiner Preferred) Job Type: Full-time Salary: ₹20,000 – ₹25,000 per month Job Summary: We are seeking a skilled and experienced STP Operation & Troubleshooting Executive to independently manage sewage and wastewater treatment plant operations. The ideal candidate should have hands-on experience in troubleshooting STP systems, a strong understanding of chemical and microbiological water parameters, and expertise in activated sludge and air treatment processes. Key Responsibilities: Independently operate, manage, and maintain the entire STP plant. Monitor and troubleshoot Activated Sludge Process (ASP), Anaerobic Sludge Digestion, and Bio Scrubber systems. Analyze water and sludge quality including BOD, COD, pH, turbidity, conductivity, and biogas parameters. Perform routine testing using lab instruments such as Spectrophotometer, BOD/COD meters, pH and Turbidity meters. Conduct daily monitoring of plant operations and process parameters. Lead weekly training sessions on STP operations and safety protocols. Collaborate with electrical and mechanical teams for routine plant maintenance. Prepare and submit monthly performance reports and interact regularly with clients. Manage manpower planning, material forecasting, and procurement. Ensure HSE compliance through regular monitoring and documentation. Take corrective and preventive actions for continuous process improvement and failure reduction. Handle troubleshooting of both aerobic and anaerobic processes including chlorination. Requirements: Experience: 2–3 years in wastewater/STP operations and troubleshooting. Education: B.Sc. Chemistry / M.Sc. Chemistry / B.E. (Chemical Engineering). Must be able to join immediately . Male candidates preferred. How to Apply: Interested candidates can contact HR – Nithya R - 9150099528 Let me know if you’d like a shorter or more targeted version for another platform! Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Health insurance Provident Fund Application Question(s): Are you an immediate joiner? Education: Bachelor's (Preferred) Willingness to travel: 100% (Preferred) Work Location: In person

To conduct physical-chemical/microbiological tests on spices, monitor CCPs, approve/reject materials, maintain samples/docs, report quality issues, ensure GMP/hygiene, handle compliance, support team, and lead troubleshooting within QA/QC processes. Required Candidate profile B.Sc./M.Sc. in Food Tech, Microbiology, Chemistry etc with 3–6 yrs QC experience in spices/FMCG. Skilled in spice testing, food safety, and handling instruments like HPLC, GCMS, moisture analyzer

Key Responsibilities Comply with the implemented Quality Management System as per ISO/IEC 17025:2017 , meeting the requirements of regulatory agencies and accreditation bodies (e.g., NABL, CPCB). Maintain confidentiality of laboratory data and uphold impartiality throughout your tenure with the organization. Ensure laboratory safety , data integrity , and adherence to Good Documentation Practices (GDP) and Good Laboratory Practices (GLP) . Manage procurement and inventory of chemicals, glassware, Certified Reference Materials (CRMs) , and other critical consumables for analysis of various water types (drinking water, ground water, surface water, industrial water, irrigation water, packaged drinking water, and packaged natural mineral water). Conduct routine and internal calibration as well as maintenance of analytical instruments used in water analysis. Perform sample preparation and chemical analysis of water parameters in accordance with relevant national/international test methods. Participate in Proficiency Testing (PT) and Inter-Laboratory Comparisons (ILC) for chemical analysis of water samples. Accurately record and enter test results into LIMS software within prescribed Turnaround Time (TAT) . Maintain log books , equipment records , and other day-to-day documentation as per QMS guidelines. Assist and participate in NABL, CPCB, or other regulatory audits related to chemical analysis of water. Perform any other task/activity assigned by management on an as-needed basis. Required Qualifications & Skills Education: B.Sc. / M.Sc. in Chemistry, Environmental Science, or related discipline. Experience: Minimum 1–3 years in an environmental or water testing laboratory. Sound knowledge of ISO/IEC 17025:2017 , NABL documentation , and regulatory compliance. Hands-on experience with analytical instruments (e.g., Spectrophotometer, pH meter, TDS meter, etc.). Familiarity with LIMS software and standard chemical testing procedures. Strong attention to detail, organization, and documentation skills. Good communication and team collaboration skills. Job Type: Full-time Pay: ₹18,000.00 - ₹28,000.00 per month Benefits: Cell phone reimbursement Health insurance Leave encashment Provident Fund Schedule: Day shift Ability to commute/relocate: Mohali, Punjab: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Do you have experience of working in NABL accredited LAB? Experience: total work: 2 years (Preferred) Work Location: In person

profile in R&D. Technical skills :- Sensory profile in R&D. All Quality control testing, UV spectrophotometer handling, Develop and update quality control procedures and work instructions. Implement and maintain quality management systems (QMS), such as ISO standards and HACCP (Hazard Analysis and Critical Control Points). Raw Material and Product Testing: Test and evaluate raw materials for quality, safety, and compliance. Perform in-process quality inspections and monitor critical control points. Analyze finished products to ensure they meet quality standards, nutritional requirements, and labeling requirements. Food Safety Compliance: Ensure adherence to food safety regulations and standards. Monitor and track product quality throughout the production process. Participate in quality management system reviews and promote quality and food safety policies. Documentation and Reporting: Maintain accurate records of quality control activities. Generate reports on quality issues and corrective actions. Collaboration and Communication: Work with other departments to identify and resolve quality issues. Communicate quality standards and procedures to all personnel. Soft Skills :- Observation Decision making Communication Multi-tasking Computer Skills RS-CIT (Word, Excel and PPT). Job Type: Full-time Pay: ₹20,000.00 - ₹28,000.00 per month Schedule: Day shift Work Location: In person