119 Wet Analysis Jobs - Page 3

Dear Candidate, We are conducting walk-in drive on 05th July (Saturday) 2025 for the positions in our Analytical Research & Development department. Job Description : Position Name: Research Chemist/Senior Research Chemist/Research Associate Experience: 1 to 5 years Qualification: M.Sc Analytical Chemistry/Organic Chemistry/M.pharm Work location: Uppal/Mallapur Walk-in Date: 05th July 2025 (Saturday) Time: 09:00 AM to 12.00 PM Venue:-Plot No. B-11/1,,,IDA Uppal,Hyderabad Key Skills and Competencies: High-Performance Liquid Chromatography (HPLC) Key Skills and Competencies: Operation and Maintenance : Proficiency in operating HPLC systems (e.g., Agilent, Waters, Shimadzu) and performing routine maintenance, calibration, and troubleshooting of equipment issues like pressure fluctuations or detector errors. Method Development and Validation : Ability to develop and optimize HPLC methods for analyzing small molecules, impurities, or degradation products, adhering to ICH guidelines (e.g., ICH Q2 for validation). Data Analysis : Expertise in interpreting chromatograms, quantifying analytes, and using software like Empower or ChemStation for data processing and reporting. Sample Preparation : Skilled in preparing samples (e.g., dissolution, extraction) for pharmaceutical or chemical analysis, ensuring reproducibility and accuracy. Regulatory Compliance : Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) for documentation, method validation, and audit readiness. Troubleshooting : Ability to diagnose and resolve issues such as peak tailing, baseline drift, or column degradation. Experience Level (1-5 Years) : 1-2 years: Basic operation, routine analysis, and data interpretation under supervision. 3-5 years: Independent method development, validation, and troubleshooting with familiarity in handling complex matrices. 2. Wet Analysis in Good Laboratory Practices (GLP) Key Skills and Competencies: Classical Analytical Techniques : Proficiency in titration (acid-base, redox, complexometric), gravimetric analysis, and other wet chemistry techniques for assay determination or impurity profiling. GLP Compliance : Strict adherence to GLP standards, including proper documentation, sample tracking, and maintaining a chain of custody for regulatory audits. Standard Operating Procedures (SOPs) : Ability to follow and draft SOPs for wet analysis methods, ensuring consistency and compliance. Quality Control : Knowledge of preparing and standardizing reagents, performing limit tests, and ensuring accuracy in quantitative and qualitative analysis. Safety and Handling : Expertise in safe handling of chemicals, waste disposal, and maintaining a contamination-free lab environment. Data Integrity : Ensuring accurate record-keeping, traceability, and error-free reporting in lab notebooks or electronic systems. Experience Level (1-2 Years) : 1-2 years: Performing routine titrations, standardization, and sample preparation under GLP guidelines. 3. Liquid Chromatography-Mass Spectrometry (LCMS) Key Skills and Competencies: Instrument Operation : Proficiency in operating LCMS systems (e.g., Thermo Fisher, AB Sciex) for qualitative and quantitative analysis, including single quadrupole, triple quadrupole, or high-resolution MS (e.g., Orbitrap). Method Development : Ability to develop LCMS methods for identifying and quantifying trace-level impurities, metabolites, or active pharmaceutical ingredients (APIs) in complex matrices. Mass Spectra Interpretation : Expertise in analyzing mass spectra, identifying molecular ions, adducts, and fragmentation patterns for structural elucidation. Sample Preparation : Skilled in sample extraction techniques (e.g., SPE, LLE) and matrix effect minimization for bioanalytical or pharmaceutical samples. Software Proficiency : Familiarity with LCMS software (e.g., Xcalibur, Analyst) for data acquisition, processing, and reporting. Regulatory Knowledge : Understanding of regulatory requirements (e.g., FDA, EMA, ICH) for bioanalytical method validation and GLP/GMP compliance. Troubleshooting : Ability to address issues like ion suppression, carryover, or instrument sensitivity. Experience Level (1-5 Years) : 1-2 years: Conducting routine LCMS analysis, sample preparation, and basic data interpretation under guidance. 3-5 years: Independently developing and validating LCMS methods, troubleshooting complex issues, and supporting drug discovery or development projects. Interested candidates can attend walk-in drive or share their profiles to saivardhan.kothuri@chemvedals.com

Company Name : Paushak Limited (Alembic Group company) Position: Executive Sr. Executive (ADL) Department: Analytical Development Group Location: Halol, Vadodara Industry: Chemical / Agro Chemical / Specialty Chemicals Experience Required: 2 to 8 Years Education: M. Sc Organic Chemistry Job Responsibilities: Prepare and standardize volumetric solutions. Handle analytical instruments including HPLC, GC , and other lab equipment. Perform wet analysis, including calibration, preventive maintenance, and troubleshooting. Conduct method development for analytical procedures. Carry out stability studies for new products. Perform in-process and finished product analysis and reporting. Maintain daily analysis records and manage chemical and instrument inventories. Oversee column management, data backup, and waste management. Handle specialty chemicals with appropriate safety and analytical protocols. Skills Required: Proficiency in handling HPLC, GC , and other laboratory instruments. Strong experience in wet analysis and method development . Expertise in handling and analyzing specialty chemicals . Strong organizational skills for managing chemical stocks, instrument parts, and documentation. Familiarity with calibration protocols and stability testing.

Role & responsibilities 1.HPLC,UPLC and GC analysis of raw material, intermediate, finish product, stability sample, equipment cleaning and distilled solvent, Analytical Method development and validation 2.HPLC,GC, UPLC calibration HPLC and GC Analysis of all in-process,Intermediate, Finish Product,Stabiltity Analysis Equipment cleaning, Distilled Solvent and Raw materials. If required then sampling of finished product. Working Standard Qualification. Calibration of HPLC and GC. GCHS. R&D Analytical Metliod Development of new molecule. Analytical Method Validation. lnstnmrent Troubleshooting

Spica Labs Pvt. Ltd. is hiring QC & QA male candidates with experience in HPLC, UV, IR, GMP, BMR review, SOPs, validation, deviations & regulatory knowledge. Send resumes to: spicalabspvtltd@gmail.com.

JOB DESCRIPTION: Department : Quality Control - API (Wet Analysis) Position : Officer Executive Experience : 01 to 05 Years Qualification : M. Sc in Chemistry Perform wet chemical analysis, including: Karl Fischer titration (KF) Potentiometric titration pH Measurements Particle Size Distribution (PSD) using Malvern Carry out daily calibration of laboratory instruments such as balances and pH meters. Ensure compliance with standard operating procedures and regulatory requirements. Maintain accurate records of all testing and calibration activities. Interested Candidates please send me resumes to pitchireddy.t@hetero.com

Key Responsibilities: Perform analysis of raw materials, intermediates, and finished products of Active Pharmaceutical Ingredients (APIs) as per approved specifications and SOPs. Operate and maintain analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, FTIR, Karl Fischer, Melting Point Apparatus, etc. Review and verify analytical data and ensure proper documentation in line with cGMP and GLP guidelines. Prepare and standardize volumetric solutions and reagents. Carry out stability studies and maintain stability data as per ICH guidelines. Ensure timely calibration of laboratory instruments. Perform method validation/transfer activities as per regulatory and internal requirements. Involve in investigations related to OOS/OOT/Deviations and CAPA implementation. Coordinate with cross-functional departments like QA, Production, and R&D for smooth workflow. Comply with all safety protocols and maintain a clean and organized lab environment. Desired Candidate Profile: Hands-on experience in analytical techniques (HPLC/GC) is a must. Good knowledge of regulatory guidelines (ICH, WHO, USFDA, etc.) Strong documentation and communication skills. Experience in a regulated API manufacturing unit is preferred.

Responsibilities: * Conduct lab tests using NABL standards for water, soil & aggregate , cement, Steel samples etc. * Ensure compliance with industry quality control procedures. Candidate Must Have M.Sc in Chemistry. Accessible workspace Travel allowance Health insurance Employee state insurance Sales incentives Annual bonus Retention bonus

Pharmaceutical Industry Raise laboratory Change control, incidents, deviations & LI wherever applicable. Review of Instrument qualification & scheduled calibration planner. Ensure proper laboratory analysis as per MOA & product specification. Required Candidate profile Mandatory - Operation & calibration of GC , HPLC, Good to have - GC-HS, FTIR, UV, AAS, KF, AUTO TITRATOR, BALANCE To maintain all record viz, consumption, Column, humidity, all instrument logbooks

Job Details: Responsible for establishing the performance of R&D formulations for water treatment applications. Creating lab SOPs for different water treatment analysis methods. Supporting the field team by performing trial sample analysis in lab. Maintaining the lab equipment, analytical records, sample inventory. Training the underworking staff for routine lab work. 1. Job Responsibilities & Duties: a. Executing application trials for product development in the water lab across various stages of treatment. b. Planning for daily experiments. c. Reading research articles and contributes to the research d. Formulation development e. Collaborating with field team to run troubleshooting experiments for market products and existing applications. f. Handling of water lab instruments including spectrophotometer, pH, TDS, ORP, COD/BOD incubator etc. g. Well aware of analytical skills including titration, preparation of standard solutions, standard calibration methods, etc. h. Results & data writing, Preparing reports & result summary. 2. Job requirements: A successful candidate will have: Qualification: BE/B.Tech, M.Sc/M.tech in Environmental Engineering/ Chemical Engineering/ water chemistry/ water technology/ analytical chemistry/ organic chemistry from a reputed institute Experience: 2+ years in water treatment lab, more specifically from a technology troubleshooting lab. - Should have basic understanding of principles behind the analysis methods - Reading and interpretation of research articles in water treatment - Thorough knowledge of water treatment, methods of analysis, product trouble shooting and various water treatment process- STP/ETP/Cooling tower/RO membrane/coagulation /Flocculation - Thorough understanding and experience in handling various chemicals used in water treatment. - Good Communication Skills - Good teamwork skills in a fast paced & challenging environment. - Sincere attitude & commitment towards job responsibilities. ***** Interested Candidates can share their profile to raksha@proklean.in *****

Roles and Responsibilities Conduct chemical testing, analysis, and inspection of raw materials as per SOP. Perform lab analysis using various instruments such as AAS (Atomic Absorption Spectrometer) and PH Meter. Carry out wet analysis on samples as per SOP Inspect raw materials against specifications and industry norms for compliance. Record test results accurately and maintain records of laboratory activities. Maintain Batch Manufacturing Records/QC records as per SOP Carry out Batch formulation Supervise Batch marking & Packing Freshers are welcome

*Comprehensive Review of Raw Data (In-process, Cleaning, Packing material, Raw material, IM, FP, and Stability) for Accuracy and Completeness. * Ensuring Data Integrity (ALCOA+ Principles). * Audit Trail Review of CDS and Non-CDS applications. * Compliance with SOPs and Specifications. * Identification of Discrepancies and Issues. * QMS (Investigations of OOS/OOT/Incident/ Deviation). * Basic knowledge of Validations. Preferred candidate profile Minimum of 3 years of working experience in quality control and operational experience with IR, UV, SOR, Titrations, Wet analysis, polarimeter, KF, MR apparatus, and Chromatography (TLC, HPLC, GC). Willing to work in Shifts(A,B&C)

Role & responsibilities- Conduct analysis of samples using HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Providing Technical support for internal and external stake holders Being the clear R&D player by working closely with cross-functional teams to drive execution across multiple projects while maintaining and achieving timelines to ensure speed to market. To conduct analysis of samples and provide inputs to R&D/QC teams Required Skill Sets: Hands on experience on HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Experience in analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Fair understanding of ISO/IEC 17025, ISO 9001, ISO14001, ISO 22000, ISO18001 Lab safety & GLP management

position 1 Job Description Sample preparation and analysis of food samples for Pesticide residue, Antibiotic residue, Aflatoxins. Method development and validation on LCMSMS and GCMSMS. Sound knowledge of instruments such as HPLC, GCMSMS and LCMSMS. Maintenance of lab records. Knowledge of ISO 17025:2017standard. position 2 Sample preparation and analysis of food samples for Aflatoxins, Preservative, Antioxidants, Colors. Method development and validation on HPLC. Sound knowledge of instrument HPLC. Maintenance of lab records. Knowledge of ISO 17025:2017standard Position 3 Wet chemical analysis of food and water samples. Instrumental analysis of food samples on HPLC, UV-Vis spectrophotometer. Volumetric solution preparation and its standardization. Distillation for food analysis. Maintenance of lab records. Knowledge of ISO 17025:2005 standard.

Role & responsibilities 1. Understands and follows safety requirements within work area to identify and escalate potential hazards and also executes CAPA's for safety observations. 2. Adheres to equipment/ instrument safety procedures and understand associated energies to be isolated and execute LOTO. 3. Understand and follow safety requirements in handling material/glassware. 4. Demonstrates ability to perform physical test/physical parameter verification/ thermal test/ spectroscopy/ Electro-chemical techniques and required non-complex & complex tests and can demonstrate the same for auditors. 5. Understands and executes analytical solution preparation steps as explained in the record of analysis. 6. Recognizes abnormalities and reports malfunctioning of instruments and performs basic maintenance in line with requirements. 7. Plans cleaning of Analytical instruments & calibration and ensures timely completion. 8. Understands and adheres to written procedures. 9. Demonstrates ability to explain/ articulate procedures related to own work areas. 10. Recognizes failures in execution and report incidents, events. 11. To follow safety norms and adhere with company policy. 12. To follow the Quality Policy & Contamination prevention policy of the company. 13. Demonstrates high discipline & orientation to detail while inspecting each sample. 14. Demonstrates complete ownership of end-result of quality check. 15. Analyses raw material/ packaging/ final product, etc. or performs in-process checks Continuously acquires new skills to perform quality check with higher accuracy and prepare for any internal and external audits.

"Key responsibilities: Perform analysis, report raw data, ensure data tracing, submit reports, address reviewer comments, follow GLP, report incidents/deviations, review data accuracy, provide training, and handle events as per SOP."

1) Testing in-coming raw materials material (Non ferrous Metals) and finished product (Non-ferrous oxide) for all parameters. 2) Data entry and record keeping as per quality SOPs and ISO standards 3) Reporting to the QC Head on analysis results Required Candidate profile BSc (minimum) with 4-5 minimum years of experience in analytical chemistry and lab testing, lab instrument handling.

Key Roles & responsibilities: A reputed Railway product manufacturer seek to hire an Operational Excellence Engineer within the Quality Assurance Team to participate in continuous improvement and efficiency projects, focusing on products, systems, operations and processes. Defines, designs, and implements process improvement as part of organizations Operational Excellence, supporting business in establishing "best practice". Responsible for the creating Quality assurance plans (QAPs) for Indian Railways, Inspection Test Plans (ITPs), Manufacturing Process Plans (MPP) Responsible for RDSO , RITES & Third Party inspection handling & documentations Responsible for the creating Quality documents (Both Export & Indian Market). Ensures integration and alignment both vertically and horizontally across organization, within areas of safety, quality, delivery, productivity, cost and process efficiency. Facilitate and coach improvement teams, establishes and maintain performance metrics to track program success. Lead in Lean health checks, apply Lean methodologies such as PDCA, and perform Lean program audits and streamlining processes. Implement standard work process/procedures, visual factory and error proofing mechanisms. Provide technical leadership on Operational Excellence/Lean systems and tools. Responsible for making SOPs and their implementations. Create, maintain and refine a Lean toolkit that can include 5S, Kaizen, quick change over, value stream mapping, mistake proofing and line balancing, Muda Walk, KANBAN, TEAMWOOD, SMED, POKA Yoke. Requirements: 1 to 3 years of exp. BE/BTech/Mtech in Mechanical/Industrial Engineering. Railways Industry experience with respect to inspection handling is preferred. Experience with Lean Manufacturing techniques, e.g. leading Kaizen events, Continuous improvement, Six Sigma, Process / Value stream mapping, FMEA, Fish Bone. Certified Six Sigma green belt will be preferred. Good understanding of industrial standards and risk management practices. Good technical capabilities, communication skills, teamwork abilities and initiative. Proficient in Microsoft Excel, Word, and PowerPoint

Job description Working in analytical method developments by using various Wet analysis techniques (Like KF, UV-Vis, Autotitrator, FT-IR etc.) Expected to be aware of basics in analytical chemistry (basic analytical techniques Theory and application)as well as handling of laboratory equipment/ instruments with basic understanding. Ability to plan, handle and analyze the regular samples independently. Awareness on other techniques (HPLC,GC etc.) Conduct analytical research and development for products. To perform analysis for various regulatory queries such as carryover study, method equivalency, column equivalency etc using instruments like HPLC/ GC, GC-HS, GC-MS To perform reaction monitoring for online support to CRD, PD Lab, Pilot Plant and Plants as per requirement of organization Trouble shooting on analytical instruments like HPLC, GC, UV etc. Interpretation of analytical raw data and maintain Documentation in ARD Skills profile : HPLC GC/GC HS/ GC-MS Karl Fisher Auto titrator C-MS, NMR Knowledge of cGMP and cGDP, ICH guidelines Interested candidates share resume on anuverma@scllifesciences.com or what's app on 9988339860.

We are hiring for multiple roles in the QC Department! Join us at Global Calcium Pvt. Ltd. a leading pharmaceutical manufacturer, and be part of a growing team committed to quality and innovation. Open Positions (Multiple Vacancies): QC ICP-MS Analyst (2 openings) Hands-on experience with ICP-MS instrumentation Knowledge of elemental impurity analysis and related regulatory guidelines QC – DMF Support (2 openings) Exposure to DMF preparation, review & support documents Understanding of regulatory documentation and compliance standards QC – Analytical Validation Support (2 openings) Knowledge of method validation techniques (HPLC/GC/UV) Experience in handling validation protocols and reports QC – Wet Analysis (2 openings) Proficient in classical wet chemistry techniques Experience in raw material and finished product testing Eligibility Criteria: B.Sc / M.Sc in Chemistry or related fields 1 to 4 years of relevant pharmaceutical QC experience Good understanding of cGMP practices and regulatory compliance Willingness to work in a fast-paced manufacturing environment Walk-in Interview Details: Venue: Global Calcium Pvt. Ltd., Unit III, 19 & 19B, Sipcot industrial complex, Phase - 1, Dharga, Hosur Date: 14th June 2025 Time: 9:30 AM to 11:00 AM Documents to Carry: Resume, Recent Photograph, Last 3 Months' Payslips, Educational & Experience Certificates, ID Proof Note: Only candidates with relevant experience in the pharmaceutical QC domain will be considered. Role & responsibilities

Opportunity with SGS India for the position of Chemist (Wet Chemistry) | Location - Ahmedabad Note: This position would be on 3rd Party Payroll. Company Profile: Established in 1878, SGS transformed grain trading in Europe by offering innovative agricultural inspection services. SGS is the world's leading inspection, verification, testing and certification MNC. We are recognized as the global benchmark for quality and integrity. With more than 96,000 employees, we operate a network of more than 2,700 offices and laboratories around the world. We cater quality services to 9 Businesses in India like Consumer & Retail Services, Oil & Gas, Industrial services, AFL, Minerals etc. Kindly visit our Global Website: www.sgs.com India Website: www.sgsgroup.in Experience - Fresher to 1-2 Years Education - M. Sc in Chemistry Walkin Details - 12th June and 13th June Time - 9:30 am - 4:30 pm Location - Ahmedabad, Gujarat Following is the Job Description for Chemist (Wet Chemistry): To perform sample preparation by using appropriate method. Assist Section In-charge for new method development and method validation to upgrade lab capability. Handling of CRM and stability check of CRM. Development, modification, verification and validation of methods Result entry in SLIM. Internal verification of equipment and equipment maintenance. Responsible for method validation To assist QAC and Section In-charges to maintain calibration status and their records. Verify Instrument maintenance and Calibration of Chemical and instrument lab area. Ensure compliance with mandatory local and other laws pertaining to health safety environment protection, within the lab and outside surroundings, compliance to SGS OI procedures Interested Candidates please share your updated CVs on fleur.dsouza@sgs.com

Research and development Required Candidate profile Quality Control

Experience: 3-8 years Location: Navi Mumbai Role & responsibilities Batch analysis and wet analysis. Should have expertise in analytical testing as per in house method / pharmacopoeia. Sound knowledge and handling of HPLC (Preferably Chromeleon software), Dissolution, UV spectrophotometer and other Analytical instruments. Should have well verse with ICH guidelines, cGMP, Data integrity. Should have knowledge of QMS related activity (i.e. Deviation, incidence, Change control, OOS, OOT). Knowledge of wet testing as per pharmacopeia. Hands on testing batch analysis using various techniques like HPLC, GC, Dissolution, UV, FTIR, Friability, Disintegration etc.

Candidate must have experience from chemical manufacturing industry.

JOB RESPONSIBILITIES --------------------------------------------------------------------------------------------------- 1) Support for analytical method development and validation. 2) HPLC and GC-Instrumentation, handling and trouble shoot 3) Calibration of HPLC and GC 4) Literature survey. 5) Preparation of SOPs, validation protocol and report. 6) Support for regulatory required testing. 7) Wet analysis 8) Stability analysis, API testing and verification of methods.

Role & responsibilities HPLC GC Wet chemistry Stability Study GLP awareness Analytical Method Validation