59 Job openings found

10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
🔬 Quality Testing & Analysis Perform routine and non-routine chemical analyses on raw materials, in-process samples, and finished goods using standard laboratory methods. Operate and validate analytical instruments such as HPLC, GC, UV-Vis, FT-IR, Karl Fischer titrator and other relevant equipment. Record, calculate, interpret and report accurate analytical results, ensuring data integrity and ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
2.40 LPA TO 4.00 LPA
GC–MS Analyst – Roles & Responsibilities Operate and maintain Gas Chromatography–Mass Spectrometry (GC-MS) systems for qualitative and quantitative analysis. Perform sample preparation, extraction, derivatization, and dilution as per approved methods. Develop, optimize, and validate GC-MS analytical methods in compliance with regulatory guidelines. Analyze chromatograms and interpret mass spectra using reference libraries (e.g., NIST). Conduct instrument ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
11.00 LPA TO 12.00 LPA
Position:       ADL Executive Location:       Mundra near by Kutch Experience:    5 - 10 Years Industries:      Chemicals  Responsibilities: Perform routine and non-routine analysis using HPLC and Gas Chromatography (GC) Conduct wet lab testing including titrations, assay, dissolution, and chemical analysis Prepare, standardize, and handle reagents, solutions, and reference standards Ensure calibration, validation, and ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
4.20 LPA TO 4.80 LPA
Instrument Handling: Proficiently operate sophisticated instruments like HPLC, GC, GC-MS/MS, AAS, ICP-MS, and FTIR. Sample Analysis: Conduct testing for various products, including food, beverages, pharmaceuticals, and environmental samples. Quality Control: Ensure accuracy and reliability in reports, adhering to standard operating procedures (SOPs). Method Development/Validation: May involve setting up and validating analytical methods for ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
2.60 LPA TO 4.00 LPA
Key Responsibilities: Perform routine and non-routine analysis using LC-MS or LC-MS/MS techniques for pharmaceutical, biological, or chemical samples. Conduct method development, optimization, and validation as per ICH or regulatory guidelines. Prepare standards, reagents, QC samples, and analytical test samples according to protocols and SOPs. Operate and maintain LC-MS instruments (e.g., Agilent, Waters, Thermo, Sciex). Interpret ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.80 LPA TO 2.40 LPA
01-03-25   HPS/2025/127 Lab Chemist (Spectometer) Male 1 1 to 3 Bsc/Diploma mech Key responsibilities may include: Sample preparation: Accurately weighing, diluting, and preparing samples for analysis using appropriate techniques depending on the sample matrix and the spectrometer type.    Spectrometer operation: Setting up and operating the spectrometer, including selecting appropriate parameters like wavelength, slit width, and scan range.    Data acquisition: Collecting spectral data from ...
1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Instrumental and Chemical analysis of Raw, intermediate and finished products as per INHOUSE, IP, BP, USP, JP, EP specifications.   Preparation and Standardization of volumetric solutions, updating and control of reference standards Record and Preparation of working standards & Record.   Responsible for Analytical method development for FP and Cleaning samples and validation of ...
4 Opening(s)
1.0 Year(s) To 5.0 Year(s)
1.00 LPA TO 4.00 LPA
Knowledge of Chemical Analysis, HPLC, GC, UV, IR, AAS, FTIR & other Lab Instruments.Able to perform routine analysis, Method Development in HPLC, GC, also perform Validations.Aware of Regulatory requirements, Basic knowledge of Documentation Audit Having an experience  3-5 year in pharma industries / GLC, HPLC exp, audit handling local as well ...
2 Opening(s)
4.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.00 LPA
Key Responsibilities: ·         Manage day-to-day operations of the Pharma Instrumentation Section. ·         Plan, supervise, and execute testing of APIs, recipients, and formulations using HPLC and other advanced instruments. ·         Ensure strict adherence to NABL, pharmacopeia (USP/IP/BP/EP), ICH, and CDSCO/WHO guidelines. ·         Perform and supervise method development, method validation, verification, and system suitability tests. ·         Maintain, calibrate, and troubleshoot instruments including HPLC, UPLC, GC, UV-Vis, FTIR, ...
1 Opening(s)
1.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
The job description is as below: To perform High Performance Liquid Chromatography analysis for various pharmaceutical tests including Related Substances, in compliance with 21 CFR Part 11 and cGMP guidelines. The role includes calibration, troubleshooting, integration, and data review activities related to HPLC.   Key Responsibilities: Perform routine and non-routine HPLC analysis for Assay, Related Substances, Content Uniformity, and other quality ...

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