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)
0 To 0.6 Year(s)
1.68 LPA TO 1.80 LPA
A Chemist Trainee assists senior chemists with lab tasks like preparing solutions, conducting experiments, analyzing samples, and maintaining equipment, focusing on learning protocols, safety, and documentation for raw materials, intermediates, and finished products, requiring a B.Sc/M.Sc in Chemistry and strong analytical skills for quality control or R&D roles.
Key Responsibilities:
Laboratory Assistance: Perform tests, ...
2 Opening(s)
2.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
The job description is as below:
Have to carry out microbiological testing, BET testing, sterility testing and like for Drug & Pharma, Medical Device, AYUSH and Food products as per respective regulatory Guidelines or any such task assigned.
Have to work for protocol preparation, report preparation, SOP Preparation and revise on there ...
2 Opening(s)
1.0 Year(s) To 7.0 Year(s)
Not Disclosed by Recruiter
Responsibilities:
Independently plan, execute, and monitor laboratory-scale reactions for new product development or process improvement.
Troubleshoot reaction-related issues and optimize parameters to achieve desired yields and purity.
Conduct analytical testing using spectroscopy techniques (IR, NMR, UV, etc.) and interpret data for structural confirmation.
Maintain detailed experiment records, observations, and analytical results in lab notebooks.
Support ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.88 LPA TO 3.00 LPA
Key responsibilities
Conduct physical and chemical tests on coal samples, including proximate analysis, ultimate analysis, and GCV (Gross Calorific Value).
Use and maintain laboratory equipment, ensuring it is calibrated and functioning correctly.
Sample and analyze other materials like input chemicals, by-products, and waste.
Prepare laboratory solutions, compounds, and reagents.
Maintain detailed records of tests, sample ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
6.00 LPA TO 7.00 LPA
Job title:Quality Assurance Chemist
Name of job holder:
Department/service:QA/QC
Signature job holder & date:
Signature hierarchical head & date:Manager - QA
Signature functional head & date:Head - QM
A. Purpose /Role of the job /: Describe in 1 phrase what contribution the job is expected toMake to the organisation’s objectives Quality Assurance of Finished Goods (SAN/ABS/ASA/PS) ...
4 Opening(s)
1.0 Year(s) To 8.0 Year(s)
1.50 LPA TO 6.00 LPA
Key Responsibilities:
Analytical Operations:
Perform routine and non-routine analysis using HPLC, GC, UV and other instruments.
Conduct and support analytical method validations as per regulatory requirements.
Review and approve analytical data, test reports, and batch release documents.
Ensure proper calibration and qualification of laboratory instruments.
QMS & Compliance:
Manage Quality Management System (QMS) activities including:OOS, Deviations, CAPA, ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.40 LPA TO 5.00 LPA
The Project Coordinator is responsible for planning, tracking, and coordinating pharmaceutical laboratory projects across departments such as R&D, Quality Control, Regulatory Affairs, and Production. The role ensures timely execution of tasks, documentation, and compliance with industry standards and project deadlines.
🎯 Key Responsibilities:
Coordinate day-to-day activities of pharmaceutical lab projects (R&D, method ...
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 ...