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)
10.0 Year(s) To 20.0 Year(s)
11.00 LPA TO 12.00 LPA
• Lead and oversee the Residue Analysis & Instrumentation section of the laboratory.• Plan, manage, and review residue analysis of pesticides, antibiotics, veterinary drugs, mycotoxins, heavy metals, and other contaminants in food samples.• Operate, supervise, and maintain advanced analytical instruments, including:o LC-MS/MSo GC-MS/MSo ICP-MS / ICP-OESo HPLC, GC, AAS, UV-Vis, ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
3.60 LPA TO 4.80 LPA
Sample Analysis: Performing analysis of routine samples including food, pharma, Ayush (traditional medicine products), water, and soil for parameters like pesticide residues and aflatoxins using GC-MS/MS and LC-MS/MS instruments.
Instrument Operation & Maintenance: Operating, calibrating, and performing routine maintenance and troubleshooting on GC-MS/MS and other instruments like GC, HPLC, and LC-MS/MS.
Documentation and Compliance: Preparing ...
1 Opening(s)
4.0 Year(s) To 10.0 Year(s)
4.20 LPA TO 5.40 LPA
Quality Control:
Ensuring the quality of pharmaceutical intermediates and APIs through various testing and analysis methods.
Lab Analysis:
Using analytical instruments like HPLC, GC, and others to analyze samples and ensure product quality.
Documentation:
Maintaining accurate records of tests, results, and other QA-related documents.
Process Improvement:
Contributing to the improvement of QA processes and procedures.
Compliance:
Ensuring that all ...