15 Opening(s)
2.0 Year(s) To 15.0 Year(s)
2.00 LPA TO 10.00 LPA
Sampling of all raw materials, packing material, finished product as per their sampling plan.
Testing of all raw materials, packaging materials, in-process products & finished products.
HPLC/GC analysis of in process & FG & its documentation, as well as calibration of HPLCs/GCs and balance. Handling the head space analysis. Additionally, can perform ...
2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 10.00 LPA
Provide analytical support for maintaining in-process control and product quality.Analysis of In-process samples and Finished Product (Syrup).Analysis of Cleaning validation and verifications samples.Documenting the activities performed online for GMP & GLP.Performed all analytical technique in Tablets, Capsules manufacturing.Responsible for Preventive maintenance of HPLC.Testing of all finish dosage form SyrupDocumentation(R.M, F.P ...
2 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 4.50 LPA
Job Description:? Should have strong communication skill? Handling & Calibration of instruments like HPLC, GC, KF, IR, UV, Viscosity,Tintometer? Sampling and analysis of of raw material as well as finish good? ETP sample analysis – pH, COD, TDS. MLSS , TS , TSS? Good Knowledge of physical as well as ...
5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Sampling of all raw materials, packing material, finished product as per their sampling plan.
Testing of all raw materials, packaging materials, in-process products & finished products.
HPLC/GC analysis of in process & FG & its documentation, as well as calibration of HPLCs/GCs and balance. Handling the head space analysis. Additionally, can perform ...
6 Opening(s)
3.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
Provide analytical support for maintaining in-process control and product quality.Analysis of In-process samples and Finished Product (Syrup).Analysis of Cleaning validation and verifications samples.Documenting the activities performed online for GMP & GLP.Performed all analytical technique in Tablets, Capsules manufacturing.Responsible for Preventive maintenance of HPLC.Testing of all finish dosage form SyrupDocumentation(R.M, F.P ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
7.00 LPA TO 12.00 LPA
? To assist in developing & implementing various quality control tests like HighVoltage, Partial Discharge, tracking and erosion test, Tensile & ultimateelongation, Hot elongation, Dielectric strength.? Preparing & maintaining various audit & Inspection reports like OHSAH & ISO.? Handling customer needs and requirements to develop effective QC process? Ensure incoming ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
1.20 LPA TO 1.32 LPA
A Store Helper in a steel plant supports the Store Keeper cum Supervisor by managing the physical inventory of heavy raw materials, spare parts, and finished goods . They ensure the safe loading, organized stacking, and accurate movement of materials while keeping the warehouse clean and strictly adhering to industrial ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable).
Review and approve analytical results, COAs, test reports, and raw data.
Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.).
Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.).
Review and update SOPs, STPs, GTPs, ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable).
Review and approve analytical results, COAs, test reports, and raw data.
Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.).
Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.).
Review and update SOPs, STPs, GTPs, ...
4 Opening(s)
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, Analytical Report for raw material, finish product and packing material.
Assistance in preparation of SOP of various departments/ preparation of draft SOPs.
During plant round QA Executive to verify documents as per cGMP and GLP norms.
Line Clearance activities for manufacturing and packaging ...