1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 3.00 LPA
We are hiring a Quality control chemist in Palanpur.
Post: Quality control chemist
Location: Palanpur
Education: Bsc. in chemistry, Msc. in chemistry.Experience: minimum 1 year in API pharmaceutical industries’.Salary: Up to 25k CTC
Required skills:Minimum 1year of experience in pharmaceutical company.Handling & calibration of instrument like HPLC, GC, KF, UV, melting point/boiling point.Sampling and analysis ...
1 Opening(s)
0 To 2.0 Year(s)
1.80 LPA TO 2.40 LPA
Job Description :
26/03/2024
HPS/2024/173
Qc executive
Male
1
0 to 2
DME/B.Tech
Qc executive for Plastic sheet line : We need a guy who should manage quality control of incoming raw material, packing material, online qc inspection on the production line, Qc of finished goods, Qc reports and documentation. Should know about all about ISO.
HPLC (Operation and ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 3.50 LPA
Duties and Responsibilities: • Hands on experience of all handling lab instrument like HPLC, GC and UV.• Checking Of Method of Analysis, Specification and Protocol.• Checking Of Finish Product Certificate of Analysis (COA).• Handling of daily and monthly calibration of all instruments.• Handling of Stability products.• Prepare and Maintain Reference Standard, ...
5 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.50 LPA
Key Responsibilities:
Design synthetic routes for novel agrochemical leads and intermediates.
Execute multi-step organic synthesis, reaction optimization, and route scouting.
Conduct structure–activity relationship (SAR) studies in collaboration with biology teams.
Purify and characterize compounds using modern analytical techniques (NMR, LC-MS, HPLC, GC, IR).
Support scale-up trials from lab to pilot plant for promising leads and ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.50 LPA
? HPLC/GC Analysis of In-process, Intermediates, raw material, packing material and FinishProduct samples as per defined test procedure.? Chemical Analysis of In-process, Intermediates, raw material, packing material and FinishProduct samples as and when required.? Sampling of intermediate, finished product and raw material samples as and when required.? To maintain Raw ...
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 ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
12.00 LPA TO 16.00 LPA
Must be m.sc/ M.pharma with 15-20 Year experience in commercial Lab Pharmaceuticals products Testing
Responsible for ensuring the execution of all types of analytical activities
(related to LC-MS/MS, GC-MS/MS, HPLC, GC, ICP-MS, Wet analysis, Microbiology) including planning, work allotment, analysis, trouble shooting and reporting of the performed work.
Responsible for ensuring the optimum ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
2.40 LPA TO 3.60 LPA
A Chemist in a Direct Reduced Iron (DRI) plant is responsible for chemical analysis of raw materials and finished products, quality control and assurance, monitoring chemical processes, and maintaining lab equipment to ensure the safe and efficient production of DRI for steelmaking. Key duties include conducting tests on raw materials like ...
1 Opening(s)
3.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 6.00 LPA
Analytical Method Development: Develop, optimize, and troubleshoot analytical methods for assay, dissolution, related substances/impurities, and residual solvents.
Method Validation: Execute analytical method validation as per ICH guidelines, including accuracy, precision, specificity, linearity, range, robustness, and system suitability.
Instrument Operation: Hands-on experience with HPLC, GC, UV-Vis, FTIR, and Karl Fischer titrators, including instrument ...
1 Opening(s)
18.0 Year(s) To 20.0 Year(s)
16.00 LPA TO 18.00 LPA
Position: QC Head
Location: Daman
Experience: 18 - 20 Years
Industries: Pharma
Responsibilities:
Lead and manage the overall Quality Control function and QC laboratory.
Ensure compliance with cGMP, GLP, ICH, WHO and regulatory requirements.
Oversee testing and release of raw materials, packing materials, in-process and finished products.
Review and approve specifications, analytical reports, SOPs, ...