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)
3.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 6.00 LPA
Job Summary:
We are looking for a skilled QC Chemist with hands-on experience in HPLC & Gas Chromatography for a pharmaceutical testing laboratory. The candidate will be responsible for routine analysis, method execution, and ensuring compliance with regulatory standards.
Key Responsibilities:
Perform analysis using HPLC and GC/GC-FID as per standard methods • Prepare ...
1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 10.00 LPA
Responsibility:
Review of Analytical Method Validation, Verification, Vendor Qualification, Cleaning validation and Method transfer protocols and reports.
Review of method development and routine stability analysis data.
Review of certificate of analysis and stability data sheet.
To guide team member for development of novel and cost-effective analytical methods.
To perform all type of analysis like Method ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QC Lab Chemsit
Location: Jhagadia near by ankleshwar
Experience: 1 - 5 Years
Industries: Chemical
Responsibilities:
Test raw materials, in-process samples, and finished products as per specifications and SOPs.
Perform wet chemical analysis, titration, pH, moisture, assay, density, etc.
Handle laboratory instruments such as pH meter, UV, Karl Fischer, HPLC/GC, as ...
1 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 6.00 LPA
Perform routine quality control analysis of raw materials, packing materials, in-process and finished products.
Operate and maintain HPLC and GC instruments for analytical testing.
Perform sample preparation, testing and documentation as per approved SOPs and specifications.
Review analytical results and ensure compliance with specifications.
Maintain proper laboratory records, logbooks and analytical worksheets.
Follow GMP, GLP ...
1 Opening(s)
0 To 1.0 Year(s)
1.20 LPA TO 1.80 LPA
The Asst Production Chemist is responsible for planning, supervising, and executing manufacturing activities to ensure products are produced safely, efficiently, and in compliance with cGMP, ISO 13485 (where applicable), Medical Device Rules (MDR) 2017, approved procedures, and company quality standards. The role includes manpower supervision, production planning, documentation, equipment utilization, ...
8 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 6.00 LPA
Description:
Position: Officer/Sr.Officer - QC
Location: Vapi
Experience: 2 – 5 Year
Industries: Pharma Formulation
Responsibilities:
Perform analysis of Raw Materials, Finished Products, Stability samples, and Method Validation samples as per approved procedures.
Operate and handle sophisticated laboratory instruments such as HPLC, Dissolution Apparatus, and UV-Visible Spectrophotometer.
Handle QC laboratory ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Key Responsibilities
Perform analysis of raw materials, in-process samples, finished products, and stability samples.
Operate and maintain laboratory instruments such as HPLC, GC, UV, FTIR, and other analytical equipment.
Prepare, review, and maintain QC documentation, test reports, and laboratory records.
Follow Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and data integrity requirements.
Ensure compliance ...
1 Opening(s)
7.0 Year(s) To 14.0 Year(s)
8.00 LPA TO 14.00 LPA
Responsible to collect the raw ingredients, EMP(Environmental monitoring program )sample, Packaging, in process samples and finished product samples as per sampling plan and conduct the test as per AN methods for salmonella, Enterobacter sakazakii, Escherichia coli, Total bacterial count, Staphylococcus aureus, shigella, Listeria monocytogen, coliforms, yeast & mold, SRC tec. ...
3 Opening(s)
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Key Responsibilities:
Perform analysis of Raw Materials (RM), In-Process Samples, Finished Products (FP), and Stability Samples.
Operate analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, FTIR, and Dissolution Apparatus.
Prepare and standardize reagents, solutions, and reference standards.
Maintain analytical records, laboratory notebooks, and test reports as per cGMP and GLP requirements.
Perform calibration and routine ...