1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
4.80 LPA TO 6.00 LPA
A Senior Lab Chemist (Ferro) in a pipes manufacturing or steel industry company is responsible for leading the quality control (QC) operations, analyzing the chemical composition of raw materials (ore, coal, flux) and finished ferroalloys (FeMn, SiMn, FeCr) to ensure they meet stringent industry standards (ISO/BIS) for pipe production. They often ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Sr. Engineer - Quality
Location: Valsad
Experience: 5 - 8 Years
Industries: Electronics
Responsibilities:
Develop and maintain quality standards and procedures
Perform incoming, in-process, and final inspections
Lead root cause analysis (8D, Fishbone, 5 Whys) and implement CAPA
Improve process quality using SPC, Kaizen, and Six Sigma
Handle customer complaints and warranty issues
Conduct ...
4 Opening(s)
6.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 3.60 LPA
A Ferro Chemist in a steel manufacturing company analyzes raw materials (ore, coal), intermediate products, and finished ferroalloys (FeMn, SiMn) to ensure quality standards. They operate laboratory instruments like spectrometers and AAS for wet/instrumental analysis, maintain lab safety, and prepare technical reports for production optimization.
Key Responsibilities
Analytical Testing: Analyze chemical composition (e.g., carbon, ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 9.00 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 test as per AN methods for salmonella, Enterobacter sakazakii, Escherichia coli, Total bacterial count, Staphylococcus aureus, shigella, Listeria monocytogen, coliforms and various yeast & mold.
•Responsible for analysis ...
4 Opening(s)
5.0 Year(s) To 10.0 Year(s)
3.60 LPA TO 4.80 LPA
A Production Shift Incharge oversees daily manufacturing operations, ensuring production targets are met, quality standards are maintained, and safety protocols are strictly followed. Key responsibilities include leading the production team, troubleshooting machinery issues, managing resources efficiently, and submitting detailed reports to management.
Key Responsibilities
Operational Leadership: Manage and supervise production staff during the assigned ...
3 Opening(s)
1.0 Year(s) To 4.0 Year(s)
1.80 LPA TO 3.00 LPA
Key Responsibilities
Testing and Analysis: Conduct raw material, in-process, finished product, and stability testing using HPLC, GC, UV-Vis, FTIR, and wet chemistry techniques.
Documentation & Compliance: Maintain accurate, timely records in LIMS and lab notebooks per GMP/GLP standards.
Instrument Calibration: Calibrate and maintain laboratory equipment (e.g., pH meters, refractometers, titrators).
Investigations: Investigate Out-of-Specification (OOS) results, deviations, and perform ...
20 Opening(s)
4.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 6.00 LPA
Position: Engineer/Sr. Engineer - Production
Location: Hajipir - Kutch
Experience: 4 - 8 Years
Industries: Chemical
Responsibilities:
Operate and monitor chemical production processes as per SOPs.
Ensure production targets are achieved with required quality standards.
Handle batch processing / continuous chemical operations.
Maintain process parameters such as temperature, pressure, flow, and ...
1 Opening(s)
15.0 Year(s) To 23.0 Year(s)
50.00 LPA TO 70.00 LPA
Key Responsibilities Strategic & Business Leadership Develop and execute the business unit strategy in alignment with the company’s longterm vision. Identify growth opportunities in domestic and international markets for soft drink concentrates. Lead product innovation and portfolio diversification to meet changing consumer preferences and regulatory standards. ...
2 Opening(s)
0 To 1.0 Year(s)
2.00 LPA TO 2.04 LPA
Position: IPQA Trainee
Location: Daman
Experience: Fresher
Industries: Pharma
Responsibilities:
Monitor manufacturing processes to ensure compliance with quality standards.
Perform in-process inspections and record observations during production.
Verify batch documentation, logbooks, and process parameters.
Identify deviations, non-conformances, and initiate corrective actions.
Coordinate with production and QA teams for quality improvement.
Ensure adherence to ...
10 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Exposure of Handling F & D activities in OSD.
An F&D (Formulation and Development) Pharma job involves designing, developing, and optimizing new drug formulations (tablets, capsules, injectables, liquids) or improving existing ones. Key responsibilities include conducting pre-formulation studies, lab-scale trials, stability testing, and ensuring regulatory compliance (GMP/GLP) during scale-up to commercial manufacturing