1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QA Officer
Location: Vapi
Experience: 3 - 4 Years
Industries: Pharma API
Responsibilities:
Review QC raw data, BMRs, STPs, and specifications.
Monitor compliance with cGMP, GLP, and documentation practices.
Conduct GMP training sessions and maintain related records.
Handle deviations, change control, CAPA, and non-conformance.
Perform self-inspections, audits, and ensure ISO ...
1 Opening(s)
9.0 Year(s) To 11.0 Year(s)
8.00 LPA TO 10.00 LPA
Key Responsibilities:
Manage and oversee all Quality Control activities for formulation products.
Ensure compliance with cGMP, GLP, and regulatory guidelines.
Review and approve analytical reports, COA, STP, and specifications.
Handle instrument operations like HPLC, GC, UV, Dissolution apparatus, etc.
Ensure calibration, validation, and maintenance of QC instruments.
Coordinate with QA, Production, and R&D for smooth operations.
Handle ...
10 Opening(s)
2.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 8.00 LPA
🔹 Job Purpose
To perform and monitor granulation activities in solid oral dosage (OSD) manufacturing while ensuring compliance with cGMP, safety, and quality standards.
🔹 Key Responsibilities
⚙️ Production / Operation
Operate granulation equipment such as RMG, FBD/FBE, blender, etc.
Execute wet / dry granulation processes as per BMR (Batch Manufacturing Record)
Set machine parameters and ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.68 LPA TO 4.80 LPA
A Ferro Chemist in a steel/ferroalloy company analyzes raw materials (ore, coal, coke) and finished products (FeMn, SiMn, FeCr) to ensure quality standards. They use instruments like AAS, XRF, and spectrometers to test composition, monitor furnace processes, and generate technical reports, typically requiring a B.Sc./M.Sc. in Chemistry.
Key Job Responsibilities:
Analytical Testing: Conduct chemical ...
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, ...
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. ...
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