1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
14.00 LPA TO 20.00 LPA
Position: Manager - QC
Location: Sarigam near by Vapi
Experience: 15 - 20 Years
Industries: Chemical
Responsibilities:
QC management and planning
Ensure that the test methods are updated and validated.
Overview / monitoring of analysis of Raw materials and Finish Goods.
Chemicals /glassware inwards and instrument procurement require for analysis.
Responsible for the timely ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: QC Chemist (Dahej)
Location: Dahej
Experience: 4 - 5 Years
Industries: Chemical
Responsibilities:
To conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods or stability samples.
To calibrate, validate, or maintain laboratory equipment.
To compile laboratory test data and perform appropriate analyses.
He should ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QC Executive
Location: Sachin - Surat
Experience: 2 - 4 Years
Industries: Chemical
Responsibilities:
Effectively perform chemical analysis techniques specifically using HPLC, GC, Karl Fischer, Melting Point, IR, and UV-Vis instrumentation.
Completes documentation relating to material analysis and enters data into database/software systems.
Assist with production activities as required.
Laboratory environment requiring the ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Highlights
Department: Health, Safety, Environment & Quality (HSEQ)
Reporting To: Assistant Manager – QA/QC
Experience Required: 4–6 Years
Qualification: B.Sc in Quality or Engineering
Core Responsibilities:
Laboratory analysis of raw materials, finished goods & waste samples
Calibration & troubleshooting of analytical instruments
Documentation as per ISO 9001 standards
SOP, checklist & compliance management
In-process & finished product analysis
Inventory management ...
10 Opening(s)
2.0 Year(s) To 8.0 Year(s)
5.50 LPA TO 6.50 LPA
Position: Executive/Sr. Executive - QC
Location: Vapi
Experience: 2 - 8 Years
Industries: Pharma API
Responsibilities:
Effectively perform analysis techniques specifically using HPLC, GC, Karl Fischer, Melting Point, IR, and UV-Vis instrumentation.
Completes documentation relating to material analysis and enters data into database/software systems.
Assist with production activities as required.
Laboratory environment requiring ...
10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
🔬 Quality Testing & Analysis
Perform routine and non-routine chemical analyses on raw materials, in-process samples, and finished goods using standard laboratory methods.
Operate and validate analytical instruments such as HPLC, GC, UV-Vis, FT-IR, Karl Fischer titrator and other relevant equipment.
Record, calculate, interpret and report accurate analytical results, ensuring data integrity and ...
10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
🔬 Quality Testing & Analysis
Perform routine and non-routine chemical analyses on raw materials, in-process samples, and finished goods using standard laboratory methods.
Operate and validate analytical instruments such as HPLC, GC, UV-Vis, FT-IR, Karl Fischer titrator and other relevant equipment.
Record, calculate, interpret and report accurate analytical results, ensuring data integrity and ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
🔬 Job Responsibilities
✔ Quality testing of Raw Materials, Intermediates & Finished Goods ✔ Sampling as per guidelines ✔ Testing as per specifications & SOPs ✔ Recording & analyzing test data ✔ Preparation & verification of standard solutions ✔ Calibration & verification of lab instruments (pH meter, conductivity meter, balance, etc.) ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
🔑 Key Responsibilities
GMP Compliance
Ensure effective implementation of GMP guidelines across production, QA, QC, warehouse, and utilities.
Monitor day-to-day GMP activities and identify non-conformances.
Support GMP audits (internal, customer, and regulatory).
Documentation & Records
Prepare, review, and control GMP documents such as SOPs, formats, logs, and registers.
Ensure proper documentation practices (GDP) are followed.
Maintain training, deviation, ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities
Conduct routine chemical and physical tests on incoming raw materials, in-process samples, and finished products in accordance with SOPs and quality standards.
Perform analytical techniques including titration, pH measurement, and instrument-based analysis (e.g., UV-Vis, chromatography as required).
Accurately record, analyze, and interpret data; prepare test reports and maintain detailed laboratory documentation.
Ensure ...