1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
2.16 LPA TO 2.64 LPA
A Junior Chemist works under the supervision of senior scientists or lab managers to conduct routine laboratory tests, prepare chemical solutions, and manage quality control data.
Job Overview
Role Type: Entry-level to mid-level
Typical Education: B.Sc. or M.Sc. in Chemistry (Organic, Inorganic, Analytical, or Industrial)
Core Goal: Support research, product development, or quality control ...
- Jr Chemist Job Keywords Comma Seprated Junior Chemist
- Jr. Chemist
- Chemist
- Assistant Chemist
- Trainee Chemist
- Graduate Chemist
- Laboratory Chemist
- Lab Chemist
- Junior Analytical Chemist
- Analytical Chemist
- Junior Qc Chemist
- Quality Control Chemist
- Qc Chemist
- Junior Qa Chemist
- Quality Assurance Chemist
- Qa Chemist
- Junior Lab Analyst
- Laboratory Analyst
- Chemical Analyst
- Junior Chemical Analyst
- Lab Assistant
- Laboratory Assistant
- Lab Technician
- Chemical Lab Technician
- Quality Control Technician
- Testing Chemist
- Production Chemist
- Process Chemist
- Industrial Chemist
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, ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: QC Executive
Location: Silvassa
Experience: 2 - 6 Years
Industries: Pharma
Responsibilities:
Perform sampling and testing of raw materials, in-process and finished products.
Conduct chemical/physical analysis as per SOPs and specifications.
Maintain QC records, logbooks, worksheets, and test reports.
Operate and maintain laboratory instruments and equipment.
Handle OOS/OOT investigations and support CAPA activities.
Ensure compliance ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 20.00 LPA
Lead and manage the complete Quality Control laboratory operations.
Supervise QC testing of Raw Materials, Packaging Materials, In-Process Samples, Finished Products and Stability Samples.
Ensure analytical testing is performed as per approved specifications, STPs, pharmacopoeial and regulatory requirements.
Manage analytical instruments such as HPLC, GC, UV, FTIR, Dissolution, KF, pH Meter, TOC and ...
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 ...
1 Opening(s)
6.0 Year(s) To 7.0 Year(s)
6.00 LPA TO 7.00 LPA
Position: QC Executive
Location: Bhimpore - Daman
Experience: 6 - 7 Years
Industries: Medical - Device
Responsibilities:
Analytical Instrumentation & Testing
Perform analysis and troubleshooting of HPLC, GC-HS, FT-IR, UV, Dissolution Apparatus, and other laboratory instruments.
Ensure the proper calibration and maintenance of laboratory instruments as per SOPs.
Review and interpret analytical ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: QC Executive (Reviewer)
Location: Vapi
Experience: 4 - 6 Years
Industries: Pharma
Responsibilities:
Experience in Method Validation and Stability Studies.
Review of electronic data, audit trails, and backup systems.
Expertise in qualification and calibration of analytical instruments such as HPLC, GC, ICP-MS, AAS, FTIR, and UV.
Hands-on experience in ICP-MS operation, ...
5 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 5.00 LPA
Key Responsibilities
Process Development:
Design and execute multi-step organic synthesis experiments to develop new and innovative routes for API synthesis.
Conduct literature searches and patent reviews to identify non-infringing and commercially viable synthesis routes.
Optimize reaction parameters such as temperature, pressure, time, and solvent to improve yield, purity, and reduce costs.
Technology Transfer:
Prepare and document ...
2 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 5.00 LPA
Key Responsibilities
Process Development:
Design and execute multi-step organic synthesis experiments to develop new and innovative routes for API synthesis.
Conduct literature searches and patent reviews to identify non-infringing and commercially viable synthesis routes.
Optimize reaction parameters such as temperature, pressure, time, and solvent to improve yield, purity, and reduce costs.
Technology Transfer:
Prepare and document ...