1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Urgent Requirement for CHEMIST/OFFICER for Incharge product handling & dispatch for Reputed Steel plant at jharsuguda location.
Urgent Requirement for CHEMIST/OFFICER for Incharge product handling & dispatch for Reputed Steel plant at jharsuguda location.
Urgent Requirement for CHEMIST/OFFICER for Incharge product handling & dispatch for Reputed Steel plant at jharsuguda location.
Urgent Requirement ...
4 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Job brief
We’re looking for a chemist to join our team and help us build safe, high-quality products. You will conduct various tests on chemical products, analyze their compounds and refine their composition.
To be successful in this role, you’ll need extensive knowledge of techniques like distillation, crystallization and titration and hands-on ...
4 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Job brief
We’re looking for a chemist to join our team and help us build safe, high-quality products. You will conduct various tests on chemical products, analyze their compounds and refine their composition.
To be successful in this role, you’ll need extensive knowledge of techniques like distillation, crystallization and titration and hands-on ...
4 Opening(s)
Not Mentioned To 1.0 Year(s)
1.00 LPA TO 1.50 LPA
Qualification: Bsc / Msc in chemistry with 0 to 2 yrs experience in micro chemist profile.
Ready to work at Boiser location in Maharashtra
Professional Skills :
Self confident and hard working.
Ability to work independently as well as part of team.
Willingness and ability to pick up new technical skills.
Ability to adapt any work ...
1 Opening(s)
0 To 3.0 Year(s)
3.00 LPA TO 3.50 LPA
Position: Production Chemist/Officer/Executive
Location: Vapi
Experience: 0 - 3 Years
Industries: Pharma API
Responsibilities:
Handling API production activities as per BMR/BPR
Monitoring process parameters and maintaining batch records
Ensuring compliance with GMP and safety norms
Coordination with QA/QC and Engineering departments
Maintaining proper documentation as per regulatory requirements
Requirements :
Logical thinking.
Organizing.
Good in communication.
Basic ...
2 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 5.00 LPA
Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
Perform line clearance and in-process checks.
Ensure compliance with cGMP, GDP, and SOP requirements.
Handle deviations, change control, CAPA, OOS, and OOT investigations.
Prepare, review, and update SOPs and QA documents.
Conduct GMP audits and shop floor inspections.
Monitor documentation and maintain data integrity.
Coordinate with Production, ...
1 Opening(s)
0 To 3.0 Year(s)
1.80 LPA TO 2.40 LPA
1. Position- R&D Chemist/Officer2. Qualification- M. Sc /M. Pharm3. Experience-3-4 yrs.4. Responsibility? Handling of analytical instruments like HPLC, UV, titration, pH meter, Rheometer etc? Carry out the analytical development, analytical method validation or analytical workand prepare the reports for bulk, finish and rawmaterials.? Prepare stability protocols, schedules and carryout the ...
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 ...
4 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Perform routine analysis of raw materials, in-process, and finished products
Operate and handle analytical instruments such as HPLC, GC, Karl Fischer, UV, Particle Size Analyzer, etc.
Ensure testing as per approved specifications, SOPs, and pharmacopeial requirements
Maintain proper documentation, test records, and compliance with GMP/GLP
Basic understanding of pharmaceutical formulations and related quality requirements
Support ...
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, ...