87 Job openings found

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, ...

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