2 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 3.00 LPA
1 To follow all safety rules and standards. Participate in safety tool box talk.Ensure compliance of SOP, work permit systems and environment care2 To ensure the use of job specific tools in good condition and tested 3 To do 5s activities in work place . 4 To attend class room ...
2 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 3.00 LPA
1 To follow all safety rules and standards. Participate in safety tool box talk.Ensure compliance of SOP, work permit systems and environment care2 To ensure the use of job specific tools in good condition and tested 3 To do 5s activities in work place . 4 To attend class room ...
1 Opening(s)
3.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 6.00 LPA
π Key Responsibilities:
β
Handle complete shift production activities β
Monitor batch charging, reaction parameters, filtration, drying & packing β
Supervise operators and contract manpower β
Ensure adherence to SOP, BMR & safety guidelines β
Maintain production logbook & shift reports β
Coordinate with QA/QC, Maintenance & EHS departments β
Handle ...
10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
π¬ 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 ...
6 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 6.00 LPA
Job Description: Quality Control EngineerQualification: BE Mechanical / BE Fabrication / BEMetallurgy/Diploma Mechanical or FabricationExperience: 3-5 years for BE and 5 to 7 years for DiplomaArea of exposure/ competencyο Supporting to QA / QC In Charge for Quality Management System Handling.ο Coordinating Third party inspection and its associated activities.ο Laboratory ...
10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
π¬ 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)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
π§ Key Responsibilities
Operate and monitor Blister Packing Machines (Alu-Alu / Alu-PVC).
Perform machine setup, changeover, and format adjustments as per production plan.
Ensure proper feeding of materials like PVC, Aluminum foil, and printed foils.
Conduct in-process checks and maintain batch records as per SOP.
Ensure compliance with cGMP, safety, and quality standards.
Troubleshoot minor mechanical ...
1 Opening(s)
6.0 Year(s) To 15.0 Year(s)
5.00 LPA TO 15.00 LPA
ο· Proper Understanding and Knowledge to troubleshoot Process and UtilityEquipment’s like Compressor, Chiller, Cooling Tower, water Treatment Plant.ο· Knowledge of Preventive Maintenance and Breakdown Maintenance.ο· Shift Handling in Maintenance.ο· Good Understanding of the Documentation.ο· Should be Involved in MTTR (Mean Time to Repair) and MTBF (Mean TimeBetween Failure) Improvement Projects.ο· ...
100 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
π§ͺ Production Department – Diploma / B.Sc / M.Sc Chemistry (2–5 Years) | 50 Positions
Role: Shift Operator / Production Executive
Qualification: Diploma Chemical / B.Sc / M.Sc Chemistry Experience: 2–5 years
Key Responsibilities
Field operation of reactors, centrifuge, pumps, dryers
Charging, sampling, filtration & packing activities
Follow SOP, GMP & safety practices
Maintain shift documentation
Report abnormalities ...
2 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 2.00 LPA
Key Responsibilities
Assist in implementation and monitoring of GMP, SOPs, and quality systems
Support preparation, review, and control of QA documentation
Assist in batch record review and compliance checks
Participate in internal audits and inspection readiness activities
Support handling of deviations, change controls, and CAPA
Assist in raw material, in-process, and finished goods release documentation
Coordinate with ...