10 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 6.00 LPA
Monitoring of manufacturing related activity performed in Mfg facility.To maintain proper planning, scheduling and achievement of production with optimum utilization of resources.To preparation, review and implementation of all necessary standard operating procedure(SOP).To preparation and review of batch manufacturing record and protocol.Training given to all concern persons in their respective areas.To ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 4.00 LPA
Position: QC Officer
Location: Vadodara
Experience: 1- 3 Years
Industries: Pharma
Responsibilities:
Responsible for Documentation work in QC Department
Candidate must have knowledge of HPLC/GC
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, packing activities and ...
1 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 1.80 LPA
Position: Trainee QC
Location: Daman
Experience: 0 - 1 Year
Industries: Pharma
Responsibilities:
Responsible for Documentation work in QC Department
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, packing activities and Procurement ...
10 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 6.00 LPA
Monitoring of manufacturing related activity performed in Mfg facility.To maintain proper planning, scheduling and achievement of production with optimum utilization of resources.To preparation, review and implementation of all necessary standard operating procedure(SOP).To preparation and review of batch manufacturing record and protocol.Training given to all concern persons in their respective areas.To ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QC Officer
Location: Bhopal
Experience: 2- 4 Years
Industries: Pharma
Responsibilities:
Responsible for Documentation work in QC Department
knowledge of Chemical Analysis Sections
Candidate must have knowledge of HPLC/GC.
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, packing ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.40 LPA
Position: Production Executive (DCS)
Location: Mehsana
Experience: 3 - 5 Years
Industries: Pharma - API
Responsibilities:
Equipment Handling, Online BMR/BPR filling, Distillation Process, having exposure of handling CF, multi mill, AGNFD, FBD equipment.
Responsible for shift production quantity & quality
Responsible for ...
3 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 3.00 LPA
Position: Production Chemist (DCS)
Location: Mehsana
Experience: 1 - 3 Years
Industries: Pharma
Responsibilities:
Knowledge of BMR Specification, GMP compliance, Area Clearance, process check and batch result, troubleshooting, Co-ordination with QC/QA & other dept.
Responsible for manpower work distribution in shift ...
3 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 3.60 LPA
We are hiring a Production chemist, Production Officer in Palanpur.
Post: Production chemist, Production Officer
Location: Palanpur
Education: Bsc. in chemistry, Msc. in chemistry.Experience: minimum 1-5 year in API pharmaceutical industries’.Salary: Up to 30k CTC
Facilities: Canteen and also transport
Required skills: to be responsible for batch start up activity, monitoring, calibration of balance andother instruction ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Executive - QC(QMS)
Location: Sarigam near by Vapi
Experience: 5 - 7 Years
Industries: Pharma - Formulation
Responsibilities:
Responsible for Documentation work in QC(QMS) Department
knowledge of Chemical Analysis Sections
Candidate must have knowledge of HPLC/GC.
Responsible for manufacturing the batch as per MOM or BMR.
Shall Handling Change control ,Deviation , ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 7.00 LPA
Monitoring all processes in process & FG quality results and trends
Reporting periodic status on quality function periodically and formats as defined to operations and top management
Maintaining all documents as defined for integrated QMS/ EMS/ TS
Undertaking RCA for recurring failure of processes / products followed by evolving CAPA in consultation with ...