1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QC Officer
Location: Vapi
Experience: 1 - 3 Years
Industries: Chemical
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)
1.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QC Officer
Location: Vapi
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 Procurement of ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Executive/Sr. Executive - Warehouse
Location: Palej - Bharuch
Experience: 2 - 4 Years
Industries: Chemical
Responsibilities:
Better planning of daily work, optimum utilization of manpower.
Control of contract workmen for better utilization.
Proper calibration of m/c, Proper cleaning of the suction line and fluidized pad.
Monitor and maintain the dedusting ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Sr. Officer/Executive - QA
Location: Silvassa
Experience: 5 - 7 Years
Industries: Pharma
Responsibilities:
To control, distribute, retrieve and maintenance of the master documents/records, log books, Issuance of analytical worksheets to Quality Control, OOS (Out Of Specification) format and track the same, To maintain the inward/ outward records in the documentation ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 4.00 LPA
Position: QA Officer
Location: Vapi
Experience: 2 - 5 Years
Industries: Pharma
Responsibilities:
Documentation & Record Review:
Review specifications, sampling instructions, test methods, and analytical reports.
Review and approval of Batch Manufacturing Record (BMR), Batch Packing Record (BPR), Master Formula Record (MFR), and Equipment Qualification Records.
Review completed Batch ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 7.00 LPA
Position: Manager/Asst. Manager - Purchase
Location: Vadodara
Experience: 4 - 5 Years
Industries: Pharma
Responsibilities:
Should able to handle day to day Purchase activities like Pharma raw material, packing, control inventory/non-inventory items, develop vendors for Quality goods.
Excellent understanding of Procurement Process & the current Best Practices ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Asst. Manager – External Preparation(P)
Location: Pariya - Vapi
Experience: 10 - 15 Years
Industries: Pharma
Responsibilities:
Production & Compliance:
Oversight of External Preparations, and Oral Liquid Finished Formulations
Ensure adherence to batch manufacturing records (BMR), batch packing records (BPR), and standard operating procedures (SOPs).
Monitor ...
1 Opening(s)
5.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Executive/Asst. Manager - QC(P)
Location: Vapi
Experience: 5 - 12 Years
Industries: Pharma
Responsibilities:
Analytical Operations:
Perform and supervise analysis of Raw Materials (RM), Packing Materials (PM), and Finished Goods (FG).
Operate and maintain analytical instruments:- HPLC, GC, UV-Vis, FTIR, Dissolution Apparatus
Ensure compliance with ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Officer/Sr. Officer - Dispatch
Location: Daman
Experience: 3 - 5 Years
Industries: Pharma
Responsibilities:
Dispatch Planning & Execution:
Plan and execute dispatches of finished goods (domestic/international) as per schedule.
Coordinate with production, QA, QC, and warehouse teams to ensure readiness of materials for dispatch.
Create and process outbound ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 3.50 LPA
Position: Production Officer
Location: Vapi
Experience: 3 - 5 Years
Industries: Pharma
Responsibilities:
Perform the Cleaning of Equipment as per ECR.
To follow the cGMP practice.
Charge the batch as per approved batch manufacturing record.
Preparation of Standard operating procedure.
Before batch charging ensure the dispensed raw materials received as per BMR/BPR.
Ensure BMR/BPR/ECR instruction are ...