1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
Position: Production Manager
Location: Vapi
Experience: 12 - 15 Years
Industries: Pharma - API
Responsibilities.
Overall responsible for planning and maintenance of optimum inventory of raw materials, in –process and finished goods.
To ensure the products are manufactured and stored according to pre-approved instructions to ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 2.76 LPA
Position: Plant Operator
Location: Vapi
Experience: 4 - 5 Years
Industries: Pharma API
Responsibilities:
Oversee consumption of raw materials, yield, and finished product quality.
Allocate equipment for production and ensure safe operation of equipment.
Safely discharge and treat effluents.
Ensure proper storage and safety of raw materials, work-in-process, ...
1 Opening(s)
10.0 Year(s) To 20.0 Year(s)
7.00 LPA TO 7.80 LPA
Oversee Quality Control, Quality Assurance, and Validation processes. Manage regulatory documentation and obtain FDA approvals for new products. Review and verify Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Ensure product quality and consistency, maintaining accountability for output standards. Monitor and improve product yields across all SKUs. Lead ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 3.60 LPA
A Stores Manager in an aluminum plant is responsible for managing inventory, raw materials, and finished goods, ensuring smooth operations by tracking incoming/outgoing stock, optimizing inventory control procedures, and maintaining accurate records. Key duties include conducting regular stock checks to identify shortages, placing orders for replenishment, using software to monitor inventory levels, ...
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)
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)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 3.00 LPA
Production Responsibilities:
Supervise day-to-day production activities in the SS tube manufacturing unit.
Plan and allocate resources, machinery, and manpower to achieve production targets.
Monitor machine performance, downtime, and efficiency.
Coordinate with maintenance for machine upkeep and breakdown handling.
Ensure proper handling of raw material, in-process, and finished goods.
Maintain production records and generate daily production reports.
Quality ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 2.40 LPA
Position: QC Officer
Location: Degam - Vapi
Experience: 1– 2 Years
Industries: Plastic
Responsibilities:
Line clearance during manufacturing and packing activities.
Testing of incoming material (RM & PM), Semi-Finished and Finished Goods as per specification.
IN process Inspection.
Redispatch Inspection.
Preparation of dimensional report.
Shift Handling.
Attending ...
2 Opening(s)
1.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 3.00 LPA
1) Ensure that lab cleanliness and safety standards are maintained.2) Develop and qualify new testing methods.
3) Train other analysts to perform laboratory procedures and assays.4) Perform visual inspections of finished products.5) Participate in internal assessments and audits as required.
6) Identify and troubleshoot equipment problems.7) Evaluate new technologies and methods to make recommendations regarding their use.8) Serve as a ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.50 LPA TO 3.00 LPA
Review and approval of artwork.
Validate, Checking, analysis and maintain data for samples before final dispatch of each product.
Vendor audit and online proof verification and personal visit if required.
Prepare document of Export Po, Product information sheet, finished product specification.
Follow up from Party for approval of finished goods sample before dispatch.
Sample approved ...