1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 3.00 LPA
Your Key Responsibilities
● In-Process Quality Supervision ○ Supervise quality inspection activities on the shop floor ensure products meet defined quality standards during production. ○ Monitor machine output and verify that molded parts meet dimensional, visual, and functional specifications. ● Product Inspection and Defect Control ○ Inspect finished plastic products for ...
1 Opening(s)
1.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 3.50 LPA
Your Key Responsibilities ●
Machine Operation & Material Handling ○ Operate injection molding machines as per assigned production work orders. ○ Start, stop, and monitor machine cycles during production. ○ Load plastic granules into the hopper and inform the Shift Engineer in advance when the raw material is about to finish. ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: EHS Manager
Location: Vapi
Experience: 10 - 12 Years
Industries: Pharma - API
Responsibilities:
Ensure compliance with EHS regulations, Factory Act, GPCB, and Pollution Control Board requirements.
Manage statutory approvals, hazardous waste disposal, and EHS documentation.
Conduct risk assessments (HAZOP/HIRA), incident investigations, and implement CAPA.
Handle GMP, regulatory, safety, and customer audits and ensure ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
Position Overview
We are looking for a QMS Engineer (Executive) with experience in pharmaceutical formulation (OSD) to manage and maintain the Quality Management System (QMS) in compliance with regulatory requirements such as ICH, WHO-GMP, USFDA, and EU-GMP.
Key Responsibilities
1. Documentation Management
Prepare, review, and control SOPs, STPs, formats, and policies
Ensure proper document lifecycle ...
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)
6.0 Year(s) To 8.0 Year(s)
3.60 LPA TO 4.80 LPA
An Incharge Shift Operations for a steel manufacturing company manages daily production, safety, and personnel within a specific shift to meet targets, specifically in areas like SMS (Steel Melting Shop), DRI (Direct Reduced Iron), or rolling mills. Key responsibilities include supervising staff, monitoring process parameters (furnace/casting), troubleshooting equipment, ensuring SOP compliance, ...
1 Opening(s)
15.0 Year(s) To 25.0 Year(s)
15.00 LPA TO 20.00 LPA
A Head of Automobile Department in a steel manufacturing company (or Head - Automobile Maintenance) is responsible for the strategic management, maintenance, and operation of all heavy earth-moving equipment (HEMM), commercial vehicles, and material handling machinery within the steel plant.
Key Responsibilities
1. Maintenance Strategy & Execution
Preventive & Breakdown Maintenance: Direct day-to-day preventive, predictive, ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Highlights
Department: Health, Safety, Environment & Quality (HSEQ)
Reporting To: Assistant Manager – QA/QC
Experience Required: 4–6 Years
Qualification: B.Sc in Quality or Engineering
Core Responsibilities:
Laboratory analysis of raw materials, finished goods & waste samples
Calibration & troubleshooting of analytical instruments
Documentation as per ISO 9001 standards
SOP, checklist & compliance management
In-process & finished product analysis
Inventory management ...
5 Opening(s)
0 To 5.0 Year(s)
1.50 LPA TO 5.00 LPA
🔹 Key Responsibilities:
Execute day-to-day operations in aseptic and sterile manufacturing areas
Monitor LVP production activities in compliance with SOPs, cGMP, and regulatory guidelines
Operate and maintain critical equipment including autoclaves, filling machines, and sterilizers
Ensure strict adherence to safety, quality, and environmental standards
Prepare, review, and maintain batch production records and related documentation
🔹 Qualifications ...