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 ... 
								
							2 Opening(s)
									 
									2.0 Year(s) To 7.0 Year(s)								
							
									 
									3.00 LPA TO 6.00 LPA								
							
									 
Experience:
2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements
 
JOB PURPOSE
Generic
Implement Quality Assurance activities for Pharmaceutical at Ankleshwar adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality of products to meet with customers’ requirements, living Group’s ... 
								
							2 Opening(s)
									 
									10.0 Year(s) To 15.0 Year(s)								
							
									 
									8.00 LPA TO 10.00 LPA								
							
									REQUIREMENTS
Education / Experience
Education:
Graduate / Post Graduate in Pharmacy or Chemistry
Experience:
2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements
 
JOB PURPOSE
Generic
Implement Quality Assurance activities for Pharmaceutical at Ankleshwar adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality ... 
								
							2 Opening(s)
									 
									2.0 Year(s) To 7.0 Year(s)								
							
									 
									2.00 LPA TO 3.00 LPA								
							
									REQUIREMENTS
Education / Experience
Education:
Graduate / Post Graduate in Pharmacy or Chemistry
Experience:
2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements
 
JOB PURPOSE
Generic
Implement Quality Assurance activities for Pharmaceutical at Ankleshwar adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality ... 
								
							2 Opening(s)
									 
									2.0 Year(s) To 7.0 Year(s)								
							
									 
									3.00 LPA TO 7.00 LPA								
							
									REQUIREMENTS
Education / Experience
Education:
Graduate / Post Graduate in Pharmacy or Chemistry
Experience:
2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements
 
JOB PURPOSE
Generic
Implement Quality Assurance activities for Pharmaceutical at Ankleshwar adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality ... 
								
							1 Opening(s)
									 
									15.0 Year(s) To 20.0 Year(s)								
							
									 
									8.00 LPA TO 12.00 LPA								
							
									
Job summary
The Head of Laboratory is responsible for leading all lab operations, ensuring accurate and timely chemical and physical testing of all materials involved in the steelmaking process. This role involves managing personnel, overseeing equipment maintenance, ensuring compliance with quality standards (e.g., ISO), and collaborating with production to drive continuous ... 
								
							1 Opening(s)
									 
									8.0 Year(s) To 12.0 Year(s)								
							
									 
									12.00 LPA TO 13.00 LPA								
							
									Job Summary :
A professional with 8 to 12 years of experience in mould design,responsible for developing high-precision moulds and fixtures for various productrequirements. This role involves performing mould flow analysis, leading trials, andaddressing design-related challenges. The focus is on continuous improvement tooptimize tool performance, cycle time, and product quality. Expertise ... 
								
							3 Opening(s)
									 
									1.0 Year(s) To 3.0 Year(s)								
							
									 
									3.00 LPA TO 5.00 LPA								
							
									Key Responsibilities:
Adhere to GMP and GDP:
Ensure all activities are performed in accordance with SOP (Standard Operating Procedures) and regulatory requirements for GMP and GDP.
Maintain compliance with safety, quality, and environmental standards during production processes.
Final Quality Check and Approval:
Conduct final quality checks and approval for finished products, including components, 2D/3D bags, ... 
								
							2 Opening(s)
									 
									5.0 Year(s) To 7.0 Year(s)								
							
									 
									3.60 LPA TO 4.80 LPA								
							
									 
25.07.25
113594
HPS/2025/442
Quality / BOPP / FIBC Engineer
Male
2
5 to 7
DME / CIPAT / BA
Gandhidham-1 &  Sanand-1
8 Hours+ Accommodation+chargeable food
Quality Control:
Inspecting raw materials, in-process production, and finished FIBC and BOPP bags for defects, dimensional accuracy, and adherence to specifications. 
 
Testing:
Conducting various tests like tensile strength, UV testing, and other relevant quality checks. 
 
Process Optimization:
Identifying areas ... 
								
							1 Opening(s)
									 
									5.0 Year(s) To 10.0 Year(s)								
							
									 
									6.00 LPA TO 10.00 LPA								
							
									DUTIES & RESPONSIBILITIES: Leading and accessing the Quality Improvement Projects (QIP), lean implementation, continual improvement and six sigma projects across JLL factories. Active team member of quality system design (SOP, Inspection, Safety, QA manual, Analysis. PQP, QFD) and responsible person for implementation of the same. Responsible for factory auditing (Own/3P) ...