3 Opening(s)
0 To 2.0 Year(s)
0.00 LPA TO 2.00 LPA
Testing knowledge of all types of pigments testing.
Having good knowledge testing of offset ink, liquid ink, UV ink and water base ink.
Handling of instrument like X rite Spectrophotometer, TRM, UV Machine, IGT printer, KPP Automatic ink proofer & muller machine etc.
Prepare test report and maintain excel sheet.
Maintain all type of ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable).
Review and approve analytical results, COAs, test reports, and raw data.
Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.).
Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.).
Review and update SOPs, STPs, GTPs, ...
3 Opening(s)
1.5 Year(s) To 6.0 Year(s)
3.00 LPA TO 7.00 LPA
Key Responsibilities:
1. Method Development & Validation
Develop analytical methods for assay, dissolution, related substances, and stability testing.
Conduct method validation as per ICH guidelines (accuracy, precision, specificity, linearity, robustness).
Optimize and troubleshoot existing analytical methods.
2. Instrument Handling
Operate analytical instruments such as HPLC, GC, UV, FTIR, KF, Dissolution Apparatus, etc.
Perform daily calibration and ensure ...
3 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 4.50 LPA
Process Excellence: Analyze and optimize manufacturing steps (e.g., granulation, blending, compression, coating, filling) to improve yield, throughput, and cycle time using continuous improvement methodologies.
Troubleshooting & RCA: Quickly diagnose and resolve technical issues, equipment malfunctions, and production deviations, performing Root Cause Analysis (RCA) and implementing CAPAs (Corrective and Preventive Actions).
Equipment & ...
2 Opening(s)
1.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 6.00 LPA
Perform scheduled Preventive Maintenance (PM) and rapid troubleshooting on AHUs, Chillers, Boilers, and associated mechanical and electrical controls.
Maintain validated cleanroom conditions, including monitoring pressure cascades and supporting HEPA filter integrity checks.
Document all maintenance activities accurately within the CMMS according to cGMP/SOP requirements.
Assist in HVAC Qualification (IQ/OQ/PQ) activities.
2-6 years of HVAC ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 8.00 LPA
Oversee day-to-day production activities for formulation batches as per approved BMR/BPR.
Ensure compliance with cGMP, GDP, and regulatory guidelines (WHO, EU, USFDA, MHRA as applicable).
Monitor production planning, batch scheduling, material requirement, and manpower allocation.
Coordinate with QA, QC, Warehouse, Engineering, and RA for smooth production operations.
Review and ensure timely completion of batch ...
5 Opening(s)
2.0 Year(s) To 13.0 Year(s)
39.00 LPA TO 43.00 LPA
Job Description-
Job Title: Warehouse OperatorLocation: USA
Experience Required: 2 years -13 yearsEmployment Type: Full-time
Shift- second shift
Job Purpose:
Job Responsibilities:
Inspect carriers/trailers of inbound and outbound shipments.
Directs and escorts drivers always when on the facility.
Receives and unloads freight, checks for damaged goods, verifies items and quantities received with BOL, Packing List, PO, etc.
Moves materials as required for ...
1 Opening(s)
0 To 4.0 Year(s)
2.50 LPA TO 3.20 LPA
A Quality Control (QC) Chemist's job is to perform qualitative and quantitative analysis on materials throughout the manufacturing process to ensure products meet quality standards. Key responsibilities include testing raw materials, in-process samples, and finished products, documenting findings, maintaining laboratory equipment, ensuring compliance with regulations like cGMP, and investigating quality deviations.
Key responsibilities
Conduct ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: QA Officer
Location: Saykha near by Bharuch
Experience: 3 - 6 Years
Industries: Chemical
Responsibilities:
Ensure current versions of all GMP documents are in use across departments.
Prepare, revise, and control SOPs and related quality documents.
Implement and enforce Good Documentation Practices (GDP).
Prevent retention of ...
4 Opening(s)
2.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 6.00 LPA
Direct Material Sourcing: Procure Active Pharmaceutical Ingredients (APIs), excipients, and primary/secondary packaging materials, ensuring compliance with all cGMP/pharmacopeial standards.
Engineering/CAPEX Procurement: Manage the end-to-end procurement of capital equipment, plant machinery, utilities (HVAC, WTP), and engineering services for facility projects and maintenance.
Vendor Management: Identify, qualify, and manage a robust base of local and international suppliers. Conduct vendor audits and ...