• +3 years Chemistry laboratory experience in a Pharmaceuticals industry
• Must be willing to work Night shift and weekends
• Attention to detail
• Microsoft Office experience essential
• Highly organized and works well under pressure and tight deadlines
+3 years Chemistry laboratory experience in a Pharmaceuticals industry
• Must be willing to work Night shift and weekends
• Attention to detail
• Microsoft Office experience essential
• Highly organized and works well under pressure and tight deadlines
• +3 years Chemistry laboratory experience in a Pharmaceuticals industry
• Must be willing to work Night shift and weekends
• Attention to detail
• Microsoft Office experience essential
• Highly organized and works well under pressure and tight deadlines
RESPONSIBILITIES
• Sampling of Raw materials, Packing materials, and analysis of Raw Materials, Packaging materials, Bulk, In-Process and Final Products.
• Particulate matter testing.
• Proper documentation and report generation.
• Daily Verification of Lab instruments
• Preparation of Standard Solutions – Volumetric and testing reagents
• Maintain and manage the QC documents and logs
• Testing of Trials and Stability Products
• Report any OOs to the QC Manager
• Perform method validation and instrument validation
• Clean, maintain and prepare supplies and work areas.
• Accurate Stock Control Management through the Sample receiving Register of all incoming materials.
• Waste Disposal and management.
• Set up, adjust, calibrate, operate, maintain and trouble shoot laboratory equipments.
RESPONSIBILITIES
• Sampling of Raw materials, Packing materials, and analysis of Raw Materials, Packaging materials, Bulk, In-Process and Final Products.
• Particulate matter testing.
• Proper documentation and report generation.
• Daily Verification of Lab instruments
• Preparation of Standard Solutions – Volumetric and testing reagents
• Maintain and manage the QC documents and logs
• Testing of Trials and Stability Products
• Report any OOs to the QC Manager
• Perform method validation and instrument validation
• Clean, maintain and prepare supplies and work areas.
• Accurate Stock Control Management through the Sample receiving Register of all incoming materials.
• Waste Disposal and management.
• Set up, adjust, calibrate, operate, maintain and trouble shoot laboratory equipments.
RESPONSIBILITIES
• Sampling of Raw materials, Packing materials, and analysis of Raw Materials, Packaging materials, Bulk, In-Process and Final Products.
• Particulate matter testing.
• Proper documentation and report generation.
• Daily Verification of Lab instruments
• Preparation of Standard Solutions – Volumetric and testing reagents
• Maintain and manage the QC documents and logs
• Testing of Trials and Stability Products
• Report any OOs to the QC Manager
• Perform method validation and instrument validation
• Clean, maintain and prepare supplies and work areas.
• Accurate Stock Control Management through the Sample receiving Register of all incoming materials.
• Waste Disposal and management.
• Set up, adjust, calibrate, operate, maintain and trouble shoot laboratory equipments.
