"• Follow cGMP and GLP practices in Quality Control Lab. • To perform the qualification of working standard. • To Maintain Inventory management for all chemicals, solvents and labo…
"• Receipt of Raw Material for main Pharma stores. • SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. • To check the environmental pa…
Follow cGMP and GLP practices in Quality Control Lab. • To follow safety procedure in qc department. • To analyze the Sample of in process validation and finish product on instrume…
Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by r…
To perform In-process Quality Assurance for the process / products being manufactured and packed in Main Pharma Block (Tablet / Capsule). To ensure Quality and cGMP compliance of t…
1) Develop robust and reliable analytical methods for finished products. Prepare detailed method development reports and summaries in compliance with regulatory guidelines. 2) Anal…
1) Develop robust and reliable analytical methods for finished products. Prepare detailed method development reports and summaries in compliance with regulatory guidelines. 2) Anal…
1) Planning of analytical activity for assign Projects. 2) Review of Routine (F & D) and stability sample analysis as assign Projects and compilation. 3) Review of Specifications a…
- Liaison with Food & Drugs Control Administration, Gandhinagar/circle offices/CDSCO for various applications including but not limited to Product Permissions for manufacturing COP…
- Method development and report preparation. - Routine F&D and stability sample analysis. - Method development and report preparation - Analytical method verification of assigned p…
Major Purpose Of The Job: 1. Negotiation with vendor for lowest price. 2. New vendor development for alternate source. 3. SAP operation. 4. Market information. 5. Resolving day to …
Major Purpose of the Job: - Analytical Method Development by HPLC for all Project. - Routine HPLC Analysis for Raw Material, Intermediate, in process and Final API as per the Speci…
Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by r…
Major Purpose of the Job: - Analytical Method Development by HPLC for all Project. - Routine HPLC Analysis for Raw Material, Intermediate, in process and Final API as per the Speci…
Follow cGMP and GLP practices in Quality Control Lab. •To perform the qualification of working standard. •To Maintain Inventory management for all chemicals, solvents and laborator…
1) Method development and report preparation. 2) Routine F&D and stability sample analysis. 3) Method development and report preparation 4) Analytical method verification of assign…
"• Receipt of Raw Material for main Pharma stores. • SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. • To check the environmental pa…
To prepare and review the PQRs. • To compile the quality attributes & In-Process parameter in PQR as per current version of SOP. • To verify & review of Ingredient manufacture name…
The Senior Manager – Purchase to Pay (P2P) is responsible for managing the end-to-end P2P process, including purchase requisition, procurement, vendor onboarding, invoice processin…
Verify Receipt of Raw Material & Packaging Material for stores. • Verify SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. • Verify th…