Officer

Sr. No.Responsibilities1.0Monitoring of Line clearance activity.1.1Line clearance of area and Equipment's as per checklists of SOP at various stages of manufacturing and packing activity.2.0Monitoring of in process activity.2.1In Process control as per mentioned in SOP and batch records at various stages of manufacturing and packing activity.3.0Monitoring of...

1)Opening & Closing of RM/PM Store.   2)Handling of documents.   3)Dispensing of RM/PM    4)Handling of Material. Verify the requisition slip.Collect the material as per requisition slip from rack. Verify the cleanliness of dispensing area /RLAF/Weighing balance/ Utensils etc (Not Limited).Verify the Temperature/RH/Differential pressure of RLAF/...

1Hands on Working experience of Analytical Method Validation/Verification of Pharma API & Products2Able to prepare AMV Protocols and Reports3Sound Knowledge on GC / HPLC Instrumentation.4Able to perform AMV Indigenously on GC / HPLC Instrument.5Basic trouble shooting capability in GC / HPLC instrument..6Cleaning and Operation of instruments...

Documents handlingTraining coordination with other department and QC and documents keeping Responsible for documentation tracking,keeping and retrival

Participation & review Qualification activity and related document in shop floor.Doing Requalification activity with document.Preparation of CPV report and data of batches.Responsible for Preparation of Media Fill report and Product process report.Responsible for review of Shop floor QMS documents like Deviation, Change control, Investigation, SOPs, Risk...

1Sampling of     Raw Material as per SOP.2Basic Knowledge of Instruments used in Raw Material analysis, UV, SOR, Autotitrator, KF apparatus, etc.3Activity recording as per GLP norms4Submitting of Raw Material samples after sampling in QC.5Sampling of     Packing Material as per SOP whenever required.6Cleaning and Operation of instruments /equipments...

Calibration of QC Instruments Working standard Preparation, issuance, & Management Volumetric solution preparation & Standardization Bench Reagent & Indicator preparation To perform Daily Inspection of QC lab with reference to GLP Checklist Daily Temperature & Humidity recording To handling glassware calibration activity To follow Good Documentation...

Liquid Inhalation manufacturing vial filling washing Liquid manufacutring and cleaning GMP GMR document filling capa

Position: Officer/Sr. Officer/ExecutiveDepartment: R&D analytical (API)Experience: 0-5 years of experience in Analytical method development and method Validation.Job description: 1. Sound Practical Knowledge of HPLC method development, method validation for Assay and Related substance of Active Pharmaceutical Ingredient.2. Characterization of newly...

Purchase orders generations, Negotiations, delivery follow ups, Cordination with internal and external stake holders. MS office & SAP knowledge is must.