1 - 4 Years
to Ensure Cgmp Compliance At Different Stages I.e. Raw Material/packing Material Dispensing, Manufacturing and Packing Activities
to Grant Line Clearance for Start-up of the Activities (raw Material and Packing Material Dispensing, Manufacturing of Medicament and Gelatin Preparation Stage, Encapsulation, Drying, Polishing, Visual Inspection, and Primary & Secondary Packing Stages).
to Responsible for Sampling of Wash Water and in Process Materials as per Batch Manufacturing Record or Validation Protocols and Release/reject of Material as per Analysis Report.
in Process Inspection of Physical Parameter of the Dosage Forms At Different Stages (manufacturing and Packing).
to Review of all Documents of Respective Areas (manufacturing and Packing).
to Calibrate Weighing Balances as per Frequency and Daily Review of Balance Verification Records
to Ensure that the Respective Standard Operating Procedures are Followed for Every Activity.
to Ensure that the Environmental Conditions are Monitored in Respective Areas of the Operation and the Conditions Meet to Recommended Limits
to Physically Verify the Incoming Raw and Packing Materials.
to Ensure that the Current Revision of Document is In- Force. (no Obsolete Copy with Users).
to Collection, Storage and Controlling of Control Samples & Stability Samples as per Requirements.
issuance, Retrieval and Destruction of Stereos as per Approved Procedure.
|Salary||4 Lac To 5 Lac P.A.|
|Industry||Manufacturing / Production / Quality|
|Work Experience||1 - 4 Years|
|Contact Person||Mrs. Neelam|
|Address||Head Office: 39, Ist Floor, Neelam Flyover Market, N.I.T|