S Kant Healthcare Ltd Hiring For Tablet Production
S Kant Healthcare Ltd Hiring For Tablet Production
Required at S Kant Healthcare Ltd. Vapi Gujarat

Officer / Executive – Tablet Production 

Qualification – B.Pharm / M.Pharm

Experience – 3-6 Years.                                                                                                                                Job description:

  • Job distribution to workmen.
  • Receipt of dispensed raw material from stores.
  • To check and issue the issued raw materials after taking into the area prior to issue for production process.
  • Generation of labels of In-process, semi finished and finished products.
  • Getting line clearance from QA before starting the next product.
  • Co-ordination with QC & maintenance department.
  • Supervision of Compression, Coating and Capsule area.
  • Performing in process checks as per BMR of the product.
  • Returning of balance/rejected empty capsule/raw material to raw material store.
  • Destruction of Non-recoverable recovery and records of the same.
  • Monitoring on production process, In-process checks and changeover time
  • Reporting the Production Head and QA head for any GMP incidence.
  • Investigating deviations and GMP incidences.
  • On line B.M.R. filling. Final yield reconciliation after each stage before proceeding to next step.
  • Performance check of weighing scale and maintaining records of it.
  • Maintaining Equipment logs of machines.
  • Maintaining record of Punches and dies.
  • Maintaining Environmental records.
  • Ensure cleanliness of area, equipment, instrument, filters of risers of AHU , punch and dies
  • Monitoring of productivity.
  • Maintaining records of approved semi finished product store.
  • Workers attendance and overtime records.
  • Training of workmen.
  • Batch creation and TRF generation in Pharmacloud system.
  • To follow the instructions as per SOP, to maintain discipline in the department and to adhere to GMP requirements.
  • Ensure the implementation and compliance with GMP aspects as trained on.
  • Ensure compliance with integrity of data as trained on.

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