To allocate the work among operators on a daily basis on machines/work center / shifts and
prepares shift schedules.
To supervise the production activities on a day-to-day basis guiding the operators and trouble
shooting for smooth operation of machines/processes.
To help prepare documentation like Batch Manufacturing Records, protocols etc.
Working in tablets, capsules & dry syrup production department.
Maintaining of all documents related to manufacturing areas as per cGMP.
Preparation of daily production report and man power allocation.
Active calculation and batch reconciliation on various stages.
In process checking on various intermediate stages.
Review of batch manufacturing record and other documents for its completion of various
intermediate and final stages.
Handling of validation batches.
Co-operating in internal and external audits.
Written the BPR’S (Batch production records).
To ensure all activities should maintaining GMP & following SOP.
Equipment cleaning log books.
Preparation of Batch manufacturing record.
Quality maintain in process area.
Overall inspection of in process manufacturing area and records on observation sheet and get
comply be online basis.
Sampling of intermediates & finished product for QC testing.
Can handle effectively tablets (granulation, compression & coating), capsules manufacturing
& various production related activities.
To handle the material complaint along with seniors and communicate the complaint to the
production manager & development dept.
Filling of deviation from in case of any deviation in the process.
Handling of whole shop floor in a shift in relation to the production job.
Dispensing of material which are required for manufacturing operation.
|Experience||6 - 9 Years|
|Salary||3 Lac To 4 Lac 50 Thousand P.A.|
|Industry||Manufacturing / Production / Quality|
|Key Skills||Production Chemist Pharmacy|
|Contact Person||Vidyadhar Tiwari|
|Address||Ward No. 1, Oppo. Govt. School|