Machine Operator
Aja Pharmaceutical Company
Total years of experience :10 years, 10 Months
Good experience in Sterile Compounding, Component Preparation of Autoclave, CIP, SIP, Filter Integrity and Bulk Filtration.
•Effectively Operating Pharmaceutical Machinery such as Bosch+Ströbel Filling, Labelling & Cartoning Machines, Uhlmann Cartoning Machine, IWK Bottle and Tube Cartoning Machine, Mettler-Toledo Garvens, Antares Vision Serialization+Aggregation Machine, Pratham Leaflet Folding Machine and other machinery.
· Good experience in Sterile Compounding, Component preparation of Mobile Vessel, Autoclave, CIP, SIP, Filter Integrity and Bulk Filtration.
· Effectively operating machines such as Bausch+Ströbel Sterile Filling, Labelling, Cartoner & Serialization Printing+Aggregation Machines.
· Operated various manufacturing equipment, Filling and Packaging Machinery.
· Good experience in Sterile Compounding, Component preparation of Mobile Vessel, Autoclave, CIP, SIP, Filter Integrity and Bulk Filtration.
· Good experience in operating machines such as Bausch+Ströbel Sterile Filling, Labelling, Cartoner & Serialization Printing Machines.
· Operated various manufacturing equipment in Sterile Compounding.
The Job Responsibilities Includes: -
•Working with high end machine equipment’s for a mass production of a firm.
•Monitoring machine health regularly to prevent any damage to it.
•Performing regular checks and maintaining and adjusting according to the conditions given.
Sterile Formulation Production and Packing Operator’s
•Good experience in Sterile Compounding, Component preparation like Autoclave, CIP, SIP, Filter Integrity and Bulk Filtration.
•Good experience in operating machines like Steril Filling, Labelling, Cartoner & Bundle Wrapper.
•Operated various manufacturing equipment in Sterile Compounding.
•Submit WFI or WPU rinse water sample to microbiology lab for approval and received report
•Prepare filter wetting solutions and Bubble Point test Hydrophilic and Hydrophobic filters for Manufacturing.
•Dispose of waste after filling process is finish weighing recording and attaching data or records to Batch record.
•Setup preparation cleaning and autoclaving components used in aseptic manufacturing operations.
•Prepares equipment by performing sterile Cleaning-In-Place, (CIP), Servicing-In-Place (SIP), and cleaning Out-of-Place (COP), conducting operator inspection performing preventive maintenance checks.
•Operated Palltronic Flowstar IV Filter for Integrity test Instrument use for forward flow rate, .
•Autoclave used to sterilize equipment high pressure saturated steam at NLT 121 °C (249°F) for validated cycle depending on the size of the load.
•Completed manufacturing documents with accuracy and completeness.
•Diligently maintain safety and quality standards.
•Performed machine and electronic sensor challenges, metal detector challenges, checkweigher challenges, removal torque testing and fill weight verifications.
•Perform every half an hour ensure that ongoing is comply with the procedure and standard.
•Checked all incoming components against batch record.
•Verify line clearance completed required line clearance checklist prior to start-up.
•Completed the required section of batch record in accordance to cGMP and SOP standards.
•Being responsible for Production Line Machineries Start-up And shutdown all productions line.
•Maintain the correct packaging specification for each different part.
•Performed the basic maintenance for the machine.
•Maintain a clean and organized designated work area at all time.
OSD Formulation Production and Packing Operator’s
•Good experience in operating machines in Compression & Coating Operation.
•Manufactures batches of tablets and capsules under supervision.
•Operates KILIAN plus 150 Compression machine Romaco Kilian 420 Automatic Compression.
•Perform In process checks every half an hour to ensure that ongoing process is comply with the procedures and standards.
•Perform major and minor changeover.
•Perform CIP for batch changeovers.
•Prepare documents and assist supervisor for Line clearance.
•Submit rinse water samples to microbiology lab for approval and receive reports.
•Receive raw material from dispensing section.
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