1.0 PURPOSE: The purpose of this procedure is to prevent errors, establish a procedure describing the activities and requirements for accomplishing returned liquid / blend control and supply the lines with correct blends / liquid.
2.0 SCOPE: This procedure applies to Chemical Area operations, Liquid Area operations, Production and Quality Control Department operations.
3.0 RELATED PROCEDURES: ALL-SOP-001- Line Startup and Line Clearance Procedure.
4.0 RESPONSIBILITY:
4.1 Scheduler, Line lead and Machine Operator are responsible for following this procedure.
4.2 Quality Control Inspectors are responsible for auditing compliance to this SOP.
4.3 Liquid Material Handler in Areas 110, 108, Lead and Material Handlers in Area 113, Chemical
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The liquid / blend is then sent to the Chemical Department, where it will be inspected for remaining shelf life (noted in the Release Tag as Expiration). If not expired, the liquid / blend is to be staged in the in Area 108, pending Q.C. release or Q.C. evaluation and or final disposition. Then stored in Area 110, from there, it is taken to production by the Liquid Material Handler from area 108 and or the Line Material Handlers.
6.2 All acetones are staged in area 113, from there, the Liquid Handler from Area 110 will take the acetone to the lines and will retrieve all unused acetone, weighing and measuring the gallons using a dipstick with gallon graduation marks, and return ticket completed and returned back to 113 for storage by the Area 110 Material Handler only.
6.3 Liquid components that are on “Hold” pending color matching or in need of adjustments are to be staged in the Chemical Container 102 area, pending Q.C. release or Q.C. evaluation and or final adjustment. Once the color is matched, the liquid / blend is sent to Area 110 for staging until production calls for the Item Number for a Work Order. If the liquid / blend expires while staged in area 110, the liquid / blend is to be evaluated by Q.C. and an extensión granted depending on the evaluation results.
6.4 Liquid components that are on permanent hold pending color matching or in need of
| State how the health and safety control equipment relevant to the work should be used in accordance with the given instructions.
6. The mixtures were then correctly disposed of, and steps 1. and 2. were repeated.
1.What parts of the supply chain are most closely involved with the situation in this case? What is the responsibility of each part in order to maintain smooth flow of material?
| Describe how the health and safety control equipment relevant to the work should be used in accordance with the given instructions.
There are two kinds of aspects in this case, one is the current cleaning process and the other is the new cleaning process.
Once inverted, built-up gas was released by turning the stopcock to its opened and closed positions. This was repeated for about four times in one minute intervals. Then the layers were allowed to settle until a separation between liquids could be observed. Due to the low density of the product, the top layer was to be extracted. The bottom layer was carefully and slowly extracted out of the separatory funnel.
(TCO 3) The Franc Zeppo Venture manufactures a product that goes through two processing departments. Information relating to the activity in the first department during April is given below:
Specific – The three batches will be imported from the USA to AndersonBrecon UK where it will be stored until satisfactory completion of Analytical testing and regulatory files in place. Once these tasks have been completed A Qualified Person (QP) will have to review and the release the batches before they can be placed on the European market.
Depending on the Work Order, the cap, tube container may change, thus, you must make sure to follow the BOM & WO.
The facility must have a way to independently verify the source strength and activity provided by the manufacturer. Source strength and activity measurement must be done with a well ionization chamber and electrometer or other suitable instrument with a calibration directly traceable to the National Institute of Standards and Technology (NIST). Calibrated survey instruments must also be available for use at and back up survey meter must be readily available in case of primary instrument failure. The facility must have instrumentation to perform periodic sealed-source leak testing. Appropriate local shielding, storage facilities, transportation containers, manipulation devices, and storage containers for emergency use must also be available. A computerized treatment planning system for volumetric image guidance (CT, ultrasound, etc), applicator reconstruction, and isodose computation must be available to calculate point doses, to generate isodose distributions, and to compute dose-volume statistics.
1. What parts of the supply chain are most closely involved with the situation in this case? What is the responsibility of each part in order to maintain a smooth flow of material?
More information is needed regarding other materials used by Manufacturing, Inc, other components needed by ProFish, the distance of the ProFish warehouse(s) to the manufacturing facilities, and the nature of the relationship and availability of the shipping company or companies utilized by ProFish and its suppliers (at all tiers) in order to more effectively determine potential interruptions in the transportation of the materials/components. This Value Stream Map, while somewhat useful in tracking this particular component, is far from complete in terms of providing a full analysis of the company (Rother & Shook, 2003).
Sufficient references samples of the starting materials and products need to be retained for future examination of the batch if necessary.
If a perpetual inventory record of Raw Material A is maintained on a LIFO basis, the March 16 issue will consist of:
The flavoured, concentrate is transferred to a 12,000 litre storage tank, containing a chilled syrup solution. The tank is chilled to around 2°C.