Abd Allah Mohamed Zaki

IPC SupervisorFull Time

• Job Details:When the product from one process is transferred to other process, the yield should be compared with set targets. If problems or deviations are observed the remarks and reasons are mentioned. If the deviation is not within the acceptable limits further manufacturing process should be continued only after QA / QC clearance and proper records should be maintained. The processing status should be appropriately documented.

IPC SpecialistFull Time

• Job Details:Follow up : Weighing or measuring of active pharmaceutical ingredients or excipients should be done under the suitable conditions which do not affect their conformity of use.  Appropriate and calibrated equipment / instrument should be used. Prior to use in manufacturing process, verify all the materials against the batch manufacturing record.  Materials should be appropriately controlled to prevent unauthorized use.  Following information being available on the label:- Material Name, Material Code, Control No.  Weight or volume of material in the new container and Re-test date.

Ipc SpecialistFull Time

• Job Details:Check environmental monitoring it should be performed and record must be maintained. Check the area of cleanliness, all unwanted material of previous batches should be absent.  Check that the blisters are free from knurling defects, strips for alignment defects & empty pockets. Check that the packing materials are received from approved vendors. Check that the packing material should be tested by quality control dept and status labels. Check the status labels on equipment, area & in-process containers. Check the Name, Strength, Volume and Composition on the printed packing material.  Check the over printing quality on the primary & secondary packing material  Check the Batch coding details on primary and secondary pack (B. No, Mfg./date, Exp./date, /bar code, etc.) Check the Text matter on the printed label, foil, carton & shipper etc. Check the Pharmacopeial status of the material used in the preparation of product. Check the Mfg. License number printed on the packing material. Check the mandatory information printed according to drugs act and rules on pre-printed packing materials. Check and confirm that the storage condition details are available in the packaging materials are according to particular product and same condition should be available on all printed items. Check the directions for use are available on the packaging items and warnings or caution against wrong administration is  provided in the packing items. Ensure checkers are performing their activity in a proper way. Verify the records for online entries. Sampling should be done according to SOPs.