Experience

SifuTutor

• Malaysia
• Education Administration Programs
• 1 - 100 Employee

• Private Tutor

  • Jul 2022 - Present

  Shah Alam, Selangor, Malaysia 1) Provide one-on-one educational assistance on Quranic subjects on online class scheduled weekly. 2) Promptly update schedule, Evaluation Form, and submit Student Progress Report in SifuTutor Mobile App. 3) Successfully improve students’ skills and understanding by analysing students’ performance and create a new learning strategy according to their knowledge, age level and learning capacity.



Idaman Pharma Manufacturing Sdn. Bhd.

• Malaysia
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Internship Trainee

  • Mar 2023 - Aug 2023

  Kedah, Malaysia 1) Conduct Requalification of Hirayama Autoclave using Kaye Intelligent Resistant Temperature Device (IRTD) and Kaye High Temperature Reference (HTR). 2) Successfully implemented and organized Wash Water Monitoring Programme for solid and galenical products, according to ISPE Guide: Cleaning Validation Lifecycle – Applications, Methods, and Controls, to reduce the change over time in cleaning validation. 3) Maintain and improve data governance and assist in identifying the gap between… Show more 1) Conduct Requalification of Hirayama Autoclave using Kaye Intelligent Resistant Temperature Device (IRTD) and Kaye High Temperature Reference (HTR). 2) Successfully implemented and organized Wash Water Monitoring Programme for solid and galenical products, according to ISPE Guide: Cleaning Validation Lifecycle – Applications, Methods, and Controls, to reduce the change over time in cleaning validation. 3) Maintain and improve data governance and assist in identifying the gap between validated process and current process in small-scale projects such as Process Parameter Data 2023, Validated Equipment Revision 15. 4) Study and monitor pilot batch manufacturing process of Cetirizine products in production area according to Batch Manufacturing Record (BMR) for the purpose of trial formulation prior registration and review by NPRA before being commercialized. 5) Guide and monitor process validation of manufacturing process for solid and galenical products in production department according to PIC/S Guidelines: Guide to Good Manufacturing Practice for Medicinal Products, PE 009-16 (Annex 15: Qualification and Validation), 01 Feb 2022 to ensure homogeneity and uniformity of the products. 6) Closely monitor the sampling plans for cleaning validation of manufacturing and filling equipment in production area according to Annexure 7-Sampling location of equipment rev00, 2023. 7) Improve data governance of Holding Time Study for solid and galenical products in accordance with Annex 4: General Guidance on Holding Time Study; World Health Organization (WHO). 8) Conduct capability analysis, Cpk of data weight for solid products to measure the performance of process for continuous improvement within the specifications. 9) Review and revise procedures as required by the standards and regulatory requirements for process and product control aligning with industry standards such as ISO 14001, ISO 45001, ISO 9001:2015, ISO 17025, IS0 37001 and MS2424. Show less