Laporan Praktik Kerja Profesi Industri Farmasi di Lembaga Farmasi TNI Angkatan Udara Drs. Roostyan Effendie, Apt. Bandung

Abstract

Background: According to the prevailing pharmacist competency standards in Indonesia, pharmacists in the industrial sector must be proficient in formulating and manufacturing pharmaceutical preparations that comply with applicable standards. This includes every aspect of their work adhering to Good Manufacturing Practice (GMP). The ultimate goal is to ensure the quality, safety, efficacy, and overall quality of pharmaceutical products. Furthermore, pharmacists are also required to collaborate effectively within an organization, build strong interpersonal relationships across different departments, and keep up with the latest scientific and technological developments. To cultivate prospective pharmacists with these competencies, the Pharmacist Professional Program (PSPPA) at the Faculty of Pharmacy, Universitas Sumatera Utara, equips them with industrial work practice.. Objective: this professional work practice in the industry is to enhance the author’s understanding of the role, function, position, and responsibilities of a pharmacist within a pharmaceutical company. Additionally, this practical work provides an opportunity for the author to learn the principles of GMP and to directly compare their application in a real-world setting. Summary: The Pharmacist Professional Work Practice (PKPA) was conducted at Indonesian air force army pharmacuetical institute Drs. Oostyan Effendie.m Apt from January 2 to February 28, 2025. During the program, the author observed and participated in various activities, including simulating cell culture processes from cell to finished product, conducting quality control, attending various training sessions, learning about aseptic techniques, understanding the air handling system, and managing post-production waste. Conclusion: Indonesian air force army pharmacuetical institute Drs. Oostyan Effendie.m Apt has implemented every aspect of the Good Manufacturing Practice (GMP) guidelines at its Cell and Human Tissue- Based Product Processing Facility. The production flow, from beginning to end, is well-executed, and the product quality and uniformity are guaranteed in every batch produced. Each activity has its own Standard Operating Procedure (SOP), which is regularly evaluated, and personnel receive periodic training to ensure they are competent in their respective fields.