Laporan Praktik Kerja Profesi Apoteker Industri Di PT. Kimia Farma Plant Jakarta

Abstract

Background: The pharmaceutical industry is a business entity that has a permit in accordance with the provisions of laws and regulations to carry out the activities of making drugs or drug ingredients. Therefore, the demands on the pharmaceutical industry are increasing because the role of the pharmaceutical industry is very important in terms of producing safe, efficacious and quality drugs. Quality, safe and effective drugs are produced through the process of implementing CPOB (Good Manufacturing Practices for Drugs). Objective: To understand the duties and roles of pharmacists regarding Good Manufacturing Practices in industry. Method: Research or PKPA activities were carried out by participating in work practice activities in the pharmaceutical industry of PT. Kimia Farma Plant Jakarta and comparing work practices carried out in the field with good manufacturing practice guidelines (CPOB). Results: PKPA activities at PT. Kimia Farma Plant Jakarta were carried out from September 9 to November 13, 2024. In general, there are two PKPA activities at PT. Kimia Farma Plant Jakarta, namely the provision of induction by departments related to pharmaceutical work at PT. Kimia Farma Plant Jakarta such as the PPIC, QC, QA, storage, packaging, engineering and maintenance departments, central weighing, HR and accounting and waste processing, and production. The implementation of CPOB at PT. Kimia Farma Plant Jakarta can be seen in various aspects of activities such as aspects of the quality system, personnel, and so on. Conclusion: The level of PT. Kimia Farma Tbk. Plant Jakarta has implemented aspects of CPOB well. This is proven by obtaining a CPOB certificate. Prospective pharmacists get a real picture of the implementation of CPOB at PT. Kimia Farma Tbk. Plant Jakarta in the form of implementing aspects of quality management, personnel, buildings and facilities, equipment, sanitation and hygiene, production, quality control, self-inspection and quality audit, handling complaints about products, product recalls and returned products, documentation, and qualification and validation.