Laporan Praktik Kerja Profesi Industri Farmasi di PT. Daewoong Biologics Indonesia Cikarang
Report on Professional Work Practice of Pharmacists Industry at PT Daewoong Biologics Indonesia Cikarang
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
PT. Daewoong Biologics Indonesia 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: PT. Daewoong Biologics Indonesia 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.

