ABSTRAKPraktek Kerja Profesi PKP di PT. Actavis Indonesia dilakukan pada tanggal 18 July ndash; 9 Septembet 2016. Tujuan pelaksanaan PKP untuk memperoleh gambaran dan pengalaman mengenai peran profesi apoteker di industri farmasi, khususnya dalam bidang pemastian mutu. Industri farmasi adalah badan usaha yang memiliki izin dari Menteri Kesehatan untuk melakukan kegiatan pembuatan obat atau bahan obat. Industri farmasi wajib memenuhi persyaratan Cara Pembuatan Obat yang Baik CPOB . Kegiatan yang dilakukan selama PKP antara lain pengenalan secara umum mengenai PT. Actavis Indonesia; induksi ke departemen yang berkaitan dengan pekerjaan kefarmasian yaitu gudang, AMD Pharmtech, Production Planning Inventory Control PPIC , Produksi Multi Product Facility MPF , Quality Control QC , Quality Assurance QA , Scientific Affairs SCA , serta Engineering dan EHS. Actavis Indonesia merupakan salah satu industri farmasi yang telah menerapkan pedoman CPOB dalam setiap kegiatan yang dilakukan, baik dalam proses produksi, pengawasan dan pemastian mutu, serta kegiatan lain yang terkait.

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ABSTRACTProfession internship at PT. Actavis Indonesia held on July 18th to September 9th 2016. The aim of profession internship to obtain an overview and experience of professional role of pharmacists in pharmaceutical industry, particularly in a quality assurance. Pharmaceutical industry is a corporation that has a license from Minister of Health to manufacturing of drugs or drug materials. Pharmaceutical industry is obliged to comply with the requirements of Good Manufacturing Practice for Pharmaceuticals GMP . Activities conducted during profession internship among other general introduction about PT. Actavis Indonesia induction into department which related pharmacy that are Warehouse, AMD Pharmtech, Production Planning Inventory Control PPIC , Production of Multi Product Facility MPF , Quality Control QC , Quality Assurance QA , Scientific Affairs SCA , and Engineering and EHS. Actavis Indonesia is the one of pharmaceutical industry which has implemented the GMP guidelines in each of activities, both in production process, control and quality assurance, and other related activities.