Supervisor Qualification, Validation & Calibration (Qa)

Company Description: Infion Pharma is an Indonesian pharmaceutical company located in Pandaan, East Java, was established on 2010. With the main vision of making Indonesia self reliante and self sufficient in healthcare. So the quality of the Indonesian's health became more assured, through the presence of Infion Pharma product which high quality and international standardized. Infion Pharma at present produces only ethical products and are planning to expand to other range of various therapeutic areas. With the continuous development, expected to be more and more new products that could be offered and can bring positive benefits to the people. Besides to reach the domestic products, Infion Pharma is also active to sell their products to other countries. This expansion proves that Indonesian products are also able to compete in global markets, so that the positive benefits of the products can be enjoyed by more and more people both domestically and internationally. With all the experience, facilities, technology, human resources, as well as the standardization that has been owned, Infion Pharma is interested in partnership opportunity with other manufactures, having capabilities in product portfolio in key of therapeutic areas. This synergy will be a compliment for us to broaden our product ranges together with our partners include marketing and distribution partners,pharmaceutical companies and MDDI ( Medical Device and Diagnostic Industry ) manufactures from the worldwide. Infion believes that every single partnership will generate multiple benefits for many entities. Infion will consistently pursue collaboration with high quality global healthcare companies such Bernofarm in Indonesia and Daewoong in Korea to provide high quality healthcare solutions for Indonesian and global community. :

• Memastikan bahwa semua aktivitas validasi, kalibrasi, dan kualifikasi dilakukan sesuai dengan peraturan cGMP, kebijakan internal, dan prosedur
• Mengembangkan dan memeligara program validasi, kalibrasi, dan kualifikasi yang komprehensif untuk peralatan, fasilitas, dan sistem yang digunakan dalam proses produksi farmasi
• Mengembangkan dan memehhara prosedur operas standar (SOP) untuk kegiatan validasi, kalibrasi, dan kualifikasi
• Melakukan penilaian risiko dan menentukan strategi kalibrasi, dan kualifikasi yang sesuai