Registration Officer (Apoteker) Jobs

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. :

• Review dossier kelengkapan dokumen yang diperlukan untuk registrasi baik alkes maupun obat
• Update terhadap Peraturan yang terkait registrasi alkes maupun obat
• Menyiapkan seluruh kelengkapan dokumen termasuk materi leaflet untuk produk yang akan didaftarkan
• Melakukan follow up ke departemen terkait terkait dokumen yang dibutuhkan untuk registrasi
• Review raw data dan data penunjang lainnya terkait laporan yang akan disubmit ke BPOM