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Analytical Assistant Scientist Jobs

Company

Dexa Group

Address Kota Bekasi, Indonesia
Employment type FULL_TIME
Salary
Category Praktisi Medis,Manufaktur Farmasi
Expires 2023-08-30
Posted at 9 months ago
Job Description
Company Description: In 1969, apt. Drs. Rudy Soetikno, a young pharmacist serving in the Indonesian Army, noted the scarce supply of medicine around him. To alleviate this situation, he decided to utilise his knowledge of medicine, setting up a small pharmacy with friends to produce tablets. This small pharmacy rapidly acquired a reputation for producing highly effective prescription drugs, facilitating its expansion into other pharmaceuticals, facilities, and markets. By 1978, its products were available across all parts of Indonesia. Its name, “Dexa”, was derived from the Greek word for ten, a symbol of perfection. Thus began Dexa Group, now among Southeast Asia’s largest pharmaceutical providers and a key strategic asset for Indonesia. The group applies its expertise in discovery, formulation, manufacturing, and marketing to supply highly sophisticated pharmaceuticals, nutraceuticals, supplements, and herbal medicines throughout Southeast Asia. It still maintains its trademark relentless emphasis on producing medicines of the highest quality. In fact, Dexa Group also works closely with the Indonesian Pharmaceutical Association to improve compliance standards across the entire industry. :
Merencanakan dan melakukan kegiatan penelitian dan pengembangan (litbang) di laboratorium Analytical untuk memperoleh metode analisis bahan baku & produk jadi sediaan farmasi yang valid, data hasil pengujian sampel formulasi dan data stabilita produk jadi yang mengacu pada regulasi pengembangan produk, sesuai dengan project dan target yang telah ditetapkan. Melakukan transfer knowledge metode analisa Analytical kepada site pengguna metode.
Responsibilities
  • Melakukan pengembangan, validasi dan transfer metode analisa, melakukan pengujian sampel formulasi, melakukan studi stabilita
  • Mempersiapkan dan memastikan kelengkapan penyiapan dokumen teknis yang dibutuhkan untuk registrasi produk
  • Memastikan compliance di area kerja, terlibat aktif dalam persiapan, pelaksanaan dan follow up hasil audit internal dan eksternal, improvement project, serta program lainnya yang terkait dengan pembangan individu, section, atau organisasi.
  • Membuat perencanaan penelitian mulai dari kebutuhan material, kebutuhan alat dan biaya beserta timeline dan eksekusinya (pengembangan, validasi dan transfer metode analisa, studi stabilita)
  • Melakukan identifikasi, menyusun, merevisi, dan/atau mengusulkan dokumen panduan kerja yang dibutuhkan, serta memelihara dokumen dan record di area kerja.