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OSD Production Supervisor

PT. Daewoong Pharmaceutical Indonesia Bekasi, Jawa Barat

Deskripsi pekerjaan

PT. Daewoong Pharmaceutical Indonesia merupakan perusahaan manufaktur farmasi terkemuka bagian dari Daewoong Group yang berdedikasi menghasilkan produk kesehatan berkualitas tinggi. Fasilitas modern kami di Cikarang Timur, Jawa Barat, berdiri dengan standar operasional yang ketat dan profesional. Sebagai OSD Production Supervisor, Anda akan memegang peran kunci dalam memastikan efisiensi, keamanan, dan kepatuhan lini produksi sediaan padat oral (oral solid dosage). Tugas utama Anda meliputi penyiapan dan peninjauan dokumen GMP, pembuatan serta revisi SOP produksi, pengelolaan data manufaktur sesuai prinsip integritas data ALCOA, serta pengawasan jalannya proses produksi dan penanganan masalah teknis mesin secara tepat.

Tanggung jawab: Prepares/reviews various GMP documents related to manufacturing. Creates/revises and reviews SOPs related to production.; Manages the generated manufacturing related data as per the ALCOA principle of conduct during the entire life-cycle to comply with data integrity. Checks that the intermediate product production was carried out as per the related SOP and manufacturin; Checks if the equipment issue during the process and trouble-shooting is being appropriately carried out. Creates/revises the production equipment Recipe as an intermediate manager. Reviews whether the manufacturing batch record has been appropriatel.

Tanggung jawab

  • Prepares/reviews various GMP documents related to manufacturing. Creates/revises and reviews SOPs related to production.
  • Manages the generated manufacturing related data as per the ALCOA principle of conduct during the entire life-cycle to comply with data integrity. Checks that the intermediate product production was carried out as per the related SOP and manufacturin
  • Checks if the equipment issue during the process and trouble-shooting is being appropriately carried out. Creates/revises the production equipment Recipe as an intermediate manager. Reviews whether the manufacturing batch record has been appropriatel

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