QC Staff

    Ditayangkan 15/October/2016




    Responsibilities :
    • Prepare SOP, test procedure and QC  document
    • Perform QC Routine Analysis, and stability study.
    • Perform Analytical method validation (chemical, microbiology, bioassay and  in vivo).
    • Prepare Analytical method validation  protocol &  report.
    Requirements :
    • Maximum 30 years old.
    • Candidate must be possess at least diploma or bachelor degree in Biology,Microbiology, Chemical, Veterinary,  or Pharmacy.
    • Candidate has experience at least 1 or 2 years in Quality control.
    • Having knowledge of Pharmaceutical industry.
    • Fluently communicate in English by written and verbal.
    • Willing to trained and study Biotechnology.
    *CV and application letter must be in English.

    Tutup pada 29/October/2016

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    Jalan Rawa Gelam V Blok L kav 11-13, Jatinegara Cakung, Special Capital Region of Jakarta, Indonesia

    Deskripsi Perusahaan

    PT Etana Biotechnologies Indonesia has one of affiliate company Indonesia will invest in building a biosimilar Plant, where a drug substance (host cell) and manufacturing process will be carried out own (Locally manufacturer). Our portfolio consists of a wide range of biosimilars in the fields of hormone. Furthermore, looking forward to involved in the development of front-edge biotech products and has an impressive track record of major scientific discoveries.

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