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DESKRIPSI PEKERJAAN

 
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.
 
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Deskripsi Perusahaan

PT Etana Biotechnologies Indonesia

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.