QC Stability & Analytical Development Supervisor


  • Pharmacist with at least 2 years experiences
  • Responsible, hard worker, fast learner, and strong leadership
  • Able to work individually and with team as well
  • Have received training and understand the Good Manufacturing Practices (CPOB)
  • Fluent in English both speaking and writing

Job Description:

  • Responsible for managing and supervising all activities related to product stability testing and analytical method.
  • Review monthly reports related to protocol of stability testing and analytical method report .
  • Review SOP/Form/List related to test and its related stability testing report and analytical method.
  • Review related to Worksheet for stability testing report and analytical method.
  • Review monthly reports regarding temperature of stability room, review verification data of measuring instruments (analytical balance, ph meter, meter conductivity, termohygrometer, etc) and evaluation report if any deviation founded.
  • Prepare SOP related to test and its related supporting activities in laboratorium.
  • Make a PJE (Application for Engineering Services) if there is damage or modification that can be done by an internal technician.
  • Provide training and qualify subordinates.
PT Medifarma Laboratories

Medifarma Laboratories is a pharmaceutical company based in Indonesia and an affiliate of United Laboratories, Inc., the biggest pharmaceutical company in the Philippines and a sister company of Darya-Varia Laboratoria, Indonesia. With its head office in Depok, on the southern outskirts of Jakarta, Indonesia’s capital, the Medifarma production facility is located in a complex that houses such big-name multinational pharmaceutical companies as Bayer Health Care, Glaxo Smith Kline, Pfizer, etc.