Company Description
SK plasma, located in Jakarta, Indonesia, is a developer of plasma-derived medicine aimed at promoting human health and protecting the environment. The company focuses on plasma fractionation business and offers essential plasma-derived products to treat diseases like congenital immunodeficiency diseases and hemophilia, contributing to the well-being of human lives.
Role Description
- Implementing methods to inspect, test and evaluate products and production equipment.
- Ensuring that products adhere to quality standards.
- Preparing reports by collecting, analyzing and summarizing data.
- Tracking products through the manufacturing process to guarantee that each part of the process is correct.
- Performing detailed and recorded inspections of final products so the products are up to industry and company standards.
Qualifications
- Minimum Bachelors Degree in Pharmacy, Biotechnology, or any related fields.
- Minimum 3 years experience working at Quality Department in Pharmaceutical Companies.
- Working experience in Korean Pharmaceutical Company is preferred
- Experience working and communicate with KEMENKES and BPOM.
- Familiarity with Local and International Quality Standards.
- Problem Solving & Root Cause Analysis.
- Required Languages : Bahasa Indonesia, and fluent in English is a must.
- Fluent in Korean Language is a plus point.
