Qa Site Regulatory Senior Staff

• Create schedule and tracking Registration Dossier which is submitted to the Regulatory Department
• Prepare, create and complete QA documents related to the Registration Dossier to support the needs of the Regulatory Department in terms of product registration
• Handling and documented all quality documents in the quality assurance department including but not limited to level 1 and 2 quality documents, validation documents, risk assessments, audit documents, CAPA, and batch record.

Requirements

• Have min. Bachelor Degree in Pharmacy, Biology, or Biotechnology
• Have min. 2 years of experience in the Pharmaceutical Industry
• Excellent skills in prioritizing and time management
• Fluent in English (both written and spoken)
• Able to work independently (self-motivated) and within a complex team environment
• Willing to be stationed in East-Jakarta​
• Willing to work with limited resources in a Start-Up Environment
• Willing to work with overtime if needed