Experience

PT Actavis Indonesia

• Indonesia
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Quality Assurance

  • Oct 2021 - Present

  - Control QA documentation in accordance with procedures- Coordinate the storage and destruction of QA documents- Provide QA documents required for registration and audit purposes- Review, follow up and upload the requisition of new or modify item or formula requisition in QAD system- Assist in coordination of data collecting for Quality Metrics, Quality Council and other activities related to Quality System responsibility- Review, edit and control all SOPs created in the EDMS (Electronic Document Management System)- Handle Change Control related to documentation changing

• Production

  • Oct 2017 - Oct 2021

  - Create Master Batch Record and Master Packaging Record- Create other supporting document for production process- Handle Change Control related to production documentation changing- Follow up CAPA related to production- Ensure implementation of CAPA on production document



PT Glaxo Wellcome Indonesia

• Internship

  • Mar 2017 - Apr 2017

  Quality Control Section, Quality Department Quality Control Section, Quality Department



Hidup Baru Pharmacy

• Internship

  • Feb 2017 - Feb 2017



South Jakarta Regional Health Department

• Internship

  • Jan 2017 - Jan 2017



University of Indonesia

• Indonesia
• Higher Education
• 700 & Above Employee

• Laboratory Assistant

  • Jan 2016 - May 2016

  Pharmaceutical Laboratory Pharmaceutical Laboratory



University of Indonesia

• Indonesia
• Higher Education
• 700 & Above Employee

• Laboratory Assistant

  • Sep 2015 - Oct 2015

  Pharmacokinetics and Pharmacology Laboratory Pharmacokinetics and Pharmacology Laboratory