● Monitor the supply chain from commercial to production.
● Monitor production plan.
● Monitor RM and PM status.
● Contact person between factories and companies.
● Document all production department’s data.
● Contact person between production departments and regulatory and QC departments.
● Daily report to the production manager.
● Monitor the handling of deviations, controlling changes, and corrective action issues to determine the task of the mentioned cases.
● Follow up on day-to-day production status from the office.
● Monitor all required materials to prevent production stop.
● Prepare required production documents.
Requirements
● At least two years in medicinal companies.
● Familiar with GMP concepts and principles.
● Familiar with pharmacology process equipment.
● Familiar with documentation principles (BMR, BPR, CTD, Protocol, writing SOP, log book, etc.).
● Familiar with production principles
● Teamwork ability.
● Ability to integrate with job description and daily report.
● Familiar with the definition of quality guarantee and control (validation, quality tools, etc.).
● Fluent in ICDL especially Excel and PowerPoint.
● UI level in English.