گروه دارویی داریان سلامت

منتشر شده 6 سال پیش

Job Description

This position is reporting to Quality Assurance Manager. Main Responsibility: • Responsible for gathering and archiving project documents (drawings, progress reports, licenses, …) based on GMP rules and regulations which will be determined by QA Manager. • Supports and participates in cross-functional projects when assigned/appropriate. • Maintaining and improving quality of workflows and procedures. • Planning and performing for internal audits and self-inspection. • Following up with internal and external audit outcome.

Requirements

- Education: Having BS / MS in Chemistry or Microbiology or Pharmacy. - Experience: Minimum 3 years of experience in a pharmaceutical manufacturing products in a GMP environment. - Fluent in English. - Good at MS Office. - Frequent travelling ability.

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