Job Description

Description

Responsibilities

Support quality documentation activities, including reviewing, organizing, and updating SOPs, batch records, and logbooks under supervision.

Assist with quality investigations by gathering data, supporting root‑cause analysis, and helping track CAPA actions.

Perform routine GMP checks, such as verifying documentation completeness, monitoring training compliance, and supporting audit or inspection preparation.

Minimum Requirements

Enrolled in bachelor’s degree program related to Science, ideally pharmaceuticals.

  • Experience with MS Office, etc.
  • Motivated self-starter, operates independently, etc.
  • Strong communication skills, etc. 
  • Relationship with Others/Scope of Position

    Interact with other team members and cross functionally as needed

    DISCLAIMER:

    The above statements are intended to describe the gen...

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