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.
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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