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 general nature and level of work being performed by employees assigned to this classification.
They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.