Project Intern

Department: Quality Management Systems (QMS)

Primary Area: Quality Systems, Documentation Management, Training Management & Risk Management

Responsibilities:

The intern should be able to:

• Understand the overall Quality Management System (QMS) framework and its interaction with site operations.
• Understand applicable Abbott Quality Policies, cGMP requirements, and site quality procedures.
• Support management of controlled documents including SOP issuance, revision, review, and archival activities.
• Participate in training management activities through ISOtrain and related systems.
• Support Quality Risk Assessment (QRA) activities and risk management processes.
• Understand document control requirements and Good Documentation Practices (GDP).
• Assist in review and maintenance of Site Master File and Site Quality Manual.
• Track QMS activities, training compliance, SOP periodic reviews, and risk management actions.
• Support quality system improvement initiatives and compliance monitoring activities.
• Independently complete a defined QMS-related project.

Specifications:

• Pharm D
• Fresh or prior internship experience in the same industry

Duration:

• 5 - 6 months