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