JOB DESCRIPTION:
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
The base pay for this position is
N/A
In specific locations, the pay range may vary from the range posted.
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Not Applicable