QA & Validation Intern

Mallinckrodt Pharmaceuticals • Port Allen, LA

1d • Onsite

About The Position

The QA and Validation Projects Intern will learn the regulations, standards, and guidance that support both pharmaceutical and medical devices manufacturing and quality systems. This individual will support the Quality at the Port Allen, LA manufacturing facility in a wide range of functions including Management of Change (MOC) action items execution support, technical writing, compiling data, and creating dashboards for trending. In addition, in this role the individual has a unique opportunity to work on continuous improvement projects to support the Port Allen, LA manufacturing facility’s transformation initiatives through Kaizen initiatives. This includes learning lean manufacturing principles for improvement.

Requirements

• Must be currently enrolled in an undergraduate or graduate program.
• Experience in self-leading a project
• Experience in working in a team environment.
• Knowledgeable in Microsoft applications (Word, PowerPoint, Excel, Outlook)
• Time management
• Technical writing
• Computer applications
• Organizational Skills
• Presentation Skills

Responsibilities

• Quality Systems (QS) Project Coordination including tracking status of open projects and actions, calling meetings, and assistance with completion of open actions.
• Automate/ Optimize Quality System Reports for improved tracking
• Record retention optimization project, includes assisting with indexing GMP documents for preparing for offsite storage, scanning GMP documents for retention in the eDMS and organization of the document control room.
• Create a trending dashboard for Notice of Events for timely trend identification.
• Assist with streamlining hold process updates.

What This Job Offers

• Career Level: Intern
• Education Level: No Education Listed