Quality Engineering Intern
About The Position
Quality Engineer 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 Validation execution support, technical writing, compiling data, and records. 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.
- Actively enrolled in a relevant field of study such as Biology, Chemistry, Biochemistry, Biochemical Engineering, or other Life Sciences.
- Experience in self-leading a project
- Experience in working in a team environment
- Knowledgeable in Microsoft applications (Word, PowerPoint, Excel, Outlook)
Responsibilities
- Author basic validation protocols, validation execution, and data compilation.
- Assist with Documentation Scanning and Management
- Drive closures functions related to Kaizen initiatives
- Compile Data and Action Item into Metric Templates
- Adhere to Keenova’s Safety Requirements
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What This Job Offers
Career Level
Intern
Education Level
No Education Listed
