Quality Engineering Intern

Job Title

Quality Engineering Intern

Requisition

JR000015690 Quality Engineering Intern (Open)

Location

Port Allen, LA

Additional Locations

Job Description Summary

Job Description

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.

 

Key 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

Minimum Requirements:

Education and Experience:

• 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)

Skills/Qualifications:

• Time management

• Technical writing

• Computer applications

• Organization

• Leading presentations

 

Relationship with Others/Scope of Position:

The Quality Engineer intern will work with various functions at the Port Allen, LA manufacturing facility including Site Quality, Quality Control, Manufacturing Operations, Materials Management, Maintenance/Metrology, and Administration. This position may work with other members of the global Quality organization.

Working Conditions: onsite role; 5 days/week onsite

 

Disclaimer:  The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications.  Management reserves the right to change or modify such duties as required.

 

#LI-GN1

At Keenova, we believe that no one should be alone in their pursuit of better health. This purpose drives us as we pair quality therapeutics with human support—showing up in big moments and small to help patients find comfort and confidence.

 

We bring deep expertise and resolve to every therapeutic area we serve, including immunology, urology, men’s health, orthopedics, critical care, and pediatric endocrinology. We work with patients, care partners, and physicians to help them navigate healthcare system complexity and access therapies that make a meaningful difference.

 

We are Keenova—keen to solve, keen to serve. Learn more at www.keenova.com.