Intern, Quality Systems
Insulet
This listing was originally posted on Insulet's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
Insulet started in 2000 with an idea and a mission to enable our customers to enjoy simplicity, freedom and healthier lives through the use of our Omnipod® product platform. In the last two decades we have improved the lives of hundreds of thousands of patients by using innovative technology that is wearable, waterproof, and lifestyle accommodating.
We are looking for highly motivated, performance driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!
Insulet Corporation (NASDAQ: PODD) is an innovative medical device company dedicated to making the lives of people with diabetes easier. Through its OmniPod Insulin Management System, Insulet seeks to expand the use of insulin pump therapy among people with insulin-dependent diabetes. Insulet's Delivery Systems business also partners with global pharmaceutical and biotechnology companies to tailor the OmniPod technology platform for the delivery of subcutaneous drugs across multiple therapeutic areas.
Responsibilities:
The main role will be to support a Green Belt project focused on document optimization and efficiency improvement. Responsibilities include assisting with process analysis, documentation updates, and workflow enhancements.
Review & update master documents list based on the actions identified by process owners either documents to be adopted as is, document requires content change or document not applicable.
Review the details of changes proposed by process owners for those documents requires content change and ensure that they are inline with global procedure/global practices. In case of any contradictions, appropriately communicate those to process owners.
Support local change admin by reviewing change orders on PLM and provide relevant inputs i.e., change order acceptable or rejected, to change admin for their action.
Support training specialist by ensuring all approved document trainings are adequately assigned to relevant user groups.
Follow up & track progress of document approval on PLM.
Assist in the development of quality metrics dashboard & key performance indicators used for operational review meetings.
Minimum Requirements:
Currently pursuing Bachelors in Industrial Engineering, quality management or manufacturing, or any related field preferably in the last study semester.
Possess excellent communication (both verbal and written), leadership, and interpersonal skills.
Critical thinking and problem-solving skills, with high attention to detail, especially in terms documentation review.
Ability to multitask and be able to contribute positively as and individual and as a team player.
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