About the role#
This Engineering Co-Op position supports engineering tasks for existing products, product testing, and line extensions. You will work on-site in Grand Rapids, Michigan, to help the team meet project timelines and maintain regulatory standards.
What you'll do#
- Support the preparation and testing of products for Device Master Records (DMRs).
- Assist with validation documentation per FDA guidelines.
- Work on product improvement projects to meet project deadlines.
- Perform engineering product prototyping and testing.
- Help maintain compliance with FDA, Good Manufacturing Practices (GMP), and ISO standards.
What you'll need#
- Current enrollment as a junior or senior in an applicable engineering bachelor's degree program.
- Knowledge of medical device design and development processes.
- Proficiency with standard computer software and CAD software.
- Ability to work with mathematical concepts and apply them to practical situations.
- Solidworks experience is desired.
- Experience with plastic component manufacturing processes, such as injection molding, is preferred.
- Previous experience in a medical device, pharmaceutical, or plastics manufacturing facility is a plus.
Location & details#
- Location: Grand Rapids, Michigan.
- Work modality: On-site.
- Employment type: Full-time.
- Compensation: Paid position.
- Term: Rolling.
About AirLife
AirLife manufactures consumable breathing products for the medical sector. The company specializes in respiratory care, anesthesia, and patient monitoring equipment. It maintains a broad portfolio that serves environments ranging from emergency response to home care. Founded in 1981, the company is based in Grand Rapids, Michigan. It employs between 5,001 and 10,000 people.
How to get in at AirLife
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