COOK Medical Fall 2024 Quality Engineering Co-op -Bloomington, Indiana

Requisition ID 2024-14307
Posting Date 1 week ago(4/3/2024 11:52 AM)
Job Location(s)
Bloomington IN United States
Travel
Less than 10%
Position Type
Internship
Company
Cook Inc - Bloomington
Category
Co-Op

Overview

The Fall Engineering Co-op Program is a paid co-op experience located in Bloomington, Indiana. We offer a 16-week rotation with assignments in Manufacturing Engineering. This position includes a housing stipend, 401(k), fitness center access, learning events, capstone presentation, and more. All Co-op positions are assigned a direct mentor and each position provides real-world experience with meaningful projects in the medical device manufacturing industry.  

Responsibilities

• Engineering CO-OPs may be involved in projects in the following areas: Equipment Application; Device Development; Manufacturing Support; New Technology Support and Development/ Process Control; Process Validation; Product Development; Quality Engineering; Project Engineering; Systems Support: Research and Technical Writing
• Produce engineering deliverables/documents; Provide analysis of recommended solutions to any obstacles or problems during production
• CO-OPs are assigned a direct mentor who provides a unique perspective of life at Cook. Mentors are chosen from Engineers and all mentors are responsible for guidance for their CO-OPs
• Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements
• Must maintain all training requirements for the position, while seeking out opportunities for continuous development and growth

Qualifications

- Engineering Co-Ops may be involved in projects in the following areas: Process Validation; Test Method Validation; Sustaining; Production; Continuous Improvement; Process Technology; Manufacturing Transfer; Supplier;    Engineering Test Lab; Research and Development; Quality Engineering  
- Utilize engineering knowledge to produce project deliverables / documents 
- Adhere to the Quality Management System (QMS) and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements 
- Must maintain all training requirements for the position, while seeking out opportunities for continuous development and growth 

- Must work and interact effectively and professionally with and for others throughout various levels of the global organization 
- Must strictly adhere to safety requirements 
- Maintain regular and punctual attendance 
- Must maintain company quality and quantity standards 
- Must have effective communication skills and ability to work in collaborative and independent work situations and environments with minimal supervision 
- Ability to remain calm and receptive in fast paced situations 

 

Minimum Work Experience/Educational Requirements / Qualifications: 

- College or University Junior or Senior preferred working towards a bachelor's degree in Engineering (Graduate students also considered)  
- Minimum GPA of 3.0 
- Must provide proof of enrollment in an accredited college or university 

 

Physical Requirements: 

- On-site and hybrid positions that work under general office environmental conditions 
- Sitting for extended periods, utilizes close visual acuity for working with computers, equipment, etc. 
- Personal protective equipment including safety glasses, lab coat and gloves may be required in some areas associated with this position 

- Must be able to perform the essential functions of the job, subject to reasonable accommodation requirements under the ADA.   

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