We are committed to providing reasonable accommodations for individuals with disabilities in our job application process. If you need assistance or an accommodation during the application or recruitment process due to a disability you may contact us at . We will treat all requests for accommodations discreetly.
*Note: There is no Visa sponsorship being offered for this position.
Kimball Electronics does not accept agency resumes. Please do not forward resumes to any recruiting alias or employee. Kimball Electronics is not responsible for any fees related to unsolicited resumes.
Position Overview
The mission of the Manufacturing Engineer Intern is to lead the development implementation of new manufacturing processes support existing manufacturing processes verify and drive improvements while meeting goals of quality cost and delivery for our customers.
Quick Summary
The ME Intern is responsible for developing assembly processes creating detailed manufacturing work instructions and testing procedures in support of regulatory addition this position supports continuous improvement by performing product/process analysis for quality improvements cost reductions and improved efficiency.
To be successful you must be self-motivated possess excellent communication skills time/project management skills a positive attitude be able to keep timely consistent and accurate records of work and train manufacturing our business it is critical the candidate can demonstrate a solid understanding of the importance of quality.
Basic Background Requirements
This position will require:
- Enrolled in a 4-year degree program in Engineering or Engineering Technology (Mechanical Electrical Biomedical)
- 3 months to 3 years relevant intern work experience with knowledge of a variety of production methods and materialspreferred
- Validation experience process and equipment qualification (IQ OQ PQ) Test Methods & R&Rs
- Process development/characterization experience
- Ability to analyze data using statistical methods
- Ability to compose professional documentation (Write protocols work instructions etc.)
- Ability to manage time and projects effectively while setting and meeting aggressive schedules
- Ability to analyze and solve problems utilizing root cause analysis tools
- Quality minded person with a focus on making data driven decisions
- Ability to understand business legal and regulatory requirements
- Ability to learn regulatory requirements FDA 21 CFR 820/GMP Medical Device Regulations
Key Performance Objectives
Required Experience:
Intern
We are committed to providing reasonable accommodations for individuals with disabilities in our job application process. If you need assistance or an accommodation during the application or recruitment process due to a disability you may contact us at . We will treat all requests for accommodations...
We are committed to providing reasonable accommodations for individuals with disabilities in our job application process. If you need assistance or an accommodation during the application or recruitment process due to a disability you may contact us at . We will treat all requests for accommodations discreetly.
*Note: There is no Visa sponsorship being offered for this position.
Kimball Electronics does not accept agency resumes. Please do not forward resumes to any recruiting alias or employee. Kimball Electronics is not responsible for any fees related to unsolicited resumes.
Position Overview
The mission of the Manufacturing Engineer Intern is to lead the development implementation of new manufacturing processes support existing manufacturing processes verify and drive improvements while meeting goals of quality cost and delivery for our customers.
Quick Summary
The ME Intern is responsible for developing assembly processes creating detailed manufacturing work instructions and testing procedures in support of regulatory addition this position supports continuous improvement by performing product/process analysis for quality improvements cost reductions and improved efficiency.
To be successful you must be self-motivated possess excellent communication skills time/project management skills a positive attitude be able to keep timely consistent and accurate records of work and train manufacturing our business it is critical the candidate can demonstrate a solid understanding of the importance of quality.
Basic Background Requirements
This position will require:
- Enrolled in a 4-year degree program in Engineering or Engineering Technology (Mechanical Electrical Biomedical)
- 3 months to 3 years relevant intern work experience with knowledge of a variety of production methods and materialspreferred
- Validation experience process and equipment qualification (IQ OQ PQ) Test Methods & R&Rs
- Process development/characterization experience
- Ability to analyze data using statistical methods
- Ability to compose professional documentation (Write protocols work instructions etc.)
- Ability to manage time and projects effectively while setting and meeting aggressive schedules
- Ability to analyze and solve problems utilizing root cause analysis tools
- Quality minded person with a focus on making data driven decisions
- Ability to understand business legal and regulatory requirements
- Ability to learn regulatory requirements FDA 21 CFR 820/GMP Medical Device Regulations
Key Performance Objectives
Required Experience:
Intern
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