Automation Engineer

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 View email address on click.appcast.io. 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. Benefits 3 weeks of PTO starting your 1st year in addition to 10 paid holidays. Potential for annual profit sharing bonus based on company performance. Major health, dental, vision, and complementary insurances offered starting day 1. 50% match on your first 6% of 401k contribution with opportunity for an employer contribution annually. Quick Summary As Automation Engineer, you will ensure that all automated manufacturing processes align with validation strategies and quality procedures. You will assist in the development of vision and programming standards and source‑code reviews for automated equipment. You will provide guidance to suppliers on new equipment builds, analyze production equipment performance, and develop plans to increase yield from underperforming inspections. The ability to manage competing projects while keeping accurate records is crucial. Demonstrating a solid understanding of the importance of quality and documentation is critical. You will work with Allen Bradley PLCs, Cognex Vision systems, and Fanuc Robots. Mastery of at least one of those systems is preferred. Basic Background Requirements 2+ years of experience in Automated Manufacturing. Validation experience, process and equipment qualification (IQ, OQ, PQ). Knowledge of Test Methods is a plus. Compose professional documentation (write protocols, work instructions, engineering studies, etc.). Manage time and projects effectively while setting and meeting ambitious schedules. Knowledgeable on regulatory requirements, FDA 21 CFR 820/GMP Medical Device Regulations. Working knowledge of Minitab. Knowledge of statistical techniques and sampling for process validation and process monitoring is desired. Key Performance Objectives Short Term (0 to 3 months) Learn KEIND Quality system requirements. Train on processes required to validate processes in the KEIND quality system. Build relationships with others. Begin training on the manufacturing line and the technology in use on the Automated Equipment. Maintain customer‑specific system documentation in support of FDA regulatory requirements. Midterm (3 to 6 months) Begin to audit current validations and identify solutions. Develop an understanding of completing engineering changes on the Automated Equipment and maintaining the validated state of the equipment. Learn and adopt Kimball Electronics philosophies and culture. Long term (6 to 12 months) Identify process improvement areas and develop a plan to implement those improvements. Write and complete test method validation and equipment qualifications. Demonstrate understanding of and attend training to FDA 21 CFR 820/GMP Medical Device Regulations. Kimball Electronics is a proud equal‑opportunity employer and considers qualified applicants without regard to race, color, religion, sex, national origin, ancestry, age, genetic information, sexual orientation, gender identity, marital or family status, veteran status, medical condition or disability or any other characteristic protected by applicable federal, state, or local law. We will consider qualified candidates with arrest and conviction records, consistent with applicable law, including the San Francisco Fair Chance Ordinance for roles based in San Francisco. #J-18808-Ljbffr Kimball Electronics