Quality Engineer
Culver Tool and Engineering LLC - Plymouth, IN
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Ready to Elevate Your Career? Join SpiTrex CTE! At CTE, we offer more than just a job-we provide an environment where you can push boundaries, fuel your curiosity, and advance your career. We are committed to supporting your growth with unique programs designed to help you do your best work while maintaining a healthy work-life balance. Here's 5 ways that CTE makes a difference: Training/Career Development Bamboo's Path Track and WorkForge Learning Management System offer education for advancement when and where needed. Work/Life Harmony with Flextime Have an appointment or emergency pop up and you don't want to use your PTO? No worries! Use "Time Off without Pay" option of up to 3 hours and then make up missed time during the week. CTE Perks Whether it's Donut Friday, lower cost vending, monthly events, food trucks, book reading incentives called "CTE Reads", or FriYAY Fridays...CTE strives to maintain a positive culture and support our employees. CTE Incentives Employee referrals, 401(k) with 50% company match (up to 10% contribution), bonuses...but that's just the beginning! What if we told you there's more? We believe in keeping some surprises for your imagination. Get ready for a journey that goes beyond expectation! Health Benefits CTE provides vision, life insurance, and short-term disability insurance at NO COST to our employees. Medical and dental insurance with HSA is offered first of the month after hire. There is also a no-cost medical option through Schumacher Family Medicine. 1st Shift: Monday to Thursday, 6AM - 3PM; Friday, 6AM - 10AM Essential Functions: Facilitate standardized inspection and sample size methodology based on risk, process capability. New product involvement Inspection reduction based on process, production, or feature inspection issues for existing product Interact with In-process Inspection and Final Inspection, issue identification and resolution. MRB member, determine conformity of suspect parts Identifying failure modes and enacting countermeasures Audit quality processes and inspection methods Involved in CAPA's, Quality Alerts, Retraining and data collection as needed Oversight of CMM programming schedule as directed Participate in project management as needed Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements Other work-related tasks as assigned Competency: Mastery in Process Capability, lean inspection methodology Strong emphasis on understanding of GD+T Ability to comply with Quality System requirements Strong Understanding of statistical analysis Problem-Solving prowess Must be respectful and display a positive attitude Working knowledge of ISO 13485 Strong computer skills (MS Office) Educational Requirements: High School Diploma or GED preferred Experience: Minimum 3-5 years of Medical Device experience in Quality setting preferred Benefits Include: Medical, Vision and Dental Insurance Short-Term Disability Life Insurance 401(k) - 50% company match (up to 10% contribution) Paid vacation days Paid holidays
Created: 2026-03-04