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Quality Engineer

Job in Plymouth, Marshall County, Indiana, 46563, USA
Listing for: SpiTrex Orthopedics
Full Time position
Listed on 2026-02-18
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Engineering, Quality Technician/ Inspector, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Ready to Elevate Your Career? Join Spi Trex 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 Work Forge 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 ISO
    13485, 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
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