Quality Engineer

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  "last_changed_at": "2026-05-30T06:06:30.474Z",
  "active_status": "active"
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  "location": {
    "raw": "Plymouth, Indiana, 46563, United States",
    "city": "Plymouth",
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    "country": "United States",
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    "confidence": 0.95
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  "inferred_at": "2026-06-06T10:25:19.208Z",
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    "location": {
      "city": "Plymouth",
      "state": "Indiana"
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    "jobOpeningName": "Quality Engineer",
    "departmentLabel": "Quality",
    "employmentStatusLabel": "Full-Time"
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    "location": {
      "city": "Plymouth",
      "state": "Indiana",
      "postalCode": "46563",
      "addressCountry": "United States"
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    "datePosted": "2026-04-16",
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    "description": "<p><span style=\"font-size: 12pt; font-weight: bold\">Build More Than a Job—Build a Career at SpiTrex CTE</span></p>\n<p>At SpiTrex CTE, we invest in our people. You’ll find opportunities to grow, real flexibility, and a culture that values balance, development, and teamwork.</p>\n<p><br></p>\n<p><span style=\"font-weight: bold\">Why join CTE?</span></p>\n<ul>\n<li><span style=\"font-weight: bold\">Career Growth:</span><span> </span>Ongoing training and development through Bamboo Path Track &amp; WorkForge</li>\n<li><span style=\"font-weight: bold\">Flexibility:</span><span> </span>Flextime options that support real life</li>\n<li><span style=\"font-weight: bold\">Culture:</span><span> </span>Team events, Donut Fridays, food trucks, and more</li>\n<li><span style=\"font-weight: bold\">Rewards:</span><span> </span>Referral bonuses, quarterly bonuses, and a 401(k) with 50% company match (up to 10%)</li>\n<li><span style=\"font-weight: bold\">Benefits:</span><span> </span>No-cost vision, life, and short-term disability; dental &amp; medical with HSA or PPO options</li>\n</ul>\n<p><br></p>\n<p>Ready to grow with a company that values you? <span style=\"font-weight: bold\">Join SpiTrex CTE.</span></p>\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\"><br><span> </span></span><span><span style=\"color: rgb(0, 112, 192)\">1st Shift: Monday to Thursday, 6AM - 3PM; Friday, 6AM - 10AM</span></span></p>\n<p><br></p>\n<p><span style=\"font-weight: bold\">Essential Functions:</span></p>\n<ul>\n<li>Facilitate standardized inspection and sample size methodology based on risk, process capability.</li>\n<li>New product involvement</li>\n<li>Inspection reduction based on process, production, or feature inspection issues for existing product</li>\n<li>Interact with In-process Inspection and Final Inspection, issue identification and resolution.</li>\n<li>MRB member, determine conformity of suspect parts</li>\n<li>Identifying failure modes and enacting countermeasures</li>\n<li>Audit quality processes and inspection methods</li>\n<li>Involved in CAPA’s, Quality Alerts, Retraining and data collection as needed</li>\n<li>Oversight of CMM programming schedule as directed</li>\n<li>Participate in project management as needed</li>\n<li>Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements</li>\n<li>Other work-related tasks as assigned</li>\n</ul>\n<p><br></p>\n<p><span style=\"font-weight: bold\">Competency:</span></p>\n<ul>\n<li>Mastery in Process Capability, lean inspection methodology</li>\n<li>Strong emphasis on understanding of GD+T</li>\n<li>Ability to comply with Quality System requirements</li>\n<li>Strong Understanding of statistical analysis</li>\n<li>Problem-Solving prowess</li>\n<li>Must be respectful and display a positive attitude</li>\n<li>Working knowledge of ISO 13485</li>\n<li>Strong computer skills (MS Office)</li>\n</ul>\n<p><br></p>\n<p><span style=\"font-family: arial, helvetica, sans-serif\"><span style=\"font-weight: bold; text-decoration: underline\">Educational Requirements:</span> <br></span></p>\n<p><span style=\"font-family: arial, helvetica, sans-serif\">High School Diploma or GED preferred</span></p>\n<p><br></p>\n<p><span style=\"text-decoration: underline\"><span style=\"font-family: arial, helvetica, sans-serif; font-weight: bold\">Experience:</span></span></p>\n<p><span style=\"font-family: arial, helvetica, sans-serif\">Minimum 3-5 years of Medical Device experience in Quality setting preferred</span></p>\n<p><br></p>\n<p><span style=\"font-family: arial, helvetica, sans-serif\"><span style=\"font-weight: bold; text-decoration: underline\">Benefits Include:</span><br></span></p>\n<ul>\n<li><span style=\"font-family: arial, helvetica, sans-serif\"><span>Medical, Vision and Dental Insurance</span><br></span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif\"><span>Short-Term Disability</span><br></span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif\"><span>Life Insurance</span><br></span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif\"><span>401(k) - 50% company match (up to 10% contribution)</span><br></span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif\"><span>Paid vacation days</span><br></span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif\"><span>Paid holidays</span></span></li>\n</ul>",
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    "employmentStatusLabel": "Full-Time"
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