QA Post Market Engineer (All Levels)

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  "last_changed_at": "2026-05-31T17:46:16.164Z",
  "active_status": "active"
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{
  "language": "en",
  "location": {
    "raw": "Gainesville, FL, Gainesville, Florida",
    "city": "Gainesville",
    "region": "FL",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.9
  },
  "salary_max": 0,
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  "inferred_at": "2026-06-06T10:57:35.186Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Gainesville, FL, Gainesville, Florida",
      "city": "Gainesville",
      "region": "FL",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.9
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
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  "workplace_type": "on_site",
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{}

{
  "id": "508555",
  "job": {
    "id": "515312",
    "division": {
      "id": "210",
      "name": "Advita Ortho"
    },
    "department": {
      "id": "11427",
      "name": "Quality"
    },
    "requisition_id": "EXAC0852",
    "structure_custom_group_one": null
  },
  "url": "https://advitaortho.pinpointhq.com/en/postings/1446803b-fe04-4d35-886e-2d04a3c7bf5b",
  "path": "/en/postings/1446803b-fe04-4d35-886e-2d04a3c7bf5b",
  "title": "QA Post Market Engineer (All Levels) ",
  "benefits": "",
  "location": {
    "id": "5732",
    "city": "Gainesville",
    "name": "Gainesville, FL",
    "province": "Florida",
    "postal_code": "32653"
  },
  "deadline_at": null,
  "description": "<div><!--block-->The QA Post Market Engineer supports post-market surveillance activities by performing product complaint investigations, root cause analysis, and product evaluations. This role plays a key part in ensuring compliance with regulatory requirements, driving continuous improvement, and maintaining the quality and safety of products in the field.</div>",
  "compensation": null,
  "reporting_to": "Director Post Market Surveillance",
  "workplace_type": "onsite",
  "benefits_header": "",
  "employment_type": "full_time",
  "workplace_type_text": "Onsite",
  "compensation_maximum": null,
  "compensation_minimum": null,
  "compensation_visible": false,
  "employment_type_text": "Full Time",
  "key_responsibilities": "<ul><li><!--block-->Conduct complaint investigations, including product analysis, testing, and root cause determination in accordance with company procedures</li><li><!--block-->Apply sound engineering principles and problem-solving techniques to evaluate product issues</li><li><!--block-->Perform risk assessments and complaint trend/history reviews</li><li><!--block-->Escalate findings appropriately and collaborate with cross-functional teams to ensure thorough investigations</li><li><!--block-->Document all investigation activities in compliance with internal procedures and regulatory standards</li><li><!--block-->Support ongoing product improvement efforts for orthopedic implants and instruments</li><li><!--block-->Assist with quality system processes, including CAPAs, HHEs, and NCRs</li><li><!--block-->Contribute to meeting departmental metrics and performance goals</li><li><!--block-->Support internal and external audits related to complaint handling</li><li><!--block-->Draft investigation summaries and responses for customers, as needed</li><li><!--block-->Assist in developing and updating procedures, work instructions, and technical documentation</li><li><!--block-->Participate in continuous improvement initiatives and team training efforts</li><li><!--block-->Ensure adherence to the company Quality System and applicable FDA/ISO regulations</li></ul>",
  "compensation_currency": null,
  "compensation_frequency": null,
  "skills_knowledge_expertise": "<div><!--block--><strong>Education:</strong></div><ul><li><!--block-->Bachelor’s degree in Engineering required (Mechanical or Biomedical preferred); Master’s degree a plus</li></ul><div><!--block--><strong>&nbsp;Experience:</strong></div><ul><li><!--block-->Foundational knowledge of engineering principles such as mechanical design, GD&amp;T, CAD, materials, and analysis methods</li><li><!--block-->Experience or exposure to root cause analysis, risk assessment, and technical documentation</li><li><!--block-->Prior experience in a medical device or FDA-regulated environment preferred</li><li><!--block-->Familiarity with FDA/ISO quality systems preferred</li></ul><div><!--block--><strong>Functional/Technical Knowledge, Skills and Abilities Required:</strong></div><ul><li><!--block-->Strong written and verbal communication skills</li><li><!--block-->Detail-oriented with a high level of accuracy in data analysis and documentation</li><li><!--block-->Excellent organizational and time management skills</li><li><!--block-->Ability to work both independently and collaboratively in a team environment</li><li><!--block-->Problem-solving mindset with the ability to apply technical principles creatively</li><li><!--block-->Proficiency in Microsoft Office applications</li></ul><div><!--block--><br></div>",
  "key_responsibilities_header": "Key Responsibilities",
  "skills_knowledge_expertise_header": "Skills Knowledge and Expertise"
}