Regulatory Affairs Specialist (Hybrid - Austin, TX)

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  "last_changed_at": "2026-05-31T17:51:58.500Z",
  "active_status": "active"
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{
  "language": "en",
  "location": {
    "raw": "On-X Life Technologies, CryoLife - Austin, Austin, TX, United States",
    "city": "Austin",
    "region": "TX",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
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  "inferred_at": "2026-06-06T10:08:08.868Z",
  "launch_scope": {
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    "included": true,
    "language": "en",
    "location": {
      "raw": "On-X Life Technologies, CryoLife - Austin, Austin, TX, United States",
      "city": "Austin",
      "region": "TX",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
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{
  "Id": "9d629162-8c18-444d-9f63-0ca1c72d53e9",
  "Title": "Regulatory Affairs Specialist (Hybrid - Austin, TX)",
  "Distance": null,
  "Featured": false,
  "FullTime": true,
  "Locations": [
    {
      "Id": "e4e9736a-7729-5454-bcf5-06e26fe41ecc",
      "Address": {
        "City": "Austin",
        "Line1": "1300 East Anderson Lane",
        "Line2": "Bldg. A",
        "State": {
          "Code": "TX",
          "Name": "Texas"
        },
        "Country": {
          "Code": "USA",
          "Name": "United States"
        },
        "PostalCode": "787521731"
      },
      "Coordinates": {
        "Latitude": 30.334395716251297,
        "Longitude": -97.68948865090935
      },
      "DisplayName": false,
      "LocalizedName": "CryoLife - Austin",
      "SourceOfTruth": 1,
      "DisplayAddress": true,
      "DisplayLocationId": false,
      "DisplayDescription": true,
      "LocalizedLocationId": null,
      "DisplayStreetAddress": true,
      "LocalizedDescription": "On-X Life Technologies"
    }
  ],
  "MatchScore": 1,
  "PostedDate": "2026-04-30T14:28:49.367Z",
  "JobCategoryName": "Regulatory Affairs",
  "JobLocationType": 0,
  "OpportunityType": 0,
  "BriefDescription": "The Regulatory Affairs (RA) Specialist is responsible for developing regulatory strategies, preparing U.S. and international submissions, and obtaining and maintaining approval for products to markets worldwide. Additionally, the RA Specialist is responsible for assessment of device changes for regulatory implications and for performing regulatory activities in support of implementing these device changes.  The RA Specialist will work independently and manage their own regulatory projects.",
  "MatchedLocations": [],
  "RequisitionNumber": "REGUL002421"
}