bluedoor data·Job Postings API·bluedoor.sh ↗

HomeCompaniesEduu Fa Us2 Oraclecloud Com CX 1Engineer III, Product Design

Engineer III, Product Design

Eduu Fa Us2 Oraclecloud Com CX 1 · Southington, CT, United States; Southington Plant · On Site · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyEduu Fa Us2 Oraclecloud Com CX 1
TitleEngineer III, Product Design
Normalized title-
Department / teamEngineering
LocationSouthington, CT, United States
Work modelOn Site
Employment typeFull Time
Salary-
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-03-27 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Eduu Fa Us2 Oraclecloud Com CX 1.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Oracle Recruiting Cloud / Fusion HCM.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Southington.Open
Department jobsActive postings in Engineering.Open
Work model jobsActive On Site postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyEduu Fa Us2 Oraclecloud Com CX 1
Source8b426a0a-f74a-41be-9961-6d7f8bb6b558
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description Position Summary The Senior Engineer, Product Development will support the Research and Development engineering team within ICU Medical’s Consumables business unit which includes Vascular Access. As part of this team, you will have a pivotal role in the development, and implementation of new products using specialized knowledge and skills typically acquired through advanced education. There will be an emphasis on Systems Engineering. The Senior Engineer can plan, lead and complete projects/matters of intermediate to high complexity working independently or with a team. Receives technical mentorship on complex problems, but independently resolves using new, improved or novel approaches and solutions. The Senior R&D Engineer will be expected to serve as the subject matter expert on a variety of topics. They will drive actionable project level tasks while adhering to established design control processes and good engineering and documentation practices. The Senior Engineer will be enthusiastic to develop their Product Development core competencies as well as their ability to direct, coach, mentor and align a cross functional team as needed. Essential Duties & Responsibilities Contributes to project planning: milestones, schedules, budgets, key decisions Defines Systems Architecture, Document Hierarchy and DHF structure Identifies and familiarizes with relevant clinical research, competitive landscape and prior art Plans and executes Voice of the Customer activities, defines and translates User Needs to Design Input Technical Specifications Defines applicable standards and regulations Leads risk management activities such as Hazard Analysis Contributes to design and process failure and effects analyses (DFMEA and PFMEA) Maintains requirement, risk management, and verification / validation traceability Invents practical solutions that advance the state of the art Collaborate with Design and Manufacturing Engineers to develop functional prototypes Plans feasibility, verification and validation activities in collaboration with cross functional team Performs characterization as required: establishes test plans, writes test protocols and methods, and authors test reports with data analysis and technical conclusions. Provides technical support to regulatory, sales, marketing and other functional areas as needed. Work on special assignments as they arise Engages others, promotes, and participates in Environmental, Health, and Safety initiatives, focusing on continuous improvement. Experience with root cause analysis, CAPA and NCR processes. Experience with global medical device regulations including FDA 510k and EU MDR (Medical Device Regulation) Knowledge & Skills Ability to quickly learn new concepts and technologies Proven hands-on experience developing medical devices in a gated development process Knowledge of manufacturing processes: extrusion, injection molding, machining, metal forming, common joining methods, inspection, etc. Experimental, computational and analytical skills such as DFSS tools, MiniTab software and statistical methods including design of experiments (DOE) Familiarity with ISO standards, including 13485, 14971, 62366, and 10555. Comfortable in clinical environments and understands product application: use cases, anatomy, physiology, biological interactions Good interpersonal, verbal and written communications skills. Minimum Qualifications, Education & Experience Must be at least 18 years of age Bachelor of Science degree from an accredited college or university in Mechanical or Biomedical Engineering or a related field. Minimum of four years' experience required. Advanced degree in related field preferred. Work Environment This is largely a sedentary role. This job operates in a professional office environment and routinely uses standard office equipment. May require travel up to 20% of the time Company ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges. With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings. We're ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you: Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization. The industry’s broadest IV smart pump offering covering large volume, pain management, and ambulatory needs. IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company. Significant US IV solutions manufacturing and supply capabilities. ICU Medical EEO Statement: ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status. If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at [email protected]. We are committed to providing equal access and opportunities for all candidates. ICU Medical EEO Policy Statement Know Your Rights: Workplace Discrimination is Illegal Poster ICU Medical CCPA Notice to Job Applicants

Full job record

Job IDfce4bb83db5e51c2f85a2be0b34fc1224b814dda
Org IDe310c35a-2ac5-4d1d-8128-a90883b48415
Source ID8b426a0a-f74a-41be-9961-6d7f8bb6b558
Board ID8b426a0a-f74a-41be-9961-6d7f8bb6b558
Provideroracle_hcm
Provider Job Key998
TitleEngineer III, Product Design
Normalized Title
Statusactive
Activeyes
Location TextSouthington, CT, United States; Southington Plant
DepartmentEngineering
Team
Employment Typefull_time
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionCT
CitySouthington
Salary RawDescription Position Summary The Senior Engineer, Product Development will support the Research and Development engineering team within ICU Medical’s Consumables business unit which includes Vascular Access. As part of this team, you will have a pivotal role in the development, and implementation of new products using specialized knowledge and skills typically acquired through advanced education. There will be an emphasis on Systems Engineering. The Senior Engineer can plan, lead and complete projects/matters of intermediate to high complexity working independently or with a team. Receives technical mentorship on complex problems, but independently resolves using new, improved or novel approaches and solutions. The Senior R&D Engineer will be expected to serve as the subject matter expert on a variety of topics. They will drive actionable project level tasks while adhering to established design control processes and good engineering and documentation practices. The Senior Engineer will be enthusiastic to develop their Product Development core competencies as well as their ability to direct, coach, mentor and align a cross functional team as needed. Essential Duties & Responsibilities Contributes to project planning: milestones, schedules, budgets, key decisions Defines Systems Architecture, Document Hierarchy and DHF structure Identifies and familiarizes with relevant clinical research, competitive landscape and prior art Plans and executes Voice of the Customer activities, defines and translates User Needs to Design Input Technical Specifications Defines applicable standards and regulations Leads risk management activities such as Hazard Analysis Contributes to design and process failure and effects analyses (DFMEA and PFMEA) Maintains requirement, risk management, and verification / validation traceability Invents practical solutions that advance the state of the art Collaborate with Design and Manufacturing Engineers to develop functional prototypes Plans feasibility, verification and validation activities in collaboration with cross functional team Performs characterization as required: establishes test plans, writes test protocols and methods, and authors test reports with data analysis and technical conclusions. Provides technical support to regulatory, sales, marketing and other functional areas as needed. Work on special assignments as they arise Engages others, promotes, and participates in Environmental, Health, and Safety initiatives, focusing on continuous improvement. Experience with root cause analysis, CAPA and NCR processes. Experience with global medical device regulations including FDA 510k and EU MDR (Medical Device Regulation) Knowledge & Skills Ability to quickly learn new concepts and technologies Proven hands-on experience developing medical devices in a gated development process Knowledge of manufacturing processes: extrusion, injection molding, machining, metal forming, common joining methods, inspection, etc. Experimental, computational and analytical skills such as DFSS tools, MiniTab software and statistical methods including design of experiments (DOE) Familiarity with ISO standards, including 13485, 14971, 62366, and 10555. Comfortable in clinical environments and understands product application: use cases, anatomy, physiology, biological interactions Good interpersonal, verbal and written communications skills. Minimum Qualifications, Education & Experience Must be at least 18 years of age Bachelor of Science degree from an accredited college or university in Mechanical or Biomedical Engineering or a related field. Minimum of four years' experience required. Advanced degree in related field preferred. Work Environment This is largely a sedentary role. This job operates in a professional office environment and routinely uses standard office equipment. May require travel up to 20% of the time Company ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges. With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings. We're ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you: Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization. The industry’s broadest IV smart pump offering covering large volume, pain management, and ambulatory needs. IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company. Significant US IV solutions manufacturing and supply capabilities. ICU Medical EEO Statement: ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status. If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at [email protected]. We are committed to providing equal access and opportunities for all candidates. ICU Medical EEO Policy Statement Know Your Rights: Workplace Discrimination is Illegal Poster ICU Medical CCPA Notice to Job Applicants
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://eduu.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/998
Apply URLhttps://eduu.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/998
First Seen At2026-05-31 18:05:41Z
Last Seen At2026-06-06 11:30:59Z
Last Checked At2026-06-06 11:30:59Z
Last Changed At2026-06-06 11:30:59Z
Inactive At
Source Posted At2026-03-27 17:17:01Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=eduu.fa.us2.oraclecloud.com|CX_1/date=2026-06-06/2026-06-06T11-30-48-802Z-02da400d3e34bd1db18cdfe149518dda26c990ccfdb9448688626151b7fcd9a3.json
Event Fields
{
  "content_hash": "fcaea5bc1a81b2c2242b2750964fb1ec907769a83e6da7180b296cc9467bc1fa",
  "source_hash": "7abfa3da713c90824f6d12dc4ff9d7b0c3c89d55ef414ca5b181b2cdf018ffad",
  "last_changed_at": "2026-06-06T11:30:59.118Z",
  "active_status": "active"
}
Parsed Structured
{
  "language": "en",
  "location": {
    "raw": "Southington, CT, United States",
    "city": "Southington",
    "region": "CT",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T11:30:59.073Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Southington, CT, United States",
      "city": "Southington",
      "region": "CT",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": "on_site",
  "salary_currency": null
}
Extensions
{}
Native Structured
{
  "detail": {
    "Id": "998",
    "Title": "Engineer III, Product Design",
    "media": [],
    "skills": [],
    "JobType": null,
    "Category": "Engineering",
    "JobGrade": null,
    "JobLevel": null,
    "JobShift": "First Shift",
    "WorkDays": null,
    "WorkHours": null,
    "WorkYears": null,
    "Department": null,
    "HotJobFlag": false,
    "StudyLevel": "Bachelor's Degree",
    "WorkMonths": null,
    "WorkerType": null,
    "GeographyId": 300000002504704,
    "JobFamilyId": 300000006850117,
    "JobFunction": "R&D",
    "JobSchedule": "Full time",
    "BusinessUnit": null,
    "ContractType": null,
    "Organization": null,
    "TrendingFlag": true,
    "workLocation": [
      {
        "Country": null,
        "Region1": null,
        "Region2": null,
        "Region3": null,
        "Building": null,
        "Latitude": "41.60691",
        "Longitude": "-72.87352",
        "LocationId": 300000386333803,
        "PostalCode": null,
        "TownOrCity": null,
        "AddressLine1": null,
        "AddressLine2": null,
        "AddressLine3": null,
        "AddressLine4": null,
        "LocationName": "Southington Plant"
      }
    ],
    "ContentLocale": "en",
    "HiringManager": null,
    "LegalEmployer": null,
    "RequisitionId": 300000531693881,
    "WorkplaceType": "On-site",
    "BusinessUnitId": 300000002477166,
    "OrganizationId": 300000002477166,
    "GeographyNodeId": 300000480425871,
    "JobFunctionCode": "R&D",
    "LegalEmployerId": 300000005961469,
    "PrimaryLocation": "Southington, CT, United States",
    "RequisitionType": "Non-Confidential",
    "NumberOfOpenings": null,
    "WorkplaceTypeCode": "ORA_ON_SITE",
    "BeFirstToApplyFlag": false,
    "otherWorkLocations": [],
    "secondaryLocations": [],
    "ExternalContactName": null,
    "ShortDescriptionStr": "The Senior Engineer, Product Development will support the Research and Development engineering team within ICU Medical’s Consumables business unit which includes Vascular Access. As part of this team, you will have a pivotal role in the development, and implementation of new products using specialized knowledge and skills typically acquired through advanced education. There will be an emphasis on Systems Engineering.",
    "ExternalContactEmail": null,
    "ExternalPostedEndDate": null,
    "OtherRequisitionTitle": null,
    "requisitionFlexFields": [],
    "ApplyWhenNotPostedFlag": false,
    "DomesticTravelRequired": null,
    "ExternalDescriptionStr": "<p><strong>Position Summary</strong></p>\n<p>The Senior Engineer, Product Development will support the Research and Development engineering team within ICU Medical’s Consumables business unit which includes Vascular Access.&nbsp;As part of this team, you will have a pivotal role in the development, and implementation of new products using specialized knowledge and skills typically acquired through advanced education. There will be an emphasis on Systems Engineering.</p>\n<p>The Senior Engineer can plan, lead and complete projects/matters of intermediate to high complexity working independently or with a team. Receives technical mentorship on complex problems, but independently resolves using new, improved or novel approaches and solutions. The Senior R&amp;D Engineer will be expected to serve as the subject matter expert on a variety of topics. They will drive actionable project level tasks while adhering to established design control processes and good engineering and documentation practices.&nbsp;</p>\n<p>The Senior Engineer will be enthusiastic to develop their Product Development core competencies as well as their ability to direct, coach, mentor and align a cross functional team as needed.&nbsp;</p>\n<p>&nbsp;</p>\n<p><strong>Essential Duties &amp; Responsibilities</strong></p>\n<ul>\n <li>Contributes to project planning: milestones, schedules, budgets, key decisions</li>\n <li>Defines Systems Architecture, Document Hierarchy and DHF structure</li>\n <li>Identifies and familiarizes with relevant clinical research, competitive landscape and prior art</li>\n <li>Plans and executes Voice of the Customer activities, defines and translates User Needs to Design Input Technical Specifications</li>\n <li>Defines applicable standards and regulations</li>\n <li>Leads risk management activities such as Hazard Analysis</li>\n <li>Contributes to design and process failure and effects analyses (DFMEA and PFMEA)</li>\n <li>Maintains requirement, risk management, and verification / validation traceability</li>\n <li>Invents practical solutions that advance the state of the art</li>\n <li>Collaborate with Design and Manufacturing Engineers to develop functional prototypes</li>\n <li>Plans feasibility, verification and validation activities in collaboration with cross functional team</li>\n <li>Performs characterization as required: establishes test plans, writes test protocols and methods, and authors test reports with data analysis and technical conclusions.</li>\n <li>Provides technical support to regulatory, sales, marketing and other functional areas as needed.</li>\n <li>Work on special assignments as they arise</li>\n <li>Engages others, promotes, and participates in Environmental, Health, and Safety initiatives, focusing on continuous improvement.</li>\n <li>Experience with root cause analysis, CAPA and NCR processes.</li>\n <li>Experience with global medical device regulations including FDA 510k and EU MDR (Medical Device Regulation)</li>\n</ul>\n<p style=\"margin-left:0.5in\">&nbsp;</p>\n<p><strong>Knowledge &amp; Skills</strong></p>\n<ul>\n <li>Ability to quickly learn new concepts and technologies</li>\n <li>Proven hands-on experience developing medical devices&nbsp;in a gated development process</li>\n <li>Knowledge of manufacturing processes: extrusion, injection molding, machining, metal forming, common joining methods, inspection, etc.</li>\n <li>Experimental, computational and analytical skills such as DFSS tools, MiniTab software and statistical methods including design of experiments (DOE)</li>\n <li>Familiarity with ISO standards, including 13485, 14971, 62366, and 10555.</li>\n <li>Comfortable in clinical environments and understands product application: use cases, anatomy, physiology, biological interactions</li>\n <li>Good interpersonal, verbal and written communications skills. &nbsp;</li>\n</ul>\n<p style=\"margin-left:0.5in\">&nbsp;</p>\n<p><strong>Minimum Qualifications, Education &amp; Experience&nbsp;</strong></p>\n<ul>\n <li>Must be at least 18 years of age</li>\n <li>Bachelor of Science degree from an accredited college or university in Mechanical or Biomedical Engineering or a related field.&nbsp;</li>\n <li>Minimum of four years' experience required. Advanced degree in related field preferred.</li>\n</ul>\n<p style=\"margin-left:0.5in\">&nbsp;</p>\n<p><strong>Work Environment&nbsp;</strong></p>\n<ul>\n <li>This is largely a sedentary role.&nbsp;</li>\n <li>This job operates in a professional office environment&nbsp;and&nbsp;routinely uses standard office equipment.&nbsp;</li>\n <li>May require travel up to 20% of the time</li>\n</ul>\n<p>&nbsp;</p>",
    "ObjectVerNumberProfile": null,
    "PrimaryLocationCountry": "US",
    "CorporateDescriptionStr": "<p class=\"MsoNormal\">ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges.</p>\n<p class=\"MsoNormal\">With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.</p>\n<p class=\"MsoNormal\">We're ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you:</p>\n<ul style=\"margin-top:0in\">\n <li>Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.</li>\n <li>The industry’s broadest IV smart pump offering covering large volume, pain management, and ambulatory needs.</li>\n <li>IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company.</li>\n <li>Significant US IV solutions manufacturing and supply capabilities.</li>\n</ul>\n<p class=\"MsoNormal\"><b>ICU Medical EEO Statement:</b></p>\n<p class=\"MsoNormal\">ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status.&nbsp;</p>\n<p class=\"MsoNormal\">If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at [email protected]. We are committed to providing equal access and opportunities for all candidates.</p>\n<div>\n <p class=\"MsoNormal\"><span><a href=\"https://www.icumed.com/media/lwkcbbam/icu-medical-eeo-policy-statement-2025.pdf\" target=\"_blank\" rel=\"nofollow\">ICU Medical EEO Policy Statement</a></span></p>\n <p class=\"MsoNormal\"><a href=\"https://www.icumed.com/media/0mrnh211/know_your_right_2023-2.pdf\" target=\"_blank\" rel=\"nofollow\"><span>Know Your Rights: Workplace Discrimination is Illegal Poster</span></a><span></span></p>\n <p class=\"MsoNormal\"><a href=\"https://www.icumed.com/media/1qwexl5a/icu-medical-job-applicant-privacy-notice-october-2024.pdf\" target=\"_blank\" rel=\"nofollow\"><span>ICU Medical CCPA Notice to Job Applicants</span></a></p>\n</div>",
    "ExternalPostedStartDate": "2026-03-27T17:17:01+00:00",
    "ExternalQualificationsStr": "",
    "InternalQualificationsStr": "",
    "OrganizationDescriptionStr": "",
    "primaryLocationCoordinates": [
      {
        "Latitude": "41.60022",
        "Longitude": "-72.87813",
        "CountryCode": "US",
        "GeographyId": 300000002504704,
        "GeographyNodeId": 300000480425871
      }
    ],
    "ExternalResponsibilitiesStr": "",
    "InternalResponsibilitiesStr": "",
    "InternationalTravelRequired": null
  },
  "list_job": {
    "Id": "998",
    "Title": "Engineer III, Product Design",
    "JobType": null,
    "Distance": 1774569600000,
    "JobShift": null,
    "Language": "US",
    "WorkDays": null,
    "JobFamily": null,
    "Relevancy": 3,
    "WorkHours": null,
    "Department": null,
    "HotJobFlag": false,
    "PostedDate": "2026-03-27",
    "StudyLevel": null,
    "WorkerType": null,
    "GeographyId": 300000002504704,
    "JobFunction": null,
    "JobSchedule": null,
    "BusinessUnit": null,
    "ContractType": null,
    "ManagerLevel": null,
    "Organization": null,
    "TrendingFlag": true,
    "workLocation": [
      {
        "Country": null,
        "Region1": null,
        "Region2": null,
        "Region3": null,
        "Building": null,
        "Latitude": 41.60691,
        "Longitude": -72.87352,
        "LocationId": 300000386333803,
        "PostalCode": null,
        "TownOrCity": null,
        "AddressLine1": null,
        "AddressLine2": null,
        "AddressLine3": null,
        "AddressLine4": null,
        "LocationName": "Southington Plant"
      }
    ],
    "LegalEmployer": null,
    "MediaThumbURL": null,
    "WorkplaceType": "On-site",
    "BusinessUnitId": 300000002477166,
    "OrganizationId": 300000002477166,
    "PostingEndDate": null,
    "LegalEmployerId": 300000005961469,
    "PrimaryLocation": "Southington, CT, United States",
    "WorkDurationYears": null,
    "WorkplaceTypeCode": "ORA_ON_SITE",
    "BeFirstToApplyFlag": false,
    "WorkDurationMonths": null,
    "otherWorkLocations": [],
    "secondaryLocations": [],
    "ShortDescriptionStr": "The Senior Engineer, Product Development will support the Research and Development engineering team within ICU Medical’s Consumables business unit which includes Vascular Access. As part of this team, you will have a pivotal role in the development, and implementation of new products using specialized knowledge and skills typically acquired through advanced education. There will be an emphasis on Systems Engineering.",
    "requisitionFlexFields": [],
    "DomesticTravelRequired": null,
    "PrimaryLocationCountry": "US",
    "ExternalQualificationsStr": null,
    "ExternalResponsibilitiesStr": null,
    "InternationalTravelRequired": null
  },
  "detail_meta": {
    "url": "https://eduu.fa.us2.oraclecloud.com/hcmRestApi/resources/latest/recruitingCEJobRequisitionDetails?expand=all&onlyData=true&finder=ById;Id=%22998%22,siteNumber=CX_1",
    "http_status": 200,
    "content_type": "application/json",
    "response_bytes": 10754
  },
  "detail_errors": []
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/fce4bb83db5e51c2f85a2be0b34fc1224b814dda?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/e310c35a-2ac5-4d1d-8128-a90883b48415JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/8b426a0a-f74a-41be-9961-6d7f8bb6b558JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/fce4bb83db5e51c2f85a2be0b34fc1224b814dda/eventsJSON