bluedoor data·Job Postings API·bluedoor.sh ↗

HomeCompaniesHcjy Fa Us2 Oraclecloud Com CX 1Regulatory Affairs Senior Specialist

Regulatory Affairs Senior Specialist

Hcjy Fa Us2 Oraclecloud Com CX 1 · IN-Gurgaon, Gurgaon, Haryana, IN · On Site · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyHcjy Fa Us2 Oraclecloud Com CX 1
TitleRegulatory Affairs Senior Specialist
Normalized title-
Department / teamCompliance, Risk & Legal
LocationHaryana, IN, United States
Work modelOn Site
Employment typeFull Time
Salary-
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-06-02 / 2026-06-02
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Hcjy 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 Haryana.Open
Department jobsActive postings in Compliance, Risk & Legal.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

CompanyHcjy Fa Us2 Oraclecloud Com CX 1
Source063b269b-849a-4216-8d0d-8fc4f7efa6f5
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description Support new product registrations and license renewals for medical device and fertility products in India, Sri Lanka, and Nepal, ensuring compliance with applicable local regulatory requirements. Act as the primary regulatory liaison with external consultants, distributors, and local health authorities, coordinating all regulatory‑related communications, submissions, responses, and follow‑ups. Ensure timely progression of regulatory activities, proactive issue resolution, and alignment between internal stakeholders and external parties to support uninterrupted market access and regulatory compliance. Responsibilities Provide regulatory input and guidance for assigned countries on regulatory‑related matters. Ensure product registrations are reviewed, maintained, and renewed in accordance with local regulatory requirements. Provide regular updates to the management team on product registration and renewal status and proactively propose action plans in the event of delays. Collaborate closely with regional and global teams on regulatory documentation and Regulatory Information Management Systems (RIMS). Prepare, coordinate, and submit regulatory applications to local health authorities and/or distributors, as appropriate. Support regulatory strategy development for new products, product changes, and market expansions in assigned countries. Track and monitor regulatory timelines and commitments, escalating risks and constraints proactively to minimize delays. Coordinate with Quality, Manufacturing, Supply Chain, and Commercial teams to ensure regulatory compliance and uninterrupted product supply. Maintain awareness of local regulatory updates, guidelines, and new regulations, including their implementation and impact on the business. Establish and maintain relationships with local medical device industry associations and participate in discussions on regulatory policies, where applicable. Support internal regulatory audits as well as external regulatory or compliance audits, as required. Support other relevant regulatory affairs activities as assigned. Travel: 5 % Qualifications Knowledge, Skills and Abilities: 3 -5 years of experience in Medical Device Regulatory Affairs Knowledge on GDPMD would be an advantage Knowledge on post market reporting would be an advantage Mandatory knowledge for regulatory submission in India Additional knowledge of regulatory environment in Sri Lanka and Nepal would be an advantage Work Environment: Office based Experience: 3 – 5 years experience in Medical Device Industry Education: Bachelor’s degree in any Science related field

Full job record

Job IDb3c132c99af4f0e43a92fe8b9a7c87ee70be5300
Org IDfd5c005d-2102-408b-80a5-9404893f9b97
Source ID063b269b-849a-4216-8d0d-8fc4f7efa6f5
Board ID063b269b-849a-4216-8d0d-8fc4f7efa6f5
Provideroracle_hcm
Provider Job Key10238
TitleRegulatory Affairs Senior Specialist
Normalized Title
Statusactive
Activeyes
Location TextIN-Gurgaon, Gurgaon, Haryana, IN
DepartmentCompliance, Risk & Legal
Team
Employment Typefull_time
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionIN
CityHaryana
Salary RawDescription Support new product registrations and license renewals for medical device and fertility products in India, Sri Lanka, and Nepal, ensuring compliance with applicable local regulatory requirements. Act as the primary regulatory liaison with external consultants, distributors, and local health authorities, coordinating all regulatory‑related communications, submissions, responses, and follow‑ups. Ensure timely progression of regulatory activities, proactive issue resolution, and alignment between internal stakeholders and external parties to support uninterrupted market access and regulatory compliance. Responsibilities Provide regulatory input and guidance for assigned countries on regulatory‑related matters. Ensure product registrations are reviewed, maintained, and renewed in accordance with local regulatory requirements. Provide regular updates to the management team on product registration and renewal status and proactively propose action plans in the event of delays. Collaborate closely with regional and global teams on regulatory documentation and Regulatory Information Management Systems (RIMS). Prepare, coordinate, and submit regulatory applications to local health authorities and/or distributors, as appropriate. Support regulatory strategy development for new products, product changes, and market expansions in assigned countries. Track and monitor regulatory timelines and commitments, escalating risks and constraints proactively to minimize delays. Coordinate with Quality, Manufacturing, Supply Chain, and Commercial teams to ensure regulatory compliance and uninterrupted product supply. Maintain awareness of local regulatory updates, guidelines, and new regulations, including their implementation and impact on the business. Establish and maintain relationships with local medical device industry associations and participate in discussions on regulatory policies, where applicable. Support internal regulatory audits as well as external regulatory or compliance audits, as required. Support other relevant regulatory affairs activities as assigned. Travel: 5 % Qualifications Knowledge, Skills and Abilities: 3 -5 years of experience in Medical Device Regulatory Affairs Knowledge on GDPMD would be an advantage Knowledge on post market reporting would be an advantage Mandatory knowledge for regulatory submission in India Additional knowledge of regulatory environment in Sri Lanka and Nepal would be an advantage Work Environment: Office based Experience: 3 – 5 years experience in Medical Device Industry Education: Bachelor’s degree in any Science related field
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://hcjy.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/10238
Apply URLhttps://hcjy.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/10238
First Seen At2026-06-02 11:20:58Z
Last Seen At2026-06-06 18:54:57Z
Last Checked At2026-06-06 18:54:57Z
Last Changed At2026-06-06 11:19:22Z
Inactive At
Source Posted At2026-06-02 08:29:27Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=hcjy.fa.us2.oraclecloud.com|CX_1/date=2026-06-06/2026-06-06T18-54-41-336Z-a5965b54189b18264a41117402013b6b0f9a2ca665e465fc49b0f52e26911a85.json
Event Fields
{
  "content_hash": "92459320844043bc9cbcf21eb0ee887c272b865f6ca5ad60c31dda049a7526c7",
  "source_hash": "5444588e8c280c2e1a7557eced01f29f39af9bf6571996317c1b2bce5881a40d",
  "last_changed_at": "2026-06-06T11:19:22.080Z",
  "active_status": "active"
}
Parsed Structured
{
  "language": "en",
  "location": {
    "raw": "IN-Gurgaon, Gurgaon, Haryana, IN",
    "city": "Haryana",
    "region": "IN",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.9
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T18:54:57.308Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "IN-Gurgaon, Gurgaon, Haryana, IN",
      "city": "Haryana",
      "region": "IN",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.9
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": "on_site",
  "salary_currency": null
}
Extensions
{}
Native Structured
{
  "detail": {
    "Id": "10238",
    "Title": "Regulatory Affairs Senior Specialist",
    "media": [],
    "skills": [],
    "JobType": null,
    "Category": "Compliance, Risk & Legal",
    "JobGrade": null,
    "JobLevel": null,
    "JobShift": null,
    "WorkDays": null,
    "WorkHours": null,
    "WorkYears": null,
    "Department": null,
    "HotJobFlag": false,
    "StudyLevel": null,
    "WorkMonths": null,
    "WorkerType": null,
    "GeographyId": 300000157689179,
    "JobFamilyId": 300000239489011,
    "JobFunction": "Regulatory Affairs ",
    "JobSchedule": "Full time",
    "BusinessUnit": null,
    "ContractType": null,
    "Organization": null,
    "TrendingFlag": true,
    "workLocation": [
      {
        "Country": "IN",
        "Region1": null,
        "Region2": "Haryana",
        "Region3": null,
        "Building": null,
        "Latitude": "28.47894",
        "Longitude": "77.09193",
        "LocationId": 300000027311044,
        "PostalCode": "122002",
        "TownOrCity": "Gurgaon",
        "AddressLine1": "01-B, Ground Floor, Tower B",
        "AddressLine2": "Global Business Park",
        "AddressLine3": "Guru Dronacharya Metro Station",
        "AddressLine4": null,
        "LocationName": "IN-Gurgaon"
      }
    ],
    "ContentLocale": "en",
    "HiringManager": null,
    "LegalEmployer": null,
    "RequisitionId": 300000420595574,
    "WorkplaceType": "On-site",
    "BusinessUnitId": 300000015798292,
    "OrganizationId": 300000039524046,
    "GeographyNodeId": 100002189498561,
    "JobFunctionCode": "RA",
    "LegalEmployerId": 300000015801661,
    "PrimaryLocation": "Gurgaon, Haryana, India",
    "RequisitionType": "Professional",
    "NumberOfOpenings": null,
    "WorkplaceTypeCode": "ORA_ON_SITE",
    "BeFirstToApplyFlag": false,
    "otherWorkLocations": [],
    "secondaryLocations": [],
    "ExternalContactName": null,
    "ShortDescriptionStr": "Lead product registration, renewals, and all activities related to regulatory for India, Sri Lanka and Nepal.",
    "ExternalContactEmail": null,
    "ExternalPostedEndDate": null,
    "OtherRequisitionTitle": null,
    "requisitionFlexFields": [
      {
        "Value": "CooperSurgical",
        "Prompt": "Company",
        "ControlType": "SingleChoiceList",
        "SequenceNumber": 18
      }
    ],
    "ApplyWhenNotPostedFlag": null,
    "DomesticTravelRequired": null,
    "ExternalDescriptionStr": "<p style=\"margin:0in;text-align:justify;\"><span lang=\"EN-SG\">Support new product registrations and license renewals for medical device and fertility products in India, Sri Lanka, and Nepal, ensuring compliance with applicable local regulatory requirements. Act as the primary regulatory liaison with external consultants, distributors, and local health authorities, coordinating all regulatory‑related communications, submissions, responses, and follow‑ups. Ensure timely progression of regulatory activities, proactive issue resolution, and alignment between internal stakeholders and external parties to support uninterrupted market access and regulatory compliance.</span></p>",
    "ObjectVerNumberProfile": null,
    "PrimaryLocationCountry": "IN",
    "CorporateDescriptionStr": "",
    "ExternalPostedStartDate": "2026-06-02T08:29:27+00:00",
    "ExternalQualificationsStr": "<p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Knowledge, Skills and Abilities:</strong></span></p><p style=\"margin:0in;\">&nbsp;</p><ul style=\"list-style-type:disc;\"><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">3 -5 years of experience in Medical Device Regulatory Affairs</span></li><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Knowledge on GDPMD would be an advantage</span></li><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Knowledge on post market reporting would be an advantage</span></li><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Mandatory knowledge for regulatory submission in India</span></li><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Additional knowledge of regulatory environment in Sri Lanka and Nepal would be an advantage</span></li></ul><p>&nbsp;</p><p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Work Environment:</strong></span></p><ul style=\"list-style-type:disc;\"><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Office based</span></li></ul><p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Experience:</strong></span></p><ul style=\"list-style-type:disc;\"><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">3 – 5 years experience in Medical Device Industry</span></li></ul><p style=\"margin:0in;\">&nbsp;</p><p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Education:</strong></span></p><ul style=\"list-style-type:disc;\"><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Bachelor’s degree in any Science related field</span></li></ul><p>&nbsp;</p>",
    "InternalQualificationsStr": "<p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Knowledge, Skills and Abilities:</strong></span></p><p style=\"margin:0in;\">&nbsp;</p><ul style=\"list-style-type:disc;\"><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">3 -5 years of experience in Medical Device Regulatory Affairs</span></li><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Knowledge on GDPMD would be an advantage</span></li><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Knowledge on post market reporting would be an advantage</span></li><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Mandatory knowledge for regulatory submission in India</span></li><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Additional knowledge of regulatory environment in Sri Lanka and Nepal would be an advantage</span></li></ul><p>&nbsp;</p><p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Work Environment:</strong></span></p><ul style=\"list-style-type:disc;\"><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Office based</span></li></ul><p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Experience:</strong></span></p><ul style=\"list-style-type:disc;\"><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">3 – 5 years experience in Medical Device Industry</span></li></ul><p style=\"margin:0in;\">&nbsp;</p><p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Education:</strong></span></p><ul style=\"list-style-type:disc;\"><li><span style=\"font-size:10.0pt;\" lang=\"EN-US\">Bachelor’s degree in any Science related field</span></li></ul><p>&nbsp;</p>",
    "OrganizationDescriptionStr": "",
    "primaryLocationCoordinates": [
      {
        "Latitude": "28.47737",
        "Longitude": "77.06914",
        "CountryCode": "IN",
        "GeographyId": 300000157689179,
        "GeographyNodeId": 100002189498561
      }
    ],
    "ExternalResponsibilitiesStr": "<ul style=\"list-style-type:disc;\"><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Provide regulatory input and guidance for assigned countries on regulatory‑related matters.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Ensure product registrations are reviewed, maintained, and renewed in accordance with local regulatory requirements.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Provide regular updates to the management team on product registration and renewal status and proactively propose action plans in the event of delays.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Collaborate closely with regional and global teams on regulatory documentation and Regulatory Information Management Systems (RIMS).&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Prepare, coordinate, and submit regulatory applications to local health authorities and/or distributors, as appropriate.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Support regulatory strategy development for new products, product changes, and market expansions in assigned countries.</span></p></li></ul><p style=\"line-height:15.0pt;margin:0in;\">&nbsp;</p><ul style=\"list-style-type:disc;\"><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Track and monitor regulatory timelines and commitments, escalating risks and constraints proactively to minimize delays.</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Coordinate with Quality, Manufacturing, Supply Chain, and Commercial teams to ensure regulatory compliance and uninterrupted product supply.</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Maintain awareness of local regulatory updates, guidelines, and new regulations, including their implementation and impact on the business.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Establish and maintain relationships with local medical device industry associations and participate in discussions on regulatory policies, where applicable.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Support internal regulatory audits as well as external regulatory or compliance audits, as required.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Support other relevant regulatory affairs activities as assigned.</span></p></li></ul><p style=\"margin:0in;\">&nbsp;</p><p style=\"margin:0in;\">&nbsp;</p><p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Travel:</strong>&nbsp;</span></p><p style=\"margin:0in;\"><span lang=\"EN-US\">5 %</span></p>",
    "InternalResponsibilitiesStr": "<ul style=\"list-style-type:disc;\"><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Provide regulatory input and guidance for assigned countries on regulatory‑related matters.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Ensure product registrations are reviewed, maintained, and renewed in accordance with local regulatory requirements.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Provide regular updates to the management team on product registration and renewal status and proactively propose action plans in the event of delays.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Collaborate closely with regional and global teams on regulatory documentation and Regulatory Information Management Systems (RIMS).&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Prepare, coordinate, and submit regulatory applications to local health authorities and/or distributors, as appropriate.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Support regulatory strategy development for new products, product changes, and market expansions in assigned countries.</span></p></li></ul><p style=\"line-height:15.0pt;margin:0in;\">&nbsp;</p><ul style=\"list-style-type:disc;\"><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Track and monitor regulatory timelines and commitments, escalating risks and constraints proactively to minimize delays.</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Coordinate with Quality, Manufacturing, Supply Chain, and Commercial teams to ensure regulatory compliance and uninterrupted product supply.</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Maintain awareness of local regulatory updates, guidelines, and new regulations, including their implementation and impact on the business.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Establish and maintain relationships with local medical device industry associations and participate in discussions on regulatory policies, where applicable.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Support internal regulatory audits as well as external regulatory or compliance audits, as required.&nbsp;</span></p></li><li><p style=\"line-height:15.0pt;\"><span style=\"font-size:10.0pt;\" lang=\"EN-SG\">Support other relevant regulatory affairs activities as assigned.</span></p></li></ul><p style=\"margin:0in;\">&nbsp;</p><p style=\"margin:0in;\">&nbsp;</p><p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Travel:</strong>&nbsp;</span></p><p style=\"margin:0in;\"><span lang=\"EN-US\">5 %</span></p>",
    "InternationalTravelRequired": null
  },
  "list_job": {
    "Id": "10238",
    "Title": "Regulatory Affairs Senior Specialist",
    "JobType": null,
    "Distance": 1780358400000,
    "JobShift": null,
    "Language": "US",
    "WorkDays": null,
    "JobFamily": null,
    "Relevancy": 8,
    "WorkHours": null,
    "Department": null,
    "HotJobFlag": false,
    "PostedDate": "2026-06-02",
    "StudyLevel": null,
    "WorkerType": null,
    "GeographyId": 300000157689179,
    "JobFunction": null,
    "JobSchedule": null,
    "BusinessUnit": null,
    "ContractType": null,
    "ManagerLevel": null,
    "Organization": null,
    "TrendingFlag": true,
    "workLocation": [
      {
        "Country": "IN",
        "Region1": null,
        "Region2": "Haryana",
        "Region3": null,
        "Building": null,
        "Latitude": 28.47894,
        "Longitude": 77.09193,
        "LocationId": 300000027311044,
        "PostalCode": "122002",
        "TownOrCity": "Gurgaon",
        "AddressLine1": "01-B, Ground Floor, Tower B",
        "AddressLine2": "Global Business Park",
        "AddressLine3": "Guru Dronacharya Metro Station",
        "AddressLine4": null,
        "LocationName": "IN-Gurgaon"
      }
    ],
    "LegalEmployer": null,
    "MediaThumbURL": null,
    "WorkplaceType": "On-site",
    "BusinessUnitId": 300000015798292,
    "OrganizationId": 300000039524046,
    "PostingEndDate": null,
    "LegalEmployerId": 300000015801661,
    "PrimaryLocation": "Gurgaon, Haryana, India",
    "WorkDurationYears": null,
    "WorkplaceTypeCode": "ORA_ON_SITE",
    "BeFirstToApplyFlag": false,
    "WorkDurationMonths": null,
    "otherWorkLocations": [],
    "secondaryLocations": [],
    "ShortDescriptionStr": "Lead product registration, renewals, and all activities related to regulatory for India, Sri Lanka and Nepal.",
    "requisitionFlexFields": [],
    "DomesticTravelRequired": null,
    "PrimaryLocationCountry": "IN",
    "ExternalQualificationsStr": null,
    "ExternalResponsibilitiesStr": null,
    "InternationalTravelRequired": null
  },
  "detail_meta": {
    "url": "https://hcjy.fa.us2.oraclecloud.com/hcmRestApi/resources/latest/recruitingCEJobRequisitionDetails?expand=all&onlyData=true&finder=ById;Id=%2210238%22,siteNumber=CX_1",
    "http_status": 200,
    "content_type": "application/json",
    "response_bytes": 13626
  },
  "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/b3c132c99af4f0e43a92fe8b9a7c87ee70be5300?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/fd5c005d-2102-408b-80a5-9404893f9b97JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/063b269b-849a-4216-8d0d-8fc4f7efa6f5JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/b3c132c99af4f0e43a92fe8b9a7c87ee70be5300/eventsJSON