Home › Companies › Hcjy Fa Us2 Oraclecloud Com CX 1 › Regulatory 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
| Field | Value |
|---|---|
| Company | Hcjy Fa Us2 Oraclecloud Com CX 1 |
| Title | Regulatory Affairs Senior Specialist |
| Normalized title | - |
| Department / team | Compliance, Risk & Legal |
| Location | Haryana, IN, United States |
| Work model | On Site |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
| Posted / first seen | 2026-06-02 / 2026-06-02 |
| Changed / last seen | 2026-06-06 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Hcjy Fa Us2 Oraclecloud Com CX 1. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Oracle Recruiting Cloud / Fusion HCM. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Haryana. | Open |
| Department jobs | Active postings in Compliance, Risk & Legal. | Open |
| Work model jobs | Active On Site postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Hcjy Fa Us2 Oraclecloud Com CX 1 |
| Source | 063b269b-849a-4216-8d0d-8fc4f7efa6f5 |
| ATS provider | Oracle 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 ID | b3c132c99af4f0e43a92fe8b9a7c87ee70be5300 |
| Org ID | fd5c005d-2102-408b-80a5-9404893f9b97 |
| Source ID | 063b269b-849a-4216-8d0d-8fc4f7efa6f5 |
| Board ID | 063b269b-849a-4216-8d0d-8fc4f7efa6f5 |
| Provider | oracle_hcm |
| Provider Job Key | 10238 |
| Title | Regulatory Affairs Senior Specialist |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | IN-Gurgaon, Gurgaon, Haryana, IN |
| Department | Compliance, Risk & Legal |
| Team | — |
| Employment Type | full_time |
| Workplace Type | on_site |
| Remote Policy | — |
| Country | United States |
| Region | IN |
| City | Haryana |
| Salary Raw | 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 |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://hcjy.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/10238 |
| Apply URL | https://hcjy.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/10238 |
| First Seen At | 2026-06-02 11:20:58Z |
| Last Seen At | 2026-06-06 18:54:57Z |
| Last Checked At | 2026-06-06 18:54:57Z |
| Last Changed At | 2026-06-06 11:19:22Z |
| Inactive At | — |
| Source Posted At | 2026-06-02 08:29:27Z |
| Source Updated At | — |
| Raw Payload Uri | s3://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;\"> </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> </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;\"> </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> </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;\"> </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> </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;\"> </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> </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. </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. </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. </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). </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. </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;\"> </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. </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. </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. </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;\"> </p><p style=\"margin:0in;\"> </p><p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Travel:</strong> </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. </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. </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. </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). </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. </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;\"> </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. </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. </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. </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;\"> </p><p style=\"margin:0in;\"> </p><p style=\"margin:0in;\"><span style=\"font-size:11.0pt;\" lang=\"EN-US\"><strong>Travel:</strong> </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=descriptionJSONGET https://api.bluedoor.sh/job-postings/v1/orgs/fd5c005d-2102-408b-80a5-9404893f9b97JSONGET https://api.bluedoor.sh/job-postings/v1/sources/063b269b-849a-4216-8d0d-8fc4f7efa6f5JSONGET https://api.bluedoor.sh/job-postings/v1/jobs/b3c132c99af4f0e43a92fe8b9a7c87ee70be5300/eventsJSON