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Regulatory Affairs Intern

Inovapharma · Taguig City, 1634, Philippines · Active · BambooHR

Job facts

FieldValue
CompanyInovapharma
TitleRegulatory Affairs Intern
Normalized title-
Department / teamMarketing
LocationTaguig City
Work model-
Employment typeInternship
Salary-
Statusactive
ATS providerBambooHR
Posted / first seen2026-01-29 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Inovapharma.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through BambooHR.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Taguig City.Open
Department jobsActive postings in Marketing.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

CompanyInovapharma
Sourcebb1bb99b-7531-4e19-9814-ce0ff27b4d36
ATS providerBambooHR

Description

The Company iNova is a different kind of health company. We are leading the way to better health by delivering innovative, patient-centric products that improve the lives of people around the world. Our diverse portfolio of iconic, market-leading consumer health brands and prescription medicines are backed by science and distributed in over 75 markets across Asia, Australia, New Zealand, Middle East & Africa and Europe. Experience the iNova difference today. The Opportunity We currently have an opportunity for a Regulatory Affairs Intern to join our Marketing team on an internship basis. Reporting to the Senior Regulatory Affairs Manager, core focus of the role is to support the Regulatory Affairs team by assisting in day-to-day regulatory tasks, document preparation, product monitoring, and administrative activities. The internship provides hands-on exposure to Philippine FDA processes, regulatory operations, and pharmaceutical industry practices. Key accountabilities and performance indicators include: Schedule product applications (Prior approval variations & Promo Application). Assist in emailing the FDA for scheduling using the Integrated Application Form. Handle document pick-up from the FDA. Secure schedule for document pick-up at the FDA Office in Alabang. Compile necessary documents for applications (promo, variations). Aid in collating and compiling documentary requirements for applications. Provide timely updates on product and promo renewals (CPR, Promos). Assist in updating the renewal timeline for CPRs and Promos (90 days before expiration). Tasks may change or be updated periodically based on demand and workload. About You To be successful in this role, you will possess the following BS Pharmacy student currently completing internship requirements. Good academic standing. Strong attention to detail, organization, and communication skills. Willingness to learn and adapt in a fast-paced regulatory environment. Additional Requirements / Working Conditions Adhere to company values at all times If you wish to be part of an energetic team within a thriving organisation, focused on bringing innovative products to market, please  APPLY TODAY!  We want you to join us in our pursuit of healthy living!

Full job record

Job IDf7ff84e088715d682d1dd0e5a381607c6458896a
Org ID8a57373f-82a3-4e47-8a8b-2b264c275ef2
Source IDbb1bb99b-7531-4e19-9814-ce0ff27b4d36
Board IDbb1bb99b-7531-4e19-9814-ce0ff27b4d36
Providerbamboohr
Provider Job Key487
TitleRegulatory Affairs Intern
Normalized Title
Statusactive
Activeyes
Location TextTaguig City, 1634, Philippines
DepartmentMarketing
Team
Employment Typeinternship
Workplace Type
Remote Policy
Country
Region
CityTaguig City
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://inovapharma.bamboohr.com/careers/487
Apply URLhttps://inovapharma.bamboohr.com/careers/487
First Seen At2026-05-30 06:03:53Z
Last Seen At2026-06-06 10:20:06Z
Last Checked At2026-06-06 10:20:06Z
Last Changed At2026-05-30 06:03:53Z
Inactive At
Source Posted At2026-01-29 00:00:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=bamboohr/board=inovapharma/date=2026-06-06/2026-06-06T10-20-03-296Z-aae16d32cb37378fa22edae6586773c56ef57d5d51cc80c549d1385874fe531c.json
Event Fields
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  "active_status": "active"
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Parsed Structured
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Extensions
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Native Structured
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    "description": "<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">The Company </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">iNova is a different kind of health company. We are leading the way to better health by delivering innovative, patient-centric products that improve the lives of people around the world. Our diverse portfolio of iconic, market-leading consumer health brands and prescription medicines are backed by science and distributed in over 75 markets across Asia, Australia, New Zealand, Middle East &amp; Africa and Europe. Experience the iNova difference today. </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\"> </span><br><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">The Opportunity </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">We currently have an opportunity for a Regulatory Affairs Intern to join our Marketing team on an internship basis. </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\"> </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Reporting to the Senior Regulatory Affairs Manager, core focus of the role is to support the Regulatory Affairs team by assisting in day-to-day regulatory tasks, document preparation, product monitoring, and administrative activities. The internship provides hands-on exposure to Philippine FDA processes, regulatory operations, and pharmaceutical industry practices. </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\"> </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">Key accountabilities and performance indicators include: </span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Schedule product applications (Prior approval variations &amp; Promo Application). </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Assist in emailing the FDA for scheduling using the Integrated Application Form. </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Handle document pick-up from the FDA. </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Secure schedule for document pick-up at the FDA Office in Alabang. </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Compile necessary documents for applications (promo, variations). </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Aid in collating and compiling documentary requirements for applications. </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Provide timely updates on product and promo renewals (CPR, Promos). </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Assist in updating the renewal timeline for CPRs and Promos (90 days before expiration). </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Tasks may change or be updated periodically based on demand and workload. </span></li>\n</ul>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\"> </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">About You </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">To be successful in this role, you will possess the following </span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">BS Pharmacy student currently completing internship requirements. </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Good academic standing. </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Strong attention to detail, organization, and communication skills. </span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Willingness to learn and adapt in a fast-paced regulatory environment. </span></li>\n</ul>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\"> </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">Additional Requirements / Working Conditions </span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Adhere to company values at all times </span></li>\n</ul>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\"> </span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">If you wish to be part of an energetic team within a thriving organisation, focused on bringing innovative products to market, please <span style=\"font-weight: bold\">APPLY TODAY! </span>We want you to join us in our pursuit of healthy living! </span></p>",
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}
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