Regulatory Specialist

SUN PHARMA

📍Taguig, National Capital Region, Philippines
Posted May 22, 2026

Job Overview

Position

Regulatory Specialist

Company

SUN PHARMA

Location

Taguig, National Capital Region, Philippines

Work Type

On-site

Job ID

li-4414061775

Job Description

We are seeking for a detail-oriented and proactive
Regulatory Specialist
to join our team. In this role, you will be responsible for ensuring that all pharmaceutical products comply with local regulatory requirements and company standards. You will work closely with cross-functional teams, external partners, and regulatory agencies—IPO, DOH, Local Laboratories and FDA.

Key Responsibilities

  • Assist the Regulatory Department by ensuring the availability of all the company and product documents on file for FDA inspection and requests, as needed.

  • Assist in maintaining the trademark (TM) registrations, ensuring that TMs are maintained in the IPO system.

  • Maintain EDPS Certificate and ensures timely quality submission of reports to the DOH.

  • Submission of monthly reports as required.

  • Safekeeping of retention samples, COAs, logbooks required by the FDA, and facilitating the local assay for all the commercial products.

Qualifications

  • Bachelor’s degree in Pharmacy

  • Licensed Pharmacist preferred (but not required depending on experience).

  • Minimum 5 year of experience as a company pharmacist within a pharmaceutical industry handling drug products.

  • Preferably with knowledge on FDA inspection, basic company and product documents, and trademarks.

  • Advantage if with experience in FDA submissions and Quality Assurance

  • Excellent documentation, writing/drafting letters and various reports.

Interview Prep

AI-powered insights to help you prepare

Key Skills

Required:
Preferred:

Practice Questions

💡Technical Questions (3)
  • 1.How do you ensure the accuracy and timeliness of your EDPS Certificate reports and monthly submissions to the DOH?
  • 2.Can you walk me through your process for organizing and safekeeping FDA-required documents like retention samples, COAs, and logbooks?
  • 3.What is your understanding of maintaining trademark registrations within the IPO system, and how would you handle upcoming renewals?
🎯Behavioral Questions (3)
  • 1.Tell me about a time you had to prepare for a regulatory agency inspection. How did you handle the pressure and ensure compliance?
  • 2.Describe a situation where you had to collaborate with external partners or cross-functional teams to meet a tight regulatory deadline.
  • 3.Give an example of a time your attention to detail caught a significant error in a regulatory document or report before submission.
🧩Situational Questions (2)
  • 1.You discover that a batch of retention samples for a commercial product is missing just days before a scheduled FDA inspection. What do you do?
  • 2.A cross-functional team member is unresponsive to your urgent requests for a document needed for an upcoming DOH submission. How do you handle this?

Resume Keywords

Make sure these keywords appear on your resume

Regulatory ComplianceFDA SubmissionsDOH ReportingTrademark RegistrationIPO SystemEDPS CertificateRetention SamplesCompany PharmacistQuality AssuranceDocument SafekeepingRegulatory InspectionCross-functional Collaboration

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