RIO Execution Hub Sr Associate
@ Pfizer

Makati, National Capital Region, Philippines
$120,000
On Site
Full Time
Posted 7 hours ago

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Job Details

Overview

The RIO Execution Hub Sr Associate role at Pfizer provides critical regulatory support to international country and cluster regulatory teams. This role spans portfolio phases from initial registration applications and lifecycle management to product withdrawal.

Main Responsibilities

  • Ensure timely delivery of local M1 dossier components
  • Perform quality review and approval of dossier builds
  • Support simple HA query responses and local audit readiness
  • Partner with regional teams for tenders, out-of-stock reporting, and launch planning
  • Coordinate regulatory input for submissions and lifecycle regulatory activities

Local Document Authoring & Submission Prep

Author and review M1 local documents including cover letters, variations, and MA applications. Collaborate with labeling hubs and clusters/countries to update labels and artwork in alignment with local requirements.

Portfolio and Non-Portfolio Support

The role includes providing regulatory support for lower to medium complexity activities and contributing subject matter expertise to projects impacting people, technology, and processes within the RIO Hubs.

Qualifications & Skills

  • B.S. or equivalent experience in Pharmacy, Life Sciences, Business, or IT
  • Advanced to fluent English; multilingual skills are a plus
  • Proven technical aptitude with quick learning of new software and regulations
  • Advanced Microsoft Office skills and familiarity with regulatory standards
  • Experience in pharma regulatory, quality, or compliance fields preferred

Key Skills/Competency

  • Regulatory
  • Dossier
  • Compliance
  • Lifecycle
  • Submission
  • Audit
  • Pharma
  • Quality
  • Microsoft Office
  • Coordination
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How to Get Hired at Pfizer

🎯 Tips for Getting Hired

  • Research Pfizer's culture: Understand their mission, values, and regulatory focus.
  • Customize your resume: Highlight pharma and regulatory experience.
  • Showcase technical skills: Emphasize Microsoft Office and dossier management.
  • Prepare for interviews: Review regulatory requirements and compliance scenarios.

📝 Interview Preparation Advice

Technical Preparation

Review current regulatory guidelines.
Practice dossier management skills.
Brush up on Microsoft Office proficiency.
Study pharma compliance standards.

Behavioral Questions

Describe a time handling tight deadlines.
Explain a conflict in regulatory coordination.
Discuss problem solving in ambiguous situations.
Share how you ensure quality submissions.

Frequently Asked Questions