Regulatory Hub Associate (Hybrid) Dossier & Lifecycle

Biopharma Careers; Philippines; Hybrid; PHP 800,000 - 1,200,000; Full time

Job summary

Pfizer is seeking an IDM RIO Execution Hub Associate/Sr Associate to provide regulatory support across international country clusters. The role spans initial registrations through lifecycle management to product withdrawal, coordinating with Hub Managers and country teams for timely, compliant submissions.

The ideal candidate has a pharmacy degree, fluent English, and strong MS Office skills, with pharma regulatory experience. The role offers hybrid work arrangements within a global team.

Qualifications

• Advanced to fluent English required.
• Proven MS Office proficiency.
• Familiarity with pharmaceutical organizational structures and regulatory standards.
• Understanding of country/cluster regulatory requirements.
• Relevant pharma regulatory/quality experience preferred.

Responsibilities

• End-to-end management of multi-regional regulatory dossiers for assigned clusters/countries.
• Support initial registrations and lifecycle management through product withdrawal.
• Coordinate with Hub Submission/Dossier Managers and regional teams for timely submissions.
• Provide status updates on regulatory information for launch planning and audits.

Skills

Fluent English

MS Office

Regulatory knowledge

Pharma industry familiarity

Korean (multilingual)

Education

B.S. Pharmacy

Job description

Pfizer is seeking an IDM RIO Execution Hub Associate/Sr Associate to provide regulatory support across international country clusters. The role spans initial registrations through lifecycle management to product withdrawal, coordinating with Hub Managers and country teams for timely, compliant submissions.

The ideal candidate has a pharmacy degree, fluent English, and strong MS Office skills, with pharma regulatory experience. The role offers hybrid work arrangements within a global team.