Execution Hub Associate

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

Job Description

The IDM RIO Execution Hub Associate/Sr Associate is responsible for providing regulatory support to the International country and/or cluster Regulatory teams.

The Execution Hub Associates/Sr Associates work across portfolio phases from initial registration applications, lifecycle management through to product withdrawal. They support numerous regulatory activities that include but are not limited to;

• M1 dossier components (local document authoring and/or coordination)
• Simple local only HA query responses,
• Provide support for general x-functional activities to country Regulatory teams for tenders, out-of-stock reporting, Annual Product Quality Review, risk minimization plans, and coordination of regulatory input for launch planning.

It is expected that this role partners closely with the Country Regulatory Strategist and Hub Submission/Dossier Managers to enable timely, high-quality submissions and sustained compliance. This includes but is not limited to:

• Identification of regulatory requirements (for the in-scope submission categories defined),
• Authoring, delivery and/or coordination of local, submission-ready documents and
• The quality review/approval of the Dossier provided by Hub Submission/Dossier Managers (for the in-scope submission categories defined).

JOB RESPONSIBILITIES

RIO Execution Hub Associate/Sr Associate is focused on end-to-end management of multi-regional, regional and national regulatory dossiers for assigned cluster/country/therapeutic area/products, both initial registration applications and ongoing lifecycle management through to product withdrawal. Associated functions are engaged to provide smooth operational performance and process efficiency.

This role executes the GRS mission by delivering against goals, executing initiatives, implementing new opportunities, and filling gaps related to the production of regulatory International and operational support. A key component of this role is the implementation of portfolio execution efficiencies, identification and escalation of quality and compliance issues or emerging risks detected during the management of the Cluster/Country submissions under his/her responsibility.

Success in this role is measured by the timeliness, quality, compliance, and efficient delivery of critical on-the-job deliverables, bringing efficiencies to the organization.

In some regions/clusters, the RIO Execution Hub can execute the role of Hub Submission Manager, while in others should closely partner with Hub Submission Manager.

Key Accountabilities include:

General accountabilities (For reference only)

• Ensure timely delivery of local M1 dossier components
• Perform Quality review/approval of the Dossier build Table of Contents provided by Hub Submission/Dossier Managers (for the in-scope submissions under his/her responsibility).
• Can provide support for simple tenders, out-of-stock reporting, Annual Product Quality Review, risk minimization plans, and regulatory information status for launch planning.
• Provide support for local audit readiness activities, Dear Healthcare Professional Communication (DHPC) responses, and responses to medical info requests as requested
• Partner with Growth submission managers and Regional Submission Hubs to meet growth application delivery in line with International Commercial knots prioritisation and OP plans.
• Partner with Submission Hubs to meet GRS lifecycle prioritisation for CMC and Labelling changes.

Local document authoring & submission prep (For reference only)

Author and review of M1 local documents (cover letters, variations, MA applications), and relevant translations.

May engage with Labeling Hubs and clusters/countries on Labels and Artwork updates to include local requirements, ensuring alignment with approved text and supporting launch activities.

Support clusters/countries with authoring of simple HA query responses e.g., admin related requests, and coordinate with relevant SMEs/functions (e.g., CMC) to address more complex HA queries, based on CRS query response strategy.

Portfolio – Non Portfolio Support (qualitative examples)

Associate

Business Experiences:
Provides regulatory support to lower complexity regulatory activities in the assigned country/Cluster (mainly for commercial lifecycle through to product withdrawal) and applies technical experience to impact business results.

Non-Portfolio Experiences:
Provides input to projects requested within RIO Hubs

Senior Associate

Business Experiences:
Provides regulatory support to lower to medium complexity regulatory activities in the assigned country (Initial applications, commercial lifecycle through to product withdrawal, simple tenders, audits, launch planning support) and applies technical experience to impact business results.

Non-Portfolio Experiences:
Provides subject matter expert (SME) input to projects that impact people, technology, and/or processes within RIO Hubs, GI&PE and GRS.

QUALIFICATIONS / SKILLS

B.S. Pharmacy; equivalent relevant professional experience will be considered.

Advanced to Fluent English language required. Multilingual skills (i.e. Korean) desirable.

Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards.

Advanced Microsoft Office Suite skills.

Familiarity with pharmaceutical organizational structures, systems, and culture is preferred.

An understanding of country/cluster regulatory requirements and trends is preferred.

Relevant experience within pharma, in Regulatory, quality and/or compliance fields preferred.

Working habits (qualitative examples)

Associate

Colleague who requires management oversight on daily work and support in problem solving.
Demonstrates technical expertise which aids in task-based execution.

Senior Associate

Self-initiates problem solving and is able to navigate ambiguous situations impacting RIO through to results. Recognizes when escalation is required.
Demonstrates technical expertise which aids submission execution.

Work Location Assignment:Hybrid

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .

Regulatory Affairs