Global Regulatory Submissions Hub Associate

Pfizer; Philippines; Hybrid; PHP 600,000 - 900,000; Full time

Job summary

Pfizer in the Philippines is seeking an IDM RIO Execution Hub Associate/Sr Associate to provide regulatory support to international country and cluster teams. You will work across registration applications, lifecycle management through to product withdrawal, coordinating local document authoring and HA responses.

The role partners with Country Regulatory Strategist and Hub Submission Managers to ensure timely, high-quality submissions, regulatory readiness, and ongoing compliance across regions.

Qualifications

• 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.

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.
• 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.

Skills

English proficiency

Multilingual (Korean)

MS Office

Pharma regulatory knowledge

Quality/compliance

Regulatory systems

Education

B.S. Pharmacy

Tools

MS Office Suite

Job description

Pfizer in the Philippines is seeking an IDM RIO Execution Hub Associate/Sr Associate to provide regulatory support to international country and cluster teams. You will work across registration applications, lifecycle management through to product withdrawal, coordinating local document authoring and HA responses.

The role partners with Country Regulatory Strategist and Hub Submission Managers to ensure timely, high-quality submissions, regulatory readiness, and ongoing compliance across regions.