Job Description

Job Description

The RIO Execution Hub Team Lead oversees a team of Hub Managers and Specialists who support regulatory operations across countries and clusters. This role ensures timely, high-quality regulatory submissions and sustained compliance throughout the product lifecycle—from initial applications to product withdrawal. Responsibilities include:

  • Leading regulatory dossier management and lifecycle activities.
  • Acting as the primary contact for issue resolution and escalation.
  • Supporting cross-functional regulatory needs (e.g., tenders, out-of-stock reporting, launch planning).
  • Overseeing local document authoring, health authority query responses, and audit readiness.
  • Partnering with the RIO Submissions Hub Team Manager to ensure submission quality and compliance.
  • Driving operational performance, process efficiency, and continuous improvement.

Education Qualifications

  • Bachelor’s or Master’s degree (e.g.,Pharmacy, MS, MBA) in a scientific, technical, or information management discipline.

Required Competencies

  • Regulatory Expertise: Deep understanding of global, regional, and cluster regulatory requirements. Preferably 10 years or more experience in regulatory affairs in Pharmaceutical Industry, with experience across different market within Asia.
  • Leadership: Proven experience in leading regulatory strategy and operations teams.
  • Business Acumen: Strong judgment, planning, and decision-making skills.
  • Communication: Ability to convey complex information clearly to diverse audiences.
  • Change Management: Experience in implementing business change and managing cross-site teams.
  • Collaboration: Skilled in relationship-building across functions and cultures.
  • Compliance & Quality: Commitment to audit readiness, SOP adherence, and KPI tracking.
  • Innovation & Agility: Ability to adapt in real-time, foster continuous improvement, and drive results.
  • Technical Proficiency: Experience with submission and portfolio management, including eCTD and dossier publishing.
  • Project management: Proven capability to successfully manage Projects. Formal Certifications will be an added advantage

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.

Regulatory Affairs


Job Details

Role Level: Mid-Level Work Type: Full-Time
Country: Philippines City: Makati National Capital Region
Company Website: https://www.pfizer.com/?source=Linkedin Job Function: Operations Management
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


About the Company

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