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Rio execution hub manager

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Pfizer

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Location:
Philippines , Makati City

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Category:
IT - Administration

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

At Pfizer, we are committed to bringing medicines to the world at a faster pace without compromising on excellence and integrity. Adhering to both local and global regulations is crucial, and the constantly evolving regulatory landscape demands forward-thinking and meticulous attention to detail. Your dedication and expertise are vital in expanding and accelerating patient access to Pfizer's medicines and vaccines.

Job Responsibility:

  • Assist in the preparation, publication, tracking, and quality control of regulatory submissions, ensuring compliance with document management standards
  • Coordinate activities related to enterprise-wide regulatory management systems and provide guidance on moderately complex projects
  • Apply skills and discipline knowledge to contribute to departmental work, making decisions to resolve moderately complex problems and developing new options
  • Work independently on assignments, seeking directional review for unusual or complex problems, and review the work of colleagues in a mentor role
  • Guide operational teams in managing projects, preparing resource forecasts, and identifying areas for improvement in products, processes, or services
  • Act as a point person for regulatory agency interactions, including preparation of briefing packages and strategy for meetings, inspections, and responses to agency letters
  • Understand and challenge scientific arguments, identify regulatory scientific data needs, and solve regulatory issues to influence the development of new global products and improvements to existing products
  • Manage registrations of existing customer products in compliance with applicable regulations and support global team efforts to ensure high-quality, compliant submissions
  • Provide daily regulatory support to Global Product Development teams and lead the logistics involved with regulatory Clinical Trial Application (CTA) submissions
  • Manage the preparation of registration packages, responses to deficiency letters, and suggest system improvements to reduce cycle time and increase efficiency

Requirements:

  • BA/BS with at least 4 years of experience or MBA/MS with at least 2 years of experience or PhD/JD with any years of experience
  • Demonstrated experience in regulatory affairs, research and development, or quality assurance/compliance
  • Experience working directly with regulatory agencies
  • Strong knowledge of the drug development process, regulatory affairs, CTA, and submissions management
  • Sound knowledge of applicable portions of agency guidance documents and regulations
  • Ability to exercise good judgment within company policy and health authority regulations with good negotiation skills
  • Excellent written and interpersonal communication skills

Nice to have:

  • Master's degree with relevant pharmaceutical experience, particularly in the lifecycle management of approved applications
  • Proven ability to manage multiple projects and deadlines
  • Proficiency in regulatory submission software and tools
  • Excellent organizational and time management skills
  • Strong attention to detail and accuracy

Additional Information:

Job Posted:
February 20, 2026

Employment Type:
Fulltime
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