RIO Execution Hub Sr. Associate Apply locations: Colombia - Bogota - Suba | Time type: Full time | Posted on: Posted 2 Days Ago | Job requisition id: 4940116 Use Your Power for Purpose We are committed to delivering medicines to the world with greater speed, without compromising on excellence and integrity. Navigating both local and global regulations is crucial, and the dynamic regulatory landscape demands innovative thinking and meticulous attention to detail. Your unwavering dedication and specialized knowledge will play a pivotal role in broadening and hastening patient access to Pfizer's medicines and vaccines. What You Will Achieve Job Summary: The RIO Execution Hub Sr Associate provides regulatory support to the international or regional regulatory teams. They work across portfolio phases from initial registration to product withdrawal, supporting activities such as M1 dossier components, local HA query responses, tenders, out-of-stock reporting, and launch planning. This role partners closely with the Country Regulatory Strategist and Hub Submission/Dossier Managers to ensure timely, high-quality submissions and compliance. Responsibilities include identifying regulatory requirements, authoring and coordinating documents, and reviewing dossiers for quality. Job Responsibilities: The role involves end-to-end management of regulatory dossiers for various regions and products, ensuring operational efficiency, compliance, and quality. Success is measured by timeliness, quality, and efficiency of deliverables. Key accountabilities include: - Ensuring timely delivery of local M1 dossier components - Performing quality review of dossiers - Supporting tenders, out-of-stock reports, and launch planning activities - Supporting audit readiness and communication responses - Collaborating with submission managers and hubs for application delivery and lifecycle management Additional duties involve authoring local documents, engaging with labeling teams, and providing SME input to projects impacting RIO hubs and GRS. Minimum Requirements: - B.S./B.Scs. in Pharmacy, Life Sciences, Business, or IT; relevant experience considered - Advanced to fluent English; multilingual skills are a plus - Strong technical aptitude and quick learning ability - Advanced Microsoft Office skills - Knowledge of pharmaceutical organizational structures and regulatory requirements - Experience in pharma, regulatory, quality, or compliance fields preferred Working Habits: Self-initiates problem solving, navigates ambiguity, recognizes escalation needs, and demonstrates technical expertise to support submission execution. EEO & Employment Eligibility: Pfizer is committed to equal employment opportunities regardless of race, color, religion, sex, sexual orientation, age, gender identity, national origin, or disability. #J-18808-Ljbffr