RIO Execution Hub Sr. Associate
Hybrid · Makati City, Metro Manila, Philippines
Job Summary
Provide operational regulatory support to International country and/or cluster Regulatory teams across portfolio phases from initial registration applications to lifecycle management and product withdrawal. Coordinate M1 dossier components and local submission activities; prepare simple local HA query responses; support cross-functional activities for tenders, out-of-stock reporting, Annual Product Quality Review, risk minimization plans, and regulatory input for launch planning. Collaborate with the Country Regulatory Strategist and Hub Submission/Dossier Managers to enable timely, high-quality submissions and sustained compliance, including identification of regulatory requirements and authoring/coordination of local, submission-ready documents with quality review of dossiers.
Required Qualifications
- B.Pharm/BA/BS with 2+ years of experience in regulatory affairs or a regulated industry
- Demonstrated knowledge of the current health regulatory framework for drug regulatory procedures
- Excellent verbal and written communication skills in English
- Proficient in MS Office Suite
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