Rio Execution Hub Manager
2 days ago
JOB SUMMARYThe RIO Execution Hub Manager is responsible for providing regulatory support to the international country and/or cluster regulatory teams.The Hub Managers work across portfolio phases from initial applications, through the commercial lifecycle, to product withdrawal.
They support various regulatory activities, including but not limited to:M1 dossier components (local document authoring and/or coordination)Simple local-only HA query responsesProviding support for general cross-functional support to country regulatory teams for tenders, out-of-stock reporting, annual product quality review, risk minimization plans, and coordination of regulatory input for launch planning.This role acts as the initial point of contact for the assigned country/cluster under his/her responsibility, liaising with the country regulatory strategist, hub submission manager/dossier manager, and other key stakeholders.It is expected that this role partners closely with the country regulatory strategist and hub submission/dossier managers to enable timely, high-quality submissions and sustained compliance.
Responsibilities include but are not limited to:Identification of regulatory requirements (for the in-scope submission categories)Authoring, delivery, and/or coordination of local, submission-ready documentsQuality review/approval of the dossier provided by hub submission/dossier managers (for the in-scope submission categories)JOB RESPONSIBILITIESThe RIO Execution Hub Manager manages end-to-end regulatory dossiers for multiple regions, focusing on initial registration and ongoing lifecycle management until product withdrawal.
The role involves engaging with functions to ensure operational efficiency and compliance.Success is measured by the timeliness, quality, compliance, and efficiency of deliverables, aiming to bring organizational efficiencies.Depending on the region/cluster, the manager may also serve as the Hub Submission Manager or partner closely with one.Key AccountabilitiesGeneral accountabilities (for reference only):Ensure timely delivery of local M1 dossier componentsAct as the initial contact point for the assigned cluster/country for the RIO execution team and key stakeholdersProvide regulatory support for cross-functional activities related to tenders, out-of-stock reporting, product reviews, risk plans, and launch coordinationSupport audit readiness activities, including audit interviews, DHPC responses, and medical info requestsAssist country strategists with cross-functional meetings on launch plansPerform quality review/approval of dossier build tables of contentsPartner with growth submission managers and regional hubs to deliver growth applications and support international commercial prioritiesSupport lifecycle prioritization discussions and local document authoring for applications and variationsCoordinate with labeling hubs on label and artwork updatesAssist with simple HA query responses and coordinate with SMEs for complex queriesBusiness ExperiencesProvide regulatory support across the product lifecycle, applying technical expertise to impact business resultsLead regulatory support in challenging environmentsAct as a regulatory expert across clusters/regions, consolidating activities and collaborating with cross-functional teamsNon-Portfolio ExperiencesRepresent RIO in improvement projects and leadership roles within transformation initiativesRequirementsB.S.
/B.Sc.
in Pharmacy, Life Sciences, Business, or IT; relevant experience consideredFluent English required; multilingual skills are a plusProven ability to learn new software, regulations, and standardsAdvanced MS Office skillsUnderstanding of pharmaceutical organizational structures and regulationsExperience in pharma regulatory, quality, or compliance fieldsWorking HabitsSelf-initiating, problem-solving, able to navigate ambiguity, and recognize when escalation is neededDomain expertise that drives execution and impacts business outcomesExperience in matrix management and risk mitigationPfizer is an equal opportunity employer and complies with all applicable legislation in each jurisdiction.
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RIO Execution Hub Manager
1 week ago
Sydney, New South Wales, Australia Pfizer Full timeJOB SUMMARYThe RIO Execution Hub Manager is responsible for providing regulatory support to the International country and/or cluster Regulatory teams.The Hub Managers work across portfolio phases from initial applications, commercial lifecycle through to product withdrawal. They support numerous regulatory activities that include but are not limited to;- M1...
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RIO Execution Hub Manager
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Sydney, New South Wales, Australia Pfizer Full timeJOB SUMMARYThe RIO Execution Hub Manager is responsible for providing regulatory support to the International country and/or cluster Regulatory teams.The Hub Managers work across portfolio phases from initial applications, commercial lifecycle through to product withdrawal. They support numerous regulatory activities that include but are not limited to;- M1...
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