Organizational Relationship(s)Works closely with local PCO BU teams in country and internal stakeholdersWorks closely with above country support as GRA-I LatAm Regional Hub, Hub Regulatory Strategists, GRA Product Strategists, Submissions Management, GCMC, Medical managers and other relevant support areas involved in product registration and product lifecycle management processesPosition PurposeParticipate in the planning of Regulatory strategies for products submissions and lifecycle to products under responsibilityCoordinate and execute activities related to dossier planning and submission -paper and/or electronic- for initial registration and maintenance of Drug products including product renewals for the assigned portfolio(s), These activities include HA query management.Interact with key internal stakeholders, such as Hub Regulatory Strategists, GRA Product Strategists, Submissions Management, GCMC, Quality, PGS and third-party vendors (as applicable), to ensure the regulatory strategies are executed according to the plan in order to permit the business continuity.Support the Regulatory Affairs Sr. Managers and Managers (as applicable), in the definition and execution of the regulatory strategies of assigned portfoliosWork in collaboration across the region to deliver efficiencies in regulatory submissions and processes.Primary ResponsibilitiesPossess understanding of the market regulatory requirements, as well as the regulatory processes.Coordinate the activities assigned, related to Drug Product submissions and license maintenance to Health authoritiesWork in partnership with in country Regulatory teams and key stakeholders including but not limited to the Regional Regulatory Hub Strategy (RRHS), Regulatory Operations, GRA, GPD, GCMC, GSCPM, to ensure the development and implementation/execution of regulatory strategies, to ensure submissions are ready to file, to permit the business continuity and to provide the necessary information to ensure internal systems and databases are updated.Coordinate the routine monitoring of BoH website for information related to drug product registration, line extensions and post-approval changes status. Understand local regulations and trends.Ensure that he/she keeps current with the agency legislations, as well as updates the regulatory information on LatAm SP & Pfizer systems/databases (as applicable).Coordinate and execute the review of submission ready dossiers, ensuring that assigned submissions fully meet the local regulatory requirements. This includes BoH query response.Support bidding processes by providing updated regulatory documents, as applicable. Collaborate with local team for the work required with local BoH by elaborating documents, e-mails, phone contacts and meetings for following-up processes of registration approval and product lifecycle.Keep updated regulatory electronic systems and tools to share accurate regulatory information with local and above country areas (GCMC, Hubs, local teams, etc.).Evaluate BoH regulations and its changes, keeping informed as per local processes to the Regulatory team and above country stakeholders.Review and approval of promotional materials (as applicable), ensuring the compliance with the due SOPs and local requirements.Collaborate with the labeling and artworks approval processes (as applicable), according to Pfizer procedures and local regulations.Complete departmental training in a timely manner to address corporate and regulatory needs. As applicable, contribute to local regulatory initiatives promoting a culture aligned with Pfizer values and which supports compliance, innovation.Technical Skill RequirementsKnowledge of local sanitary legislations and regulatory environment, including Clinical Trials Applications requirements (as applicable)Technical and scientific knowledge of human pharmaceutical productsProficiency in the English languageCommunication and negotiation skillsProblem SolvingGoals orientedUnderstanding stakeholder needs. Customer-orientedNetwork and alliance building/ peer relationshipsStrong quality and compliance orientationAnalytical ThinkingAbility to work under pressureAdaptabilityPlanningOrganizedTeam playerChange agileQualifications (i.e., preferred education, experience, attributes)Education: Pharmacist graduated or life science degreeLocal Regulatory experience– minimum 4 years of experience as Regulatory Affairs Analyst (Human Medicinal Products)Demonstrable local Regulatory experience including knowledge of NCEs and Biological products submission processes, CTAs applications (as applicable) and product life cycle management activities.Proven ability to consistently deliver on time and quality standards.Proven ability to manage complex regulatory issues EEO (Equal Employment Opportunity) & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.Regulatory Affairs
