Senior Regulatory Affairs Director, South Latam Cluster Lead And Head Of Brazil

Leadership and Strategic RoleLead and manage the cluster (Brazil and Argentina Region) / country team in the development of regulatory strategies for registration of new products and line extensions, and their lifecycle management.

Ensure that the team provides input into global and regional development and regulatory strategies to provide optimal support for meeting regional and country business objectives.Responsible for the leadership, development, and performance management of the Cluster / country team to achieve company objectives and culture.

Develop and enhance the capabilities and capacities of the team through the identification and implementation of training and development needs.Ensures that all regulatory activities in the country are managed in compliance with Pfizer standards and international / local regulations.Internal PartnershipsDevelop strong partnerships within the country (e.g., Country Manager, Medical, Marketing, Supply Chain, Quality), and above-country functions (e.g., GCMC, GRS Regulatory Hubs, Regulatory Operations) and above-country GRS Categories and Regional Teams to facilitate the development and implementation of regulatory strategies to expedite the registration of new products, line extensions and life-cycle optimization.Provide strategic contribution to the country (PCO) leadership team – anticipate what Regulatory needs to contribute to achieve business objectives, e.g., BU Strategic and Operating plans.Collaborate with the Country lead to align on regulatory positions on pan-portfolio or policy topics for communication to in-country internal and external stakeholders.Operational ExcellenceEnsure internal regulatory processes and procedures are followed according to Pfizer policies and procedures and support compliant regulatory activities.Assure local licenses in country under responsibility are maintained (e.g., Marketing Authorizations) in compliance with local regulations and following corporate policies, regulatory processes, and SOPs (e.g. CMC change control, product labelling, single channel of communication, etc.).

QualificationsScientific Degree – such as life sciences or chemistry.A higher degree (MSc, MBA or PhD) may be an advantage but is not essential.General management experience and previous line management and leadership experience at senior management level is essentialExtensive experience in regulatory affairs preferably for more than 10 years, in human medicines.Proven ability to manage complex regulatory issues.Demonstrable knowledge across the Drug, Discovery, Development, and commercialization lifecycle, with proven examples of contribution.Proven ability to consistently deliver with agility to time, cost, and quality standards.Demonstrable experience of effective delivery in a complex matrix environment.Fluency in both English and Portuguese is required.SkillsStrong leadership qualities and management skills, including talent development, team working, problem solving, communication and interpersonal skills.In depth knowledge of national / regional regulatory legislation and guidelines.

Understanding of business and financial environment, drug development process, local healthcare system and challenges and opportunities of the pharmaceutical industry.Knowledge and understanding of quality systems, processes, audit, and inspections.Ability to influence at all levels in the organization and build networks internal and externally.Organizational RelationshipsReports to VP.

Head of Regulatory Sciences, Emergin MarketsMember of Brazil Leadership TeamMember of Extended local Commercial Leadership team (as applicable)External RelationshipsResponsible for developing and enhancing relationships with key external entities (HA's / BoH, RKOL's, etc.).

Manage the HA / BoH interface throughout the product development and product lifecycle, developing a long-term and positive relationship characterized by Integrity, Quality, Compliance and Leadership.Represents the Company at the local Regulatory Authority(ies) and lead the conversation in support to the achievement of Country Regulatory priorities aligned to country / regional advocacy / strategic plan.Partner with Regulatory Policy to develop and reinforce Pfizer regulatory positions with external stakeholders and understanding of the external environment.Understand local regulations and developing trends in the local regulatory environment of the country under responsibility and provide assessment of the impact to key stakeholders.Leverage regulatory intelligence / landscape knowledge to support the development and implementation of regulatory and business strategies, and decision making.Influence on new legislation initiatives that could positively impact the business.Active participation in the local Trade Association(s) and effective communication to key stakeholders of key issues that could impact regulatory strategies or the business.Other Job DetailsWork Location Assignment : On-site 2-3x / week or as needed by the business.Last date to apply for job : August 13EEO (Equal Employment Opportunity) & Employment EligibilityPfizer 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