Job Description

Why Patients Need You We\'re looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines and vaccines. JOB RESPONSIBILITIES Committed to quality and excellence in compliance and conformance Accountable for maintaining the corporate change and dossier management system (PDM) regarding the status of regulatory CMC submissions with global health authorities per internal SOPs and policies. Ensures timely communication of any issues e.g. Board of Health queries to the regional teams as needed Manages multiple regions/projects/timelines of moderate complexity within a Work Team. Manages workload within the team for business continuity Work in collaboration with regulatory colleagues to ensure compliance and deliver efficiencies in the regulatory submission process. Responsible for evaluation of all CMC notifications for accuracy. Responsible for making updates in PDM Market Views for all submission types upon receipt of notification of Submission and Approval evidence Applies technical knowledge and key concepts in PDM Conformance updates. Considered as a technical resource within the work team. Demonstrates strong technical/functional knowledge w.r.t Regulatory requirements and internal process to coach direct reports on day-to-day activities Breadth of technical/functional expertise is focused on applicable discipline Acts as a mentor for the colleagues Actively shares knowledge with others within Work Team through existing knowledge sharing processes/systems. Solves moderately complex problems within area of expertise Demonstrates effective written and oral communication skills Support for updates in PDM for License withdrawals Operate to the highest conformance and quality standards Operate in line with internal SOPs and policies Encourages the participation and perspectives of all Work Team\'s members Supports developmental and training opportunities for mentees Adhere to standard turnaround timelines Escalate any potential compliance issues to management Liaise with regulatory colleagues to communicate and resolve potential issues Provide input to continuously improve and streamline the process Support periodic and ad-hoc system reports to estimate metrics Contribute to local and regional regulatory initiatives promoting a culture aligned with Pfizer values and which supports compliance, innovation and talent development and retention Assist in ensuring internal regulatory processes and procedures are well documented Assist in remediation activities Technical Skills - Knowledge and / or experience in Pharmaceutical industry in Regulatory / Quality Assurance, especially in Life cycle management or compliance. Strong quality and compliance orientation Diligence and attention to detail Prior Regulatory experience in any of the market Knowledge of regulatory practices, rules, regulations and guidelines Good communication skills Problem Solving Understanding stakeholder needs Fluent English Speaker Work Location Assignment:Flexible Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Regulatory Affairs #LI-PFE

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