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A global pharmaceutical company in Madrid is seeking a Manager, Global Labeling Lead to oversee the global labeling strategy. You will manage the labeling process for assigned products and work closely with various teams to ensure compliance with regulations. The ideal candidate has over 4 years of experience in the pharmaceutical industry and strong project management abilities. The role offers a hybrid work model.
Use Your Power for Purpose
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.
What You Will Achieve
The Manager, Global Labeling Lead (GLL) has overall accountability for global labeling strategy for their assigned products. This includes managing the end-to-end labeling process to maintain Core Data Sheets (CDS), and submission and label negotiations for US Prescribing Information (USPI), and EU Summary of Product Characteristics (EU SmPC). This role offers high visibility and the opportunity to work cross-functionally with SMEs, contribute to organizational strategic initiatives, and support Pfizer’s established products. The successful candidate should possess an eagerness to grow, an aptitude for strategic thinking, and a focus on delivering for patients.
How You Will Achieve It
Lead the development, maintenance, and implementation of high quality labeling including CDS, USPIs, EU SmPCs, and patient labeling
Manage cross-functional Labeling Team and collaborate with stakeholders including Clinical, Medical, Safety, Regulatory, and Commercial
Drive global labeling strategy through development of target labeling, scenario planning, and risk mitigation
Manage label negotiations with US FDA and EMA
Provide guidance on labeling regulations, industry best practices, and competitor label assessments
Act as the primary labeling representative on Global Regulatory Strategy Teams, Submission Working Groups, and other relevant product teams
Contribute to strategic initiatives and process improvements across the organization
Here Is What You Need (Minimum Requirements)
Bachelor’s degree in a scientific or technical discipline
Minimum of 4 years of relevant labeling experience in the pharmaceutical or biotech industry
Advanced knowledge of external labeling guidelines and regulations
Ability to successfully understand regulatory implications of product strategy with regards to the product label, assessment and practical management of associated impacts
Ability to develop strong and positive working relationships with cross-functional stakeholders and SMEs
Excellent written and verbal communication skills; complete fluency in English language
Proven strength in logical, analytical and writing ability
Strong project management skills and attention to detail
Proven ability to negotiate, influence and problem solve
Work Location Assignment:Hybrid
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