Global Strategic CMC Regulatory Lead

About the role Responsible for the CMC regulatory activities in the investigational, late phase development and/or early commercial lifecycle management of GSK products. About the responsibilities Si assicuri di leggere l'intera descrizione riportata di seguito e di candidarsi immediatamente se è sicuro/a di soddisfare tutti i requisiti.

About the role Responsible for the CMC regulatory activities in the investigational, late phase development and/or early commercial lifecycle management of GSK products. About the responsibilities * Be responsible for the global CMC regulatory activities for assigned projects and responds readily to changing events and priorities * Be responsible for CMC...

Menarini Group in Florence seeks a Head of Global Regulatory Publishing to own the global publishing strategy, technical submissions operations, and electronic document infrastructure across therapeutic areas. You will lead a global team and shape the regulatory publishing operating model. The role requires deep expertise in global electronic submissions and...

Our client is Menarini Group , a leading international pharmaceutical and healthcare company, present in 140 countries worldwide with over 17,500 employees , with a long-standing commitment to innovation, scientific excellence and improving patients’ lives. As part of the continued evolution of its Global R&D and Global Regulatory Affairs organization ,...

MENARINI Group is seeking a Performance Analysis Coordinator in Florence to transform market and competitive data into growth strategies. You will lead the Global Business Insights team, drive the BI transition to Power BI, and support top management with strategic analyses.The role requires a Master’s degree in quantitative fields, 5–7 years of...

pIn this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...

Global Strategic Portfolio Evaluation BI & CI Manager Location: Florence, Italy Contract: Permanent Role Overview We are seeking an experienced pharmaceutical professional to support global portfolio evaluation and strategic commercial decision-making for a leading international pharmaceutical organisation. This is a high-impact role combining business...

MENARINI Group in Florence, Italy, seeks a senior leader for Global Manufacturing Science & Technology to drive industrialization, process optimization and technology transfer across the product lifecycle.Reporting to the Global MS&T Lead, you will bridge R&D, manufacturing, quality and regulatory affairs, guiding cross-functional teams and CMOs to deliver...

pParexel is seeking an Regulatory Affairs Consultant - CMC for post-approval activities related to vaccines or biological products. The role collaborates across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions and timely regulatory outcomes. /ppYou will support worldwide regulatory activities, manage regulatory information...