مدير مشروع الشؤون التنظيمية CMC GlaxoSmithKline

GlaxoSmithKline

Join our Chemistry, Manufacturing and Controls (CMC) Regulatory Affairs Group within Global Regulatory Affairs at GSK, where we play an essential role in ensuring uninterrupted access to life-changing medicines for patients worldwide.

As part of the CMC Regulatory Affairs team, you ll collaborate across Global Supply Chain (GSC), Technical, Quality, and Local Operating Companies to support lifecycle management of marketed small molecules. In this exciting role, you ll help shape regulatory strategies, drive sustainability initiatives that align with GSK s 2030 environmental goals, and deliver high-impact solutions that enhance the way we manufacture and control our medicines.

At GSK, we re committed to improving the quality of human life by enabling people to do more, feel better, and live longer. As a CMC Regulatory Project Manager, you ll contribute to this mission while advancing your career in an environment that fosters collaboration, innovation, and professional growth.

Join us to help shape the future of healthcare and make a difference in the lives of patients worldwide.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.

قراءة المزيد

https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/UK--London--New-Oxford-Street/CMC-Regulatory-Project-Manager_429428-2