Amgen - IT - Administration

Senior Associate Regulatory Affairs role in Cambridge, UK, supporting UK and Ireland submissions. You will manage marketing authorisations, clinical trial documentation (IMPDs), and agency interactions with increasing autonomy. Requires degree, Veeva Vault experience, and strong regulatory projec...

Seeking a **Manager, Regulatory Affairs** in **Seoul, South Korea** to lead end-to-end **Clinical Trial Applications** and regulatory submissions. Requires a Bachelor’s in Pharmacy, 6-7 years of clinical trials experience, and 3-4 years in **Korean regulatory submissions**. Ideal candidates have ...

Amgen seeks a Global L&P Director for ELMAC ROW in Lisbon, Portugal. This strategic role requires a Doctorate with 4 years of experience or equivalent, plus 4 years of managerial/leadership experience. You will elevate learning strategy, drive digital transformation with AI and data analytics, an...

Senior Manager – Systems and Master Data Management Lead in Hyderabad, India. Lead a high-performing team ensuring enterprise Engineering, Facilities, and EHS systems are standardized, scalable, and secure. Drive master data governance and FAIR data principles while partnering with Technology and...

Amgen seeks a Regulatory Policy and Intelligence Senior Manager to drive global policy alignment and impact patient access. This US-based role requires deep regulatory expertise (FDA/EMA) and a scientific background. You will analyze emerging guidances, coordinate ICH activities, and shape Amgen’...

Amgen seeks a Japan Regulatory Strategy Manager in Tokyo to lead drug development strategies and interface with Japanese authorities. This role requires 10+ years of experience, including 5+ in Regulatory Affairs, with deep knowledge of Japan’s pharmaceutical regulations. You will drive local and...

Lead global regulatory strategy for Amgen’s obesity and chronic weight programs in Thousand Oaks, CA. Drive FDA/EMA submissions and GRTs with deep expertise in metabolic biology, cardiometabolic risk, and clinical endpoints. Requires 8–10+ years of global regulatory experience and a Doctorate or ...

Seeking a **MEA Regulatory Affairs Senior Associate** in **Cairo, Egypt** to manage labeling and packaging for Amgen’s pipeline and biosimilars. Requires 2+ years of RA experience, a pharmacist/biology background, and fluency in English & Arabic (French a plus). Drive lifecycle management, e-labe...

Global Regulatory Director Lead sought to drive strategy for obesity and Type II diabetes programs. This role requires deep expertise in metabolic biology, global submissions, and Health Authority interactions (FDA, EMA). Lead cross-functional GRTs, develop regulatory plans, and shape clinical de...

Senior Associate Regulatory Affairs sought for Amgen’s clinical studies in Mexico City. Drive local regulatory strategy and ensure compliant clinical trial authorizations under NOM-012 and COFEPRIS. Requires a Master’s in health sciences with clinical regulatory experience in Mexico. Enjoy compet...

Join our Global Commercial Operations team in Lisbon as an Associate Scrum Master. Facilitate Agile practices and sprint delivery for the ELMAC region, using Jira and SAFe frameworks. Guide a dynamic team, remove impediments, and drive continuous improvement in a cloud-first, AI-powered environme...

Join Amgen's Commercial Data Management team in Hyderabad as an MDM Associate. Support day-to-day operations of our core master data platform across key domains like Provider and Patient. This hands-on role is ideal for early-career professionals with 2-5 years' data management experience and SQL...