This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Eu Regulatory Affairs Senior Manager (Biosimilars)
Amgen seeks a Senior Manager in EU Regulatory Affairs for Biosimilars in Uxbridge, UK. You will lead regional regulatory strategy and submissions for a dynamic biosimilar portfolio. Ideal candidates possess deep biosimilars expertise, a scientific degree, and a proven track record in regulatory s...
Executive Director of Regulatory Affairs - Obesity and Related Conditions
Lead global regulatory strategy for Amgen’s obesity pipeline as Executive Director of Regulatory Affairs. Drive integrated cross-indication approaches, mentor high-performing teams, and align development pathways for metabolic and related conditions. Requires 10+ years regulatory experience with ...
Senior Manager Manufacturing Systems Engineering - Automation
Lead a team of Automation Engineers at Amgen’s advanced drug substance plant in Holly Springs, NC. This Senior Manager role requires 8+ years of Engineering experience and 2+ years of leadership. Drive automation strategy using Emerson DeltaV, Allen Bradley PLC, and Siemens DesigoCC. Enjoy a comp...
Lead global forecasting strategy for Amgen’s high-impact obesity portfolio as Senior Director. Drive evidence-based forecasts to inform investment, launch, and lifecycle decisions in a rapidly evolving therapeutic area. Requires deep biopharma forecasting expertise, leadership experience, and kno...
Join Amgen as an Intern in Medical Operations - Oncology in Mississauga, Canada. Support strategic Medical Affairs tactics, manage budgets, and coordinate scientific congresses. Ideal for students in Life Sciences or related fields with strong research skills. Gain hands-on experience in a collab...
Regulatory Affairs Manager sought by Amgen in Dun Laoghaire, Ireland. You will lead CMC regulatory strategy, manage global dossiers for MAAs and CTAs, and ensure compliance. Requires a Doctorate or Master’s with 3+ years of Regulatory CMC experience. Join a global biotech leader offering a divers...
Lead manufacturing systems innovation at Amgen in Thousand Oaks, CA. As Principal Manufacturing Systems Engineer, you will drive GMP-compliant automation projects, manage global standards, and oversee financials for core systems like Aveva PI and DeltaV. Requires a Doctorate with 2 years of leade...
Seeking a proactive **Project Management Coordinator** in Holly Springs, NC to support Operations staff. This role requires a High School diploma with 4 years of senior admin experience or an Associate's degree. Key skills include Excel, PowerPoint, SharePoint, and MS Project. Enjoy top benefits ...
Eu Regulatory Affairs Senior Manager - General Medicine
Senior EU Regulatory Affairs Manager sought to lead regional strategy and submissions for General Medicine at Amgen in Cambridge/Lisbon. Drive clinical trial and marketing applications, leveraging deep drug lifecycle knowledge and regulatory expertise. Requires a scientific degree, proven strateg...
Amgen seeks a Regulatory Affairs Manager in Cairo, Egypt to lead submissions and lifecycle management for new and established products. You need 6+ years of pharmaceutical regulatory experience, deep knowledge of FDA/EMEA guidelines, and proven people management skills. This role offers a chance ...
Lead Director of CfOR Operations at Amgen in Thousand Oaks, CA. Drive the scalable, compliant delivery of high-impact observational research (RWE) across the product lifecycle. Requires 12+ years in biotech/pharma with proven operational transformation and leadership. Enjoy top benefits, career g...
Senior Project Manager needed to drive Corporate Affairs & External Engagement for Obesity initiatives in Thousand Oaks. You will coordinate medical congresses, support leadership communications, and streamline workflows using AI. Requires a Bachelor’s degree with 6 years of experience and strong...