Location: Warsaw & Madrid/Barcelona– hybrid work Type: Full-time Join our CMC Regulatory Affairs team and work on complex projects supporting the development, registration, and lifecycle management of medicinal products. You will combine your CMC expertise with client-facing consulting, supporting
Location: Warsaw & Madrid/Barcelona– hybrid work Type: Full-time What you’ll be doing CMC Activities Lead complex CMC projects and provide strategic advice on pharmaceutical development, manufacturing, testing, lifecycle management, and global regulatory requirements; Coordinate the preparation, review, and submission
About the role Are you ready to power the business to have a bigger impact on patients lives? Embrace the novel opportunity to work at a business that puts patients first. In Early Science, we have