GE Healthcare is seeking an entry level Regulatory Affairs professional to support marketing authorization activities and lifecycle management tasks. You will assist with CPP management, documentation legalization, labeling aspects and regulatory fees, while ensuring right-first-time submissions.
Key responsibilities include supporting submissions, improving processes, and collaborating with regional and national regulatory teams to meet timelines and quality standards.
#J-18808-LjbffrGlobal Regulatory Affairs Intern — Jumpstart Submissions in Chalfont St Giles employer: MS0160 GE Healthcare Limited
At GE HealthCare, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. As a Lead QA Specialist in New Product Implementation, you will have the opportunity to work with cutting-edge technology in a global environment, ensuring compliance and quality in healthcare solutions. We are committed to your professional growth, providing continuous learning opportunities and a supportive atmosphere where your contributions can make a real impact.
Contact Details:
MS0160 GE Healthcare Limited Recruitment Team
