Global Regulatory Affairs Lead - Medical Devices

A leading life sciences consulting firm is looking for an experienced regulatory affairs professional. You'll manage regulatory submission timelines and prepare global medical device applications to ensure timely market access. A minimum of 5 years of experience and fluency in English are required. You will engage with regulatory authorities and cross-functional teams, author EU MDR-compliant documentation, and support audits to ensure ongoing compliance. This role is critical for maintaining global standards in a dynamic environment. #J-18808-Ljbffr