Regulatory Affairs Project Manager (m/f/d)

Job description

We are looking for a Regulatory Affairs Project Manager to provide strategic direction and manage product registrations across Europe, the US, and China. You will prepare premarket submissions and collaborate with international teams. Ideal candidates have significant regulatory experience and expertise in medical devices or IVDs. At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted... At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted an... regulatory affairs, project management, medical device regulatory compliance, premarket submissions, fda submission, notified body submission, regulatory

strategy, product registration, stakeholder management, cross-functional collaboration, quality management, compliance management, agile project management, life sciences knowledge, data science knowledge, english fluency, international regulatory knowledge, multitasking