Step out of your comfort zone, excel and redefine the limits of what is possible. That’s just what our employees are doing every single day – in order to set the pace through our innovations and enable outstanding achievements. After all, behind every successful company are many great fascinating people.The Senior Regulatory Affairs Specialist is responsible for US medical device premarket (510(k)) and post market activities (such as radiation and laser reports; product listing and registration) for assigned products Regulatory responsibilities include, but are not limited to, communicating with local and multi-site Regulatory Counterparts, Product Development Teams, etc and developing regulatory strategy for US market based on applicable standards, guidances
This job listing is no longer active.
Check the left side of the screen for similar opportunities.