... development process and design control Preferred qualifications: Understanding of FDA, European, and ... Scientific, our products and technologies are used to diagnose or treat a wide range of medical conditions ...

... responsible for Regulatory Affairs support of global regulatory submissions for the BSC product development ... /regulatory pathway development, testing requirements, clarification, and follow-up of submissions under ...

... responsible for Regulatory Affairs support of global regulatory submissions for the BSC product development ... /regulatory pathway development, testing requirements, clarification, and follow-up of submissions under ...

... . Participate in department systems development initiatives. Required qualifications: Minimum of a Bachelor ... and standards General understanding of product development process, design controls and quality system ...

... responsible for Regulatory Affairs support of global regulatory submissions for the BSC product development ... /regulatory pathway development, testing requirements, clarification, and follow-up of submissions under ...

... responsible for Regulatory Affairs support of global regulatory submissions for the BSC product development ... /regulatory pathway development, testing requirements, clarification, and follow-up of submissions under ...

... the development of global strategies for regulatory approval of Class I, II and III medical devices ... by working in teams of diverse and high-performing employees, tackling some of the most important ...

... direct supervision of the RA Project Manager, or Department Manager, assists in preparing moderately ... . Under the direct supervision of RA Project Manager or RA Department Manager, develops global regulatory ...