Regulatory Affairs Specialist Nobel Biocare

Nobel Biocare is a medical devices group and the world leader in innovative esthetic dental solutions with its brands Brånemark System®, NobelSpeedyT, NobelReplaceT, NobelPerfect®, NobelDirect®, Replace® Select, (dental implants) and Procera® (individualized dental prosthetics).Nobel Biocare is a one-stop shop for restorative esthetic dentistry, offering a wide range of innovative Crown & Bridge & Implant products, as well as training and education and clinically documented treatment concepts.Nobel Biocare has some 1,900 employees and recorded revenue of EUR 484 million in 2005.The Company is domiciled in Zurich, Switzerland with headquarters in Zurich and in Gothenburg, Sweden.Production takes place at four production sites located in Sweden and the USA.Nobel Biocare has direct sales organizations in 34 countries.The shares of the parent company Nobel Biocare Holding AG are listed on the SWX Swiss Exchange and on the Stockholm Stock Exchange, Sweden.We now need to further strengthen the Clinical & Regulatory Affairs Department The Regulatory Affairs Specialist will work in an international environment with authorities, officials and agencies within Europe, Americas, Asia-Pacific and report directly to the Global Director Clinical & Regulatory Affairs Department.Responsibility: You will ensure that the regulatory workflow is handled correctly and efficiently.You will also be responsible for global registrations, serve as regulatory advisor for design teams and contribute with regulatory expertise in different research projects.You will continuously investigate and keep yourself updated on requirements related to global product approvals, develop Regulatory Plans, maintain and update regulatory registrations, approval processes, standards and changes on a daily basis. Educational background: For this challenging position within Nobel Biocare we are looking for someone that has a relevant background, minimum Swedish gymnasium, with focus on technology or natural science.Furthermore, you need to have a few years of regulatory experience within the field of medical device business.Personally you are flexible, independent and can make priorities.You can take on many responsibility areas, you are service minded, a good team member and have diplomatic skills.You are also a good communicator, speak and write English fluently.A third language except Swedish is appreciated.Apply before 19th of February 2007.