Lediga jobb som Riskingenjör, risk management i Härryda

Are you currently working within Quality Engineering in health sciences or medical devices? Perhaps you are working with Clinical Evidence and seeking a different way you can make an impact on outcomes for end users? Are you looking for a role where you will not only be responsible for driving Risk Management, work at the head office where a life changing product is not only developed but also manufactured? Work with a product which changes people’s lives?Change people’s lives and love what you do! Cochlear develops world-leading medical devices that help people hear. As a top 100 medical device company and market-leader in implantable hearing devices, more people choose a Cochlear-branded cochlear implant system than any other. Our employees tell us that the number one reason they enjoy working for Cochlear is the opportunity to make a difference to people’s lives.We are seeking a Senior Risk Management Specialist to join our Quality & Regulatory department. This position reports directly to the Quality Manager. This role is responsible for driving Risk Management and Usability Engineering in the development products here at Cochlear BAS. A key focus on assuring that our products are launched not only on time, but are safe and easy-to use for our end customer.Key responsibilities: Assure that products are safe and reliable by applying state of the art Risk Management methods in cross functional co-operation in development projects.Educate the business in methods useful for the design of safe productsHandle common quality management tasks such as CAPAs and nonconformitiesProduct intelligence on status of reliability, usability and product risk prior to product launchWhy is this role right for you?You have an Engineering, Clinical or other relevant degreeYou have experience working with Risk Management or Clinical ProtocolsYou have knowledge of ISO 14971You have an understanding of design controlHave experience working with Usability EngineeringYou have worked with a Quality Management SystemYou have had exposure to product developmentYou have an interest to further learn about Product UsabilityYou are looking for a role with global exposureYou will be part of setting they key standards within the business for Risk Management including MDR.You are comfortable speaking and writing in English at a professional levelYou can feel proud that the work you do helps more people around the world to hear again and live full lives.You will enjoy spacious, modern facilities, surrounded by a beautiful forest in MölnlyckeYou will experience an engaged workplace, motivated team mates and supportive Manager  A Little Bit About CochlearCochlear’s global mission is to help people hear and be heard. Cochlear BAS is the division of Cochlear that designs and manufactures the world’s leading bone conduction and other implantable acoustic solutions. Our employees tell us that the number one reason they enjoy working for Cochlear is the opportunity to make a difference to people’s lives. Situated in Mölnlycke, 10 minutes from the city centre of Gothenburg, Sweden, the head office employs approximately 200 people whose responsibilities include research, product design and development, marketing, quality and regulatory, manufacturing, distribution and administration for our implantable acoustic products.Does this sound of interest to you? Of course it does, where else would you be able to be an integral part of helping people hear and be heard? So what are you waiting for?If you feel your skills and experience match what we have mentioned then Apply Now! Or maybe you want to learn more about Cochlear first, you can simply head to our website www.cochlear.comAs the selection and interview process is ongoing, please submit your application as soon as possible Visa mindre