**Requistion ID** : 79869 Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona’s products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona’s global headquarters is located in Charlotte, North Carolina, USA. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. **Bringing out the best in people** As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we’re looking for the best to join us. **Manager Quality Control** Do you want to join a world leading dental company that´s been shaping the industry around the world for more than a century? With our innovative solution we improve oral health worldwide. We make people smile! Join us at our Dental Sirona Implants in Mölndal / Gothenburg. What are we expecting from you? We expect you to have a passion for bringing out the best in people. You enjoy to coach and develop your team and you will work close with Manufacturing and Supply Planning to meet defined targets. The team consist of mainly Quality Technicians, and you will report into the Senior Manager Quality Assurance. We offer a truly International QA environment where you will work close with our other sites. We don´t mind if you also like to have fun at work as we value a good laughter every now and then. **Responsibilities** : + Lead Quality Control team in daily operations. + Ensure Incoming Inspection, Final Inspection and Final Release are performed according to plan. + Ensure that Quality Control processes are compliant and efficient. + Take the Lead and coordinate Non-conformity / CAPA activities. + Lead root cause investigations related to Quality Issues. + Provide QA support to Manufacturing when needed. + Actively work with Continuous Improvements of the processes linked to Quality Control. + Participate in Audits performed by internal / external parties. + Participate as QA representative in other improvement projects. **Background / Qualifications:** + An academic degree in engineering or equivalent professional background. + Experience from working in the medical device industry and have knowledge aboutISO 13485 and 21 CFR Part 820. + Experience as people manager and enjoy coaching and developing. + Excellent communication skills as the role requires close contact with several functions. + Participation in and experience of Audits from external parties. + Good communication in English as well as Swedish, both written and verbally. Personal characteristics are planning skills, attention to details and the skill to lead a team. We believe that you are a positive and social person with the ability to maintain a good relationship with local and global network. It is an advantage if you have strong focus and drive to achieve goals and targets. Good to know Please note that we will review applications continuously, so be sure to send in your application as soon as possible. We look forward hearing from you!