Job Information
Dentsply Sirona Quality Control Manager - ZH Switzerland in Zurich, Switzerland
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.
Quality Control Manager
This role is an excellent opportunity at our digital hub in Zurich and is crucial for guaranteeing the quality of new product developments, as well as for the upkeep of existing products. It involves ensuring proper product documentation and control, safeguarding data integrity, confirming software reliability, fostering trust, and promoting ongoing improvement. Our modern workplace in Zurich has a start-up feel in a mature and global organization. We offer a hybrid working model. After the onboarding period, we are looking for a presence of two to three days per week on site. Join us and help us to improve dental care in the future!
Key Responsibilities
Assure high quality of our products throughout their entire lifecycle
Work close with R&D on new product developments and maintaining existing products – SaMD and non-medical SW
Assure data accuracy and data integrity
Support product registrations
Complaint investigation in collaboration with R&D teams and customer support
CAPA and NC Management
Change Management and Document Control
Lead or participate in quality related project, where applicable
Support to quality related processes, e.g. internal audits, supplier audits, external audits, CAPA management, training and others
Requirements and Qualification
Bachelor or Master in engineering, computer science, life science or other related fields. Software background is a plus
Minimum of 5 years professional experience in new product development of medical devices, preferably SaMD; experience in quality management or regulatory affairs of medical devices, preferably in a software environment
Lead auditor qualification is benefitial
Knowledge of MDR, CFR FDA, MDSAP, ISO 14971, ISO 13485, IEC 62304
Good technical understanding of software
Excellent communication and team player skills
Independent and results-oriented way of working
Fluency in English (written and spoken) – German is a plus
With us, you can expect an attractive salary that recognizes your performance. We offer flexible working hours in a hyrbid working model to harmonize your private life and job. On top, you can expect benefits such as a free yearly dental check-up, an appealing pension scheme, working in a up to date Software Stack, etc. We also support your further training and development.