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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.

As Research and Development (R&D) Project Manager,you’ll lead technical aspects in New Product Development projects as well as Core Business Engineering. With a focus on Root Canal Treatment,you’ll be dealing with dental instruments,root filling materials and associated electrical equipment. You’ll provide leadership to R&D project teams,in close cooperation with the multidisciplinary international Project Core Team. Whilst comfortable and used to working in an international environment a local focus remains paramount for cross-functional collaboration and ongoing compliance in a fast-evolving global Regulatory environment.

Main Responsibilities

• Leads the development of new medical devices in conformance with applicable international standards as well as with the Dentsply Sirona new product development procedure.
• Leads R&D Projects for New Product Development,Core Business Engineering and MDR remediation in direct collaboration with key project stakeholders.
• Provides leadership to R&D project members and serves as R&D’s principal point of contact for the Project Management Office.
• Defines project plan,human and financial resources needed to meet project objectives applying state of the art methods and tools for project management,and project documentation.
• Collaborates closely with internal and external laboratories for Design verification and validation.
• Drives project execution in compliance with regulations,applicable standards and company procedures.
• Creates and delivers regular verbal and written project updates to Management,to the Project Management Office and to R&D.
• Delivers compliant Technical Documentation using Electronic Document Management systems in accordance with company procedures.
• Partners with internal and external stakeholders critical for effective project execution.

Requirements and Qualifications

• Bachelor’s,Master’s or PhD degree in Mechanical Engineering,Microtechnology or similar
• Minimum of 3 years (MSc or PhD) to 6 years (BSc) of relevant professional experience in a highly regulated industry
• Strong technical background,preferably in metallurgy,polymers,structural and fracture mechanics as well as manufacturing processes
• Professional experience with product development phases for highly regulated products in an international environment
• Proven track record in Project Management; experience in the Medical Device industry would be a very strong plus
• Understanding of medical device design control and international standards.
• Very good command of MS Office including MS Project
• Excellent communication and presentation skills in English (C1) and French (B2)
• Strong interpersonal skills and the ability to deal effectively with a variety of different stakeholders,both internally and externally
• Hands-on approach to product design and development
• High results-orientation coupled with flexibility in adjusting to changes in priorities,timelines,and resources
• Strong team-spirit and collaborative nature
• Excellent organizational and prioritization skills to manage several projects in parallel
• Willingness to travel (up to 10%)