Dentsply - Bar Lev, IL
posted 4 days ago
About the position
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. Reporting to the Chief Technology Officer, the Vice President Research and Development for our IPS Business Unit will lead the innovation and development of cutting-edge Implants and Prosthetic products. This role is critical for driving our company's growth and maintaining our leadership in the dental industry. The VP of R&D will oversee the entire product development lifecycle, from conceptualization through commercialization, ensuring that all products meet regulatory requirements and exceed market expectations. Additionally, the incumbent closely collaborates across Business Units to ensure the focus on Clinical Jobs to be done and treatment solutions releases. The ideal candidate will be a strategic thinker with a deep understanding of Implants and Prosthetics technology, a strong track record in R&D leadership, and the ability to foster cross-functional collaboration.
Responsibilities
- Develop and execute the R&D strategy aligned with the company's vision, ensuring continuous innovation and market leadership in Implants and Prosthetics solutions.
- Drive the company's innovation agenda by identifying emerging technologies and market trends and managing the intellectual property (IP) portfolio to protect and leverage key innovations.
- Lead the research, design, and development of new products, ensuring timely delivery of high-quality, cost-effective solutions that meet customer needs.
- Work closely with Marketing, Manufacturing, Quality, and Regulatory teams to ensure seamless product development and launch processes.
- Build, mentor, and manage a high-performing R&D team, fostering a culture of innovation, accountability, and continuous improvement.
- Ensure all R&D activities comply with relevant regulatory standards, including FDA and ISO guidelines, and oversee the preparation of technical documentation for regulatory submissions.
- Develop and manage the R&D budget, ensuring efficient use of resources while maximizing ROI.
- Present R&D updates and strategic recommendations to leadership, establish strong relationships with KOLs and OPLs.
Requirements
- Degree in Engineering, Materials Science, Biomedical Engineering, or a related field is required, advanced degree (Master's or Ph.D.) in a relevant field is strongly preferred.
- Minimum of 15 years of experience in the medical device industry, with at least 7 years in a leadership role within R&D.
- Professional certifications related to project management, quality assurance, or regulatory affairs are a plus.
- Proven track record of successful product development and commercialization in the medical device industry.
- Extensive experience working within FDA-regulated environments and managing regulatory submissions.
- Experience in managing large, cross-functional teams and budgets.
- Ability to set and execute a clear R&D vision that aligns with overall business goals.
- Deep understanding of Implants and/or Prosthetic technologies, materials science, and medical device development.
- Strong knowledge of regulatory requirements in the medical device industry, particularly FDA and ISO standards.
- Ability to drive and manage innovation, from concept to commercialization.
- Willingness to travel (20 -50% depending on location).
Nice-to-haves
- Professional certifications related to project management, quality assurance, or regulatory affairs.
Benefits
- Equal Opportunity/ Affirmative Action employer.
