Regulatory Affairs Specialist

Company: Dentsply Sirona
Location: Sarasota
Posted on: January 26, 2026

Job Description:

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 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. This position can be a hyrbid working arrangement for someone that is near one of the following locations: Sarasota, FL, Charlotte, NC, or York, PA Contributing member of cross-functional teams in support of regulatory market access activities for US, Canada, EU, and other countries. Job Responsibilities: • Prepares and submits international regulatory submissions to obtain and maintain regulatory approvals for medical devices, including 510(k) submissions and technical files for CE Marking • Maintains regulatory files and databases to ensure compliance with regulatory requirements • Reviews and interprets regulatory requirements and guidance documents to ensure compliance • Coordinates regulatory activities with internal teams and external regulatory agencies • Supports regulatory audits and inspections as SME for questions related to market access • Stays current with regulatory requirements and updates affecting medical devices • Fosters professional interactions with internal and external stakeholders through various communication channels, enhancing business relationships • Complies with company and departmental policies and administrative requirements • Performs other duties as assigned or as needed Education & Experience: • Bachelors degree in a relevant field, such as life sciences, regulatory affairs, or a related discipline • 1-5 years of experience in regulatory affairs, preferably in the medical device industry • Experience with regulatory submissions and documentation, including 510(k) submissions and CE marking • Knowledge of FDA regulations and international standards (e.g., ISO 13485, MDSAP, EU MDR) • Proficiency with Microsoft Office Suite • Proficiency with Regulatory software Key Required Skills, Knowledge, and Capabilities: • Strong attention to detail and organizational skills • Excellent communication (both written and verbal) and interpersonal skills • Ability to work effectively in a team environment • Knowledge of regulatory affairs principles and practices • Ability to critically review detailed scientific information and assess whether technical arguments are presented clearly, and conclusions are adequately supported • Willingness to learn and adapt to new processes and technologies • Regulatory registration experience within med device organizations • Prior technical writing experience and proven track record with FDA and EU regulatory submissions preferred

Keywords: Dentsply Sirona, Lehigh Acres , Regulatory Affairs Specialist, Healthcare , Sarasota, Florida