Medical Device Regulatory Specialist k & CE

Location: Sarasota, FL, US, 34243 York, PA, US, 17405 Waltham, MA, US, 2451 Charlotte, NC, US, 28277 Johnson City, TN, US, 37601 Milford, DE, US, 19963

Company: Dentsply Sirona, Inc

Requisition : 83371

Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with over a century 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 dental care. Dentsply Sirona’s headquarter is located in Charlotte, North Carolina. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. Visit  for more information about Dentsply Sirona and its products.

We are seeking an experienced and highly motivated Regulatory Affairs Specialist who will be a contributing member of a cross‑functional team in support of regulatory market access activities for US, Canada, EU, and other countries.

This postion can be located in one of the following DS facilities:
Sarasota, FL;
Charlotte, NC;
Johnson City, TN;
Milford, DE;
York, PA;
Waltham, MA

• 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

• Bachelor's 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

• 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

Dentsply Sirona is an Equal Opportunity Employer. All qualified applicants will be considered without unlawful discrimination or regard for race, color, religion, sex, sexual orientation, sexual or gender identity, national or ethnic origin, age, marital status, disability, genetic factors, military and veteran status, or any other characteristics protected by applicable local law.

All successful applicants must be eligible to work in the country the position is based.

Please note that Dentsply Sirona does not accept or respond to unsolicited requests or applications submitted by Recruitment Agencies/ Search Firms.

Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information:  .