Regulatory Affairs Specialist

Regulatory Affairs Specialist

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.

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

Key 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:

Bachelor's degree in a relevant field, such as life sciences, regulatory affairs, or a related discipline

Years and Type of Experience:

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)

Required Computer / Software Skills:

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

Equal Opportunity Employer:

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.

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

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