Senior Regulatory Affairs Specialist

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. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY.Bringing out the best in people 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.Working At Dentsply Sirona You Are Able ToDevelop faster - with our commitment to the best professional development.Perform better - as part of a high-performance, empowering culture.Shape an industry - with a market leader that continues to drive innovation.Make a difference -by helping improve oral health worldwide.This position can be a hybrid working arrangement for someone that is near one of the following Dentsply Sirona locations: Sarasota, FL; Charlotte, NC; Milford, DE; or York, PA.Job SummaryThe Senior Regulatory Specialist is a contributing member of cross-functional teams in support of regulatory market access activities for US, Canada, EU, and other countries. May support NPD and Sustaining activities for the US, Canada and EU markets. Also supports additional international registrations.Key ResponsibilitiesAssists in development and execution of regulatory strategies to obtain and maintain regulatory approvals for medical devicesPrepares and submits international regulatory submissions to obtain and maintain regulatory approvals for medical devices, including 510(k) submissions and technical files for CE MarkingMaintains regulatory files and databases to ensure compliance with regulatory requirementsProvides regulatory guidance and support to cross-functional teams throughout the product lifecycleParticipates in review of labelling and claims for the US and EU markets.Reviews and interprets regulatory requirements and guidance documents to ensure compliance Coordinates regulatory activities with internal teams and external regulatory agenciesSupports regulatory audits and inspections as SME for questions related to market accessStays current with regulatory requirements and updates affecting medical devicesFosters professional interactions with internal and external stakeholders through various communication channels, enhancing business relationshipsComplies with company and departmental policies and administrative requirementsPerforms other duties as assigned or as neededEducationBachelor's degree in a relevant field, such as life sciences, regulatory affairs, or a related disciplineYears And Type Of Experience5(+) years of experience in regulatory affairs, preferably in the medical device industryExperience with leading regulatory submissions and documentation, including 510(k) submissions and CE markingIn-depth knowledge of FDA regulations and international standards (e.g., ISO 13485, MDSAP, EU MDR)Required Computer / Software SkillsProficiency with Microsoft Office SuiteProficiency with Regulatory softwareKey Required Skills, Knowledge, And CapabilitiesStrong attention to detail and organizational skillsExcellent communication (both written and verbal) and interpersonal skillsAbility to work effectively in a team environmentKnowledge of regulatory affairs principles and practicesAbility to critically review detailed scientific information and assess whether technical arguments are presented clearly, and conclusions are adequately supportedWillingness to learn and adapt to new processes and technologiesRegulatory registration experience within med device organizationsPrior 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 receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, disability, or protected Veteran status. We appreciate your interest in Dentsply Sirona.If you need assistance with completing the online application due to a disability, please send an accommodation request to careers@dentsplysirona.com. Please be sure to include “Accommodation Request” in the subject.For California ResidentsWe may collect the following categories of personal information in connection with the submission of your resume or application materials to us for employment, and if hired, your employment with us: identifiers (e.g., name, address, email address, birthdate); personal records (e.g., telephone number, signature, education information, criminal background information, passport number and visa information); consumer characteristics (e.g., sex, marital status, veteran status, race, disability, sexual orientation); professional or employment information (e.g., resume, cover letter, employment history, background check forms, references, certifications, transcripts and languages spoken); and inferences from personal information collected (e.g., a profile reflecting abilities and aptitudes).The above categories of personal information are collected for the following business purposes: performing recruitment and hiring services; processing interactions and transactions (e.g., to comply with federal and state laws requiring us to maintain certain records, managing the workforce); and security (e.g., detecting security incidents, protecting against fraudulent or illegal activity).For additional details and questions, contact us at careers@dentsplysirona.com