π‘ Opportunity Summary
- Mid-Senior levelDentsply 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.
- 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.

Job title
Regulatory Affairs Specialist IICompany
LifelancerJob Title: Regulatory Affairs Specialist IIJob Location: Home, KS 66438, USAJob Location Type: RemoteJob Contract Type: Full-timeJob Seniority Level: Mid-Senior levelDentsply Sirona is the worldβs 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 Sironaβs products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sironaβs global headquarters is located in Charlotte, North Carolina, USA. The companyβs shares are listed in the United States on NASDAQ under the symbol XRAY.Bringing out the best in peopleAs 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 weβre 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.Regulatory Affairs Specialist II – Remote
- Leads regulatory submissions to obtain and maintain regulatory approvals for medical devices, including 510(k) submissions, and technical files for CE marking
- Provides regulatory guidance and support to cross-functional teams throughout the product lifecycle
- 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
- 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
- Bachelor’s degree in a relevant field, such as life sciences, regulatory affairs, or a related discipline
- 5(+) years of experience in regulatory affairs, preferably in the medical device industry
- Experience with leading regulatory submissions and documentation, including 510(k) submissions and CE marking
- In-depth knowledge of FDA regulations and international standards (e.g., ISO 13485)
- Proficiency with Microsoft Office Suite
- Proficiency with Regulatory software
- Strong leadership, attention to detail and organizational skills
- Excellent communication and interpersonal skills
- Ability to work effectively in a team environment
- Knowledge of regulatory affairs principles and practices
- Willingness to learn and adapt to new processes and technologies
- Leadership experience within med device organizations
- Strong organizational skills, including attention to detail
- Strong written and verbal communication
- Exceptional interpersonal skills
Expected salary
$100000 – 110000 per yearLocation
USAJob date
Fri, 25 Jul 2025 22:51:03 GMTApply for the job now!
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