Role Overview
Dentsply Sirona is hiring a entry-level Regulatory Affairs Specialist. This is a full-time role in Milford. posted 2 weeks ago. Full responsibilities, required qualifications, and the apply link are listed in the description below.
Resume Keywords to Include
Make sure these keywords appear in your resume to improve ATS scoring
Sign up free to auto-tailor your resume with all these keywords and get a higher ATS score
Job Description
Requistion ID: 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 www.dentsplysirona.com for more information about Dentsply Sirona and its products.
Summary
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
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.
Eligibility: All successful applicants must be eligible to work in the country the position is based.
Assistance: If you need assistance with completing the online application due to a disability, please send an accommodation request to accommodationrequest@dentsplysirona.com.
Agencies: Please note that Dentsply Sirona does not accept or respond to unsolicited requests or applications submitted by Recruitment Agencies/ Search Firms.
Notice on Fraudulent Job Offers: 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: careers.dentsplysirona.com.
Frequently Asked Questions
How do I apply for the Regulatory Affairs Specialist position at Dentsply Sirona?
Use the Apply button above to submit your application directly to Dentsply Sirona. Most applications take less than 5 minutes if your resume and contact details are ready, and you'll be routed to the employer's official application system to finish.
Where is the Regulatory Affairs Specialist position at Dentsply Sirona located?
This position is based in Milford. Dentsply Sirona has not indicated remote or hybrid options for this role, so candidates should plan for on-site work.
What does a Regulatory Affairs Specialist at Dentsply Sirona earn?
Dentsply Sirona has not disclosed a salary range in this posting. Many employers share specifics later in the interview process; you can also ask during a recruiter screen if compensation transparency is important to you.
When was the Regulatory Affairs Specialist role at Dentsply Sirona posted?
This role was posted on May 21, 2026 (20 days ago). It's still listed as actively hiring; we re-confirm openings against the source system multiple times per day and remove closed roles.
Is the Regulatory Affairs Specialist role at Dentsply Sirona entry-level?
Yes. This is an entry-level position. Strong candidates typically have 0-2 years of relevant work experience, internships, or significant project work. Read the full description for any specific qualification requirements Dentsply Sirona has listed.
AI-powered job search
Get every job scored to your resume
Upload your resume and get jobs ranked, your resume tailored, and employee contacts found automatically.
Get Started FreeNo credit card to start