Senior Regulatory Affairs Specialist

Bioventus LLC.; Durham (NC); On-site; USD 85,000 - 105,000; Full time

Job summary

Bioventus LLC. is seeking a Senior Regulatory Affairs Specialist in Durham, NC. In this hybrid role, you will author and submit key regulatory applications, ensuring compliance with standards for new and existing products. A Master’s degree and 3 years of experience in regulatory affairs are required. You'll guide cross-functional teams and manage compliance documentation while communicating with regulatory agencies.

This position requires national travel up to 25% of the time. Join Bioventus and make a difference in helping patients lead active lives.

Qualifications

• 3 years of experience in regulatory affairs or related position within the medical device industry.
• Experience with regulatory assessments for engineering/design changes.
• Experience preparing and reviewing documentation for regulatory submissions.

Responsibilities

• Author applications for product clearance and maintain registrations globally.
• Communicate with regulatory agencies regarding submissions.
• Review protocols for scientific validity and compliance.

Skills

Regulatory assessment

Project management

Documentation preparation

Cross-functional teamwork

Education

Master’s degree in Regulatory Affairs or related field

Job description

## Senior Regulatory Affairs SpecialistApplylocations: Durham, NCtime type: Full timeposted on: Posted 2 Days Agojob requisition id: R-2026-06-001664**Are you ready to work for a more active world?** At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our success rests on working together to achieve shared goals and rewards. Join a diverse team of global colleagues driven to help patients resume and enjoy active lives.Bioventus LLC., seeks Senior Regulatory Affairs Specialist (Durham, NC).Duties:* Author and submit applications 510(k), PMA Supplements and, Technical Documentation to receive product clearance / approvals for new products and maintain existing registrations globally.* Author and maintain Technical Files compliant to the MDD 93/42/EEC and Technical Documentation compliant to the EU MDR 2017/745.* Communicate with Regulatory Agencies regarding submissions, and changes of products, including manufacturing, design and new product development.* Serve as Subject Matter Expert to represent Regulatory during internal audits and external audits by regulatory agencies.* Review protocols and reports for scientific validity and compliance to regulatory standards and provide scientific judgement to guide cross functional teams.* Perform Regulatory Assessments for design, manufacturing, and labeling changes to ensure compliance with regulations and standards where the product is registered.* Research requirements and set priorities while maintaining project schedules. Provide guidance and oversight to team members related to regulatory compliance.* Review marketing literature for compliance with applicable regulations and company policies and procedures.Required: Master’s degree or foreign equivalent in Regulatory Affairs, Pharmaceutical Sciences or related field plus 3 years of experience in the job offered, as Regulatory Engineer or related regulatory affairs position within the medical and/or diagnostic device industry.Must have 3 years of experience with:* Regulatory assessment of engineering/design change execution.* Working with or providing guidance to cross-functional or offshore team in preparation of documents for regulatory agency submissions.* Regulatory registrations in at least 3 or more of the following agencies or regions (FDA, EMEA, Canada, LATAM, Japan, Australia).* Project management.* Preparing and reviewing documentation regarding submissions and product changes of medical devices.Must have experience working with medical device registrations compliant with Medical Device Regulation and EU Medical Device Directive.Hybrid role model position, working 3 days in office and 2 days from within normal commuting distance of the office location.National travel required 25% of the time.**Are you the top talent we are looking for?**Apply now! Hit the “Apply” button to send us your resume and cover letter.*Bioventus is committed to fostering an inclusive and diverse community of employees with a strong sense of belonging. We believe we are bettered by all forms of diversity and take pride in working with top talent from every walk of life. In the spirit of inclusivity, qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion or sexual orientation. All individuals, regardless of personal characteristics, are encouraged to apply.*