Principal Regulatory Affairs Specialist

Why Join Bracco Medical Technologies?

We care as much about our employees as we do our patients. Our culture fosters a work environment where employees can thrive, be passionate and have fun along the way. Each member of the Bracco Medical Technologies team has the power to make a difference every day!

The Principal Regulatory Affairs Specialist is responsible for developing and implementing regulatory strategies across projects, processes, and/or products. This individual partners with internal stakeholders and external consultants to optimize and execute these strategies in support of business objectives. This role provides hands‑on regulatory affairs support for new product marketing submissions and changes to existing devices, including development of regulatory requirements/strategies and preparing submissions.

In addition, this individual will represent BMT Regulatory in interactions with US and international regulators during submission reviews/approvals and audits. This individual will ensure compliance with required regulations and established corporate standards and ensure that product approvals are properly maintained. This position requires creativity/innovation with expectations of independent research and use of accepted regulatory practices in the execution of tasks to drive successful outcomes.

• Develop and execute regulatory plans and author 510(k) Premarket Notifications, EU MDR Technical Documentation, Canadian Licensing Submissions, and contribute content to Japan and China submissions.
• Coordinate cross‑functional support for worldwide registrations for global product growth and market expansion.
• Participate as regulatory representative on project teams throughout the product lifecycle. Review, edit and approve project documentation, provide strategic regulatory direction and communicate global regulatory requirements and strategy to project teams and cross‑functional partners.
• Communicate with government regulatory agencies and Notified Bodies; prepare for and lead meetings / teleconferences with external regulatory authorities, including the FDA, and support audits and inspections as assigned.
• Identify new and emerging regulations, assess potential impact(s), and recommend alternatives to ensure compliance with all standards and regulations.
• Contribute content for and review all forms of device labeling and advertising materials for compliance with FDA submissions and applicable global regulations; analyze and recommend appropriate changes.
• Serve as the primary point of contact with external regulatory consultants, when applicable, coordinating their contributions and ensuring alignment with internal regulatory strategies and timelines.
• Maintain all regulatory files ensuring documentation and registrations are complete and up to date.
• Demonstrate strong planning, organizational and time‑management skills, including the ability to work on multiple projects and adhere to timelines to achieve desired outcomes.
• Drive superior results by taking initiative, planning and implementing projects, setting priorities and holding self and others accountable to meet commitments.
• Commit to driving efficiency while maintaining quality, and ensures timely, clear communications to internal stakeholders on project status and issues.
• Support the business by communicating effectively, managing issues proactively, resolving conflicts and mitigating risks.
• Mentor, develop, and provide oversight of junior regulatory staff and provide training and guidance for cross‑functional partners.

• Bachelor's degree plus 7+ years of experience in medical device Regulatory Affairs.
• Demonstrated experience with 510(k), EU CE Marking, and Health Canada submissions.
• Understanding of FDA, EU MDD and MDR, Australia and Canada regulatory framework including how to comply with standards and regulations.
• Experience successfully leading FDA meetings, such as pre‑submissions and submission issue request meetings.
• Effective written and verbal communication skills, technical writing and editing skills.
• Ability to develop clear, concise, and timely oral and written reports, and…