Principal Regulatory Affairs Specialist - Bracco Medical Technologies

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 develops and executes regulatory strategies for medical device products, submissions, and lifecycle changes. This role provides hands-on regulatory support for new product marketing submissions, changes to existing devices, global registrations, audits, labeling, and ongoing compliance with applicable regulations and company standards.

• Develop and execute regulatory plans for product submissions, including 510(k) Premarket Notifications, EU MDR Technical Documentation, Canadian Licensing Submissions, and select Japan/China submission content.
• Serve as the regulatory representative on cross-functional project teams throughout the product lifecycle, providing strategic guidance on global regulatory requirements.
• Prepare for and support communications with regulatory agencies and Notified Bodies, including FDA interactions, submission reviews, approvals, audits, and inspections.
• Maintain complete and current regulatory files, product registrations, and supporting documentation.
• Review device labeling, advertising, and promotional materials for compliance with approved submissions and applicable global regulations.
• Monitor new and changing regulations, assess business impact, and recommend appropriate compliance actions.
• Mentor junior regulatory staff and provide regulatory guidance to cross-functional partners.

• Bachelor’s degree in Engineering, Life Sciences, Regulatory Affairs, or a related technical field.
• 7+ years of regulatory affairs experience in the medical device industry.
• Demonstrated experience preparing and supporting global regulatory submissions, including FDA 510(k), EU MDR/CE Marking, and Health Canada submissions.
• Strong understanding of FDA regulations, EU MDR, international regulatory frameworks, product lifecycle requirements, labeling review, and regulatory compliance practices.
• Experience leading or supporting FDA meetings, agency interactions, audits, inspections, and cross‑functional regulatory strategy discussions.
• Excellent technical writing, communication, project leadership, analytical thinking, and stakeholder management skills.

• Experience supporting Class II medical devices, global market expansion, or multi‑region regulatory submissions.
• Experience mentoring regulatory professionals or leading regulatory work streams without direct supervisory authority.
• Regulatory Affairs Certification or advanced degree in a relevant discipline.

The estimated base salary range for this position is $131,000–$143,000 annually. Actual compensation may vary based on relevant experience, skills, education, internal equity, and business needs.

Bracco Medical Technologies also offers a comprehensive total rewards package, including

• health benefits
• paid time off
• company holidays
• paid family leave
• retirement savings
• tuition reimbursement
• professional development opportunities

Bracco Medical Technologies is an Equal Opportunity Employer.

Employment decisions are made without regard to race, color, religion, sex, national origin, disability, protected veteran status, age, or any other characteristic protected by applicable law.

Improve people’s lives by shaping the future of prevention and precision imaging. This is our purpose. Our work impacts millions of people all over the world. Not least the more than 4,000 Bracco colleagues who work to improve lives every single day. That is quite a responsibility and something we proudly embrace. We are the Bracco Group!