Principal Regulatory Affairs Specialist

About the role

At Boston Scientific, you’ll discover a place where you can have meaningful purpose—improving lives through your life's work. In our Rhythm Management division, we offer innovative solutions for treating irregular heart rhythms and heart failure, while protecting against sudden cardiac arrest. We continue to expand into new geographies and high‑growth adjacent markets through cutting‑edge technologies.

This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

Your responsibilities will include:

• Provide regulatory guidance, training, and mentoring to Regulatory Affairs colleagues and cross‑functional partners.
• Develop global strategies for regulatory approval across all medical device classifications.
• Coordinate, author, and submit U.S. and EU regulatory filings for new and modified products—including PMAs, PMA Supplements, pre‑submissions, 510(k)s, CE Mark submissions under MDR, annual reports, and U.S. clinical investigation submissions.
• Support international submissions and registrations in partnership with BSC’s global regulatory teams.
• Respond to regulatory and clinical personnel requests related to international clinical investigation submissions.
• Build and maintain productive relationships with regulatory agency reviewers.
• Review technical and labeling documentation for regulatory submission readiness and compliance.
• Evaluate product and manufacturing changes for regulatory impact and ensure appropriate filing updates.
• Represent Regulatory Affairs on cross‑functional project teams, including new product development and continuous improvement initiatives.
• Support and lead regulatory audits as needed.
• In all actions, maintain a primary commitment to patient safety and product quality by ensuring compliance with Boston Scientific’s Quality Policy and applicable procedures.

Qualifications:

• Bachelor’s degree in a scientific or technical discipline.
• Minimum of 7 years’ experience in regulatory affairs or related field, or 5 years’ experience with an advanced degree (Master’s or PhD).
• Proven knowledge of U.S. and EU regulatory requirements for medical devices, including clinical investigations and Quality Systems standards.
• Experience authoring a variety of regulatory submissions (510(k), PMA, CE Mark under MDR, etc.).
• Solid understanding of product development, clinical development, manufacturing, and change control.
• Strong problem‑solving and research skills, along with proficiency in Microsoft Word, Excel, PowerPoint, and Adobe Acrobat.
• Previous experience in the medical device industry, specifically with Class II or III devices.
• Prior direct experience interacting with the FDA, Notified Bodies, or international regulatory authorities.
• Ability to work independently and manage multiple complex projects simultaneously.
• Demonstrated leadership, strategic thinking, and project management capabilities.
• Experience with capital equipment or software‑based medical devices.
• Strong interpersonal skills and ability to clearly communicate complex regulatory concepts.
• History of providing technical guidance, training, or mentorship within Regulatory Affairs or cross‑functional teams.

Minimum Salary: $99,100

Maximum Salary: $188,300

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non‑exempt (hourly), non‑sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements). Compensation for exempt, non‑sales roles may also include variable compensation, i.e., annual bonus target and long‑term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Nearest Major Market: Minneapolis
Job Segment: Regulatory Affairs, Medical Device, Compliance, Testing, Law, Legal, Healthcare, Technology