• Design and operationalize scalable compliance frameworks, including policies, procedures, and controls aligned with federal, state, and local requirements • Build escalation workflows so complaints requiring additional oversight are quickly identified and handled consistently • Review training materials, scripts, and workflows to ensure regulatory compliance, and collaborate on enhancements where needed • Assist in developing reporting and dashboards that translate customer service data into actionable insights for leadership • Lead risk identification, assessment, and mitigation processes across business • Maintain risk registers and control frameworks • Establish escalation and reporting structures for key risks • Design risk-based monitoring and testing programs • Define KPIs and develop reporting dashboard for leadership • Identify trends and areas for improvement across compliance and risk

• Provide strategic regulatory leadership across radiopharmaceutical clinical development programs • Develop and execute global regulatory strategies • Lead global regulatory submissions in support of clinical development, product registrations, and lifecycle management activities • Translate complex and evolving global regulatory requirements into clear, actionable strategies • Ensure regulatory alignment across functions and support the successful advancement of radiopharmaceutical programs from early development through commercialization

Title: Senior Regulatory Affairs Specialist Location: Marlborough, MA, US, 01752 Department: Legal and Regulatory Job Description: Additional Location(s): US-CA-Irvine; US-MN-Arden Hills; US-MN-Maple Grove Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. About this role: At Boston Scientific, this is a place where you can find meaningful purpose, improving lives through your life's work. We offer a collaborative culture that values diversity and prioritizes initiatives that promote awareness and inclusion, celebrating personal, cultural, and demographic differences of our customers, patients, and workforce. In the Urology division, we continually advance the quality of patient care with innovative Urology solutions. We are looking to hire an enthusiastic individual for a Senior Regulatory Affairs Specialist position (hybrid work mode) supporting our rapidly growing active implantable device portfolio. This role will be responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process, as well as developing regulatory strategies. The role requires strong US, EU, and international regulatory experience that can be leveraged to help support international expansion. In this role, you’ll be part of a high-functioning, close-knit Regulatory Affairs team responsible for support of submissions and on-going regulatory compliance through partnership with our global R&D, manufacturing, clinical, and quality teams. Work model, sponsorship, relocation: At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. We will consider candidates from the following office locations: Irvine, CA, Marlborough, MA, Arden Hills, MN, or Maple Grove, MN. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Your responsibilities will include: - Reviews change notifications and performs regulatory impact assessment for product and manufacturing changes for compliance with applicable regulations and impact to regulatory filings, and supports associated global submissions as needed - Supports the coordination, drafting, and submitting of U.S. and EU regulatory filings for new and modified Class III products   - Provides technical reviews of test protocols and reports - Assesses labeling materials, including Instructions for Use - Represents RA on cross functional project teams - Works as liaison with International BSC Regulatory colleagues on various projects, including providing support with international regulatory filings - Supports highly technical or major business segment product lines, special projects or strategic initiatives Required Qualifications: - A minimum of a Bachelor’s Degree in a scientific, technical, or related discipline - A minimum of 4 years Regulatory Affairs experience in the medical industry - Prior experience with 510(k) submissions, EU MDR or international regulatory registrations Preferred Qualifications: - Prior experience with PMA submissions or Class III submissions - Prior experience with active implantable devices, active devices, or long-term implants. - Working knowledge of FDA, EU and international regulations for medical devices - General understanding of product development process, design control and quality system regulations - Ability to simultaneously manage several projects - Proficiency with Microsoft Office - Effective research and analytical skills - Effective written and oral communication, technical writing and editing skills - Ability to work independently with minimal supervision Requisition ID: 627376 Minimum Salary: $89200 Maximum Salary: $169500 The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—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 transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn. 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. Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

• Oversees the planning, execution, and monitoring of quality and regulatory activities to ensure organizational compliance • Leads and develops a high‑performing compliance team by setting priorities, managing performance to activity, and supporting professional development • Serves as the quality knowledge expert in all related to a SaMD organization and the primary point of contact for the Agile Release Train (ART) and Compliance Teams • Works collaboratively with the ART and management team members to align quality and compliance activities with business and product goals • Promotes Lean-Agile product development principles integrates them into the Quality Management System using a risk-based approach • Identifies, assesses, and communicates quality and compliance risks, providing actionable recommendations to improve product quality and regulatory readiness • Drives continuous improvement initiatives to maintain adherence to Standard Operating Procedures (SOPs), regulatory requirements, and quality standards • Leads the creation, review, approval, and maintenance of quality documentation • Plans and manages quality management projects that support ongoing compliance and continuous improvement • Establishes, monitors, and reports on post-market quality metrics • Manages the internal audit program, guiding internal auditors and ensuring overall organizational compliance • Facilitates external audits and inspections, including Food and Drug Administration (FDA), client, and other regulatory audits, to ensure successful outcomes • Ensures execution of regulatory operations, including standards maintenance, product labeling, Unique Device Identifier (UDI) updates, and medical device reporting requirements.