Senior DesignQualityEngineer - Electrophysiology

Additional Location(s):US-MA-Waltham;
Canada-QC-Montreal; US-MN-Arden Hills

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.

We have a high-impact opportunity for a Senior Design Quality Engineer  to lead design assurance efforts for a critical medical devicein the Electrophysiology space. This role requires a self-driven professional capable of independently managing complex technical challengesanddrivingtosolutionsacross hardware,software, and system domains. The Senior Engineer willinfluence strategic quality initiatives, mentor junior engineers, and serve as a key resource in cross-functional teams to ensure product safety, regulatory compliance, anddesignrobustness.

At Boston Scientific, we value collaboration and synergy. This hybrid role is based in Waltham, MA or Arden Hills, MN and requires being on-site at least three (3) days per week. We will also consider candidates based in our Montreal, Canada location.

Relocation assistance may be available for this position at this time.

Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

• Serve as the technical authority within Quality for system integration,design decisions,risk management,andsoftwaredevelopment &validation.
• Independently lead design control activities for the Capital Equipment, including
  
  Design & Development planning, risk management, design verification, and validation efforts, with a strong focus on robustness ofsystem design and documentation.
• Collaborate closely with R&D, regulatory, manufacturing, and clinical teams toprovideexpert guidance on design and compliance matters throughout the product lifecycle.
• Own andmaintaincomprehensive risk management files (Hazard Analysis, FMEAs), ensuring robust coverage of both hardware,software, and system risks, applying advanced risk mitigation strategies to influence robust design decisions
• Lead root cause investigations and resolution of test failures,CAPAs, NCEPs, and complaints, driving corrective actions and preventive measures with minimal oversight.
• Provide mentorship and guidance to junior engineers on design assurance best practices, regulatory requirements, and quality processes.
• Proactivelyidentifygaps and opportunities for continuous improvement inproduct development processes, tools, and documentation.
• Act as a primary point of contact for design assurance during internal and external audits and regulatory inspections.
• Effectively manage multiple priorities and projects independently, demonstrating strong decision-making skills in ambiguous situations, and ability to influence project team towards quality-centric decisions and behaviors

Required Qualifications

• Bachelor's degree in Mechanical, Electrical, Software Engineering, Biomedical Engineering,or related technical discipline.
• 6+ years of experience in Quality Assurance, Design Assurance, Software Quality, or related roles in the medical device industry.
• Demonstratedexpertisein Design Controls, Risk Management (ISO 14971), Quality System Regulations (21 CFR 820), and Quality management systems (ISO 13485).
• Proven ability to independently lead complex product development projects, including software and system quality assurance activities, frominceptionthrough completion.
• Experience developing andmaintainingrisk documentation such as FMEAs and Hazard Analyses witha hardware, software and system focus.
• Strong problem-solving skills with experience leading root cause analysis and CAPA investigations.
• Excellent communication skills, capable of influencing stakeholders at all levels and leading cross-functional initiatives.
• Ability to thrive in a fast-paced environment and navigate ambiguity with sound judgment.

Preferred Qualifications

• Experience mentoring or leading junior engineers in design assurance or software/systemsengineeringactivities.
• Experience with Capital Equipment
• Knowledge of software quality standards (IEC 62304) and software/system development principles.
• Prior experience working on or supportingcardiac mapping systemsor similar complex medical device platforms.
• Strong project management skills and familiarity with agile development methodologies.

Requisition

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  vary based on actual location of the position and other pertinent factors considered in determining actual…