Design Quality Assurance Engineer II

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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.

Boston Scientific is a worldwide and diverse company who puts patients first. The Urology divisional team is on a mission to provide urologists with products that offer the best quality, functionality, and flexibility they need to treat their patients. As a Design Quality Assurance Engineer II, you’ll be at the heart of that mission by working with high-performing cross‑functional teams to primarily sustain commercialized Laser products.

You will serve as a Quality representative who can directly impact patient care by ensuring the safety, quality, post‑market performance and compliance of the Laser franchise products are maintained while continuously improving their value. You will interface with cross‑functional teams to complete sustaining projects, design control deliverables, and activities to ensure our products continue to meet state‑of‑the‑art regulatory standards and user needs.

At Boston Scientific, we value collaboration and synergy. This hybrid role is based in Marlborough, MA and requires being on‑site at least three days per week.

Relocation assistance is not 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.

• Act as an effective cross‑functional team member in supporting quality disciplines, decisions, and practices.
• Effectively work with and influence cross‑functional teams during the Design Change process to ensure proposed changes to products are systemically / thoroughly analyzed, assessed, controlled and implemented appropriately (i.e., EN 13485 / CFR
  820).
• Support planning, updating and maintenance of product Risk Management documentation (Hazard Analysis, Design FMEA, Task Analysis and Fault Tree Analysis, etc.) in compliance with Boston Scientific procedures and external standards (i.e., EN 14971).
• Support Usability Engineering and planning documentation (i.e., EN / ISO 62366 and IEC 606061-1-6).
• Interface with the core team and support manufacturing operation efforts / changes to ensure they meet or exceed internal and external requirements.
• Apply sound, systematic problem‑solving methodologies in identifying, prioritizing, communicating, and resolving quality issues in a timely manner.
• Support post‑market activities, ensuring our products meet patient, customer, product performance, and quality system expectations through risk‑based assessment of post‑market signals.
• Support internal and external regulatory audits as required.

Required Qualifications:

• Minimum of a Bachelor’s Degree in mechanical, electrical, or biomedical engineering (or other related technical discipline).
• Minimum of 2 years of related experience.
• Travel approximately