R & D Engineer III - Sustaining
Listed on 2025-12-02
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Engineering
Biomedical Engineer, Quality Engineering, Mechanical Engineer, Medical Device Industry
Additional Location(s): N/A
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 the roleJoin our Vascular R&D Sustaining team, where we are dedicated to improving and sustaining commercial products that diagnose and treat peripheral vascular disease. Our mission is to enhance patient outcomes and improve lives through a broad and advanced portfolio of therapy solutions.
We are seeking a dynamic and collaborative R&D Engineer III to support design improvements, supply continuity initiatives, and product lifecycle excellence. In this role, you will work cross‑functionally to drive design and material changes, solve complex technical challenges, and ensure our commercial devices continue to meet the highest standards of quality and regulatory compliance.
Boston Scientific requires employees to be in the local office at least three days per week and does not offer visa sponsorship or relocation assistance for this position.
Your responsibilities will include- Support product design changes to maintain or improve supply continuity, including strategy development, feasibility studies, and testing activities
- Lead or assist in root cause investigations and develop robust engineering solutions to address technical and quality-related issues
- Ensure compliance with applicable regulatory standards, including ISO 13485 and 21 CFR 820, throughout the product lifecycle
- Collaborate with cross‑functional teams, including project management, marketing, design assurance, manufacturing, and regulatory affairs, to ensure successful project execution
- Prepare and review engineering documentation such as design change analyses, test protocols, technical reports, design history file components, and regulatory submissions, and present project updates and technical insights to stakeholders
- Coordinate global engineering activities across Boston Scientific sites to align execution efforts and meet project milestones
- Bachelor's degree or higher in Mechanical Engineering, Biomedical Engineering, or a related technical field
- Minimum of 3 years’ industry experience in an engineering role
- Proven ability to synthesize technical data from various sources and make sound recommendations
- Strong problem‑solving skills and technical acumen
- Working knowledge of quality systems and regulatory standards, including ISO 13485 or 21 CFR 820
- Prior experience working in the medical device industry, preferably in a regulated R&D or sustaining engineering environment
- Experience with test method development
- Demonstrated success working within global or cross‑functional teams
- Experience with design control, risk management, and DV/DVAL activities
- Familiarity with ultrasound technology
- Knowledge of peripheral vascular anatomy and related therapies
- Strong time management and project coordination skills
Minimum Salary: $76,000
Maximum Salary: $144,400
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.
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