Quality Engineer III - Defined Term

Additional Location(s): N/ADiversity
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- 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 role:

Please note that this is a defined-term position of up to 18 months. Defined-term employees are eligible for most benefits, including paid vacation, 401K matching, and healthcare benefits.

Join the Neuromodulation post-market complaint trending team as a Quality Engineer III
- Defined Term, where we are committed to transforming customer experiences into actionable insights that improve patient outcomes across the globe. In this role, you will be responsible for monitoring, identifying, investigating, and escalating product performance signals related to our products within the Neuromodulation division. This is an exciting opportunity within the Post Market Organization to collaborate with Design Assurance, R&D, Supplier Engineering, and Manufacturing teams to ensure a comprehensive understanding of product performance and to drive continuous improvement.

Boston Scientific was recognized by Forbes as one of the Best Workplaces for Engineers in 2026, reflecting a culture where engineers do meaningful work.

Boston Scientific was also recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.

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 (3) 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.

Your responsibilities will include:

Perform complaint monitoring, statistical trending, and signal evaluation activities to identify emerging product quality and patient safety concerns

Conduct signal assessments and present findings, recommendations, and escalations to management review boards and cross-functional stakeholders

Develop, maintain, and improve complaint monitors aligned with risk management documentation, product hazards, and surveillance requirements

Execute ad hoc data analyses to support Quality, Regulatory, Clinical, Engineering, and business partner requests

Apply statistical methodologies and Statistical Process Control (SPC) techniques to evaluate product performance and identify meaningful trends

Collaborate with Risk Management teams to ensure surveillance activities remain aligned with product risks and evolving post-market requirements

Investigate data anomalies and develop recommendations to improve data quality, monitoring effectiveness, and signal detection capabilities

Communicate analytical findings to both technical and non-technical audiences through clear visualizations, presentations, and written summaries

Support audit readiness and compliance with applicable quality system and regulatory requirements

Required qualifications:

Bachelor's degree in Statistics, Engineering, Life Sciences, Biomedical Sciences, or related technical discipline

Minimum of three (3) years of professional engineering experience in medical device quality engineering, manufacturing quality, supplier quality, post-market quality, reliability engineering, or related technical role Experience working within FDA and/or ISO-regulated quality systems

Exp…