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Boston Scientific

Medical devices maker for interventional specialties

Senior Quality Engineer - Global Post Market Support, Engineering

Quality EngineeringConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A bachelor's degree in industrial engineering, statistics, sciences, or a related technical discipline is required.
  • A minimum of 5 years of experience in a quality control-related role within a regulated industry is required.
  • Experience with statistical process control and other statistical tools for quality data analysis, especially applying statistical process control to business processes, is required.
  • Experience managing cross-functional projects in a regulated environment is required.

Responsibilities

  • Establish robust process controls for complaint handling outputs to ensure alignment with customer requirements and maintain reliable process performance.
  • Apply expertise in quality control, statistical methods, and systems thinking to drive continuous improvement of the complaint handling process.
  • Evaluate the end-to-end complaint handling process, from intake through adverse event reporting, to identify systemwide dependencies, bottlenecks, and potential failure modes, and proactively mitigate risk.
  • Lead and participate in root cause investigations for recurring process failures and implement effective corrective and preventive actions.
  • Collaborate with the Complaint Handling, Post-Market Surveillance, Risk Management, and IT and Systems teams to support process effectiveness and compliance.
  • Provide technical leadership to a team of global and divisional subject matter experts responsible for monitoring the complaint handling process.
  • Coordinate with global and divisional teams to create and maintain documentation, including standard operating procedures, work instructions, and control plans, to support consistency and compliance with medical device regulatory requirements.
  • Collect, analyze, and report key complaint handling process outputs and trends to senior management.
  • Translate customer needs into process requirements for critical outputs, such as complaint codes, so downstream users have reliable information for analysis and decision-making.

Desired Qualifications

  • Experience in the medical device or pharmaceutical industry is preferred.
  • An ASQ Certified Quality Engineer certification, Lean Six Sigma certification, or similar certification is preferred.
  • Familiarity with systems thinking principles and the ability to apply them to complex business processes is preferred.
  • Working knowledge of relevant medical device regulations and standards, including the European Union Medical Device Regulation, ISO 13485, and ISO 14971, is preferred.
  • A methodical approach to data analysis is preferred.
  • The ability to present complex data to diverse audiences is preferred.
  • The ability to collaborate effectively with cross-functional teams is preferred.
  • A proactive and accountable mindset focused on delivering solutions is preferred.

About the Company

Boston Scientific

Medical devices maker for interventional specialties

Boston Scientific designs and makes medical devices used in procedures across cardiology, endoscopy, urology, and neuromodulation. Its products help doctors diagnose and treat conditions by guiding minimally invasive interventions and delivering therapies inside the body, with revenue from hospitals and clinics. The firm differentiates itself through a broad, global portfolio and heavy ongoing investment in research and development to expand capabilities and address complex health issues. Its goal is to improve patient care by providing reliable, effective medical devices and solutions that enable clinicians to perform safer, more effective procedures while growing its business.

Company size
10,001+
Company stage
IPO
Headquarters
Marlborough, MA
Founded
1979

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