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Boston Scientific

Medical devices maker for interventional specialties

Quality Systems Engineer 3 - Engineering

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeQuincy, MA, USA

About the Job

Requirements

  • A bachelor's degree and a minimum of 5 years of relevant experience, or a master's degree.
  • Working knowledge of FDA Quality Management System Regulation and ISO 13485 requirements.
  • Demonstrated technical writing skills, including the ability to develop and maintain clear, accurate, and compliant quality documentation.
  • Demonstrated ability to analyze quality data, identify trends, and determine appropriate corrective or preventive actions.
  • Experience applying risk-based approaches to quality and business decisions.
  • Ability to work in the United States without current or future employer sponsorship.

Responsibilities

  • Lead and support Quality Management System processes, including corrective and preventive action, nonconforming events, internal and external audits, and management review.
  • Ensure compliance with applicable regulatory requirements and standards, including FDA Quality Management System Regulation, ISO 13485, and ISO 14971.
  • Provide technical guidance and mentorship on complex investigations, root cause analysis, corrective actions, and effectiveness verification.
  • Support internal and external audits and regulatory inspections, including site preparation, subject matter expert readiness, responses to findings, and remediation activities.
  • Analyze quality metrics and trends to identify systemic risks, evaluate performance, and drive data-informed improvements.
  • Lead continuous improvement initiatives to enhance Quality Management System effectiveness, regulatory compliance, and operational efficiency.
  • Collaborate with engineering, operations, and cross-functional stakeholders to resolve quality issues and implement sustainable solutions.
  • Develop, review, and maintain quality procedures, work instructions, and other controlled documentation.
  • Apply risk-based decision-making to quality and compliance issues to support effective and sustainable outcomes.
  • Serve as a Quality Management System subject matter expert, providing technical guidance and training to cross-functional teams.
  • Lead quality system projects, influence stakeholders, and ensure timely, compliant, and effective execution.
  • Partner with global teams to identify opportunities and drive continuous improvement across the Quality Management System.

Desired Qualifications

  • A degree in science, engineering, or a related technical discipline.
  • A minimum of 3 years of experience in quality systems.
  • Experience with corrective and preventive action, nonconformance management, internal and external audits, and management review processes.
  • Training or certification related to ISO 13485 and FDA quality management system requirements.
  • Experience managing projects, coordinating cross-functional activities, and driving initiatives to completion.
  • Experience leading continuous improvement initiatives to enhance quality system performance and operational effectiveness.

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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