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Boston Scientific

Medical devices maker for interventional specialties

Senior Quality Systems Engineer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A bachelor's degree with at least five years of related experience, or a master's degree with at least three years of related experience.
  • Experience in a medical device manufacturing, quality, or regulatory/compliance environment.
  • Previous experience in a Supplier Quality, Supplier Engineering, or Sourcing organization.
  • Understanding of quality system requirements in 21 CFR Part 820 and ISO 13485.
  • Willingness to travel 25% of the time.
  • Technical writing and documentation skills.

Responsibilities

  • Lead cross-functional project teams, using project management best practices to coordinate activities, communicate progress, collaborate on key deliverables, and meet critical phase timelines.
  • Drive continuous improvement and globalization by gaining alignment across multiple functional departments while meeting Boston Scientific and regulatory requirements.
  • Communicate and influence across the global sourcing organization to deliver long-term strategic outcomes.
  • Assess material-controls processes continuously and rigorously, and review documentation throughout those processes to ensure compliance with global processes, FDA regulations, ISO 13485, and medical device requirements.
  • Own highly visible, global, systemic corrective and preventive actions (CAPAs) while leading through a Community of Practice.
  • Guide functional members and teams in process ownership areas, including supplier audit/approved vendor list (AVL), material qualification, procurement, supplier change, and corrective action through audit support and CAPA processes.
  • Determine and track actionable material-controls metrics and trends to ensure proper execution and effectiveness of the global process.
  • Participate in or lead appropriate Communities of Practice to ensure global processes continuously execute process outputs at the highest industry/company level and anticipate emerging regulatory lines of questioning.
  • Support site- and global-scale CAPA initiatives, continuous improvement opportunities, and projects.

Desired Qualifications

  • A degree in Science or Engineering.
  • At least five years of experience in Supplier Quality, Supplier Management, or Quality Systems.
  • Training or certifications in Quality Management System Requirements (ISO 13485) and FDA Quality System Regulation (21 CFR Part 820).
  • Project management skills.

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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