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Boston Scientific

Medical devices maker for interventional specialties

Quality Engineer 3 - Engineering

Quality EngineeringConfirmed live in the last 24 hours
Full-timeGeorge Town, Penang, MalaysiaNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Engineering, Technology, or a related Science discipline.
  • At least 5 years of relevant experience in a regulated industry, preferably medical devices.
  • Experience running and reviewing nonconforming event risk assessments and investigations.
  • Experience in quality engineering, process validation, and quality system compliance.
  • Ability to support quality and operational excellence initiatives through analytical and problem-solving skills.
  • Understanding of ISO 13485 requirements and QMSR or equivalent quality system regulations.
  • Ability to interpret, execute, and support the full validation lifecycle from planning to reporting.
  • Root cause analysis skills, including the use of Excel and Minitab for statistical analysis.
  • Experience with CAPA, NCEP, and Failure Mode Investigations.
  • Ability to develop and review validation protocols and reports.
  • Knowledge of Risk Management and BSEN 14971 requirements.
  • Knowledge of Six Sigma, statistical analysis, and Lean methodologies.
  • Experience investigating customer complaints and handling complaint processes.
  • Cross-functional collaboration and stakeholder management skills.
  • Strong written and verbal communication skills.

Responsibilities

  • Identify and resolve complex exceptions to work assignments.
  • Summarize and analyze test results or other process-related findings, draw conclusions, and make appropriate decisions.
  • Read and interpret technical drawings, procedures, and protocols.
  • Identify manufacturing process defects, including scrap, nonconforming material, and customer complaints, by dispositioning nonconforming material, assisting with primary root-cause identification, and understanding corrective and preventive actions.
  • Work with process owners to bound product stops and document release criteria when required.
  • Exercise independent authority to make product-quality decisions, including disposition of nonconforming product.
  • Participate in customer complaint investigations for areas under the role's control.
  • Document investigation findings in GCS2 analysis reports.
  • Train users on the GCS2 complaint-handling software as required.
  • Drive improvements in product and process quality.
  • Check and support execution and investigation of CAPAs, NCEP, and Failure Mode Investigations.
  • Evaluate new equipment and processes and participate in new product transfers.
  • Promote awareness of QSR and ISO/MDD standards and apply industry best practices, consulting the quality engineering manager or site QA director as final arbitrator on critical quality decisions.
  • Apply validation techniques and associated regulatory requirements, including analysis of customer feedback and complaints.
  • Review and develop process validation protocols and reports, and support other functional areas during validation activities.
  • Evaluate new equipment, processes, and chemicals with EHS for environmental impact and identify ways to eliminate or lessen those impacts.
  • Compile and analyze operational, test, and validation data to establish technical specifications and performance standards for newly designed or modified products and processes.
  • Participate in new product or technology transfers to ensure compliance with internal and regulatory requirements.
  • Apply Six Sigma, statistical analysis, and Lean principles to investigate and solve problems and improve quality.
  • Ensure laboratory equipment complies with requirements for analysis activities, including calibration, safety, and cleanliness.
  • Provide technical guidance to associate quality engineers, technicians, and inspection staff.
  • Work with suppliers, engineering disciplines within and outside the site, and customers as needed.
  • Participate in the internal auditing process.

Desired Qualifications

  • Relevant experience in the medical device industry.

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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