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Boston Scientific

Medical devices maker for interventional specialties

Quality RI FG Engineer

Inspection & Test +1Confirmed live in the last 24 hours
Full-timeGeorge Town, Penang, MalaysiaNo salary listedIn-person

About the Job

Requirements

  • An undergraduate degree in Science, Material Engineering, or a related discipline.
  • At least 5 years of experience in Quality Engineering within a regulated manufacturing environment.
  • Experience in Incoming Quality Assurance (IQA) and Outgoing Quality Inspection.
  • Experience in equipment qualification and test method validation.
  • Experience supporting material issue management and product release activities.
  • Strong stakeholder management and communication skills.
  • Experience conducting incoming raw-material inspections and finished-goods quality inspections.
  • Product-release accountability and decision-making capability.
  • Equipment and test-method validation experience.
  • Strong problem-solving and root-cause analysis skills.
  • Analytical thinking and data-driven decision-making skills.
  • Knowledge of SAP for quality and material management.
  • Ability to interpret engineering drawings.
  • Cross-functional collaboration skills.
  • Risk assessment and nonconforming-material investigation skills.
  • Knowledge of statistical analysis and quality-improvement tools.
  • Ability to work effectively with Manufacturing, Engineering, Materials, and Quality stakeholders.

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 in identifying primary root causes, and understanding corrective and preventive actions.
  • Work with process owners to bound product stops and document release criteria, as required.
  • Make decisions related to product quality, 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 GCS2 software for complaint handling, 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.
  • Apply knowledge of QSR and ISO/MDD standards, promote best industry practices, and make daily quality decisions, with 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 to eliminate or lessen environmental impacts and effects.
  • Apply knowledge of Risk Management and BS EN 14971 requirements.
  • Compile and analyze operational, test, and validation data to establish technical specifications and performance standards for newly designed or modified products and processes.
  • Participate directly in new-product or technology transfers to ensure compliance with internal and regulatory requirements.
  • Use 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.
  • Coordinate with suppliers, other engineering disciplines within and outside the site, and customers as needed.
  • Follow the internal auditing process.
  • Perform incoming quality inspections of raw materials and outgoing quality inspections of finished goods.
  • Conduct inspection and evaluation activities in the quality laboratory to ensure compliance with established specifications and quality standards.
  • Make product-release decisions and ensure released products meet quality and regulatory requirements.
  • Support material-issue investigations, containment actions, and resolution activities to maintain product quality and compliance.
  • Partner with Manufacturing, Engineering, Materials, Suppliers, and other stakeholders to drive issue resolution and continuous improvement.
  • Manage stakeholders and communicate promptly to ensure alignment, rapid decision-making, and minimal operational disruption.

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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