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Philips

Makes medical devices and personal health products

Design Quality Engineer

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeSuzhou, Jiangsu, ChinaNo salary listed

About the Job

Requirements

  • A Bachelor's degree or Master's degree in Mechanical Engineering, Electronics Engineering, Science, or an equivalent field.
  • At least 2 years of experience in Quality Engineering, Safety Engineering, R&D Engineering, or an equivalent area with a Bachelor's degree; no prior experience is required with a Master's degree.

Responsibilities

  • Create and execute comprehensive process validation strategies using statistical tools to support the transition of new products to production while meeting quality and regulatory standards, working under limited supervision.
  • Manage the design control process from eliciting and validating design inputs through verification, validation, and design transfer, ensuring adherence to regulatory and quality standards.
  • Oversee the drafting and updating of quality engineering documents, including quality plans for hardware, software, and systems, ensuring accuracy, currency, and regulatory compliance.
  • Integrate quality, reliability, and Post Market Surveillance insights into quality improvement projects across the product lifecycle to enhance product quality and reliability.
  • Assess product and system designs, review performance data, and perform root cause analysis to identify and address quality deficiencies.
  • Validate design inputs including usability, reliability, performance, manufacturability, and safety to ensure alignment with quality standards and regulatory requirements.
  • Guide risk management activities throughout the product lifecycle, ensuring risks are identified, assessed, and mitigated to uphold product safety and quality.
  • Use post-market performance data to assess product effectiveness in the field, provide feedback to manufacturing and design teams, and initiate corrective actions when necessary.
  • Prepare for quality audits and inspections, maintaining documentation and processes that demonstrate compliance with internal and external quality standards.
  • Record, manage, and execute CAPA processes, including problem identification, root cause analysis, and implementation of solutions to prevent recurrence and drive continuous improvement.
  • Apply continuous improvement techniques to enhance quality practices and maintain audit readiness and adherence to internal and external quality standards throughout the product lifecycle.
  • Build relationships with internal and external stakeholders, providing guidance and mentorship to support alignment with quality standards and project milestones.

Desired Qualifications

  • Six Sigma Green Belt certification.
  • Design Quality Management.
  • Data Analysis and Interpretation.
  • Design for Quality (DFQ).
  • Root Cause Analysis (RCA).
  • CAPA Methodologies.
  • Regulatory Requirements.
  • Privacy, Safety and Security Risk Assessment.
  • Technical Documentation.
  • Continuous Improvement.
  • Product Quality and Reliability.
  • Defect Management.
  • Design Verification Planning.
  • Design Validation Planning.
  • Product Test Design.

About the Company

Philips

Makes medical devices and personal health products

Philips makes medical equipment and software for hospitals and care providers, along with personal health products for consumers. Its hospital portfolio spans MRI and CT scanners, ultrasound, image-guided treatment systems and patient monitors, while Sonicare and Avent cover oral health and baby care. Clinical software connects medical images and patient data across care teams, and the company earns revenue from equipment, software, maintenance and consumer product sales. It works with health systems through long-term technology and service partnerships, including solutions for care at home. Founded in 1891, Philips is headquartered in Amsterdam, the Netherlands.

Company size
10,001+
Company stage
IPO
Headquarters
Andover, MN
Founded
1891

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