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Danaher

Makes tools for drug research and medical testing

Principal Engineer Supplier Quality - Supplier Quality Engineering

Quality EngineeringConfirmed live in the last 24 hours
Full-timeShanghai, ChinaNo salary listed

About the Job

Requirements

  • A degree in Electrical, Electronics, or Mechanical Engineering and 5–8 years of related Supplier Quality Management experience are preferred.
  • Broad knowledge of manufacturing operations and quality system practices in a medical device company is preferred.
  • Strong knowledge of supplier management, including supplier evaluation and supplier performance, is required.
  • Excellent verbal and written communication skills, including the ability to communicate effectively and independently with internal and external customers, are required.
  • Self-motivation and high energy are required.
  • The role requires travel 30–40% of the time, including occasional international travel.
  • Flexibility and the ability to engage in virtual meetings across time zones are required.

Responsibilities

  • Lead supplier qualification activities for new suppliers with Global Sourcing and Global Supply Chain.
  • Monitor supplier performance and review periodic quality data, reports, scorecards, and related action plans.
  • Drive resolution of complex material quality issues through root cause analysis and close collaboration with suppliers to ensure timely corrective actions, including leading failure analysis and comprehensive resolution of defective parts in the factory and field.
  • Lead continual improvement initiatives and activities such as Kaizen to improve KPIs, including working with suppliers to use PSP to identify critical few for proper root cause investigation and Poka-yoke solutions.
  • Support and participate in internal audits and ISO 9001, ISO 13485, and GMP/FDA compliance activities; contribute to supplier quality strategy planning and drive improvement initiatives.
  • Ensure China site compliance with ISO 9001, ISO 13485, FDA 21 CFR Part 820, and China NMPA requirements; support and lead internal and external audits, including preparation, execution, and timely closure of audit findings.
  • Perform other work as agreed with superiors.

Desired Qualifications

  • Familiarity with ISO 9001, knowledge of ISO 13485, FDA QSR, or China NMPA, and lead-auditor certification are advantageous.
  • Familiarity with problem-solving tools such as 5 Why root cause analysis and quality tools such as DFM, PFMEA, GR&R, Control Plan, and SPC is advantageous.

About the Company

Danaher

Makes tools for drug research and medical testing

Danaher makes instruments, tests and laboratory supplies for drug developers, researchers and clinicians, spanning the path from biological research to clinical patient diagnosis. Its businesses include Cytiva for drug manufacturing, SCIEX for chemical analysis and Beckman Coulter for laboratory testing, linking specialized tools across healthcare workflows. Customers use its equipment to study cells, produce biological medicines and analyze patient samples; the group earns money by selling instruments, reagents, software and support services through its operating companies. Danaher was established in 1984 and is headquartered in Washington, DC.

Company size
10,001+
Company stage
IPO
Headquarters
Washington, DC
Founded
1984

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