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Danaher Corporation

Principal Engineer Supplier Quality

Posted Yesterday
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In-Office
Woodlands
Senior level
In-Office
Woodlands
Senior level
The Principal Engineer, Supplier Quality drives supplier quality performance and compliance through qualification processes, audits, and resolution of quality issues, ensuring adherence to standards.
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Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At SCIEX, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

As part of SCIEX, you will help to influence life changing research and outcomes, while accelerating your potential. For more than 50 years, we have been empowering our customers to solve the most impactful analytical challenges in quantitation and characterization through ground-breaking innovation and outstanding reliability and support. You will be part of a winning team, enabled by DBS, that is passionate about helping life science experts around the world get to answers they can trust.

Learn about the Danaher Business System which makes everything possible.

The Principal Engineer, Supplier Quality is responsible for driving Quality performance of the suppliers to meet SCIEX Product Quality requirements through supplier qualification processes, supplier control processes, aligned with supplier management strategies.

This position reports to the Senior Manager Supplier Quality and is part of the QARA team located in Singapore and will be an on-site role.

In this role, you will have the opportunity to:

  • Drive improvement of quality performance of Global suppliers, for Reagent and Consumables.

  • Lead supplier qualification activities for new suppliers with Global Sourcing & Global Supply Chain.

  • Plan and execute periodic audits at suppliers' site to ensure suppliers' QMS is meeting ISO standards, FDA QMSR (GMP) and compliance to agreed process control plans

  • Monitor supplier performance, review periodic quality data/reports/scorecards and related action plans

  • Drive resolution of complex material quality issues by deep diving suppliers' root cause analysis and by working with suppliers to monitor corrective action and facilitating with internal support where required.

The essential requirements of the job include:

  • Degree in Biochemistry, Chemical Engineering, or related field with of 5-8 years related experience in Supplier Quality Management, Process Engineering is preferred

  • Demonstrated experience on the performance of audits, lead-auditor certification preferred

  • Familiar with problem solving tools such as 5 why root cause analysis, and Quality tools such as DFM, PFMEA, GR&R, Control Plan, SPC.

  • Knowledge of ISO 9001, ISO13485 and FDA 21 CFR Part 820 will be added advantage

Travel Requirements:

  • Ability to travel – 20-50%, and maybe travel on short notice

It would be a plus if you also possess previous experience in:

  • Managing suppliers including supplier evaluation and supplier performance

  • Broad knowledge of manufacturing operations and quality system practices in a Medical Device or Pharmaceutical company is preferred

SCIEX, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

#LI-TW1

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Top Skills

Control Plan
Dfm
Fda 21 Cfr Part 820
Gr&R
Iso 13485
Iso 9001
Pfmea
Spc

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