Danaher
Global Supplier Quality Engineer - Electronics
Danaher, Chaska, Minnesota, United States, 55318
Global Supplier Quality Engineer - Electronics
At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work saves livesand 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 a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. This position reports to the Sr. Director of Global Supplier Quality responsible for global supplier quality strategy and is part of the Global Supplier Quality team. The job location for this role is in-person, preferably, Chaska MN, Miami FL or Brea CA. In this role, you will have the opportunity to: Drive supplier quality strategies aligned with key commodity sourcing objectives by partnering closely with Global Commodity Management and cross-functional teams across manufacturing sites. Ensure alignment with business goals by integrating quality initiatives into sourcing decisions and long-term supplier strategies. Independently lead quality workshops and comprehensive supplier development initiatives to strengthen manufacturing process capabilities, product reliability, and supplier performance across global sites. Utilize data-driven approaches and best practices to enable sustainable improvements in supplier operations. Manage and execute supplier audits, qualifications, and ongoing performance assessments to ensure adherence to internal quality standards, customer requirements, and applicable external regulatory frameworks. Provide structured feedback and corrective action follow-up to drive accountability and continuous improvement. Serve as a strategic quality leader throughout the supplier lifecycle, including early engagement during supplier selection, influencing quality expectations during contract negotiations, and managing supplier relationships to drive long-term quality outcomes. Partner with Operational SQEs and suppliers to develop and implement robust risk mitigation plans addressing quality, compliance, and supply continuity risks. Collaborate with cross-functional teams across R&D, Procurement, Operations, Quality, and Regulatory Affairs to embed quality into all phases of the product lifecyclefrom concept through commercialization. Leverage strategic partnerships and internal collaboration to drive year-over-year improvements in supplier quality, delivery, and cost performance. The essential requirements of the job include: Bachelor's degree in technical field with 9+ years' experience or master's degree in field with 7+ years' experience or comparable Minimum 5 years of experience in supplier quality engineering or supplier development within international manufacturing environments. Strong knowledge in quality systems and tools, including risk management, CAPA, APQP, PPAP, FAI, and statistical analysis methodologies. Exceptional communication and interpersonal skills, with a proven ability to influence cross-functional teams and external suppliers. It would be a plus if you also possess: Experience in FDA-regulated or medical device manufacturing environments. Certifications such as CQE, CQA, Six Sigma, or equivalent. Familiarity with ISO13485, 21 CFR Part 820, and other relevant regulatory frameworks. The salary range for this role is $130,000-$160,000 USD range. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and Retirement Benefits to eligible employees. Beckman Coulter Diagnostics, 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. At Beckman Coulter Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. 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.
At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work saves livesand 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 a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. This position reports to the Sr. Director of Global Supplier Quality responsible for global supplier quality strategy and is part of the Global Supplier Quality team. The job location for this role is in-person, preferably, Chaska MN, Miami FL or Brea CA. In this role, you will have the opportunity to: Drive supplier quality strategies aligned with key commodity sourcing objectives by partnering closely with Global Commodity Management and cross-functional teams across manufacturing sites. Ensure alignment with business goals by integrating quality initiatives into sourcing decisions and long-term supplier strategies. Independently lead quality workshops and comprehensive supplier development initiatives to strengthen manufacturing process capabilities, product reliability, and supplier performance across global sites. Utilize data-driven approaches and best practices to enable sustainable improvements in supplier operations. Manage and execute supplier audits, qualifications, and ongoing performance assessments to ensure adherence to internal quality standards, customer requirements, and applicable external regulatory frameworks. Provide structured feedback and corrective action follow-up to drive accountability and continuous improvement. Serve as a strategic quality leader throughout the supplier lifecycle, including early engagement during supplier selection, influencing quality expectations during contract negotiations, and managing supplier relationships to drive long-term quality outcomes. Partner with Operational SQEs and suppliers to develop and implement robust risk mitigation plans addressing quality, compliance, and supply continuity risks. Collaborate with cross-functional teams across R&D, Procurement, Operations, Quality, and Regulatory Affairs to embed quality into all phases of the product lifecyclefrom concept through commercialization. Leverage strategic partnerships and internal collaboration to drive year-over-year improvements in supplier quality, delivery, and cost performance. The essential requirements of the job include: Bachelor's degree in technical field with 9+ years' experience or master's degree in field with 7+ years' experience or comparable Minimum 5 years of experience in supplier quality engineering or supplier development within international manufacturing environments. Strong knowledge in quality systems and tools, including risk management, CAPA, APQP, PPAP, FAI, and statistical analysis methodologies. Exceptional communication and interpersonal skills, with a proven ability to influence cross-functional teams and external suppliers. It would be a plus if you also possess: Experience in FDA-regulated or medical device manufacturing environments. Certifications such as CQE, CQA, Six Sigma, or equivalent. Familiarity with ISO13485, 21 CFR Part 820, and other relevant regulatory frameworks. The salary range for this role is $130,000-$160,000 USD range. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and Retirement Benefits to eligible employees. Beckman Coulter Diagnostics, 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. At Beckman Coulter Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. 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.