Sr. Supplier Quality Engineer

Danaher; Chaska (MN); On-site; USD 100,000 - 130,000; Full time

Job summary

Join a top-tier diagnostics team as a Sr. Supplier Quality Engineer at Beckman Coulter in Chaska, MN. You will enhance supplier performance through effective management and rigorous quality assurance processes in a dynamic environment committed to healthcare innovation.

Benefits

Comprehensive benefits package

Paid time off

401(k) plan

Medical/dental/vision insurance

Qualifications

• Minimum 5 years of experience in engineering, science or quality.
• Experience in supplier development activities required.

Responsibilities

• Execute supplier management plans to improve performance.
• Plan and organize supplier selections and audits.
• Develop supplier material control plans.

Skills

Supplier Qualification

Root Cause Analysis

Material Control

Quality System Audits

Education

Bachelor's Degree in Engineering or Science

Job description

Wondering what’s within Beckman Coulter Diagnostics? Take a closer look.

At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful!

Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.

The Sr. Supplier Quality Engineer for Beckman Coulter Diagnostics ensures that suppliers deliver quality products and develops supplier capability for future needs. They handle supplier selection, material qualification, control, and development activities. They investigate nonconforming materials to understand the root cause of failure and drive corrective actions internally and externally. They also plan, coordinate, and report on material projects and supplier performance.

This position is part of the Instrument Operations department located in Chaska, MN and will be an onsite role. At Beckman Coulter, our mission is to Relentlessly Reimagine Healthcare, One Diagnosis at a Time. .

You will be a part of the Supplier Quality Team and report to the Supplier Quality Manager. If you thrive in a fast-paced supporting role and want to work to build a world-class quality organization—read on.

In this role, you will have the opportunity to:

• Execute supplier management plans to improve supplier and product performance.
• Plan and organize routine and non-routine tasks such as supplier selections, qualifications, change notifications, audits, corrective actions, and supplier scorecards.
• Develop supplier material control plans as part of product qualification.
• Act as the primary supplier quality representative for root cause and corrective action analysis regarding supplier-caused manufacturing issues.
• Visit suppliers to resolve product performance concerns and recommend appropriate field actions to the product regulatory committee.

The essential requirements of the job include:

• Degree with experience in engineering, science or quality field (Bachelor 5+ yrs; Masters 3+ yrs).
• Experience in supplier qualification activities such as supplier selection, approval, material qualification, material control, and/or supplier development activities.
• Expertise in investigating nonconforming materials to understand the root cause of failure and driving corrective actions internally and externally with suppliers.
• Experience or involvement in supplier monitoring and improvement activities such as supplier performance reviews, process or quality system audits, supplier change notifications, and action plans

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

• Internal or External quality system auditing
• FDA regulated environment
• Knowledge of GDT and ability to interpret engineering drawings.

The annual salary range for this role is 100K-130K. 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 comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

#LI-NS3 #LI-Onsite

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.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at [e-mail] to request accommodation.