4.354 Jobs für Supplier Quality in Deutschland

Senior Specialist, Supplier Quality
Requisition ID:
71354
Date:
Oct 24, 2025
Location:
Eschweiler, North Rhine-Westphalia, DE
Department:
Quality
Description:
**This is a hybrid position (3 days per week) working in our office at Eschweiler, Germany. Candidates applying must be residing within a 50-mile commutable distance to the job location.**
At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
**Job Summary**
In this role you will be responsible for performing Supplier Quality activities associated with external suppliers. This role performs activities to ensure West supplier's maintain compliance with West's procedures and policies. You will interface with R&D, Sourcing, Design Quality, Regulatory and Operations Quality to drive improved supplier quality performance.
**Essential Duties and Responsibilities**
+ Establish and successfully execute supplier management plans which will align to overall business objectives
+ Maintain a strong collaborative partnership with external suppliers and cross-functional team members that facilitates organizational success for assuring high product quality and meeting business needs
**Additional Responsibilities**
+ Monitor supplier performance including incoming failures, manufacturing yields and field failures to drive Supplier Corrective Action Reports (SCARs)
+ Execute Supplier Corrective Action Requests (SCAR) with suppliers, ensuring effective and timely closure
+ Work with suppliers, R&D, and Sourcing on continuous improvement of supplier performance including supplier change request.
+ Evaluate potential new or future suppliers and support supplier selection process with the cross-functional team
+ Participate in cross-functional teams of design engineering and quality engineering to work with suppliers during product development and ensures agreement for manufacturable, cost-effective designs
+ Approves components for use in products by driving Product Approval activities with the suppliers
+ Supports Supplier evaluation, audit management and related records
+ Supports the evaluation and development of Quality Agreements and purchasing specifications with suppliers
+ Support the development of an Incoming Inspection strategy on purchased products
**Education**
+ Bachelor's Degree in Science or equivalent experience required
+ Master's Degree in Science or equivalent experience preferred
**Work Experience**
+ Minimum 5 years of quality related experience with preferred experience in pharmaceutical and/or medical device industry
+ Experience working with suppliers and supplier engagement activities
**Preferred Knowledge, Skills and Abilities**
+ Knowledge of sterilization process is preferred
+ Knowledge of cGMP, cGDP, relevant ISO standards, medical device requirements and other international regulations
+ Familiarity with MasterControl, SAP and working knowledge of statistical data analysis
+ Fluent in English
+ Thorough understanding of validation activities and risk management principles and techniques
+ Strong problem-solving and critical thinking skills
+ Negotiation skills and collaborating with suppliers
+ Ability to work under high volume production and fast changing environment
+ Willingness to work in a cross-functional team with different time zones
+ Able to comply with the company's safety policy at all times. #LI-AP1 #LI-HYBRID
**Travel Requirements**
20%: Up to 52 business days per year
**Physical Requirements**
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening.

Bring more to life.

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

At Beckman Coulter Diagnostics, 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 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. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible.

The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will serve as a critical quality liaison between Beckman Coulter and our key electronics (PCB, cables, electrical assemblies) suppliers worldwide . In close partnership with Operational SQE’s and our Sourcing Commodity Managers, you will lead efforts to develop long-term supplier partnerships to elevate supplier performance, mitigate risk, and ensure consistent delivery of high-quality electronics components to meet quality, delivery and cost objectives .  

This position reports to the Sr. Director of Global Supplier Quality responsible for glob al 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 lifecycle—from 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.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel – up to 25% globally, based on business needs

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.  

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. Check out our benefits at Danaher Benefits Info .

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. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.    

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 .

Bring more to life.

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

At Beckman Coulter Diagnostics, 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 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. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible.

The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will serve as a critical quality liaison between Beckman Coulter and our key electronics (PCB, cables, electrical assemblies) suppliers worldwide . In close partnership with Operational SQE’s and our Sourcing Commodity Managers, you will lead efforts to develop long-term supplier partnerships to elevate supplier performance, mitigate risk, and ensure consistent delivery of high-quality electronics components to meet quality, delivery and cost objectives .  

This position reports to the Sr. Director of Global Supplier Quality responsible for glob al 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 lifecycle—from 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.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel – up to 25% globally, based on business needs

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.  

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. Check out our benefits at Danaher Benefits Info .

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. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.    

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 .

Bring more to life.

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

At Beckman Coulter Diagnostics, 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 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. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible.

The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will serve as a critical quality liaison between Beckman Coulter and our key electronics (PCB, cables, electrical assemblies) suppliers worldwide . In close partnership with Operational SQE’s and our Sourcing Commodity Managers, you will lead efforts to develop long-term supplier partnerships to elevate supplier performance, mitigate risk, and ensure consistent delivery of high-quality electronics components to meet quality, delivery and cost objectives .  

This position reports to the Sr. Director of Global Supplier Quality responsible for glob al 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 lifecycle—from 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.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel – up to 25% globally, based on business needs

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.  

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. Check out our benefits at Danaher Benefits Info .

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. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.    

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 .

Bring more to life.

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

At Beckman Coulter Diagnostics, 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 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. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible.

The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will serve as a critical quality liaison between Beckman Coulter and our key electronics (PCB, cables, electrical assemblies) suppliers worldwide . In close partnership with Operational SQE’s and our Sourcing Commodity Managers, you will lead efforts to develop long-term supplier partnerships to elevate supplier performance, mitigate risk, and ensure consistent delivery of high-quality electronics components to meet quality, delivery and cost objectives .  

This position reports to the Sr. Director of Global Supplier Quality responsible for glob al 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 lifecycle—from 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.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel – up to 25% globally, based on business needs

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.  

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. Check out our benefits at Danaher Benefits Info .

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. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.    

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 .

Bring more to life.

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

At Beckman Coulter Diagnostics, 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 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. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible.

The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will serve as a critical quality liaison between Beckman Coulter and our key electronics (PCB, cables, electrical assemblies) suppliers worldwide . In close partnership with Operational SQE’s and our Sourcing Commodity Managers, you will lead efforts to develop long-term supplier partnerships to elevate supplier performance, mitigate risk, and ensure consistent delivery of high-quality electronics components to meet quality, delivery and cost objectives .  

This position reports to the Sr. Director of Global Supplier Quality responsible for glob al 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 lifecycle—from 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.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel – up to 25% globally, based on business needs

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.  

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. Check out our benefits at Danaher Benefits Info .

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. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.    

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 .

Bring more to life.

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

At Beckman Coulter Diagnostics, 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 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. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible.

The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will serve as a critical quality liaison between Beckman Coulter and our key electronics (PCB, cables, electrical assemblies) suppliers worldwide . In close partnership with Operational SQE’s and our Sourcing Commodity Managers, you will lead efforts to develop long-term supplier partnerships to elevate supplier performance, mitigate risk, and ensure consistent delivery of high-quality electronics components to meet quality, delivery and cost objectives .  

This position reports to the Sr. Director of Global Supplier Quality responsible for glob al 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 lifecycle—from 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.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel – up to 25% globally, based on business needs

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.  

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. Check out our benefits at Danaher Benefits Info .

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. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.    

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 .

Bring more to life.

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

At Beckman Coulter Diagnostics, 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 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. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible.

The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will serve as a critical quality liaison between Beckman Coulter and our key electronics (PCB, cables, electrical assemblies) suppliers worldwide . In close partnership with Operational SQE’s and our Sourcing Commodity Managers, you will lead efforts to develop long-term supplier partnerships to elevate supplier performance, mitigate risk, and ensure consistent delivery of high-quality electronics components to meet quality, delivery and cost objectives .  

This position reports to the Sr. Director of Global Supplier Quality responsible for glob al 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 lifecycle—from 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.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel – up to 25% globally, based on business needs

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.  

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. Check out our benefits at Danaher Benefits Info .

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. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.    

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 .

Bring more to life.

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

At Beckman Coulter Diagnostics, 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 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. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible.

The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will serve as a critical quality liaison between Beckman Coulter and our key electronics (PCB, cables, electrical assemblies) suppliers worldwide. In close partnership with Operational SQE’s and our Sourcing Commodity Managers, you will lead efforts to develop long-term supplier partnerships to elevate supplier performance, mitigate risk, and ensure consistent delivery of high-quality electronics components to meet quality, delivery and cost objectives. 

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 lifecycle—from 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.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel – up to 25% globally, based on business needs

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. 

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. Check out our benefits at Danaher Benefits Info.

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. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.   

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