232 Supplier Quality Engineer jobs in Minneapolis

Overview

We are seeking a detail-oriented and experienced Supplier Quality Engineer to join our dynamic team. The ideal candidate will play a crucial role in ensuring that our suppliers meet the highest quality standards, contributing to our commitment to excellence in manufacturing and product delivery. This position requires a strong background in quality management systems, supplier management, and regulatory compliance.

Duties

• Create and implement vendor quality plans through risk analysis
• Support ISO 9000 Requirements
• Make sure corrective and preventive actions are created and put in place for assigned vendors
• Perform supplier quality audits
• Identify issues with quality, perform root cause analysis and put in place corrective actions
• Take part in continuous improvement plans
• Create and submit reports for audits, inspections, etc.

Experience

• Bachelors degree in Engineering, Supply Chain or related discipline
• 4+ years in manufacturing, operations, supply chain, quality or related
• License or certifications such as CPIM, ASQ, CQE, CSCP or other related
• ISO9000, Six Sigma preferred
• Excellent problem solving skills, and rood cause analysis experience
• MRP/ERP experiences

MUST BE AUTHORIZED TO WORK IN THE US PERMANENTLY.

Must be a resident of the Minneapolis/St. Paul metro area

**Job Description Summary**
Are you ready to see your future take flight? At GE Aerospace, we are advancing aviation technologies for today and tomorrow. Your work will contribute to the production of advanced jet engines, components, and integrated systems that power commercial and military aircraft. You'll be part of a team that embraces your drive, your curiosity, and your unique ideas and perspectives. Most importantly, you'll share in our pride and purpose that affects the lives of millions around the world!
This role will drive management of change and deployment of Product Quality Planning for assigned parts/suppliers within the Organization; as well as with GE Aerospace Suppliers to ensure on time supply of production engine components, at cost and rate, that conform to General Electric Aerospace Manufacturing and Quality requirements.
The Advanced Supplier Quality Engineer will lead Standardization of tools and process to be followed throughout the business and will work closely with other functions such as Engineering, Commercial and Services to develop the strategy and effectively implement the new Aerospace standard and ensures that the assigned suppliers continually develop their Management of Change process in line with the design intent of the customer and verify their systems to ensure they are compliant with the end customer's needs.
**Job Description**
**Roles and Responsibilities**
+ Track and manage NPI quality actions driving both internal and external to support continuous improvement with APQP concepts.
+ Work developing procedures, regulations and work instructions that support APQP and AS9145 / AS13100 requirements.
+ Accountable for overall Supplier Management of Change as defined by established processes, policies, and tools for an assigned portfolio of hardware, programs and/or supplier.
+ Support new product launches to ensure that supplier quality meets the required standards Be a mentor/coach for various projects with several part families and/or different Engine Programs.
+ Lead/Develop roadmaps that lead to successful integration of Management of change Product Quality Planning into existing policies and procedures.
+ Responsible for the maintenance and communication of Source Change and/or NPI plan execution to partner pillars within the Supplier Performance & Execution, respective Commodity teams and customer program focal points. Inform the respective Commodity on progress and lessons learned to inform future strategy for supplier, part family, etc.
+ Collaborate with various leaders in different functions to understand best approach to implementing changes within NPI and Product Management
+ Train and coach individuals and teams on various elements within Production Part Approval Process (PPAP) such as FMEAs, Gage R&Rs, Control Plans, etc.
+ Collaborate with various leaders in different functions to develop and implement a review process for ensuring rigor and quality of completed deliverables.
+ Generate executive summaries that clearly indicate status, business impact and significant issues related to NPI projects, Work with cross functional teams from Internal Shops as well as External Suppliers to coach/mentor all deliverables of APQP.
+ Includes both Supplier Quality Assurance and Supplier Quality Development. Includes supplier qualifications, action plans, audits, and assisting key suppliers towards industrial standards of excellence.
+ A job at this level is likely to be an individual contributor, with proven interpersonal skills. Communication with direct colleagues and the business about design and coordination services rendered. Provides informal guidance to new team members. Explains complex information to others in straightforward situations.
+ The role operates with some autonomy but is focused on execution of activities/provision of advice within an enabling discipline covered by standard functional practices and procedures. Activities require professional judgment but may require more senior levels of guidance.
+ Provide concise, complete, and accurate documentation of inspection results relative to area of responsibility. In appropriate functional areas, this refers to supporting inspection and test status requirements defined by regulations, engineering product specifications or Control Plans, Production Part Approval Process (PPAP) approval.
+ **Travel Required on average between 25% - 40%.**
**Required Qualifications**
+ Bachelor's degree from an accredited university or college + a minimum of 5 years of manufacturing for automotive or aerospace experience.
+ Knowledge of manufacturing and production process
+ Knowledge of government compliance and quality control regulatory standards
**Desired Characteristics**
+ Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Ability to document, plan, market, and execute programs. Established project management skills.
+ Prior supplier quality management experience
+ Understanding of AS9100 - AS13100
+ Knowledge of investment casting processes
+ Knowledge of measurement techniques
+ Metrology, Inspection Methods, and Equipment
+ Understanding and interpretation of engineering drawings
+ Understanding manufacturing processes
+ Ability to work in a diverse and dynamic environment
+ Planning and prioritizing activities
+ Good communication and interpersonal skills
+ Listening skills
+ Negotiation skills
+ Ability to present data effectively
+ Problem-solving skills
+ Understanding of Health and Safety practices
+ Team working skills
+ Analytical skills
+ Experience of working in Quality Assurance
+ Experience of Supplier quality development
+ Lean skills
+ Membership of appropriate professional body
GE Aerospace offers comprehensive benefits and programs to support your health and, along with programs like HealthAhead, your physical, emotional, financial and social wellbeing. Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach from GE Aerospace; and the Employee Assistance Program, which provides 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Aerospace Retirement Savings Plan, a 401(k) savings plan with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness.
GE Aerospace (General Electric Company or the Company) and its affiliates each sponsor certain employee benefit plans or programs (i.e., is a "Sponsor"). Each Sponsor reserves the right to terminate, amend, suspend, replace or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual.
The base pay range for this position is 110,000.00 - 140,000.00. The specific pay offered may be influenced by a variety of factors, including the candidate's experience, education, and skill set. This position is also eligible for an annual discretionary bonus based on a percentage of your base salary/ commission based on the plan. This posting is expected to close on **September 6th,** **2025** **.**
#LI-AZ1
_This role requires access to U.S. export-controlled information. Therefore, for applicants who are not U.S. lawful permanent residents, U.S. Citizens, or have been granted asylee or refugee status (i.e., not a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3), otherwise known as a U.S. Person), employment will be contingent on the ability to obtain authorization for access to U.S. export-controlled information from the U.S. Government._
**Additional Information**
GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer ( . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
**Relocation Assistance Provided:** No
#LI-Remote - This is a remote position
GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Job Description
Insight Global is looking for a Senior Supplier Quality Engineer who will support global sourcing, manufacturing operations, and global quality systems by participating in global communities of practice and value improvement projects. Leads supplier audits to ensure compliance with regulatory standards, including scheduling, reporting, and follow-up actions. Conducts on-site assessments and supports evaluation of supplier changes. Applies data-driven problem-solving to resolve complex quality issues, communicates findings, and approves corrective actions. Serves as a technical lead in Global Sourcing teams, driving category objectives and strategy. Independently leads cross-functional projects to improve quality systems and processes, mentors junior engineers, and recommends updates to the Quality Management System. Builds strong relationships across teams and with suppliers to support project goals and influence business decisions. Maintains a strong commitment to patient safety and product quality by ensuring compliance with the Quality Policy and fostering a culture of quality. Drives improvement and corrective action in the quality of components sourced from outside suppliers. Provides technical support in the selection of suppliers. Develops acceptance criteria for materials. Monitors supplier performance to drive supplier corrective action, manufacturing yield issues and field failures.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: and Requirements
-Bachelor's degree in Chemistry, Biochemistry, chemical engineering or related field
- 5+ years of experience in pharmaceutical or drug combination products
-Communicates effectively and concisely pack up information to deliver key points; appropriately scales communication style and depth according to the audience.
-Ability to influence cross functional global teams spanning Design Quality Assurance, R&D, Regulatory, Supplier Engineering, and Sourcing.
Strong knowledge of FDA 21 CFR 820 and CFR 210/211. -Experience in global supplier management, ISO 13485, ISO 9001 strongly desired.
-Supplier quality experience
-Experience with manufacturing support or process development.
Ideally someone with experience in aseptic processes. null
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to

We anticipate the application window for this opening will close on - 20 Oct 2025
Position Description:
Sr. Supplier Quality Engineer for Medtronic, Inc. located in Minneapolis, MN. Responsible for communicating technical objectives between Medtronic and suppliers. Coordinate with cross-functional groups in supplier selection process. Developing and maintaining incoming inspection procedures, ensuring inspector trainings and qualifying parts for SOQ program. Responsible for Supplier Change process between Medtronic and Suppliers to evaluate and implement changes at Supplier. Responsible for Supplier and Medtronic CAPA (Corrective and Preventive Action) Supplier related Product and Process NCMR (Nonconforming Material Report) by working with the supplier to conduct root cause investigation, implement appropriate controls and perform effectiveness checks. Responsible for Supplier Maintenance and Controls, Supplier Audits, Quality Agreements, Quality Performance Reviews. Execute supplier and component qualification and validation including drafting, Control Plans, PPAP (Production Part Approval Process), Medtronic qualify plans/RIR (Receiving Inspection Requirements), and Gage R& R (Repeatability & Reproducibility), DOE (Design of Experiments), and GD&T (Geometric Dimensioning and Tolerancing). Coordinate equipment Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Process Validation, pFMEA (Process Failure Mode and Effects Analysis) and Risk Assessments of suppliers, Test Method Validations and Measurement System Analysis. Utilize failure investigation techniques, statistical quality controls, protocol & report preparation, and non-conforming product controls. Utilize GMP (Good Manufacturing Practices) for Class II and Class III medical devices to ensure quality products and outcomes. Navigate the complexities of various government and industry regulations to include FDA QSR 21 CFR 820, EU Medical Device Directive (EU MDD 93/42 EEC), ISO 13485, ISO 9001, and ISO 14971. Multiple positions available. Position is open to telecommuting from anywhere in the United States. Requires up to 25% travel to suppliers within the U.S. and internationally. #LI-DNI
Basic Qualifications:
Requires a Master's degree in Mechanical, Biomedical, Industrial, Electrical, or Manufacturing Engineering, Engineering Technology, Technology Project Management or related engineering field, and two (2) years' experience as a supplier, quality, or manufacturing engineer or related occupations; or Bachelor's degree in Mechanical, Biomedical, Industrial, Electrical or Manufacturing Engineering, Engineering Technology, Technology Project Management, or related engineering field, and five (5) years' experience as a supplier, quality, or manufacturing engineer or related occupations. Must possess at least two (2) years' experience with each of the following: Supplier Change Process evaluation and implementation; CAPA, Supplier related Product and Process NCMR; Supplier Maintenance and Controls, Supplier Audits, Quality Agreements, and Quality Performance Reviews; Supplier and component qualifications and validations, including Control Plans, PPAP, RIR, Gage R&R, DOE, and GD&T; IQ/OQ/PQ, Process Validation, pFMEA and Risk Assessments of suppliers, Test Method; Validations, and Measurement System Analysis; Failure investigation techniques, statistical quality controls, protocol & report preparation, and non-conforming product controls; GMP for Class II and Class III medical devices; FDA QSR 21 CFR 820, EU MDD 93/42 EEC, ISO 13485, ISO 9001 and ISO 14971.
Salary: $121,400 to $145,200 per year
The position reports to Medtronic, Inc., 710 Medtronic Parkway NE, Minneapolis, MN 55432.
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings

**Working Location:** **MINNESOTA, BROOKLYN PARK**
**Workplace Flexibility:** **Hybrid**
**_For more than 100 years, Olympus has focused on making people's lives healthier, safer and more fulfilling. _** **__**

Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill their desires, dreams, and lives.

Our five Core Values empower us to achieve Our Purpose:
**Patient Focus, Integrity, Innovation, Impact and Empathy.**
Learn more about Life at Olympus ( .
**Job Description**
The Senior Supplier Quality Engineer is responsible for the product-related supplier quality within a defined material segment and / or site including part approval, SCAR handling, development project support, sustaining engineering support including non-conformance handling and incoming inspection planning.
**Job Duties**
+ Develops quality assurance strategy for sourced products including suppliers and incoming inspection in cooperation with Manufacturing Quality Assurance.
+ Acts as supplier quality engineering representative in new product development projects.
+ Performs Advanced Product Quality Planning (APQP) by applying the appropriate methods including early supplier involvement into development projects and assures that required process validations are sufficiently implemented.
+ Coordinates and ensures the external component qualification/FAI process is effective.
+ Identifies gaps in suppliers' capabilities / technical project risks.
+ Accountable for incoming inspection planning.
+ Makes decisions on acceptance or rejection of sourced materials.
+ Guides inspectors regarding incoming inspections (e. g. training, standards, etc.).
+ Responsible for SCAR process as part of the NC process.
+ Leads improvement projects at the supplier.
+ Acts as primary interface to supplier regarding product related quality matters.
+ Analyzes product related supplier quality issues.
+ Is part of the material review boards.
+ Supports facility audits by outside agencies (i.e., FDA, ISO / MDSAP).
+ Supports Supplier audits as co-auditor.
+ Performs local supplier management such as supplier approval, supplier auditing, QAA negotiation and supplier evaluation if delegated by SQM.
**Job Qualifications**
**Required:**
+ Minimum requirements are a BA/BS degree or equivalent in a Life Science, Engineering, or Physical Science with an advanced technical degree.
+ Demonstrated expertise in the applied interpretation of worldwide regulatory standards and laws applicable to the IVD industry e.g., ISO, QSR, GMP, GLP, GCP, HIPAA.
+ Knowledge of and minimum 5 years' experience in supplier quality engineering.
+ High level of quality tools and methodology skills (e.g. 8D, 5-Whys, FMEA, IQ/OQ/PQ).
+ Very good written and oral communication and organizational, project management skills.
+ Technical knowledge about category supported.
+ Very good knowledge of Quality tools and methods.
+ ISO 9001 / FDA / Medical technology background.
+ Qualification in specific product group.
+ Basic project management skills.
+ Advanced English.
+ 20% travel should be expected.
**Why join Olympus?**
_We offer a holistic employee experience supporting personal and professional well-being through meaningful work, equitable offerings, and a connected culture._
**Equitable Offerings you can count on:**
+ Competitive salaries, annual bonus and 401(k)* with company match
+ Comprehensive medical, dental, vision coverage effective on start date
+ 24/7 Employee Assistance Program
+ Free live and on-demand Wellbeing Programs
+ Generous Paid Vacation and Sick Time
+ Paid Parental Leave and Adoption Assistance*
+ 12 Paid Holidays
+ On-Site Child Daycare, Café, Fitness Center**
**Connected Culture you can embrace:**
+ Work-life integrated culture that supports an employee centric mindset
+ Offers onsite, hybrid and field work environments
+ Paid volunteering and charitable donation/match programs
+ Employee Resource Groups
+ Dedicated Training Resources and Learning & Development Programs
+ Paid Educational Assistance
*US Only
**Center Valley, PA and Westborough, MA
**Are you ready to be a part of our team?**
Learn more about our benefit and incentives ( .
The anticipated base pay range for this full-time position working at this location is $93,793.00 - $126,621.00 / year, plus potential for annual bonus (subject to plan eligibility and other requirements). Olympus considers a variety of factors when determining actual compensation for this position including: level of experience, working location, and relevant education and certifications.
At Olympus, we are committed to Our Purpose of making people's lives healthier, safer and more fulfilling. As a global medical technology company, we partner with healthcare professionals to provide best-in-class solutions and services for early detection, diagnosis and minimally invasive treatment, aiming to improve patient outcomes by elevating the standard of care in targeted disease states.
For more than 100 years, Olympus has pursued a goal of contributing to society by producing products designed with the purpose of delivering optimal outcomes for its customers around the world.
Headquartered in Tokyo, Japan, Olympus employs more than 31,000 employees worldwide in nearly 40 countries and regions. Olympus Corporation of the Americas, a wholly owned subsidiary of Olympus Corporation, is headquartered in Center Valley, Pennsylvania, USA, and employs more than 5,200 employees throughout locations in North and South America. For more information, visit .
**You Belong at Olympus**
We value a workforce that reflects a wide range of perspectives, backgrounds, and experiences. We foster an environment where all employees feel valued, respected, and supported. And we provide employees with equal access to opportunities for growth and development.
**_Applicants Requesting Accommodations:_** Olympus is committed to the full inclusion of all qualified individuals. As part of this commitment, Olympus will ensure that persons with disabilities are provided reasonable accommodations for the hiring process. If reasonable accommodation is needed, please contact If your disability impairs your ability to email, you may call our HR Compliance Manager at 1-888-Olympus ( ).
**Let's realize your potential, together.**
It is the policy of Olympus to extend equal employment and advancement opportunity to all applicants and employees without regard to race, color, national origin (including language use restrictions), citizenship status, religious creed (including dress and grooming practices), age, sex (including pregnancy, childbirth, breastfeeding, medical conditions related to pregnancy, childbirth and/or breastfeeding), gender, gender identity and expression, sexual orientation, marital status, disability (physical or mental) and/or a medical condition, genetic information, ancestry, veteran status or service in the uniformed services, and any other characteristic protected by applicable federal, state or local law.
Posting Notes: | United States (US) | Minnesota (US-MN) | Brooklyn Park | Quality & Regulatory Affairs (QA/RA)

Are you ready to help us make the future?
As a **Sr. Advanced Supplier Quality Engineer** at Honeywell ACST, you will be responsible for ensuring quality throughout the supply chain and product development lifecycle. You will ensure compliance with customer requirements, all applicable laws and regulations, Honeywell sourcing requirements and engineering specifications for our products and services. This position requires close collaboration with internal teams and external providers to Honeywell.
You will work out of our Plymouth MN location on an onsite work schedule with up to 25% domestic travel.
WHATS IN IT FOR YOU?
In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays. For more information visit: Benefits at Honeywell
The annual base salary for this position is $106,000.00-$132,000.00. Please note that this salary information serves as a general guideline. Honeywell considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as market and business considerations.
Key Responsibilities:
+ Provide technical expertise and guidance to the procurement and engineering teams on quality requirements
+ Serve as supplier quality representative in development, new product introduction and manufacturing product development phases
+ Analyze supply chain risks to enact proactive risk management initiatives
+ Ensure compliance with internal and external quality standards from Honeywell and its customers
+ Own and conduct supplier audits to assess supplier capabilities and identify areas for improvement
+ Drive supplier root cause analysis and corrective actions to address quality issues and prevent recurrence
+ Collaborate with cross-functional teams to drive supplier performance improvement and resolve quality issues
+ Implement and manage First Article Inspection (FAI) program
+ Monitor supplier quality metrics to identify trends and opportunities for improvement
US CITIZENSHIP REQUIREMENTS
Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. citizen, U.S. permanent resident, or have asylum or refugee status in the U.S.
The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates.
**YOU MUST HAVE**
+ Minimum of 5+ years' experience in direct Supplier Quality Engineering
+ U.S. citizenship is required due to contractual requirements. Applicants must also be able to obtain and maintain a U.S. Government security clearance. Continued employment is contingent upon successful completion of security processing.
**WE VALUE**
+ Bachelor's degree from an accredited institution in a technical discipline such as the sciences, technology, engineering, or mathematics
+ Manufacturing experience in a fast-paced environment
+ Ability to collaborate effectively with internal/external customers.
+ Excellent interpersonal and communication skills
+ MBA or post graduate degree preferred.
+ Able to focus priorities to best impact quality metrics.
+ Experience in collaborating with technical teams.
+ Experience operating in a Quality Management system i.e. ISO 9001/13485, AS9100.
+ Six Sigma Greenbelt desired
+ Greenfield/startup experience in a technical environment.
**ABOUT HONEYWELL**
Honeywell International Inc. (NYSE: HON) invents and commercializes technologies that address some of the world's most critical challenges around energy, safety, security, air travel, productivity, and global urbanization. We are a leading software-industrial company committed to introducing state of the art technology solutions to improve efficiency, productivity, sustainability, and safety in high growth businesses in broad-based, attractive industrial end markets. Our products and solutions enable a safer, more comfortable, and more productive world, enhancing the quality of life of people around the globe.
**THE BUSINESS UNIT**
At Honeywell Advanced Connected Sustainability Technologies (ACST), our outstanding team of thinkers, innovators, and doers help make the future. We build environments and technologies that meet our customers' needs. The groundbreaking scientists, engineers, and professionals that make up our nimble group have the agility of a start-up backed with the power and investment of Honeywell.
Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.
#ACST
Honeywell helps organizations solve the world's most complex challenges in automation, the future of aviation and energy transition. As a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments - powered by our Honeywell Forge software - that help make the world smarter, safer and more sustainable.
Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.

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 Global Supplier Quality Engineer - Plastics for Beckman Coulter Diagnostics will serve as a critical quality liaison between Beckman Coulter and our key plastics 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 plastics components to meet quality, delivery and cost objectives .
This position 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, may be remote for qualified candidates.
This position reports to the Sr. Director of Global Supplier Quality responsible for glob al supplier quality strategy . If you thrive in a fast paced, broad reaching, dynamic role and want to work to build a best-in-class Global Supplier Quality organization -read on.
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.
+ Deep expertise 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.
+ Ability and willingness to travel up to 25%, 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.
Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we'll empower you to push the boundaries of what's possible.
#LI-LCS
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 .
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.
The U.S. EEO posters are available here ( .
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .

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.
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.
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
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.
#LI-GC1
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 .
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.
The U.S. EEO posters are available here ( .
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .

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 - Systems and Innovation for Beckman Coulter Diagnostics is responsible for l eading the development of best-in-class supplier quality processes, tools, and system s, with emphasis on PPAP, APQP, and the integration of automation to drive improvements throughout our global supply base .
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:
+ Design and Implement Scalable Quality Systems Develop and deploy supplier quality processes, digital tools, and intelligent workflows that incorporate best practices in APQP, PPAP, FMEA, Control Plans, and validation to drive global standardization and process efficiency
+ Enable Data-Driven Decision-Making Build dashboards, automation, and real-time analytics to enhance visibility, support proactive quality planning, and drive continuous improvement across the global supply base.
+ Provide Strategic Guidance and SME Support Act as a subject matter expert to global and site-level SQE teams, offering leadership on supplier quality planning, digital integration, and advanced quality tool utilization.
+ Lead Cross-Functional and Transformational Initiatives Drive projects focused on supplier readiness, onboarding, and long-term capability development, emphasizing scalability, lean principles, and digital transformation. Utilize application of DBS tools and kaizen methodologies to identify and implement opportunities for innovation, process simplification, and global standardization.
+ Collaborate and Cultivate Partnerships for Performance Improvement Work closely with cross-functional teams and external partners to embed smart quality systems throughout the product lifecycle and deliver sustained improvements in quality, delivery, cost, and compliance.
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
+ 5 + years of experience in supplier quality, advanced quality planning, or quality systems engineering.
+ Demonstrated expertise in APQP, PPAP, FMEA, MSA, SPC, and related quality tools within regulated manufacturing environments.
+ Experience working with or implementing digital tools, AI platforms, or automated quality systems is strongly preferred.
+ Strong project leadership, analytical, and communication skill s.
Travel, Motor Vehicle Record & Physical/Environment Requirements:
+ Ability to travel - Up to 15% globally based on business need
It would be a plus if you also possess :
+ Experience in FDA-regulated or medical device manufacturing environments.
+ 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.
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
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.
#LI-GC1
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 .
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.
The U.S. EEO posters are available here ( .
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .