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Semiconductor Quality Engineer Jobs in Minnesota

Quality Manager

Shoreview, MN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Quality Engineer (CQE), or Six Sigma Black Belt certification. * Experience in precision measurement, instrumentation, or similarly regulated manufacturing industries (semiconductor, environmental ...

Quality Manager

Saint Paul, MN · On-site

$150K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Quality Engineer (CQE), or Six Sigma Black Belt certification. * Experience in precision measurement, instrumentation, or similarly regulated manufacturing industries (semiconductor, environmental ...

Quality Manager

Shoreview, MN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Quality Engineer (CQE), or Six Sigma Black Belt certification. * Experience in precision measurement, instrumentation, or similarly regulated manufacturing industries (semiconductor, environmental ...

PDK Engineer

Bloomington, MN · On-site

$104K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

S.-based manufacturer of analog and power semiconductor devices and sensors. Proudly located in the ... Develop, QA, maintain and support PDKs with infrastructure for multiple EDA platforms. * Developing ...

PDK Engineer

Bloomington, MN · On-site

$104K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

S.-based manufacturer of analog and power semiconductor devices and sensors. Proudly located in the ... Develop, QA, maintain and support PDKs with infrastructure for multiple EDA platforms. * Developing ...

PDK Engineer

Bloomington, MN

$104K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

S.-based manufacturer of analog and power semiconductor devices and sensors. Proudly located in the ... Develop, QA, maintain and support PDKs with infrastructure for multiple EDA platforms. * Developing ...

Test Development Engineer

Bloomington, MN · On-site

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... improving quality. Interacts with product and process engineering personnel to ensure that ... Knowledge of semiconductor device physics, fabrication processes, and characterization techniques.

Product Engineer

Bloomington, MN · On-site

$90 - $127/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

R3736This position will sustain and improve product die yield for semiconductor manufacturing ... To ensure top quality, we provide employees with extensive training and use statistical process ...

Test Development Engineer

Bloomington, MN · On-site

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... improving quality. Interacts with product and process engineering personnel to ensure that ... Knowledge of semiconductor device physics, fabrication processes, and characterization techniques.

Test Development Engineer

Bloomington, MN · On-site

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... improving quality. Interacts with product and process engineering personnel to ensure that ... Knowledge of semiconductor device physics, fabrication processes, and characterization techniques.

Test Development Engineer

Bloomington, MN · On-site

$75K - $93K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... improving quality. Interacts with product and process engineering personnel to ensure that ... Knowledge of semiconductor device physics, fabrication processes, and characterization techniques.

Test Development Engineer

Bloomington, MN · On-site

$75K - $93K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... improving quality. Interacts with product and process engineering personnel to ensure that ... Knowledge of semiconductor device physics, fabrication processes, and characterization techniques.

Showing results 21-40

Semiconductor Quality Engineer information

What does a semiconductor quality engineer do?

A Semiconductor Quality Engineer is responsible for ensuring that semiconductor products meet established quality standards and specifications. They develop and implement quality control processes, perform failure analysis, and collaborate with engineering and manufacturing teams to resolve quality issues. Their work includes analyzing data, conducting audits, and driving continuous improvement in production processes to minimize defects and ensure product reliability. Ultimately, they play a crucial role in guaranteeing that semiconductor devices are safe and perform as intended for end users.

What are some common challenges semiconductor quality engineers face in ensuring product reliability?

Semiconductor Quality Engineers often encounter challenges related to rapidly evolving manufacturing processes, stringent industry standards, and the need to detect minute defects that can impact chip performance. They must work closely with cross-functional teams, including design, process, and production engineers, to implement robust quality controls and root cause analyses. Staying updated on new technologies and maintaining clear communication are essential for managing quality issues efficiently and ensuring that products meet both customer and regulatory expectations.

What are the key skills and qualifications needed to thrive as a semiconductor quality engineer, and why are they important?

To thrive as a Semiconductor Quality Engineer, you need expertise in quality assurance, semiconductor manufacturing processes, and statistical analysis, usually supported by a degree in engineering or a related field. Familiarity with tools such as Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), and quality management systems like ISO 9001 is typically required. Strong problem-solving abilities, attention to detail, and effective communication skills set outstanding candidates apart. These competencies are essential to ensure product reliability, maintain industry standards, and drive continuous improvement in semiconductor manufacturing.

What is the difference between Semiconductor Quality Engineer vs Semiconductor Process Engineer?

AspectSemiconductor Quality EngineerSemiconductor Process Engineer
Primary FocusEnsuring product quality, defect prevention, and compliance with standardsDesigning, developing, and optimizing manufacturing processes
Skills & CertificationsQuality management, testing, inspection, certifications (e.g., ISO)Process engineering, manufacturing techniques, statistical analysis
Work EnvironmentQuality labs, manufacturing floors, supplier auditsCleanrooms, fabrication facilities, process development labs
Industry UsageUsed across semiconductor manufacturing companies focusing on product qualityUsed in process development and manufacturing optimization

The Semiconductor Quality Engineer primarily focuses on maintaining and improving product quality, ensuring standards are met, and preventing defects. In contrast, the Semiconductor Process Engineer concentrates on developing and refining manufacturing processes to enhance efficiency and yield. Both roles are essential in semiconductor manufacturing but serve different aspects of the production cycle.

What are popular job titles related to Semiconductor Quality Engineer jobs in Minnesota?

For Semiconductor Quality Engineer jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Semiconductor Quality Engineer jobs in Minnesota look for?

The top searched job categories for Semiconductor Quality Engineer jobs in Minnesota are:

What cities in Minnesota are hiring for Semiconductor Quality Engineer jobs?

Cities in Minnesota with the most Semiconductor Quality Engineer job openings:

Infographic showing various Semiconductor Quality Engineer job openings in Minnesota as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% In-person job distribution.

Supplier Quality Engineer II - Direct Materials Acquisitions

Boston Scientific

Arden Hills, MN

Full-time

Re-posted 20 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz

32nd of 540 rated manufacturers


Job description

Recruiter: Spencer Gregory Hale

Supplier Quality Engineer - Direct Materials Acquisitions 

About the role:
The Global Sourcing organization at Boston Scientific is a global, passionate team that oversees a diverse network of suppliers which manufactures components or finished devices for BSC distribution. The Supplier Quality Engineer will demonstrate a primary commitment to patient safety and collaborate with cross-functional internal/external resources to continually improve our supplier's manufacturing processes. In this role, you will support products within the acquisition space with a primary focus on components and applicable accessories.

Your responsibilities include:

Supplier/Sustaining Engineering:

  • Evaluates and communicates quality issues to suppliers and applies sound, systematic problem-solving methodologies in identifying, prioritizing, and resolving quality issues. Reviews and approves supplier corrective action plans and verification of effectiveness documentation.
  • Manages sustaining quality issues, process change impacts, and design change implementations for suppliers within the Acquired Entity Quality system, the hybridized BSC-Acquired Entity Quality System, and in the BSC Quality System after products are successfully integrated.
  • Proactively assesses supplier capabilities through direct on-site visits and technical discussions. Coordinates the evaluation of proposed changes at suppliers.
  • Plans and leads supplier audits to assess compliance with regulatory standards and Boston Scientific requirements, including audit scheduling investigation, and evaluation of audit observation and findings, reporting, follow-up, and confirmation of follow-up actions.
  • Supports Design Quality Assurance with Field Action and Product Inquiry Reports by performing investigations on supplier-related or supplier-caused quality issues.
  • Investigates complaints and manages SCARs/NCEPs at component suppliers where the issue is manufacturing-related.
  • Supports Supplier Change Impact Assessments for process changes at suppliers.
  • Supports and performs Finished Good Documentation changes in support of ongoing design changes or labeling updates.
  • Leads projects and consistently hits project milestones. Creates crisp and clear project plans and develops strong contingency plans as part of project planning process.

New Product Development:

  • Support manufacturing lines of acquired entity's manufacturing line through integration of acquired company's suppliers and products into BSC's Quality System.
  • Lead the execution of material controls quality deliverables and collaborate with cross-functional new product development teams to onboard suppliers.
  • Generate and review quality plans, agreements, product specifications, component qualifications, design verification/validations, and process validations.

Quality System Champion:

  • Supports Material Controls external regulatory body audits requests as required.
  • Leads or supports Material Controls internal audit efforts.
  • Collaborates with corporate and regional supplier quality organizations on policy, procedure, and guideline development. Includes generation, review, and implementation of these documents.
  • Identifies and advises management on potential improvements to quality systems and processes in the company.
  • Champions 100% compliance to company policies and SOP's.

 

What we're looking for in you:
Minimal Qualifications:

  • BS degree in engineering or technical field with minimum of 2 years of relevant experience.
  • Experience in medical device, automotive, aeronautical, semiconductor, or other regulated industry.
  • Project management: ability to influence cross functional global teams spanning Quality, Operations, R&D, and Sourcing.
  • Experience in process validation, design controls, risk management, CAPA, SCAR.
  • Ability to work independently; organized and self-driven.
  • Articulate communicator; adept at packaging and appropriately scaling information to the intended audience.
  • Ability to rapidly learn and use new software applications (e.g., PLM, ERP).
  • Domestic and international travel up to 25%. 

Preferred Qualifications:

  • 7+ years of medical device engineering experience preferred.
  • Medical Device Industry experience
  • Drug or animal tissue experience
  • Problem Solving and Project Management experience
  • Leadership experience on a materials or service commodity team.
  • Lead auditor of quality systems experience (ISO 13485 or similar).
  • ASQ certification (CQE, CBA, SSGB, SSBB) desired.

Requisition ID: 625534 

Minimum Salary: $ 71500 

Maximum Salary: $ 135800 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions.  This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement.  The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.  


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