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Quality Engineer Associate Jobs in Minnesota (NOW HIRING)

Xylem

Quality Technician

Chaska, MN

$28/hr

Certifications an advantage including Quality Auditor, Quality Engineer, Quality Improvement Associate, Six Sigma Green Belt preferred * Quality inspection and auditing experience preferred * Ability ...

Xylem

Quality Technician

Chaska, MN · On-site

$28 - $32/hr

Certifications an advantage including Quality Auditor, Quality Engineer, Quality Improvement Associate, Six Sigma Green Belt preferred * Quality inspection and auditing experience preferred * Ability ...

Xylem

Quality Technician

Chaska, MN · On-site

$28 - $32/hr

Certifications an advantage including Quality Auditor, Quality Engineer, Quality Improvement Associate, Six Sigma Green Belt preferred * Quality inspection and auditing experience preferred * Ability ...

Xylem

Quality Technician

Chaska, MN

$28 - $32/hr

Certifications an advantage including Quality Auditor, Quality Engineer, Quality Improvement Associate, Six Sigma Green Belt preferred * Quality inspection and auditing experience preferred * Ability ...

Kognitiv Edge

Data Engineer II

Minneapolis, MN · On-site

Troubleshoot and resolve data quality, performance, reliability, and scalability issues across the ... Relevant certifications (e.g., Security+, CISSP, Azure Security Engineer Associate, CKS)

Xylem

Quality Technician

Chaska, MN · On-site

$28 - $32/hr

Certifications an advantage including Quality Auditor, Quality Engineer, Quality Improvement Associate, Six Sigma Green Belt preferred * Quality inspection and auditing experience preferred * Ability ...

Integer

Design Assurance Engineer II- Chaska

Chaska, MN · On-site

$79K - $116K/yr

Performs quality/reliability engineering activities to ensure that the design/development ... with other associates and cross functional teams. Special Skills: Strong written and oral ...

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Quality Engineer Associate information

What is the difference between Quality Engineer Associate vs Quality Technician?

AspectQuality Engineer AssociateQuality Technician
CredentialsTypically requires a bachelor's degree in engineering or related field; certifications like ASQ CQE are a plusUsually requires a high school diploma or associate degree; certifications like CQI or CQT are common
Work EnvironmentInvolves analysis, process improvement, and collaboration with engineering teamsFocuses on inspection, testing, and data collection on the production floor
Employer & Industry UsageUsed across manufacturing, aerospace, automotive, and electronics industriesCommonly employed in manufacturing and production settings

The Quality Engineer Associate and Quality Technician roles share a focus on quality assurance but differ mainly in responsibilities and required education. The associate typically engages in process analysis and improvement, while the technician concentrates on testing and inspection tasks. Both roles are vital in maintaining product quality within manufacturing industries.

What does a Quality Engineer Associate do?

A Quality Engineer Associate supports the quality assurance and control processes within manufacturing or production environments. Their responsibilities typically include inspecting products, monitoring production processes, assisting with quality audits, and helping to implement quality standards and procedures. They work closely with senior quality engineers and production teams to identify defects, resolve quality issues, and ensure that products meet required specifications. This entry-level role is a great starting point for a career in quality engineering, as it provides hands-on experience with quality systems and tools.

What engineer makes $500,000 a year?

Highly experienced engineers in specialized fields such as petroleum engineering, aerospace engineering, or certain senior roles in software engineering can earn $500,000 or more annually, often including bonuses and stock options. These positions typically require advanced skills, extensive experience, and often involve leadership or executive responsibilities.

What engineers make $200,000 a year?

Senior engineers in fields such as software, petroleum, aerospace, and electrical engineering can earn $200,000 or more annually, especially with extensive experience, advanced skills, and often in leadership or specialized roles. High salaries are common in industries with high demand for technical expertise and may require advanced degrees, certifications, or management responsibilities.

What engineers make $300,000 a year?

Senior engineers in specialized fields such as petroleum, aerospace, or software engineering with extensive experience and advanced skills can earn $300,000 or more annually. High-level roles often require advanced certifications, leadership responsibilities, and working in high-demand industries or companies.

What are some common challenges a Quality Engineer Associate might face in their daily work?

Quality Engineer Associates often encounter challenges such as balancing multiple projects with tight deadlines, interpreting complex product specifications, and effectively communicating quality standards to cross-functional teams. They may also need to troubleshoot unexpected production issues and adapt quickly to new processes or technologies. Developing strong analytical and problem-solving skills, as well as building collaborative relationships with manufacturing, engineering, and quality assurance teams, can help overcome these challenges.

What are the key skills and qualifications needed to thrive as a Quality Engineer Associate, and why are they important?

To thrive as a Quality Engineer Associate, you need a solid understanding of quality control principles, data analysis, and basic engineering concepts, usually supported by a bachelor’s degree in engineering or a related field. Familiarity with tools such as statistical process control (SPC), Six Sigma methodologies, and quality management systems (QMS) is often required, and certifications like ASQ CQE can be beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills help you collaborate across teams and address quality issues proactively. These skills are vital for ensuring product reliability, compliance with standards, and continuous improvement in manufacturing or service processes.

What does an associate quality engineer do?

An associate quality engineer supports quality assurance processes by inspecting products, analyzing data, and assisting in implementing quality improvements. They often use tools like statistical analysis and follow industry standards such as ISO or Six Sigma to ensure products meet specified requirements. This role typically involves collaboration with manufacturing and engineering teams to maintain quality standards.
What are the most commonly searched types of Quality Engineer jobs in Minnesota? The most popular types of Quality Engineer jobs in Minnesota are:
What are popular job titles related to Quality Engineer Associate jobs in Minnesota? For Quality Engineer Associate jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Quality Engineer Associate jobs in Minnesota look for? The top searched job categories for Quality Engineer Associate jobs in Minnesota are:
What cities in Minnesota are hiring for Quality Engineer Associate jobs? Cities in Minnesota with the most Quality Engineer Associate job openings:
Quality Engineer Associate jobs near you
Infographic showing various Quality Engineer Associate job openings in Minnesota as of July 2026, with employment types broken down into 75% Full Time, 8% Temporary, and 17% Contract. Highlights an 100% In-person job distribution.
Post Market Surveillance Engineer II

Post Market Surveillance Engineer II

Integer Holdings Corporation

Plymouth, MN • On-site

$76K - $98K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Integer Holdings rating

7.1

Company rating: 7.1 out of 10

Based on 40 frontline employees who took The Breakroom Quiz

369th of 527 rated manufacturers

Job description

By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success.
At Integer, our values are embedded in everything we do.
Customer
We focus on our customers' success
Innovation
We create better solutions
Collaboration
We create success together
Inclusion
We always interact with others respectfully
Candor
We are open and honest with one another
Integrity
We do the right things and do things right
What you'll do in this role:
  • The primary purpose of this job is to execute and support the Complaint Handling, Regulatory Reporting, and Post Market Surveillance processes for Integer under the direction, instruction and guidance from more experienced associates and managers in your organization. This position will be responsible for executing and providing support in the analysis, evaluation and product investigation of complaints received from external customers in a timely manner to comply with FDA 21 CFR (QSR) requirements and requirements of other regulatory bodies and countries with some instruction and guidance from more experienced associates and managers.

  • You adhere to Integer's Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements.

Post Market Complaint Handling Activities:
  • You will be responsible for accurately capturing and documenting all complaints in the complaint handling database according to internal policies and procedures.

  • You will be responsible for sending complaint acknowledgements to customers.

  • You will be responsible for tracking customer return products.

  • You will be responsible for performing complaint investigation activities with cross functional team members.

  • You will be responsible for reviewing device history records for nonconformities related to the alleged complaint.

  • You will interface with internal and external customers to gather additional information required for complaint investigations and prepare customer communication, complaint investigation reports and Customer Facing Reports, as applicable.

  • You will execute data collection, root cause investigations and resolution in support of a thorough complaint investigation related to product quality and patient safety.

  • You will play an active role in ensuring timely closure of complaint investigations to comply with requirements of FDA and other regulatory bodies and countries.

  • You may be required to handle, decontaminate, and analyze products used in the field by hospitals/end users per internal procedures and safety requirements, which will require you to have relevant vaccinations.

  • You will be responsible for performing risk assessments for products that are Integer owned designs.

  • You will be responsible for performing CAPA assessments and supporting CAPA investigations.

  • You will be responsible for assessing Adverse Event Reportability decisions in accordance with US and International regulations.

  • You will be responsible for assisting in the completion of applicable forms for submission of reportable complaints to applicable agencies.

  • You will assist in gathering complaint and ship data to support Post Market Trending, PMSRs, and PSUR's.

  • You are expected to collaborate with others in the exchange of information, ask questions and regularly check for understanding in support in your development as a Post Market Surveillance Engineer II.

Audit Support:
  • You will be responsible for supporting internal and external audits. Provide support for external regulatory inspections and customer audits. Support the timely response and closure of audit observations and findings.

Quality System Responsibilities:
  • You will perform work on projects where you will follow Integer's standard quality management system methodologies to investigate opportunities for process improvements.

  • You are expected to collaborate with others in the exchange of information, ask questions and regularly check for understanding in support of your development as an Associate Product SurveillanceEngineer.

  • You embed Quality within the Regulatory discipline - "I own Quality." You are a standard bearer for Quality in everything we do at Integer, by assuring adherence to our Quality Management System (QMS), facilitating and/or contributing to corrective and preventive actions, and contributing to the successful

attainment of our quality KPI's and journey to 5 Sigma.
  • You may perform other duties as needed and as directed by your line of supervision.

Manufacturing Excellence Imperatives:
  • Provide support of Integer's Manufacturing Excellence and Market Focused Innovation Strategies

  • Participation or Leadership in Site Hoshin Planning, Quality Planning, Validation master plans and associated quality improvement imperatives

  • Provide leadership as required for QA RA weekly and monthly metrics, supporting the walk to 5 sigma.

  • Leadership of Sustained Change ensuring customer change notifications are initiated and completed, as necessary, and supporting continuous improvement activities as required.

  • Support the standardisation of workplace organization & visual controls (5S), Manufacturing Standard Work, and robust training & certification programs where applicable.

  • Associate Engagement promoted through the adoption of standardized problem solving. methodologies, behaviour-based safety programs, and improvement idea and suggestion systems.

  • Systems & Process Optimization through adoption of principles of built in quality,

How you will be measured:
The specific measures listed below may be subject to change and are not intended to be an all-inclusive list.
  • Safety is our highest priority; you will be an active supporter of the Integer Environmental, Health & Safety programs.

  • Adhere to all Integer Values: Customer, Integrity, Candor, Inclusion, Collaboration, Innovation.

  • You will have defined Goals and Objectives specifying key projects and expected milestones to achieve.

  • Achievement of site quality KPI's

  • Innovation and ideation are critical aspects of your role, and you will be expected to generate continuous improvement suggestions and support the implementation of them.

What sets you apart:
Minimum Education and Experience:
  • You have earned, as a minimum, a bachelor's degree and have at least 1 year of relevant experience. Candidates who do not meet the education requirement may be considered if they have a minimum of 3 years' relevant experience (medical device or other regulated industry experience preferred).

Specialized Knowledge:
  • While you will have occasional support and guidance from more experienced Post Market Surveillance professionals, supervisors or managers, you will demonstrate the ability to work independently as well as collaboratively with other associates and cross functional teams.

Specialized Skills:
  • You demonstrate a solid technical aptitude with the ability to be an effective contributor to a team or produce results of a technical nature as an individual.

  • You demonstrate competencies in both written and oral communications.

  • You are highly organized and able to work and track multiple projects and complaints simultaneously.

  • You possess intermediate to advanced skills using Microsoft Office (PowerPoint, Visio, Project, Excel, Word, etc.)

  • You possess a positive, can-do attitude with an underlying belief that failure is not an option.

#IND1
Our total rewards program is designed to attract, retain, and motivate associates to contribute to Integer's success. Our compensation program includes base salary and a cash-based incentive program supporting our pay-for-performance philosophy. We provide a comprehensive benefits package with immediate eligibility including medical, dental, vision, disability, life insurance, and adoption benefits. Parental leave is available after one year. Optional employee-paid programs include supplemental life insurance, critical illness, hospital indemnity and accident insurance. Employees are immediately eligible to participate in the 401(k) plan with company matching contributions. We provide 80 hours (10 days) of company designated holidays per year plus an annual allotment of paid time off.
U.S. Applicants: Equal Opportunity Employer. In addition, veterans and individuals with disabilities are encouraged to apply.

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