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Senior Quality Process Engineer Jobs in Minnesota

Tactile Medical

Senior Quality Engineer

Minneapolis, MN · On-site

$93K - $131K/yr

The Senior Quality Engineer provides quality engineering leadership for manufacturing and post ... Review and approve process and test method validations, manage quality metrics, and oversee ...

Daikin Applied

Senior Quality Engineer

Owatonna, MN · On-site

$74K - $151K/yr

Train and teach others on quality topics including Quality Clinic Process, RCCA, Poke-yoke level ... Certified Quality Assurance Engineer, Six Sigma Black Belt, Red X Journeyman (preferred) * 6-8 ...

Baxter

Sr. Quality Engineer

Saint Paul, MN · On-site

$89K - $121K/yr

This role is responsible for ensuring that the quality of all product/process design meet all ... of senior personnel. You will help to perform engineering design evaluations and may develop a ...

Johnson Screens Inc

Senior Quality Engineer

Saint Paul, MN · On-site

$92K - $98K/yr

What You'll Do The Senior Quality Engineer is responsible for leading advanced quality initiatives ... Lead the development, implementation, and optimization of advanced quality control processes to ...

Daikinapplied

Senior Quality Engineer

Owatonna, MN · On-site

$151K/yr

Train and teach others on quality topics including Quality Clinic Process, RCCA, Poke-yoke level ... Certified Quality Assurance Engineer, Six Sigma Black Belt, Red X Journeyman(preferred) * 6-8years ...

IMRIS

Sr. Quality Engineer

Chaska, MN

$94K - $128K/yr

JOB SUMMARY TheSenior Quality Engineer is a member of the Quality Assurance team that will directly ... Actively participate in the Design Change process to ensure the proposed changes to the products ...

Ametek

Senior Quality Engineer

Jackson, MN · On-site

$83K - $113K/yr

The Senior Quality Engineer is responsible to ensure the operations adherence to organization ... Identify and implement effective process control systems to support the development, qualification ...

Danaher

Sr. Quality Engineer

New Brighton, MN · On-site

$115K - $125K/yr

The Sr. Quality Engineer is responsible for assuring the quality of processes and products by performing audits, inspections, tests, defect analysis, trend analysis, programming & troubleshooting ...

Danaher

Sr. Quality Engineer

New Brighton, MN · On-site

$115K - $125K/yr

The Sr. Quality Engineer is responsible for assuring the quality of processes and products by performing audits, inspections, tests, defect analysis, trend analysis, programming & troubleshooting ...

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Senior Quality Process Engineer information

What does a senior quality process engineer do?

A Senior Quality Process Engineer is responsible for designing, implementing, and improving processes to ensure products meet established quality standards. They analyze production systems, identify areas for improvement, and develop strategies to enhance efficiency and reduce defects. This role often involves collaborating with cross-functional teams, conducting root cause analyses, and ensuring compliance with industry regulations. Senior Quality Process Engineers also mentor junior staff and help drive continuous improvement initiatives within the organization.

How does a senior quality process engineer typically collaborate with cross-functional teams to drive process improvements?

A Senior Quality Process Engineer frequently works alongside manufacturing, design, and supply chain teams to identify inefficiencies and implement quality enhancements. This collaboration often involves leading root cause analysis sessions, facilitating process mapping workshops, and ensuring that corrective actions are communicated and adopted across departments. Effective communication and project management skills are essential, as the engineer acts as a bridge between technical and non-technical stakeholders to align quality objectives with business goals.

What is the difference between Senior Quality Process Engineer vs Quality Assurance Engineer?

AspectSenior Quality Process EngineerQuality Assurance Engineer
CredentialsBachelor's or Master's in Engineering, certifications like CQEBachelor's in Engineering, certifications like CQE or ASQ certifications
Work EnvironmentManufacturing, industrial, or production settingsProduct development, software, or manufacturing environments
ResponsibilitiesDesigning quality processes, process improvements, complianceTesting, inspection, ensuring product quality, audits

The main difference is that Senior Quality Process Engineers focus on developing and optimizing quality processes and ensuring compliance, often working on process improvements. Quality Assurance Engineers primarily focus on testing and inspecting products to ensure they meet quality standards. Both roles require similar certifications and often work in manufacturing or industrial settings, but their core responsibilities differ in scope and focus.

Is a senior quality process engineer a good career?

A senior quality process engineer is a valuable role in industries such as manufacturing, pharmaceuticals, and technology, focusing on improving product quality and process efficiency. It typically requires strong analytical skills, knowledge of quality standards like ISO or Six Sigma, and experience with process improvement tools. The role offers opportunities for advancement and specialization, making it a stable and rewarding career path for those interested in quality management and process optimization.

What are the key skills and qualifications needed to thrive as a senior quality process engineer?

To excel as a Senior Quality Process Engineer, you need a solid background in engineering principles, quality management systems, and process improvement methodologies, often supported by a bachelor's degree in engineering or a related field. Familiarity with Six Sigma, Lean tools, ISO standards, statistical analysis software, and quality auditing certifications like CQE are typically required. Strong analytical thinking, leadership, and effective communication skills set candidates apart when driving cross-functional initiatives. These competencies are crucial for ensuring product quality, regulatory compliance, and ongoing operational efficiency in manufacturing environments.

What are the most commonly searched types of Quality Process Engineer jobs in Minnesota?

The most popular types of Quality Process Engineer jobs in Minnesota are:

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

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

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

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

Senior Quality Process Engineer jobs near you
Infographic showing various Senior Quality Process Engineer job openings in Minnesota as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Senior Quality Engineer

Tactile Medical

Minneapolis, MN • On-site

$93K - $131K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago

Tactile Medical rating

8.6

Company rating: 8.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

Job description

At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses.
At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses. The Senior Quality Engineer provides quality engineering leadership for manufacturing and post-market activities supporting commercial medical devices. This role partners closely with Operations, Engineering, and Supply Chain to ensure regulatory compliance, effective risk management, and sustained product and process performance throughout the product lifecycle. Responsibilities focus on non-design quality activities, including change management, nonconformance, CAPA, complaint investigations, and continuous improvement within a regulated environment.
Responsibilities:
  • Provide quality engineering leadership and support for manufacturing, assembly, testing, packaging, and labeling operations, ensuring product quality and patient/user safety
  • Ensure ongoing compliance with FDA QSR (21 CFR 820), ISO 13485, and applicable regulatory and quality system requirements
  • Serve as the Quality representative on operations and sustaining teams, partnering cross-functionally to balance compliance, risk, and business needs
  • Lead document change requests and impact assessments to ensure changes maintain product safety, performance, and regulatory compliance
  • Lead and support nonconformance investigations, root cause analysis, disposition decisions, and CAPA activities through effective closure and verification of effectiveness
  • Apply structured problem-solving and statistical methods (e.g., 5 Whys, Fishbone, fault tree analysis, SPC) to drive data-based decisions and continuous improvement
  • Own and maintain risk management and DMR documentation for commercial products, including periodic review of complaints, nonconformance trends, and post-market signals
  • Review and approve process and test method validations, manage quality metrics, and oversee incoming material quality and acceptance activities
  • Other duties as assigned

Qualifications
Required:
  • 5+ years of experience as a Quality Engineer within the medical device industry
  • Bachelor level degree in Engineering (Mechanical, Material Science or Biomedical) or related Science

Preferred:
  • Certified Quality Engineer (CQE)
  • Certified Quality Auditor (CQA)
  • Six Sigma Belt

Knowledge & Skills
  • Strong working knowledge of 21 CFR 820, ISO 13485, ISO 14971
  • Demonstrated skills in statistical analysis
  • Strong analytical and problem-solving skills
  • Ability to work in a fast paced, dynamic and growth environment
  • Excellent interpersonal skills: ability to articulate verbally and written, review, analyze, summarize, and interpret data; draw conclusions and make appropriate recommendations and decisions; write reports; and lead or conduct teams and meetings
  • Proven ability to work with minimal direction, as well as be resourceful and independent in solving problems and multi-task effectively
  • Strong attention to detail
  • Ability to educate cross-functional peers, stakeholders, suppliers and management on quality requirements
  • Experienced with participation in audits

Our total compensation package includes medical, dental and vision benefits, retirement benefits, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness benefits and discounts. Benefits may be subject to generally applicable eligibility, waiting period, contributions, and other requirements and conditions.
Below is the starting salary or hourly range for this position, although offers may differ based on the candidate's location, job-specific knowledge, skills and experience.
US Pay Range
$93,600-$131,040 USD
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