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Senior Design Quality Engineer Jobs in Missouri (NOW HIRING)

Develop, establish, and maintain design controls, quality engineering methodologies, systems, and practices * Interact with R&D, Program Management, Manufacturing Operations and Engineering, Quality ...

$149K - $210K/yr

Our partner is looking for a Senior Design Engineer - MetaMask based in Netherlands. This is an ... Advocate for high-quality product craft and identify opportunities to improve usability ...

SENIOR DESIGN ENGINEER This position is based out of our Fenton, MO office or fully remote. About ... Surveys job sites as needed for the scope of work and quality to determine compliance with the ...

SENIOR DESIGN ENGINEER This position is based out of our Fenton, MO office or fully remote. About ... Surveys job sites as needed for the scope of work and quality to determine compliance with the ...

Description SENIOR DESIGN ENGINEER This position is based out of our Fenton, MO office or fully ... Surveys job sites as needed for the scope of work and quality to determine compliance with the ...

Senior Design Engineer

California, MO · On-site

$100 - $150/hr

Works with Sr. Designer on circuit synthesis from the transistor/resistor level up to the system level, simulation, layout supervision. * Assists ATE development with Design-For-Test methods.

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Senior Design Quality Engineer information

See Missouri salary details

$56.7K

$98.8K

$137.4K

How much do senior design quality engineer jobs pay per year?

As of Aug 27, 2026, the average yearly pay for senior design quality engineer in Missouri is $98,765.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $112,600.00 per year, depending on experience, location, and employer.

What is a senior design quality engineer?

Senior Design Quality Engineers are experienced professionals responsible for ensuring that products are designed and developed in compliance with regulatory standards and quality requirements. They work closely with design, engineering, and manufacturing teams to identify potential risks, implement quality control processes, and verify that products meet both customer expectations and industry regulations. Their role often includes reviewing design documentation, managing design validation and verification activities, and leading efforts to continuously improve product quality. Senior Design Quality Engineers typically have a strong background in engineering, quality assurance, and regulatory compliance.

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

To thrive as a Senior Design Quality Engineer, you need expertise in quality engineering principles, risk management, regulatory standards (such as ISO 13485 or FDA 21 CFR Part 820), and typically a degree in engineering or a related field. Experience with quality management systems (QMS), statistical analysis tools, and certifications like Six Sigma or ASQ CQE are highly valued. Strong problem-solving abilities, attention to detail, and effective communication skills help drive cross-functional collaboration and ensure product compliance. These skills are essential for maintaining high product quality, meeting regulatory requirements, and supporting successful product development in regulated industries.

What types of cross-functional teams does a senior design quality engineer typically collaborate with, and how does this impact daily responsibilities?

Senior Design Quality Engineers frequently work with multidisciplinary teams including R&D, manufacturing, regulatory affairs, and supply chain. This collaboration ensures that product designs meet both quality standards and regulatory requirements throughout the development lifecycle. Daily responsibilities often involve participating in design reviews, risk assessments, and process validations, as well as communicating quality feedback and facilitating corrective actions. Being proactive and adaptable is essential, as priorities can shift quickly based on project needs and compliance issues.

What is the difference between Senior Design Quality Engineer vs Design Quality Engineer?

AspectSenior Design Quality EngineerDesign Quality Engineer
CredentialsBachelor's degree in engineering, quality certifications (e.g., CQE)Bachelor's degree in engineering or related field, quality certifications optional
Work EnvironmentInvolved in complex product development, cross-functional teamsSupports design processes, quality assurance in product development
Industry UsageCommon in manufacturing, automotive, aerospaceUsed across similar industries, often as entry to mid-level role
Search & ComparisonOften compared with Design Quality Engineer for experience and responsibilities

The main difference between a Senior Design Quality Engineer and a Design Quality Engineer lies in experience, scope, and responsibilities. Senior roles typically involve more complex projects, leadership, and strategic input, while Design Quality Engineers focus on supporting design quality processes. Both roles require similar credentials and are used across manufacturing and engineering industries, but the senior position indicates a higher level of expertise and accountability.

What are popular job titles related to Senior Design Quality Engineer jobs in Missouri?

For Senior Design Quality Engineer jobs in Missouri, the most frequently searched job titles are:

What job categories do people searching Senior Design Quality Engineer jobs in Missouri look for?

The top searched job categories for Senior Design Quality Engineer jobs in Missouri are:

What cities in Missouri are hiring for Senior Design Quality Engineer jobs?

Cities in Missouri with the most Senior Design Quality Engineer job openings:

Infographic showing various Senior Design Quality Engineer job openings in Missouri as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, 3% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $98,765 per year, or $47.5 per hour.

Staff Design Quality Engineer

Jobtailor

California, MO • On-site

$90 - $130/hr

Other

Posted 9 days ago


Job description

  • Support new hardware and software medical device product development
  • Support sustaining product line activities and hardware customer quality activities
  • Serve as Design Quality Project Lead for cross-functional teams
  • Advise teams on design controls, cybersecurity, AI/ML-enabled medical device considerations, risk management, human factors and usability engineering, verification and validation, and mitigations
  • Communicate quality metrics to promote continual improvement and compliance with QMS procedures, laws, regulations, standards, and guidance
  • Develop, establish, and maintain design controls, quality engineering methodologies, systems, and practices
  • Interact with R&D, Program Management, Manufacturing Operations and Engineering, Quality Management Systems, Regulatory, Clinical, Marketing, customer-facing teams, and customers as appropriate
  • Support regulatory, notified body, FDA, internal, customer, supplier, and contract manufacturer audits
  • Support customer issue resolution and cross-functional product quality activities
Requirements
  • Bachelor's degree in engineering, life sciences, biomedical engineering, mechanical engineering, electrical engineering, software engineering, quality, or a related technical field
  • Experience in design quality engineering, quality engineering, product development, systems engineering, software quality, AI/ML quality, hardware quality, or a related role in a regulated industry
  • Experience with AI/ML-enabled medical devices, software-enabled medical devices, SaMD, clinical decision support tools, diagnostic algorithms, imaging algorithms, predictive models, or other regulated AI/ML product development
  • Strong working knowledge of medical device design controls
  • Experience owning or maintaining medical device risk management files in accordance with ISO 14971
  • Strong proficiency with 8D problem-solving tools and methods
  • Ability to understand technical details related to customer complaints, quality issues, hardware failures, manufacturing escapes, and product risk
  • Knowledge of AI/ML development and validation considerations
  • Knowledge of human factors and usability engineering principles, including IEC 62366
  • Experience with SMT, PCBA, semiconductor manufacturing, electronics manufacturing, supplier manufacturing controls, or contract manufacturer quality
  • Familiarity with cybersecurity expectations for connected medical devices
  • Familiarity with IEC 60601 electrical safety testing requirements
  • Familiarity with FDA 21 CFR Part 820 and ISO 13485
  • Strong written and oral communication skills
  • Strong cross-functional leadership and coordination skills
  • Ability to design, iterate, and optimize complex prompts for AI models
  • Candidates must be authorized to work in the United States; no immigration sponsorship is provided
  • Preferred/ideal qualifications include Class II or Class III medical device experience, additional standards knowledge, eQMS/PLM experience, CAPA and complaint investigation experience, and ASQ, Six Sigma, or RAC certification
Core Competencies

Demonstrates expertise in design quality engineering and risk management for medical devices, with a strong focus on AI/ML-enabled products and compliance with regulatory standards. Proficient in cross-functional collaboration and quality improvement methodologies to ensure product excellence.

Highest-signal resume keywords
  • Design Quality Engineering
  • Medical Device Risk Management
  • AI/ML-Enabled Medical Devices
  • Quality Management Systems Compliance
  • Cross-Functional Leadership
ATS Optimization Keywords Hard Skills
  • Design Controls
  • Quality Engineering Methodologies
  • 8D Problem-Solving Tools
  • Human Factors Engineering
  • Usability Engineering
  • ISO 14971 Compliance
  • IEC 62366 Knowledge
  • FDA 21 CFR Part 820 Familiarity
  • ISO 13485 Familiarity
  • AI Model Optimization
Soft Skills
  • Strong Written Communication
  • Strong Oral Communication
  • Cross-Functional Coordination
Certifications & Qualifications
  • ASQ Certification
  • Six Sigma Certification
  • RAC Certification
Industry Keywords
  • Medical Device Development
  • Regulated Industry Experience
  • Clinical Decision Support Tools
  • Diagnostic Algorithms
  • Predictive Models
  • Electronics Manufacturing
  • Supplier Manufacturing Controls
  • Connected Medical Devices
  • Electrical Safety Testing
  • Contract Manufacturer Quality
Tools & Technologies
  • EQMS
  • PLM
  • CAPA
  • Complaint Investigation Tools
  • Cybersecurity Standards
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