ZipRecruiter

Log In

1

Senior Design Quality Engineer Jobs in California

Medtronic

Senior Design Quality Engineer - Irvine

Irvine, CA · On-site

$95K - $128K/yr

Medtronic Neurovascular As a Neurovascular Sr. Design Quality Engineer, you will have responsibility for directly contributing to the design of life-saving Neurovascular devices. You will integrate ...

Medtronic

Senior Design Quality Engineer - Irvine

Irvine, CA · On-site

$95K - $128K/yr

Medtronic Neurovascular As a Neurovascular Sr. Design Quality Engineer, you will have responsibility for directly contributing to the design of life-saving Neurovascular devices. You will integrate ...

Philips

Senior Design Quality Engineer

San Diego, CA · On-site

$103K - $145K/yr

Job TitleSenior Design Quality Engineer In this role you Will be part of a team that is excited by the unique professional challenges that our Quality Transformation presents, has strong technical ...

Enovis

Design Quality Engineer

Carlsbad, CA · On-site

Design Quality Engineer Reports To: Director, QA | QC Location: Carlsbad, CA (Hybrid 3 days onsite 2 days remote) Business Unit Description: Bracing & Supports Job Title/High-Level Position Summary:

Enovis

Design Quality Engineer

Carlsbad, CA · Hybrid

Design Quality Engineer Reports To: Director, QA | QC Location: Carlsbad, CA (Hybrid 3 days onsite 2 days remote) Business Unit Description: Bracing & Supports Job Title/High-Level Position Summary:

next page

Showing results 1-20

All JobsDesign Quality Engineer JobsSenior Design Quality Engineer JobsSenior Design Quality Engineer Jobs in California

Senior Design Quality Engineer information

See California salary details

$59.7K

$103.9K

$144.6K

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

As of Aug 10, 2026, the average yearly pay for senior design quality engineer in California is $103,914.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,300.00 and $118,400.00 per year, depending on experience, location, and employer.

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 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 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 popular job titles related to Senior Design Quality Engineer jobs in California? For Senior Design Quality Engineer jobs in California, the most frequently searched job titles are:
What job categories do people searching Senior Design Quality Engineer jobs in California look for? The top searched job categories for Senior Design Quality Engineer jobs in California are:
What cities in California are hiring for Senior Design Quality Engineer jobs? Cities in California with the most Senior Design Quality Engineer job openings:
Senior Design Quality Engineer jobs near you
Infographic showing various Senior Design Quality Engineer job openings in California as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, and 5% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $103,914 per year, or $50 per hour.

Senior Design Quality Engineer

Circadia Health

El Segundo, CA

$120K - $160K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 3 days ago

New

Job description

About Circadia Health

Circadia Health is a growth-stage healthcare AI company on a mission to prevent avoidable hospitalizations and transform senior-care operations. Our Circadia Intelligence Platform combines:

  • Contactless sensing that monitors respiration and motion with medical-grade accuracy

  • Native predictive models that detect 85% of preventable adverse events several days in advance

  • Enterprise integrations that operationalize predictions directly inside EHR, care-coordination, billing, and compliance workflows

Today, our technology touches 40,000+ post-acute patients daily across skilled-nursing, home-health, and home-care networks. We are backed by leading healthcare and AI investors and headquartered in El Segundo, CA.


About the Role
 
Circadia Health is looking for a Senior Design Quality Engineer to establish and lead our quality engineering processes from the ground up. In this role, you will build, implement, and scale our Quality Management System (QMS) in alignment with ISO 13485 and FDA QMSR. You will take full ownership of design controls across the product lifecycle, establish robust complaint handling and CAPA workflows, and lead post-market surveillance activities. This role requires a hands-on, startup-savvy engineer who thrives in fast-paced environments.
Responsibilities

QMS Building & Implementation

  • QMS Architecture: Lead the design, implementation, and roll-out of an ISO 13485-compliant Quality Management System.
  • Process Creation: Establish and standardize core quality procedures, including document control, change management, CAPA, nonconformance, and audit readiness.
  • Compliance Standards: Ensure organizational alignment with ISO 13485 and prepare the company for FDA Inspections/Notified Body audits.

Post-Market Surveillance, Complaints & CAPA

  • Complaint Handling: Establish and execute end-to-end complaint handling processes, root-cause investigations, and medical device reporting (MDR) evaluations.
  • CAPA Leadership: Drive the CAPA and Nonconformance (NC) processes, performing thorough root-cause analyses and implementing corrective/preventive actions.
  • Post-Market Surveillance (PMS): Design and maintain the Post-Market Surveillance (PMS) system, generating PMS reports, clinical evaluation updates, and data trending summaries.

Design Controls & Product Development Support

  • Support execution and maintenance of design control activities across the product lifecycle.
  • Maintain Design History File (DHF) documentation for Circadia products.
  • Assist with preparation and review of:
    • Design inputs and outputs
    • Risk management documentation
    • Verification and validation documentation
    • Design review records
  • Track design control deliverables and coordinate documentation across teams.

Regulatory Submission Support

  • Assist in preparation of FDA submission documentation (e.g., 510(k)).
  • Support compilation and organization of testing documentation and reports.
  • Track submission deliverables and supporting evidence.

Cross-Functional Collaboration

  • Coordinate with R&D, Engineering, Customer Success, Ops and Clinical teams to collect documentation and evidence.
  • Support human factors validation and cybersecurity testing coordination.
  • Assist with third-party testing documentation collection.
Qualifications

  • Education: Bachelor's degree in Biomedical Engineering, Software Engineering,  Mechanical Engineering, or a related technical field.

  • Senior-Level Expertise: 5+ years of design quality engineering experience within the medical device or digital health industry.

  • Startup Track Record: Proven experience in a fast-paced environment where you built processes from scratch rather than executing existing ones, and are comfortable owning ambiguous, evolving work.

  • QMS Implementation: Direct experience building and implementing an ISO 13485 QMS 

  • Subject Matter Ownership: Deep, hands-on proficiency in Design Controls, Risk Management (ISO 14971), CAPA management, Complaint Handling, and Post-Market Surveillance (PMS).

Nice to Have

  • QMSR Familiarity: Direct experience or working knowledge of the FDA's updated Quality Management System Regulation (QMSR).

  • Digital Health / Hardware + Software: Experience with Software as a Medical Device (SaMD) and/or software in a medical device (SiMD), firmware/hardware integration, human factors validation, and cybersecurity.

  • Regulatory Submissions: Direct involvement in successful FDA submissions or European CE mark technical files.

  • Certifications: ASQ Certified Quality Engineer (CQE), Certified Software Quality Engineer (CSQE), or Six Sigma Green/Black Belt.

$120,000 - $160,000 a year

As a full-time [Title], you will be employed by Circadia Health, Inc. The anticipated annual base salary range for this full-time position is $[range]. The base range is determined by role and level, and placement within the range will depend on a number of job-related factors, including but not limited to your skills, qualifications, experience, and location.

Annual salary is only one part of an employee's total compensation package at Circadia Health. We also offer:

  • Meaningful employee stock options
  • 100% company-paid medical, dental, and vision coverage
  • 401(k)
  • Competitive time off with pay policies including vacation, sick days, and company holidays
  • Impact: your work will influence care decisions for tens of thousands of seniors every day.
  • Culture: hard-working, mission-driven, and collaborative - with weekly and monthly social events like yoga, beach bonfires, and Wednesday/Friday team lunches.

As a full-time Senior Design Quality Engineer, you will be employed by Circadia Health, Inc. The anticipated annual base salary range for this full-time position is $120,000 - $160,000. The base range is determined by role and level, and placement within the range will depend on a number of job-related factors, including but not limited to your skills, qualifications, experience, and location.

Annual salary is only one part of an employee's total compensation package at Circadia Health. We also offer:

  • Meaningful employee stock options
  • 100% company-paid medical, dental, and vision coverage
  • 401(k)
  • Competitive time off with pay policies including vacation, sick days, and company holidays
  • Impact: your work will influence care decisions for tens of thousands of seniors every day.
  • Culture: hard-working, mission-driven, and collaborative - with weekly and monthly social events like yoga, beach bonfires, and Wednesday/Friday team lunches.
Circadia Health is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, veteran status, or any other status protected by law.
 

Circadia Health is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, veteran status, or any other status protected by law.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
apply for this job

Apply