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Risk Management Quality Engineer Jobs (NOW HIRING)

Quality Engineer (MN)

Moundsview, MN · On-site

$80K - $120K/yr

Support risk management activities in accordance with ISO 14971 and ICH guidelines. * Participate ... quality engineering experience in pharmaceutical and/or medical device manufacturing. Required ...

Sr. Quality Engineer- NPI

Tallassee, AL · On-site

$74K - $101K/yr

The Senior Quality Engineer NPI (New Product Introduction) will play a critical role in ensuring ... Risk Management: Conduct risk assessments and implement mitigation strategies to address potential ...

Senior Quality Engineer I

Aliso Viejo, CA · On-site

$105K - $120K/yr

The Senior Quality Engineer I will support all RxSight products and will be expected to apply knowledge of process engineering, risk management, and quality engineering techniques to innovate and ...

Senior Quality Engineer I

Aliso Viejo, CA · On-site

$105K - $120K/yr

The Senior Quality Engineer I will support all RxSight products and will be expected to apply knowledge of process engineering, risk management, and quality engineering techniques to innovate and ...

Quality Engineer

Mansfield, MA · On-site

$76K - $98K/yr

Quality Engineer Location: Mansfield, MA Duration: 6+ months (possibility of extension) JOB ROLES ... Principal Risk Management Specialist This position will lead risk management related activities for ...

Principal Quality Engineer

Ontario, CA · On-site

$120K - $150K/yr

The Principal Quality Engineer will serve as a subject matter expert in regulatory compliance (e.g., ISO 13485, FDA QSR), validation strategy, and supplier quality, ensuring robust risk management ...

The Design Quality Engineer II applies Design Controls, Risk Management, and Change Control processes to support evaluation, implementation, and release of product improvements across the ACM product ...

Staff NPD Quality Engineer

Raynham, MA · On-site

$74K - $96K/yr

Risk Management, Design Verification and Validation Strategies, and Design Transfer to ... Serve as lead quality engineer on cross functional new product development projects. * Leads design ...

R+D Quality Engineer III

Versailles, OH

$66K - $86K/yr

Leads all risk management processes and creates risk management documentation for (NPD) projects ... Certified Quality Engineer (CQE), Six Sigma Blackbelt (DMAIC, DMADV), and Certified Reliability ...

Staff NPD Quality Engineer

Raynham, MA

$74K - $96K/yr

Risk Management, Design Verification and Validation Strategies, and Design Transfer to ... Serve as lead quality engineer on cross functional new product development projects. * Leads design ...

The Design Quality Engineer II applies Design Controls, Risk Management, and Change Control processes to support evaluation, implementation, and release of product improvements across the ACM product ...

Sr. Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Job Title: Sr. Quality Engineer Location: Austin, Texas Job Title/High Level Position Summary ... Lead risk management activities, including development and review of DFMEAs, PFMEAs, and risk ...

Quality Engineer

San Antonio, TX · On-site

$60K - $78K/yr

The Quality Engineer serves as a technical resource for root cause analysis, risk management, statistical analysis, process improvement, and quality system effectiveness. What You'll do: * Lead root ...

Showing results 41-60

Risk Management Quality Engineer information

See salary details

$45K

$84K

$119K

How much do risk management quality engineer jobs pay per year?

As of Aug 11, 2026, the average yearly pay for risk management quality engineer in the United States is $84,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $93,000.00 per year, depending on experience, location, and employer.

What is the difference between Risk Management Quality Engineer vs Quality Engineer?

AspectRisk Management Quality EngineerQuality Engineer
CertificationsISO 9001, Six Sigma, Risk Management certificationsISO 9001, Six Sigma, Quality Management certifications
Work EnvironmentManufacturing, aerospace, automotive, industries with risk assessment focusManufacturing, software, healthcare, quality assurance roles
Primary FocusIdentifying and mitigating risks to ensure product safety and complianceEnsuring product quality, process improvements, defect reduction

The Risk Management Quality Engineer focuses on identifying and mitigating risks to ensure safety and compliance, often working in industries like aerospace and automotive. In contrast, a Quality Engineer concentrates on improving product quality and reducing defects across various sectors. While both roles require similar certifications and work environments, their core responsibilities differ in scope and focus.

More about Risk Management Quality Engineer jobs
What cities are hiring for Risk Management Quality Engineer jobs? Cities with the most Risk Management Quality Engineer job openings:
What states have the most Risk Management Quality Engineer jobs? States with the most job openings for Risk Management Quality Engineer jobs include:
What job categories do people searching Risk Management Quality Engineer jobs look for? The top searched job categories for Risk Management Quality Engineer jobs are:
Infographic showing various Risk Management Quality Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $84,039 per year, or $40.4 per hour.

Quality Engineer (MN)

Excel Engineering Inc

Moundsview, MN • On-site

$80K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 23 hours ago


Job description

Quality Engineer (MN)
Full-time
Mounds View, MN
Description
Excel Engineering is seeking a team-oriented, highly motivated Quality Engineer for our Mounds View, Minnesota office.
As a Quality Engineer, you will provide hands-on quality engineering and compliance support to pharmaceutical and medical device manufacturing clients. This role partners with client quality, manufacturing, validation, and regulatory teams to ensure compliance with FDA, EU, and international regulations while driving continuous improvement, risk reduction, and operational excellence across the product lifecycle.
You may support multiple client sites and projects, contributing expertise in quality systems, GMP compliance, risk management, validation, audits, and remediation activities.
Primary Responsibilities
  • Support development, implementation, and maintenance of Quality Management Systems (QMS) compliant with:
  • FDA 21 CFR Parts 11, 210/211, 820 (QMSR)
  • ISO 13485, ISO 9001 (as applicable)
  • EU MDR/IVDR and EU GMP requirements
  • Author, revise, review, and approve quality documentation, including SOPs, work instructions, and quality records.
  • Ensure alignment with data integrity and documentation best practices (ALCOA+).
  • Provide quality oversight for pharmaceutical and medical device manufacturing operations.
  • Support deviations, nonconformances, investigations, and root cause analyses.
  • Lead or support CAPA development, execution, and effectiveness checks.
  • Partner with manufacturing, engineering, and automation teams to assess the quality impact of process changes.
  • Support risk management activities in accordance with ISO 14971 and ICH guidelines.
  • Participate in or lead:
  • Process validation and revalidation
  • Equipment and system qualification (IQ/OQ/PQ)
  • Computer System Validation (CSV) / Computer Software Assurance (CSA)
  • Review and approve validation protocols and reports from a quality perspective.
  • Support supplier qualification, audits, and quality agreements.
  • Review and approve change controls, ensuring regulatory and quality impact assessments are complete.
  • Assist with technology transfers and new product introductions (NPI).

Requirements
Education and Experience
  • Bachelor's degree in Engineering, Life Sciences, or a related technical field.
  • 6+ years of quality engineering experience in pharmaceutical and/or medical device manufacturing.

Required Qualifications
Strong working knowledge of:
* FDA and international GMP regulations
* ISO 13485 and/or FDA QMSR
*CAPA, deviations, change control, and risk management
  • Experience supporting audits and regulatory inspections.
  • Excellent technical writing and documentation skills.
  • Ability to write and speak in the English language.
  • Willingness to travel up to 10% of the time.

Preferred Qualifications
Consulting or multi-site support experience.
Experience with automation, manufacturing systems, or computerized systems.
Knowledge of CSA, data integrity, and validation best practices.
ASQ certification (CQE, CQA) or equivalent.
Experience supporting both pharma and medical device client.
Engineer in Training (EIT) registration or ability to obtain registration.
We offer...
Growth & Development: Ongoing continuing education, hands-on training, and opportunities to expand your skills.
Career Advancement Support: Assistance in earning professional certifications and pursuing further education.
Retirement Benefits: 401(k) plan with employer matching.
Comprehensive Health Coverage: Medical, dental, vision, and life insurance options.
Wellness Focus: Access to programs designed to support your overall well-being.
Work-Life Balance: Paid time off and flexible work environment
Flexibility & Trust: A flexible schedule and work environment built around mutual trust and accountability.
Share the Talent, Share the Rewards: We value great people recommending great people, which is why our employee referral program is designed to reward you continuously
We offer a competitive salary and great benefits. At Excel Engineering, we're proud of our positive, high-performing culture where teamwork, continuous improvement, and a service-oriented mindset help us do our best work every day. If you enjoy a fast-paced and rewarding environment, you'll love being part of our team!
Excel Engineering, Inc. is proud to be an Equal Opportunity Employer. We welcome and consider all qualified applicants without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, disability, age, veteran status, marital status, or any other protected characteristic.
We value diverse perspectives and believe they strengthen our work, our teams, and the solutions we deliver to clients. We encourage candidates from backgrounds traditionally underrepresented in engineering to apply. If you need accommodations during the application or interview process, please contact our Human Resources team at ExcelHR@exceleng.net.
Salary Description
$80,000 - $120,000 a year