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Risk Management Quality Engineer Jobs in Spring, TX

Halma plc

Quality Engineer II

Houston, TX · On-site

$68K - $88K/yr

Role Overview The Quality Engineer II is a hands-on quality professional who supports manufacturing ... Contribute to risk management activities in accordance with ISO 14971 to help identify, assess, and ...

Abbott

Quality Engineer

Houston, TX

$68K - $88K/yr

Job Title Quality Engineer Working at Abbott At Abbott, you can do work that matters, grow, and ... Lead and maintain risk management activities in accordance with ISO 14971, including hazard ...

Abbott

Quality Engineer

Houston, TX · On-site

$68K - $88K/yr

... risk management activities in accordance with ISO 14971, including hazard analysis, risk assessment, and risk control verification • Work with Microbiology and Manufacturing to ensure compliance ...

Abbott

Quality Engineer

Houston, TX

$68K - $88K/yr

Job Title Quality Engineer Working at Abbott At Abbott, you can do work that matters, grow, and ... Lead and maintain risk management activities in accordance with ISO 14971, including hazard ...

KBR

Risk Management Specialist

Houston, TX

Risk Management Specialist We are KBR At KBR, we partner with clients to provide purposeful and comprehensive science, technology and engineering solutions to governments as well as the top tier ...

KBR, Inc.

Risk Management Specialist

Houston, TX · On-site

Risk Management Specialist We are KBR At KBR, we partner with clients to provide purposeful and comprehensive science, technology and engineering solutions to governments as well as the top tier ...

NDT Global

Quality Engineer

Houston, TX · On-site

$68K - $88K/yr

... Quality Engineer is to provide expertise and advice concerning operational business process ... and risk management. The job holder independently engages with others, is technically and ...

APT Research, Inc.

Quality Engineer

Houston, TX · On-site

$68K - $88K/yr

Provides direct input to program Quality management with respect to contractor performance ... Work attire must be appropriate for the position and must not impose a safety risk / hazard to the ...

Hultec Group

Quality Engineer

Spring, TX · On-site

$64K - $82K/yr

Plant Manager | Direct Reports: 7 About the Role Hultec is looking for a hands-on Quality Engineer to own quality assurance and control within our rubber seal manufacturing operation in Houston. You ...

Hultec Group

Quality Engineer

Spring, TX

$64K - $82K/yr

Plant Manager | Direct Reports: 7 About the Role Hultec is looking for a hands-on Quality Engineer to own quality assurance and control within our rubber seal manufacturing operation in Houston. You ...

WFI International

Quality Engineer

Houston, TX · On-site

$67K - $87K/yr

The Quality Engineer is responsible for assisting the Quality Assurance Supervisor in establishing, implementing, and continually improving the performance of the Quality Management System. Primary ...

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All JobsRisk Management Quality Engineer JobsRisk Management Quality Engineer Jobs in Spring, TX

Risk Management Quality Engineer information

See Spring, TX salary details

$40K

$74.8K

$105.9K

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

As of Jul 26, 2026, the average yearly pay for risk management quality engineer in Spring, TX is $74,786.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,100.00 and $82,800.00 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.

What job categories do people searching Risk Management Quality Engineer jobs in Spring, TX look for? The top searched job categories for Risk Management Quality Engineer jobs in Spring, TX are:
What cities near Spring, TX are hiring for Risk Management Quality Engineer jobs? Cities near Spring, TX with the most Risk Management Quality Engineer job openings:
Risk Management Quality Engineer jobs near you
Infographic showing various Risk Management Quality Engineer job openings in Spring, TX as of July 2026, with employment types broken down into 1% Locum Tenens, 92% Full Time, 4% Part Time, and 3% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $74,786 per year, or $36 per hour.

Quality Engineer II

Halma plc

Houston, TX • On-site

$68K - $88K/yr

Full-time

Posted 19 days ago

Job description

Help grow a safer, cleaner, healthier future for everyone, every day.
Company description:
TeDan Surgical Innovations (TSI) designs and manufactures specialty surgical products for use in orthopedic, neuro, thoracic and spine surgeries. TSI was founded in 2006 with the goal to innovate and address evolving retraction techniques in spine surgery. We have successfully addressed the need for minimally invasive, posterior, lateral and anterior surgical approaches to the spine, and have introduced access instrumentation for neurological, orthopedic and cardiothoracic procedures. We commit to providing innovative, high-quality surgical access systems designed to optimize exposure and improve the surgeon experience.
Role Overview
The Quality Engineer II is a hands-on quality professional who supports manufacturing and post-manufacturing activities to ensure safe, effective, and compliant medical devices. This role is ideal for an engineer who enjoys solving technical problems, leading investigations, improving processes, and working cross-functionally to make measurable quality improvements. The QE II will play a visible role in driving product and process quality through failure analysis, validation support, risk-based decision-making, and data-driven continuous improvement in a fast-paced regulated environment.
Core Competencies
1. Quality & Regulatory Expertise
  • Apply working knowledge of ISO 13485, FDA QMSR, GMP/GDP, and Design Controls to support compliance across product and process activities.
  • Manage complaint investigations, CAPAs, nonconformances, and supplier corrective actions using structured root cause and risk-based methodologies.
  • Contribute to risk management activities in accordance with ISO 14971 to help identify, assess, and mitigate product and process risks.

2. Analytical & Problem-Solving Skills
  • Analyze manufacturing, quality, and post-production data to identify trends, performance gaps, and improvement opportunities.
  • Apply statistical and analytical tools such as SPC, control charts, Pareto analysis, sampling plans, and process capability analysis to monitor and improve process performance.
  • Lead or support root cause investigations and failure analysis for nonconformances, complaints, and product performance issues, and help implement effective corrective actions.
  • Develop and maintain reports, dashboards, and quality metrics that improve visibility into performance and support better decision-making.
  • Translate data into clear, actionable insights for Quality leadership and cross-functional stakeholders.

3. Process & Product Excellence
  • Review engineering, process, and supplier changes for quality impact and support validation and implementation activities.
  • Support process validation activities, including protocol development, execution, data analysis, and reporting, and perform measurement system analysis for inspection and test methods.
  • Partner with Engineering and Manufacturing to improve process capability, reduce variation, and strengthen process controls.

4. Supplier & Cross-Functional Collaboration
  • Support supplier quality activities through investigations, corrective actions, performance monitoring, and collaboration with internal and external partners.
  • Partner with Quality, Manufacturing, and Engineering to maintain process controls, inspection methods, measurement systems, and validation requirements.
  • Communicate technical findings clearly and work effectively across functions to resolve issues and advance improvement initiatives.

5. Technical Communication & Documentation
  • Prepare clear, concise technical documentation, including protocols, reports, procedures, and quality metrics.
  • Ensure traceability of complaints, CAPAs, nonconformances, supplier events, and risk management records.

6. Project & Time Management
  • Manage multiple assignments and projects effectively while balancing timelines, quality priorities, and regulatory requirements.
  • Demonstrate ownership, sound judgment, and follow-through in completing quality engineering activities with appropriate guidance.

Qualifications & Experience
  • 3-5 years of Quality Engineering experience in the medical device industry, with demonstrated support for manufacturing quality and post-market activities.
  • Experience with complaint handling, CAPA, nonconformance investigations, supplier quality, and risk-based problem-solving.
  • Strong understanding of manufacturing support, failure analysis, process validation, inspection methods, measurement system analysis, and process capability.
  • Proficiency in quality and statistical tools (Excel required; Minitab preferred); experience with dashboards or data visualization tools is a plus.
  • Ability to write clear technical documentation, including protocols, reports, and procedures.
  • Working knowledge of Design Controls, risk management, and regulated manufacturing environments.
  • Strong organizational, communication, and collaboration skills with the ability to work effectively across functions.

Education
Bachelor of Science in Biomedical Engineering, Mechanical Engineering, or a related discipline.
Additional Requirements
  • Occasional travel (5-10%).

Reasonable Accommodations
Tedan Surgical Innovations is an Equal Opportunity Employer. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions of this position.
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