Top 38 Director quality engineering Jobs in Houston, Tx

Director of Quality and Regulatory Affairs
US Med-Equip —Houston, TX
- Full-time
- 7 years
- Engineering
- Office
- Health savings account
- Health insurance
Quick Apply
10d
Director of Quality Modular
GRAYWOLF INTEGRATED CONSTRUCTION COMPANY —Humble, TX
- Engineering
- Master's degree
- Analysis skills
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Director of Quality
Superior Energy Services Wellbore Technologies Division —Houston, TX
- 5 years
- Engineering
- Office
Global Quality Director
Wellbore Integrity Solutions LLC —Houston, TX
- Management
- Engineering
- Master's degree
- Free parking
- Paid holidays
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Director, General Engineering
Alcon —Houston, TX
- Full-time
- High school
- English
- Doctor of Philosophy
- Health insurance
- Paid time off
Director I, Process/Specialty Engineering (Power)
Fluor Enterprises, Inc-FD —Houston, TX
- $160,000 - $302,000 a year
- 11+ years
- US work authorization
- Experience equivalent to degree accepted
- AD&D insurance
- Disability insurance
Director of Engineering
BSA Lifestructures Inc —Houston, TX
- Full-time
- Hybrid work
- Management
- Engineering
- 11+ years
- Free parking
- Health insurance
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Director of Gulf Coast Engineering
ZAP Engineering —Houston, TX
- $156,000 - $234,000 a year
- Weekends as needed
- Clean driving record
- Construction site
- Bachelor of Science
- AD&D insurance
- Disability insurance
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Director I, Process Engineering (Nuclear)
Fluor Enterprises, Inc-FD —Houston, TX
- $166,500 - $309,500 a year
- 11+ years
- US work authorization
- Experience equivalent to degree accepted
- AD&D insurance
- Disability insurance
Director of Efficiency & Optimization
Commercial Services —Houston, TX
- Full-time
- Analysis skills
- Bachelor's degree
- Mentoring
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Director of Service Quality
ON.energy —Houston, TX
- Hybrid work
- Up to 50% travel
- Engineering
- Office
- Paid holidays
- Health insurance
7d
Quality Assurance Director
Management Controls Inc —Houston, TX
- Computer Science
- 5 years
- Master's degree
- Paid time off
Nuclear Director I, Engineering Management
Fluor Enterprises, Inc-FD —Houston, TX
- $160,000 - $302,000 a year
- Engineering
- 11+ years
- Administrative experience
- AD&D insurance
- Disability insurance
Director of Engineering
The Falcon Group —Houston, TX
- $150,000 - $200,000 a year
- Overtime
- 7 years
- Writing skills
- Office
- AD&D insurance
- Paid holidays
Quick Apply
Nuclear Director I, Engineering Management
Fluor Corporation —Houston, TX
- $160,000 - $302,000 a year
- Engineering
- 11+ years
- Administrative experience
- AD&D insurance
- Disability insurance
Director of Engineering Delivery (Power Generation / Gas-to-Power)
Candid Intelligence —Houston, TX
- Full-time
- Hybrid work
- 11+ years
- Senior level
- Leadership
- Health insurance
- Dental insurance
Quick Apply
Deputy Director of Transportation Operations
Texas Department of Transportation —Houston, TX
- $126,000 - $165,000 a year
- Full-time
- Engineering
- Pass drug screening
- Office
- Wellness program
- Paid holidays
12d
Director – Environmental Remediation
J.S. Held LLC —Houston, TX
- $155,000 - $190,000 a year
- Full-time
- Remote
- System design
- Analysis skills
- Continuous improvement
- Commuter assistance
- Health insurance
Quick Apply
Director I, Nuclear Structural Engineering (Lead)
Fluor Enterprises, Inc-FD —Houston, TX
- $166,500 - $309,500 a year
- Word processing
- Computer literacy
- 11+ years
- AD&D insurance
- Disability insurance
Director of Engineering and Design
AUC Group LLC —Houston, TX
- Monday to Friday
- Hybrid work
- 5 years
- Writing skills
- Office
Quick Apply

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Director of Quality and Regulatory Affairs

US Med-Equip -
Houston, TX

Quick Apply

Job Details

Full-time
10 days ago

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Employee assistance program
Vision insurance
Life insurance
Referral program

Qualifications

Teamwork
Program management
Enterprise software
Master's degree
Organizational skills

Full Job Description

Director of Quality & Regulatory Affairs at “Top Workplace”

US Med-Equip LLC is seeking a strategic, tech-forward, and highly collaborative Director of Quality & Regulatory Affairs. Reporting directly to the COO, this pivotal leader will elevate our quality management framework from an internal standard to a market-defining competitive advantage.

Operating as a strategic contributor, you will be the chief architect of our transition from ISO 9001:2015 to ISO 13485 certification, establishing a gold-standard Quality Management System (QMS) optimized for a high-velocity, decentralized medical equipment rental and asset-management model. You will not just audit; you will partner with Regional Operations Directors to embed a culture of compliance, predictive risk mitigation, and safety across our nationwide footprint. Furthermore, you will leverage advanced technology to help our healthcare customers solve their own compliance, recall, and Joint Commission challenges.

A Day in the Life

Strategic QMS & ISO 13485 Establishment

· Build from the Ground Up: Evaluate, select, and spearhead the implementation of a brand-new, enterprise-grade digital QMS platform. Ensure seamless integration with US Med-Equip's proprietary logistics and tracking technologies.

· ISO 13485 Pivot: Design, document, and execute the transition from our current ISO 9001:2015 baseline to full ISO 13485 certification, tailoring clauses (traceability, cleanliness, servicing) to a non-manufacturing distribution/consignment environment.

· Customer-Facing Value: Transform compliance into a commercial advantage by developing tech-driven quality reports and insights that help hospital partners ace their own Joint Commission audits.

Decentralized Branch Operations & Safety

· Virtual Auditing & Tech Adoption: Pioneer remote virtual branch auditing protocols to maintain strict oversight of a vast, decentralized footprint of regional support centers and biomedical support pockets.

· Cross-Functional Influence: Work hand-in-hand with Regional Operations Directors to ensure tactical-level branch managers strictly execute quality, safety, and OSHA SOPs.

· Resiliency & Risk Management: Own the development and continuous improvement of risk-mitigation frameworks, including inclement weather, natural disaster preparation, and business continuity SOPs tailored by region.

Regulatory Compliance & Product Lifecycles

· Medical Device Reporting (MDR): Oversee rigorous medical device reporting processes, ensuring immaculate documentation and swift communication with regulatory bodies and manufacturing partners.

· Predictive Risk Modeling: Introduce advanced risk modeling to vet and evaluate new medical equipment and technologies prior to fleet introduction, safeguarding patient care and capital investment.

· Recall & Inquiry Response: Architect rapid-response workflow for manufacturer product recalls and complex customer quality inquiries, minimizing downtime and maximizing trust.

GOV Regulatory and Quality

· Regulatory:

· Federal Acquisition & Compliance

Familiarity with FAR (Federal Acquisition Regulation) and DFARS (Defense Federal Acquisition Regulation Supplement)
Understanding of government contract vehicle structures (GSA Schedule, IDIQs, BPAs, OTA, SBIRs)
Experience with SAM.gov registration, CAGE codes, and DUNS/UEI management
Knowledge of Buy American Act and Trade Agreements Act compliance

· Medical Device Regulatory

FDA 21 CFR Part 820 (Quality System Regulation / QSR) and the newer QMSR alignment with ISO 13485
FDA 510(k), PMA, and De Novo submission experience relevant to the equipment USME sells or services
UDI (Unique Device Identification) compliance and GUDID management
CLIA and Joint Commission standards as they apply to biomedical equipment servicing

· Quality:

· Defense & VA Healthcare

Familiarity with VA/DoD medical equipment procurement standards and VISN (Veterans Integrated Service Network) requirements
Experience with DCAA audit readiness (if we pursue DoD contracts)
Understanding of Section 508 accessibility compliance for any technology components
Knowledge of cybersecurity frameworks relevant to connected medical devices (NIST SP 800-171, CMMC if DoD-adjacent)

· Service & Maintenance Contracts

Ability to develop and maintain a quality plan that meets government contract SOW requirements
Experience writing and executing corrective/preventive action (CAPA) programs that satisfy government auditors
Calibration and preventive maintenance documentation standards (ISO 17025 awareness)

Additional Responsibilities

· Maintain updated knowledge of equipment, services, and policies through regular professional development training.

· Travel nationally as needed

· All other duties as assigned

About US Med-Equip

Recognized as a Top Workplace, US Med-Equip partners with top hospitals across the nation to provide the highest quality movable medical equipment, beds and therapeutic surfaces. USME, an Inc. 5000 Fastest Growing company, supplies and services equipment rented, maintained, and managed using the latest technology to help healthcare providers focus on their patients’ healing.

Education/Experience

· Experience: 7+ years of progressive leadership experience in Quality Assurance and Regulatory Affairs within the medical device, biomedical services, or healthcare logistics space.

· Education: Bachelor’s degree in Engineering, Biomedical Sciences, Healthcare Administration, or a related technical field. Master’s degree or relevant certifications (ASQ CQA/CQE, RAC) a strong plus.

Qualifications

· ISO 13485 Expertise: Proven track record of successfully implementing, auditing, or building an ISO 13485 framework from scratch. Experience adapting manufacturing standards to a service, rental, or asset management environment is highly preferred.

· The "Builder" Mindset: Demonstrated experience evaluating, procuring, and implementing enterprise digital QA/QMS software platforms.

· Influence Without Authority: Exceptional interpersonal skills with a proven ability to lead, coach, and drive accountability across a highly decentralized, nationwide network of operations and biomed peers.

· Tech-Savvy Auditor: Forward-thinking approach to compliance, with experience or strong capability in implementing remote virtual auditing, digital workflows, and data-driven risk modeling.

· Travel: Ability to travel strategically to branches and regional hubs, utilizing robust virtual meeting infrastructure for day-to-day oversight.

· Outstanding listening, communication, collaboration, organization and problem-solving skills

· Highest integrity and relentless commitment to delivering value to customers and co-workers

· Resourcefulness in a fast-paced environment with a readiness to embrace change

· Strong organizational, attention-to-detail, critical thinking and problem-solving skills

· Reports To: Chief Operating Officer (COO)

· Location: Houston, TX (Corporate HQ) / Hybrid with strategic travel

· Position Type: Full-Time

Benefits of Working at US Med-Equip

· Professional development and career growth

· Health, Dental, Vision & Life insurance

· Paid time off starting within the first year

· Employee assistance program

· Flexible spending account

· Health savings account

· Employee referral bonuses

· 401(k)

Benefits:

401(k)
Dental insurance
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Referral program
Vision insurance

Experience:

QMS & ISO 13485: 4 years (Preferred)
Regulatory Compliance and Product Lifecycles: 4 years (Preferred)
Defense and VA Healthcare standards: 1 year (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

director quality engineering jobs in houston, tx

Director of Quality and Regulatory Affairs

Director of Quality Modular

Director of Quality

Global Quality Director

Director, General Engineering

Director I, Process/Specialty Engineering (Power)

Director of Engineering

Director of Gulf Coast Engineering

Director I, Process Engineering (Nuclear)

Director of Efficiency & Optimization

Director of Service Quality

Quality Assurance Director

Nuclear Director I, Engineering Management

Director of Engineering

Nuclear Director I, Engineering Management

Director of Engineering Delivery (Power Generation / Gas-to-Power)

Deputy Director of Transportation Operations

Director – Environmental Remediation

Director I, Nuclear Structural Engineering (Lead)

Director of Engineering and Design

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