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Quality Systems Manager Jobs in Texas (NOW HIRING)

Zimmer, Inc.

Quality Systems Sr Engineer II

Austin, TX · On-site

$100K - $124K/yr

What You Can Expect Responsible for leading the implementation, maintenance, and continuous improvement of the Quality Management System (QMS) supporting the design, development, verification ...

SpaceX

Quality Systems Engineer (Starlink)

Bastrop, TX · On-site +1

The Quality Systems Engineer will improve the quality management system and verify compliance to ISO 9001 prescribed procedures. They will plan, schedule, and perform regular audits to drive ...

ForeFlight

Sr Quality Systems Specialist

Austin, TX · Remote

$100K - $125K/yr

Leads the introduction and/or maturation of new and/or existing quality management systems and their successful re-/certification(s) * Ability to independently develop solutions to a variety of ...

Flow Control Group

Control Systems Manager

Houston, TX · On-site

The Control Systems Manager is responsible for leading Cougar USA's Systems Production operations ... Process Improvement & Quality Assurance: * Drive continuous improvement initiatives focused on ...

Stratasys Ltd

Director of Quality Systems

Belton, TX · On-site

$140 - $210/hr

Director of Quality Systems Location: Belton, TX, US Job ID: 55287 Category: Manufacturing ... Manage quality assurance operations relative to all manufacturing departments & sites. * Ensures ...

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All JobsQuality Systems JobsQuality Systems Manager JobsQuality Systems Manager Jobs in Texas

Quality Systems Manager information

See Texas salary details

$50.3K

$91.9K

$143.5K

How much do quality systems manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for quality systems manager in Texas is $91,873.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,300.00 and $114,100.00 per year, depending on experience, location, and employer.

What does a quality systems manager do?

As a quality systems manager, your primary responsibilities are monitoring the production processes and ensuring factory machinery/goods are within company and industry requirements. Your duties include weighing, sampling, or testing products for quality and functionality. You may also report the results of quality control tests. You monitor the equipment and people involved, and help with the development and implementation of improved management systems. You are also in charge of creating a standard operating procedure for the specific plant where you work. You check that everything is running at full efficiency and the quality of merchandise is standardized.

What are the key skills and qualifications needed to thrive as a quality systems manager?

To thrive as a Quality Systems Manager, you need strong expertise in quality management principles, regulatory compliance, and process improvement, typically supported by a degree in engineering or a related field. Familiarity with ISO standards (like ISO 9001), quality management software, and certifications such as Six Sigma or ASQ Certified Manager of Quality/Organizational Excellence are commonly required. Leadership, analytical thinking, and effective communication are crucial soft skills for coordinating teams and driving continuous improvement. These skills and qualifications are essential to ensure consistent product quality, regulatory adherence, and overall organizational efficiency.

How does a quality systems manager typically collaborate with cross-functional teams to drive continuous improvement?

A Quality Systems Manager works closely with departments such as manufacturing, engineering, regulatory, and supply chain to ensure that quality standards are consistently met and improved. They often lead or participate in cross-functional meetings to identify process gaps, analyze data, and develop corrective and preventive action plans. Effective communication and project management skills are essential, as the role involves aligning diverse teams toward common quality objectives and facilitating training or audits to support compliance and improvement initiatives.

What is the difference between Quality Systems Manager vs Quality Assurance Manager?

AspectQuality Systems ManagerQuality Assurance Manager
Primary FocusDeveloping and maintaining quality management systems and processesOverseeing product testing and ensuring quality standards are met during production
CertificationsISO 9001 Lead Auditor, CQEASQ certifications, QA certifications
Work EnvironmentQuality management departments, compliance teamsProduction lines, testing labs
Industry UsageManufacturing, healthcare, aerospaceManufacturing, software, healthcare

While both roles focus on quality, the Quality Systems Manager primarily manages the overall quality management system and compliance, whereas the Quality Assurance Manager concentrates on product testing and ensuring quality during production. Understanding these differences helps in selecting the right career path or hiring the appropriate professional.

More about Quality Systems Manager jobs

What are the most commonly searched types of Quality Systems jobs in Texas?

The most popular types of Quality Systems jobs in Texas are:

What are popular job titles related to Quality Systems Manager jobs in Texas?

For Quality Systems Manager jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Quality Systems Manager jobs in Texas look for?

The top searched job categories for Quality Systems Manager jobs in Texas are:

What cities in Texas are hiring for Quality Systems Manager jobs?

Cities in Texas with the most Quality Systems Manager job openings:

Quality Systems Manager jobs near you
Infographic showing various Quality Systems Manager job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $91,873 per year, or $44.2 per hour.

Quality Systems Sr Engineer II

Zimmer, Inc.

Austin, TX • On-site

$100K - $124K/yr

Full-time

Posted 14 days ago

Job description

Zimmer Biomet is a global medical technology leader. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.


What You Can Expect

Responsible for leading the implementation, maintenance, and continuous improvement of the Quality Management System (QMS) supporting the design, development, verification, validation, and commercialization of advanced robotic surgical systems. Provides technical leadership for Document Control, Change Control, Training, audit readiness, electronic Quality Management Systems, and Quality System compliance. Partners with cross-functional teams to ensure compliance with FDA QMSR, ISO 13485, and company procedures.

How You'll Create Impact
  • Lead or support the implementation, maintenance, and continuous improvement of the Quality Management System (QMS).
  • Develop, implement, and maintain Document Control and Change Control processes aligned with FDA QMSR, ISO 13485, and company procedures.
  • Lead or support the development, implementation, and continuous improvement of the Monogram Training Program, ensuring training assignments, completion, effectiveness, and training record compliance.
  • Serve as the Quality Systems subject matter expert for Greenlight Guru and future enterprise electronic QMS platforms, such as Windchill, ETQ, CodeBeamer, etc.
  • Develop, maintain, and continuously improve Quality System procedures, work instructions, forms, templates, and records.
  • Partner with Engineering, Regulatory Affairs, Clinical Affairs, Operations, and Supply Chain to ensure Quality System compliance throughout the product lifecycle.
  • Support regulatory submissions by ensuring Quality System documentation is complete, accurate, controlled, and inspection ready.
  • Lead or support internal audits, external/certification audits, and regulatory inspections, ensuring organizational readiness and successful outcomes.
  • Coordinate audit responses and support timely implementation of corrective actions.
  • Lead or support Product Quality Signal (PQS) assessments, Health Hazard Evaluation Determinations (HHEDs), Health Hazard Evaluations (HHEs), Issue Evaluations (IEs), Nonconformance Reports (NCRs), deviations, CAPAs, root cause investigations, and other Quality System activities, including appropriate interface with product risk management processes.
  • Develop Quality System metrics and key performance indicators (KPIs) to monitor effectiveness and drive continuous improvement.
  • Lead or support Quality System harmonization initiatives with Zimmer Biomet corporate Quality Systems.
  • Provide technical leadership and mentoring to Quality Systems personnel and cross-functional teams.
  • Stay informed of FDA regulations, ISO standards, and industry best practices and implement improvements as appropriate.
  • May lead cross-functional projects and assume supervisory responsibilities as business needs evolve.
What Makes You Stand Out
  • Comprehensive knowledge of FDA QMSR, ISO 13485, document control, records management, training systems, PQS, HHED/HHE, IE, NCR/deviation, CAPA, audits, risk management, and change control.
  • Expertise with electronic Quality Management Systems (e.g., Greenlight Guru, SmartSolve, Windchill, ETQ).
  • Experience leading or supporting internal, certification, customer, and regulatory audits.
  • Excellent technical writing, communication, project management, and problem-solving skills.
  • Ability to lead cross-functional initiatives and influence without direct authority.
  • Strong analytical skills and continuous improvement mindset.
Your Background
  • Minimum Requirements:Bachelor's Degree in Engineering and 5 years of relevant experience or equivalent experience
  • 6+ years of progressive Quality Systems experience within the medical device industry highly preferred
  • Experience with FDA-regulated medical devices and ISO 13485
  • Experience leading Document Control, Change Control, Training, and Audit programs
  • ASQ Certified Quality Auditor (CQA), Certified Manager of Quality/Organizational Excellence (CMQ/OE), or equivalent certification preferred
Travel Expectations

Up to 25%

Expected Compensation Range

$100,000 - $124,000 USD / Annual


EOE

Employment Type: OTHER

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