1

Quality System Manager Jobs in Austin, TX (NOW HIRING)

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 ...

Own subsets of the Quality System related to software design controls, including but not limited to: * Software Design Control processes * Software Risk Management * Software Change Control

... system management documentation prior to project/ Activity commencement • Ensuring all project site compliance with Document Control system. • Ensuring proper turnover of complete quality control ...

... system management documentation prior to project/ Activity commencement • Ensuring all project site compliance with Document Control system. • Ensuring proper turnover of complete quality control ...

... system management documentation prior to project/ Activity commencement • Ensuring all project site compliance with Document Control system. • Ensuring proper turnover of complete quality control ...

Mentoring preparation and control of project quality system management documentation prior to project/ Activity commencement Ensuring all project site compliance with Document Control system.

This role manages the Quality System for third party manufacturing in accordance with Corporate and Divisional standards to ensure overall TPM performance and compliance. The role is responsible for ...

... system management documentation prior to project/ Activity commencement • Ensuring all project site compliance with Document Control system. • Ensuring proper turnover of complete quality control ...

... system management documentation prior to project/ Activity commencement • Ensuring all project site compliance with Document Control system. • Ensuring proper turnover of complete quality control ...

... system management documentation prior to project/ Activity commencement • Ensuring all project site compliance with Document Control system. • Ensuring proper turnover of complete quality control ...

... system management documentation prior to project/ Activity commencement • Ensuring all project site compliance with Document Control system. • Ensuring proper turnover of complete quality control ...

... system management documentation prior to project/ Activity commencement • Ensuring all project site compliance with Document Control system. • Ensuring proper turnover of complete quality control ...

... system management documentation prior to project/ Activity commencement • Ensuring all project site compliance with Document Control system. • Ensuring proper turnover of complete quality control ...

next page

Showing results 1-20

Quality System Manager information

See Austin, TX salary details

$53.5K

$97.7K

$152.6K

How much do quality system manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for quality system manager in Austin, TX is $97,746.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,800.00 and $121,400.00 per year, depending on experience, location, and employer.

What does a quality system manager do?

A Quality System Manager oversees the development, implementation, and maintenance of an organization's quality management systems. They ensure that all processes and products meet established quality standards and comply with relevant regulations. Their responsibilities include auditing processes, managing documentation, training staff on quality procedures, and driving continual improvement initiatives. By monitoring performance and addressing non-conformities, they help organizations deliver consistent, high-quality products or services.

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

To thrive as a Quality System Manager, you need a solid background in quality management principles, regulatory compliance, and process improvement, typically with a degree in engineering, life sciences, or a related field. Familiarity with ISO standards (e.g., ISO 9001), quality management software, and relevant certifications like Six Sigma or ASQ certifications is important. Strong leadership, problem-solving, and communication skills help drive cross-functional initiatives and foster a culture of continuous improvement. These skills ensure effective implementation of quality systems, compliance with industry standards, and sustained operational excellence.

What are some common challenges faced by a quality system manager when implementing new quality standards across an organization?

Quality System Managers often encounter challenges such as resistance to change from staff, aligning new standards with existing processes, and ensuring consistent understanding across departments. Building strong communication channels and providing thorough training are essential to facilitate adoption. Additionally, maintaining regulatory compliance while tailoring the system to the organization's unique needs requires careful planning and collaboration with cross-functional teams.

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

AspectQuality System ManagerQuality Assurance Manager
CertificationsISO 9001 Lead Auditor, CQEASQ CQE, Six Sigma Green/Black Belt
Work EnvironmentOversees quality management systems across departmentsFocuses on product quality and testing processes
Industry UsageCommon in manufacturing, aerospace, automotivePrevalent in manufacturing, healthcare, software
Primary FocusMaintaining and improving quality management systemsEnsuring product quality through testing and inspection

The Quality System Manager primarily manages the overall quality management system, ensuring compliance with standards like ISO 9001. The Quality Assurance Manager concentrates on product quality, testing, and inspection processes. Both roles require similar certifications and are vital in manufacturing and related industries, but their focus areas differ—system oversight versus product quality assurance.

What cities near Austin, TX are hiring for Quality System Manager jobs?

Cities near Austin, TX with the most Quality System Manager job openings:

Infographic showing various Quality System Manager job openings in Austin, TX as of August 2026, with employment types broken down into 100% Full Time. Highlights an 83% In-person, 11% Hybrid, and 6% Remote job distribution, with an average salary of $97,746 per year, or $47 per hour.

Quality Systems Sr Engineer II

Zimmer, Inc.

Austin, TX • On-site

$100K - $124K/yr

Full-time

Posted 5 days ago


Job description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging.


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