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

Neuralink

Quality Systems Engineer

Austin, TX

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

Artivion

Quality Systems Engineer I (Hybrid)

Austin, TX · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Responsible for operating the Quality Management System (QMS). To assist in providing assurance the Company operates in compliance with all required regulations and standards as determined by both ...

Artivion

Quality Systems Engineer I (Hybrid)

Austin, TX · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Responsible for operating the Quality Management System (QMS). To assist in providing assurance the Company operates in compliance with all required regulations and standards as determined by both ...

CryoLife

Quality Systems Engineer I (Hybrid)

Austin, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Responsible for operating the Quality Management System (QMS). To assist in providing assurance the Company operates in compliance with all required regulations and standards as determined by both ...

Neuralink

Quality Systems Engineer

Austin, TX · On-site

$71K - $119K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

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

Lemartec

QA/QC Manager

Austin, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Abbott

Senior Manager Supplier Quality

Austin, TX

$129K - $258K/yr

  • Medical

  • Life

  • Retirement

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 ...

Mastec Industrial

QA/QC Manager

Austin, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Lemartec

QA/QC Manager

Austin, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Lemartec

QA/QC Manager

Austin, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Lemartec

QA/QC Manager

Austin, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Lemartec

QA/QC Manager

Austin, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Lemartec

QA/QC Manager

Austin, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Lemartec

QA/QC Manager

Austin, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Lemartec

QA/QC Manager

Austin, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Abbott

Senior Manager Supplier Quality

Austin, TX

$129K - $258K/yr

  • Medical

  • Life

  • Retirement

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 ...

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Showing results 1-20

All JobsQuality System JobsQuality System Manager JobsQuality System Manager Jobs in Austin, TX

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

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

Quality System Manager jobs near you
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 Engineer

Neuralink

Austin, TX

Full-time

Re-posted yesterday

Job description

Team Description:

Join the Quality Systems Team, where our mission is to ensure compliance with applicable regulatory standards by designing scalable, efficient, and automation-driven systems. We focus on embedding compliance directly into engineering workflows rather than treating it as a manual or reactive function.

We are a team of industry-experienced professionals who apply systems thinking and creative problem-solving to build a durable compliance infrastructure that supports rapid development. Our vision is to establish internal design and quality systems that exceed FDA expectations while enabling fast iteration and deployment of complex, safety-critical software products.

Job Description and Responsibilities:

As a Quality Systems Engineer (dedicated towards Design Controls), your primary responsibility will be to design, implement, and continuously improve software-focused design control systems with regulatory compliance embedded into their architecture.

You will build systems that eliminate ambiguity, reduce manual effort, and enable rapid and reliable development of regulated medical device software. These systems will support the full software lifecycle, from requirements definition through verification, validation, risk management, and release.

You will continuously optimize these systems to improve speed, traceability, and audit readiness while supporting aggressive development timelines and frequent design changes. Your responsibilities include, but are not limited to:

  • Design and implement scalable software design controls systems aligned with IEC 62304 and FDA design control requirements (21 CFR 820.30)
  • Develop and maintain end-to-end traceability frameworks linking:
    • User needs
    • Software requirements
    • Risk controls
    • Design outputs (code, architecture)
    • Verification and validation evidence
  • Integrate software risk management into design controls, ensuring alignment with ISO 14971 principles
  • Build change control mechanisms capable of supporting:
    • Rapid iteration
    • Parallel development
    • Same-day deployment
  • Partner closely with software engineering teams to embed:
    • Compliance with CI/CD pipelines
    • Automated evidence generation
    • Controlled release processes
  • 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
    • Software Verification & Validation traceability

Required Qualifications: 

  • Bachelor's degree in Electrical Engineering, Computer Science, or a related technical field
  • Demonstrated experience designing or maintaining structured engineering or compliance systems
  • Familiarity with software development lifecycles in regulated or safety-critical environments
  • Working knowledge of:
    • Design Controls
    • Software requirements management
    • Proficiency in basic scripting, automation, or querying (e.g., Python, SQL, or equivalent)
  • Excellent written and verbal communication skills
  • Strong problem-solving mindset with the ability to think in systems rather than silos

Preferred Qualifications:

  • Familiarity with IEC 62304 (Medical Device Software Lifecycle Processes)
  • Familiarity with FDA Design Controls (21 CFR 820.30)
  • Familiarity with Design Risk Management (ISO 14971 principles)
  • 1-3 years of experience in:
    • Design Controls
    • Software Quality
    • Regulated software development

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