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Capa Jobs in Austin, TX (NOW HIRING)

Quality Engineer

Austin, TX · On-site

$71K - $92K/yr

The Quality Engineer (CAPA) is responsible for supporting and maintaining the effectiveness of the Quality Management System through ownership and oversight of Corrective and Preventive Action ...

ESD Quality Engineer

Austin, TX · On-site

$71K - $92K/yr

Define and maintain CAPA trigger criteria based on defect severity, recurrence, and risk * Lead root cause analysis and ensure appropriate corrective and preventive actions are implemented * Review ...

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks, closure documentation, and tracking of open compliance actions * Validate AI/ML-enabled GxP systems ...

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks, closure documentation, and tracking of open compliance actions * Validate AI/ML-enabled GxP systems ...

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks, closure documentation, and tracking of open compliance actions * Validate AI/ML-enabled GxP systems ...

Quality Engineer

Round Rock, TX · On-site

$67K - $86K/yr

Lead and support root cause investigations related to deviations, NCRs, CAPA, and process failures * Analyze quality and manufacturing data to identify trends, recurring issues, and opportunities for ...

Quality Engineer

Round Rock, TX · On-site

$67K - $86K/yr

Lead and support root cause investigations related to deviations, NCRs, CAPA, and process failures * Analyze quality and manufacturing data to identify trends, recurring issues, and opportunities for ...

Senior Engineer, Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Monitor and improve key quality metrics including QN aging, CAPA effectiveness, MOC cycle time, customer complaints, and product compliance performance. * Lead cross-functional Material Review Board ...

Senior Engineer, Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Monitor and improve key quality metrics including QN aging, CAPA effectiveness, MOC cycle time, customer complaints, and product compliance performance. * Lead cross-functional Material Review Board ...

Senior Engineer, Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Monitor and improve key quality metrics including QN aging, CAPA effectiveness, MOC cycle time, customer complaints, and product compliance performance. * Lead cross-functional Material Review Board ...

Senior Engineer, Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Monitor and improve key quality metrics including QN aging, CAPA effectiveness, MOC cycle time, customer complaints, and product compliance performance. * Lead cross-functional Material Review Board ...

Senior Engineer, Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Monitor and improve key quality metrics including QN aging, CAPA effectiveness, MOC cycle time, customer complaints, and product compliance performance. * Lead cross-functional Material Review Board ...

These processes include but are not limited to receiving inspection, in-process inspection, final inspection, first article inspection (FAI), internal auditing, CAPA and feedback to management. The ...

Senior Engineer, Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Monitor and improve key quality metrics including QN aging, CAPA effectiveness, MOC cycle time, customer complaints, and product compliance performance. * Lead cross-functional Material Review Board ...

Lead root cause investigations, CAPA initiatives, and risk management activities * Champion Lean Manufacturing, Six Sigma, Kaizen, and continuous improvement programs * Build, mentor, and develop a ...

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Capa information

See Austin, TX salary details

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$41

$69

How much do capa jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for capa in Austin, TX is $41.38, according to ZipRecruiter salary data. Most workers in this role earn between $31.37 and $48.12 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a CAPA specialist?

A CAPA specialist is responsible for investigating quality issues, identifying root causes, and implementing corrective and preventive actions to ensure ongoing compliance and product integrity. Their typical day involves reviewing nonconformance reports, collaborating with cross-functional teams, documenting findings, and tracking the progress of CAPA initiatives using specialized software. CAPA specialists also prepare reports for audits and may facilitate meetings to drive continuous improvement activities. This role often requires balancing multiple projects and deadlines in a regulated environment, making organizational and communication skills crucial for success.

What are the key skills and qualifications needed to thrive in the CAPA position, and why are they important?

To thrive as a CAPA (Corrective and Preventive Action) specialist, you need expertise in quality management systems, root cause analysis, and compliance with industry standards, typically backed by a degree in engineering, life sciences, or a related field. Familiarity with CAPA software, regulatory frameworks (such as ISO 13485 or FDA 21 CFR Part 820), and document control systems is essential. Strong analytical thinking, attention to detail, and effective communication skills are vital soft skills for this role. These skills ensure effective problem-solving and sustained compliance, which are essential for maintaining product quality and meeting regulatory requirements.

What is a CAPA?

A CAPA (Corrective and Preventive Action) job involves identifying, investigating, and resolving quality issues in industries like manufacturing, healthcare, and pharmaceuticals. CAPA professionals analyze root causes of defects or process failures and implement corrective actions to prevent recurrence. They ensure compliance with regulatory standards, document findings, and improve overall quality management systems. Their role is critical in maintaining product safety, efficiency, and regulatory adherence.

What cities near Austin, TX are hiring for Capa jobs? Cities near Austin, TX with the most Capa job openings:
Infographic showing various Capa job openings in Austin, TX as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $86,061 per year, or $41.4 per hour.

Quality Engineer

Flex

Austin, TX • On-site

$71K - $92K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary

Summary:


The "Quality Engineer" will be based in Austin, TX reporting to Adriana Russell.

What a typical day looks like:

Maintaining quality engineering programs, standards and improvements within the organization. The Quality Engineer (CAPA) is responsible for supporting and maintaining the effectiveness of the Quality Management System through ownership and oversight of Corrective and Preventive Action activities, quality investigations, root cause analysis, risk assessments, and continuous improvement initiatives. This role partners with cross-functional teams to ensure quality issues are thoroughly investigated, appropriately mitigated, and effectively resolved while maintaining compliance with applicable regulatory, customer, and organizational requirements. The position serves as a key driver of quality system effectiveness, operational excellence, and regulatory compliance.

The experience we're looking to add to our team:

  • Leads and facilitates Corrective and Preventive Action (CAPA) activities from initiation through closure, ensuring compliance with internal procedures, customer requirements, and applicable regulatory standards.
  • Conducts thorough investigations using structured problem-solving methodologies such as 5 Whys, Fishbone Diagram, Fault Tree Analysis, Is/Is Not Analysis, and other root cause analysis tools.
  • Evaluates quality system data, manufacturing metrics, audit findings, customer complaints, nonconformances, and trend analyses to identify systemic issues requiring corrective action.
  • Ensures root cause investigations are scientifically sound, data-driven, and supported by objective evidence. Develops and initiates standards and methods for inspection, testing and evaluation.
  • Develops, reviews, and approves correction, corrective action, and preventive action plans to address identified quality issues and prevent recurrence.
  • Coordinates cross-functional teams including Manufacturing, Supplier Quality, Engineering, Regulatory Affairs, Operations, and Customer Quality to drive timely CAPA execution.
  • Assesses quality events and nonconformances for CAPA applicability utilizing risk-based decision-making methodologies.
  • Devises sampling procedures and designs and develops forms and instructions for recording, evaluating and reporting quality and reliability data.
  • Develops and implements methods and procedures for disposition of discrepant material and devises methods to assess cost.
  • Directs workers engaged in measuring and testing product and tabulating data concerning materials, product or process quality and reliability.
  • Compiles and writes training material and conducts training sessions on quality control activities.
  • Holds up Product Engineers and Quality Program Managers with customer interfaces as necessary on quality related issues.
  • Assures data availability and integrity for all quality related data. Consolidates and reports quality results.
  • Initiates corrective action requests as needed and tracks to satisfactory completion.
  • Assists with development and implementation of quality audits.
  • In charge of developing, applying, revising and maintaining quality standards for processing materials into partially finished or finished products.
  • Designs and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and/or production equipment.
  • Explores reports and returned products and recommends corrective action.
  • Establishes program to evaluate precision and accuracy of production equipment and testing, measurement and research of equipment and facilities.
  • Approves product, process and equipment qualifications.
  • Provides liaison to various regulatory bodies.
  • Participates in customer, internal, supplier, certification body, and regulatory audits and inspections.
Qualifications:
  • Typically requires a Bachelor's degree in related field or equivalent experience.
  • Typically requires 6 years of experience in engineering in the high technology electronics industry or related field.
  • Experience with Corrective and Preventive Action (CAPA), Nonconformance Management, Complaint Handling, Change Control, and Risk Management processes.
  • Strong knowledge of Quality Management Systems (QMS) and applicable regulatory requirements including FDA 21 CFR Part 820, ISO 13485, and ISO 14971.
  • Experience with electronic Quality Management Systems (eQMS) and quality data analysis tools.
  • Strong project management, organizational, and communication skills with the ability to manage multiple priorities simultaneously.
  • Experience supporting regulatory inspections, customer audits, and compliance activities preferred.
  • Knowledge of medical device manufacturing, contract manufacturing, or highly regulated industries preferred.
  • Demonstrated ability to influence cross-functional teams and drive quality improvements without direct authority.
  • Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations and permutations.
  • Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory and factor analysis.
  • Ability to interpret an extensive variety of technical instructions in mathematical or diagram form, and deal with several abstract and concrete variables.
  • Use of the following tools may be required:
  • Electronic Assembly: color code, component, schematics. May require various PCB operations.
  • Testing: oscilloscope, cable and harness testing, trouble shooting, component testing, logic analyzer.
  • Inspection: bare board, systems, components, cable and harness, microscope, measuring tools.
  • Mechanical & Electrical Tools: taps and dies, alignment tools, measuring tools. Office skills: telephones, data entry, office software to include, word processing, spreadsheet and presentation package.
  • Demonstrates operations and technical skills and understanding of Flex's functional standards.
  • Demonstrates working knowledge of functional concepts and a solid understanding of Flex policies and procedures. Typically requires some knowledge of computerized electronic test equipment and programming.
  • Demonstrates advanced functional and technical skills and basic process skills. Demonstrates advanced/thorough knowledge of the function and Flex business.
  • Typically requires skill and troubleshooting, and diagnostics, and overview of the entire test process and the ability to train others.
  • Demonstrates advanced operations, technical and people and/or process skills as well as customer (external and internal) relationship skills. Demonstrates expert knowledge of the function and a thorough understanding of Flex and related business. Demonstrates knowledge of multiple functional technologies/ processes, industries or functions and understanding of interdependencies of such processes at the site.

What you'll receive for the great work you provide:

  • Full range of medical, dental, and vision plans
  • Life Insurance
  • Short-term and Long-term Disability
  • Matching 401(k) Contributions
  • Vacation and Paid Sick Time
  • Tuition Reimbursement

Application Deadline:

Applications for this job position will be accepted for at least five days following the job posting start date below and continuing until the end date below or until the position is filled. This posting may close sooner due to application volume.

Job Posting Start Date 07-24-2026 Job Posting End Date 08-08-2026 Job CategoryQuality

Is Sponsorship Available?

NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

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About Flex Personnel

Sourced by ZipRecruiter

The Flex Team is made up of Staffing Industry experts committed to serving the needs of businesses and workers by bringing people together. We are guided by our Core values Integrity, Courtesy, and Respect. At Flex we bring Businesses and People together. We carefully assess both the needs of our Business clients and the complete profiles of each candidate, and then make the connections we believe will be most mutually beneficial. With offices in select markets throughout the Country, We are continually expanding our industry reach nationwide.

Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Dallas, TX, US

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