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Capa Jobs in Austin, TX (NOW HIRING)

Deloitte

System Test and Validation Lead

Austin, TX · On-site +1

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 ...

Deloitte

System Test and Validation Lead

Austin, TX · On-site +1

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 ...

Deloitte

System Test and Validation Lead

Austin, TX · On-site +1

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 ...

The Goodkind Co

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 ...

The Goodkind Co

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 ...

Entegris

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 ...

Entegris

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 ...

Entegris

Senior Engineer, Quality Engineer

Austin, TX

$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 ...

Entegris

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 ...

Entegris

Senior Engineer, Quality Engineer

Austin, TX

$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 ...

TransPak

Quality Manager

Manor, TX · On-site

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 ...

Entegris

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 ...

Sterling Engineering Inc.

Quality Director

Austin, TX · On-site

$145K - $165K/yr

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 ...

Stark Pharma Solutions Inc

CQV Engineer

Austin, TX · On-site

Analyze validation data, investigate deviations, support root cause analysis, and implement CAPA activities. * Collaborate with Engineering, Manufacturing, Validation, Quality Assurance, and ...

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How much do capa jobs pay per hour?

As of Aug 13, 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 are popular job titles related to Capa jobs in Austin, TX?

For Capa jobs in Austin, TX, the most frequently searched job titles are:

What job categories do people searching Capa jobs in Austin, TX look for?

The top searched job categories for Capa jobs in Austin, TX are:

What cities near Austin, TX are hiring for Capa jobs?

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Capa jobs near you
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 Assurance Release Specialist

The Goodkind Co

Round Rock, TX • On-site

Full-time

Posted 23 days ago

Job description

Overview
Reporting to the QA Supervisor, the Quality Assurance Release Specialist is responsible for batch disposition and quality systems oversight to ensure products meet internal, customer, and regulatory requirements prior to release to market. This role applies risk-based decision-making and technical evaluation of manufacturing, quality, and compliance data to support product release, investigation activities, and continuous improvement initiatives.
The position is responsible for managing quality system processes including deviations, non-conformance reports (NCRs), CAPA, and change control, ensuring issues are appropriately investigated, documented, and resolved in accordance with GMP requirements. This role also supports data trending, root cause analysis, and cross-functional quality improvement efforts to strengthen process reliability and compliance readiness.
About Us
Founded in 2010 and based in the Austin area, Goodkind is a leading manufacturer of clean and green personal care and beauty products. Goodkind specializes in natural deodorant, skincare, and facial care products. The company has a wealth of experience in the formulation of these products and can develop according to a variety of guidelines from consumer organizations such as Ecocert to EWG, to retailers such as Credo or Sephora.
Goodkind is a certified B Corporation. As such, we balance purpose and profit, considering the impact of decisions across associates, customers, suppliers, community, and the environment. Goodkind believes by following this central multi-stakeholder approach, we are creating optimal value for each stakeholder while leaving the world a better place.
What You'll Do
  • Review and approve batch production records and supporting quality documentation prior to product release
  • Evaluate manufacturing and quality data to identify deviations, trends, atypical results, and potential product quality risks
  • Manage and support investigations related to NCRs, deviations, and CAPA activities
  • Support change control processes, including quality impact and risk assessments
  • Review Certificates of Analysis (COAs) and product specifications for release approval
  • Ensure calibration status and related quality system requirements are compliant prior to batch disposition
  • Analyze and trend quality data to identify recurring issues and support continuous improvement initiatives
  • Escalate quality or compliance risks that may impact product disposition or regulatory compliance
  • Collaborate cross-functionally with QA, QC, Manufacturing, and Operations to resolve quality system issues
  • Maintain accurate, complete, and audit-ready quality records and documentation
  • Support internal and external audits and regulatory inspections
  • Perform additional duties as assigned

Requirements
What We Require
  • Bachelor's degree in Chemistry, Biology, Engineering, Life Sciences, or related field (or equivalent experience)
  • 3+ years of Quality Assurance experience in a regulated manufacturing environment
  • Strong working knowledge of GMP requirements and quality systems
  • Experience with batch record review and product release activities
  • Experience managing deviations, NCRs, CAPA, and change control processes
  • Ability to perform root cause investigations and apply risk-based decision-making
  • Experience reviewing manufacturing and quality data for compliance and product impact
  • Strong written and verbal communication skills
  • Strong attention to detail, organization, and documentation practices
  • Ability to work independently and manage multiple priorities in a fast-paced environment
Preferred Qualifications
  • Experience in OTC, pharmaceutical, cosmetic, or personal care manufacturing
  • Experience with ERP systems, eQMS platforms, and Redzone
  • Familiarity with FDA regulations, ISO standards, and data integrity principles
  • Experience supporting audits, inspections, and validation activities
Key Skills & Competencies
  • Batch release and disposition decision-making
  • Root cause analysis and risk assessment
  • Quality systems management (NCR, CAPA, deviations, change control)
  • Data analysis and trend evaluation
  • Regulatory compliance and GMP knowledge
  • Critical thinking and problem-solving
  • Cross-functional collaboration
  • Technical documentation and investigation writing
  • Accountability and sound judgment

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