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Capa Engineer Jobs in Texas (NOW HIRING)

Quality Engineer II

Allen, TX · On-site

$67K - $86K/yr

This role leads CAPA and risk assessment activities, supports supplier quality programs, manages engineering projects, and ensures compliance with regulatory standards through audits and validations.

MANUFACTURING ENGINEER

Rosenberg, TX · On-site

$80K - $100K/yr

Participate in deviation investigations, root cause analysis, CAPA implementation, and change ... Ensure engineering documentation complies with FDA and current Good Manufacturing Practice (cGMP ...

Quality Engineer

Brenham, TX

$60K - $78K/yr

Are you a driven Quality Engineer ready to take the next step in your career and make a meaningful ... Drive CAPA activities and ensure timely closure of corrective and preventive actions. * Maintain ...

Quality Engineer

Brenham, TX · On-site

$60K - $78K/yr

Are you a driven Quality Engineer ready to take the next step in your career and make a meaningful ... Drive CAPA activities and ensure timely closure of corrective and preventive actions. * Maintain ...

Quality Engineer

Brenham, TX · On-site

$60K - $78K/yr

Drive CAPA activities and ensure timely closure of corrective and preventive actions. * Maintain ... Work closely with Manufacturing Engineering and Operations to implement sustainable process ...

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

Quality Engineer

Waco, TX · On-site

$63K - $82K/yr

Monitor corrective and preventive action (CAPA) effectiveness. * Participate in management review ... Bachelor's Degree in Engineering, Quality, Manufacturing, Industrial Technology, or related ...

Quality Engineer

Waco, TX · On-site

$63K - $82K/yr

Monitor corrective and preventive action (CAPA) effectiveness. * Participate in management review ... Bachelor's Degree in Engineering, Quality, Manufacturing, Industrial Technology, or related ...

Quality Engineer

Waco, TX · On-site

$63K - $82K/yr

Monitor corrective and preventive action (CAPA) effectiveness. * Participate in management review ... Bachelor's Degree in Engineering, Quality, Manufacturing, Industrial Technology, or related ...

Quality Test Engineer

Dallas, TX

$71K - $92K/yr

Develop, implement, and verify Corrective and Preventive Actions (CAPA). * Monitor corrective ... Test Engineering * Develop, validate, and improve electrical and functional test procedures.

FormFactor is seeking a Process Engineer to support and improve photolithography and etch processes ... Perform root cause analysis and implement corrective and preventive actions (CAPA). * Support ...

Showing results 21-40

Capa Engineer information

See Texas salary details

$36.3K

$94.8K

$128.1K

How much do capa engineer jobs pay per year?

As of Aug 9, 2026, the average yearly pay for capa engineer in Texas is $94,798.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,300.00 and $108,500.00 per year, depending on experience, location, and employer.

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

To thrive as a CAPA Engineer, you need a solid background in quality engineering, root cause analysis, and process improvement, typically supported by a degree in engineering or a related technical field. Familiarity with CAPA management systems, quality standards such as ISO 13485 or ISO 9001, and tools like Six Sigma or FMEA is highly valuable. Strong problem-solving abilities, attention to detail, and effective communication skills distinguish top performers in this role. These competencies ensure effective identification, documentation, and resolution of quality issues, helping organizations maintain regulatory compliance and deliver high-quality products.

What is a CAPA engineer?

A CAPA (Corrective and Preventive Action) Engineer is responsible for identifying, investigating, and resolving quality issues in manufacturing or engineering processes. They analyze root causes of defects, implement corrective measures, and develop preventive strategies to ensure compliance with industry regulations. CAPA Engineers work closely with cross-functional teams to improve product quality, streamline processes, and maintain regulatory compliance. They also document findings, track action plans, and support continuous improvement initiatives to reduce future risks.

What are the main daily responsibilities of a CAPA engineer?

A CAPA Engineer's daily responsibilities typically include investigating potential or actual nonconformities, conducting root cause analyses, and developing corrective and preventive action plans to resolve and prevent future issues. They also collaborate closely with cross-functional teams such as manufacturing, quality assurance, and regulatory affairs to ensure solutions are practical and compliant with industry standards. Additionally, CAPA Engineers monitor the progress and effectiveness of implemented actions, prepare documentation for audits, and participate in continuous process improvement initiatives. This role is crucial for maintaining the highest quality standards and ensuring compliance in regulated industries such as medical devices or pharmaceuticals.

What are the most commonly searched types of Capa Engineer jobs in Texas? The most popular types of Capa Engineer jobs in Texas are:
What cities in Texas are hiring for Capa Engineer jobs? Cities in Texas with the most Capa Engineer job openings:
Infographic showing various Capa Engineer job openings in Texas as of July 2026, with employment types broken down into 93% Full Time, 4% Part Time, and 3% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $94,798 per year, or $45.6 per hour.

Quality Engineer II

Nordsonhcm

Allen, TX • On-site

$67K - $86K/yr

Full-time

Re-posted 18 days ago


Job description

Nordson Medical, a global leader in Interventional Solutions, Fluid Components, and Surgical Solutions, is seeking an experienced and highly motivated individual to join our team. We are committed to creating a diverse and inclusive workplace, and we are looking for candidates who share that same commitment.

Summary of the role

As a member of our team, you will have the opportunity to work in a dynamic and collaborative environment, where your ideas and contributions will be valued and respected.

Summary

The Senior Quality Engineer is responsible for maintaining and improving the Quality Management System (QMS) across the product lifecycle-from design and development to manufacturing and post-production. This role leads CAPA and risk assessment activities, supports supplier quality programs, manages engineering projects, and ensures compliance with regulatory standards through audits and validations.

Key Responsibilities

  • Lead CAPA investigations and risk assessments for new and existing products.
  • Demonstrates strong project management skills by effectively leading CAPA, product, and process improvement initiatives from initiation through sustained implementation, delivering measurable business impact.
  • Demonstrates strong expertise in validation, including protocol development, execution, and lifecycle management for equipment, processes, and systems in compliance with regulatory requirements.
  • Support daily manufacturing activities and resolve line issues.
  • Develop and maintain quality systems, procedures, and documentation.
  • Provide technical support for incoming inspection and lot release testing.
  • Manage customer complaints and non-conformance investigations.
  • Lead internal and external audits (FDA, ISO, MDD).
  • Oversee supplier quality activities including audits and corrective actions.
  • Support engineering teams in product development and process improvements.
  • Conduct statistical analysis, validation testing, and Gage R&R studies.
  • Mentor junior quality staff and provide training as needed.

Qualifications

  • Bachelor's degree in engineering, science, or related technical field.
  • Minimum of 3-5 years of quality engineering experience in regulated industries (medical device or pharmaceutical preferred).
  • Experience with ISO 13485, ISO 14971, FDA QSR, IEC 60601, and related standards.
  • Proficiency in statistical tools and software (Minitab preferred).
  • ASQ certifications (CQE, CQA) and Six Sigma Green/Black Belt preferred.
  • Demonstrates working knowledge of sterilization methods and controls and their impact on product quality, including validation, change control, and compliance requirements (preferred).
  • Excellent communication, technical writing, and project management skills.
  • Ability to travel up to 10%.

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Interested?

If you are interested in being a part of a team and creating an inclusive and diverse workplace, please apply online with your CV.

About Nordson Medical

At Nordson MEDICAL, you don't have to be a doctor to help save lives. We are the global expert in the design, development, and manufacturing of complex medical devices and component technologies. By joining our team today, you will help us bring innovative ideas to life. Nordson MEDICAL is a global team that works to create components for life-saving medical devices. We offer a supportive culture in a growing and dynamic work environment. Whether you're just beginning your career or you're a seasoned professional, there's a place for you to belong at Nordson MEDICAL. We offer hourly and salary positions in production, maintenance, customer service, quality, engineering, and more. We actively invest in our teams to help you build your skillsets and advance your career.