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Capa Jobs in Arizona (NOW HIRING)

Principal R&D Engineer

Tempe, AZ ยท On-site

$55 - $65/hr

Investigation & CAPA * Medical Device Regulatory Compliance Education: * Advanced degree in Mechanical Engineering, Biomedical Engineering, Materials Science, Physics, Chemistry, Chemical Engineering ...

New

Quality Engineer I

Goodyear, AZ

$70K - $90K/yr

Responsible to assist in containment activities when reactive issues arise and ensure all customer issues (CAPA's, etc.) are addressed, filed,and documented in a timely manner. * Participate and lead ...

Quality Engineer I

Goodyear, AZ ยท On-site

$70K - $90K/yr

Responsible to assist in containment activities when reactive issues arise and ensure all customer issues (CAPA's, etc.) are addressed, filed, and documented in a timely manner. * Participate and ...

Product Quality Engineer II (Onsite)

Scottsdale, AZ ยท On-site

$72K - $93K/yr

Manage 8D and RCA teams to perform corrective and preventive actions (CAPA/APEX) from internal and external sources (RMA). * Create First Article Inspection Plans (FAIR) and production part approvals ...

Pipe Layer

Gilbert, AZ

$19 - $25/hr

La funcion principal de un Capa de Tuberia es realizara tareas de colocacion de tuberias que involucran trabajo fisico (colocacion, union, envoltura, sellado) en sitios de trabajo de construccion ...

Conduct root cause analysis (RCA) and implement effective Corrective and Preventive Actions (CAPA). * Sound understanding of the build and functionality of aero engine and sub-modules. * Experience ...

Experience with root cause analysis tools (e.g., 8D, Fishbone, 5 Whys) and CAPA processes * Proficiency in Microsoft Office and quality data/reporting tools * Strong analytical, communication, and ...

Quality Manager

Mesa, AZ ยท On-site

$100K - $120K/yr

Experience with root cause analysis tools (e.g., 8D, Fishbone, 5 Whys) and CAPA processes * Proficiency in Microsoft Office and quality data/reporting tools * Strong analytical, communication, and ...

Supports the maintenance and continuous improvement of the overall quality system or a specific procedure, including management review, CAPA management, internal quality audits, quality self ...

Quality Assurance Supervisor

Goodyear, AZ ยท On-site

$55K - $90K/yr

Supports the maintenance and continuous improvement of the overall quality system or a specific procedure, including management review, CAPA management, internal quality audits, quality self ...

Supports the maintenance and continuous improvement of the overall quality system or a specific procedure, including management review, CAPA management, internal quality audits, quality self ...

Supports the maintenance and continuous improvement of the overall quality system or a specific procedure, including management review, CAPA management, internal quality audits, quality self ...

Quality Assurance Supervisor

Goodyear, AZ ยท On-site

$55K - $90K/yr

Supports the maintenance and continuous improvement of the overall quality system or a specific procedure, including management review, CAPA management, internal quality audits, quality self ...

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Capa information

See Arizona salary details

$14

$40

$68

How much do capa jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for capa in Arizona is $40.94, according to ZipRecruiter salary data. Most workers in this role earn between $31.04 and $47.61 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 job?

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 the most commonly searched types of Capa jobs in Arizona? The most popular types of Capa jobs in Arizona are:
What are popular job titles related to Capa jobs in Arizona? For Capa jobs in Arizona, the most frequently searched job titles are:
Infographic showing various Capa job openings in Arizona as of July 2026, with employment types broken down into 91% Full Time, 3% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $85,157 per year, or $40.9 per hour.
Principal R&D Engineer

Principal R&D Engineer

Three Point Solutions

Tempe, AZ โ€ข On-site

$55 - $65/hr

Contractor

Posted 2 days ago

New


Job description

Job Title: ย ย ย ย ย ย ย  Principal R&D Engineer

Client: ย ย ย ย ย ย ย ย ย ย ย  Medical Device Manufacturing Company

Duration: ย ย ย ย ย ย ย  8.5 Months (Possibility of Extension)

Location: ย ย ย ย ย ย ย  Tempe, AZ 85281

Shift: ย ย ย ย ย ย ย ย ย ย ย ย ย ย  1st Shift

Description:

  • Lead the development, validation, and optimization of medical device manufacturing processes.
  • Design and execute process characterization, validation (IQ/OQ/PQ), DOE, and TMV activities.
  • Analyze manufacturing data using statistical methods to drive process improvements and solve complex engineering problems.
  • Collaborate with cross-functional teams to support product development, manufacturing readiness, and commercialization.
  • Conduct root cause investigations and implement corrective actions using DMAIC, 5 Whys, and Lean Six Sigma methodologies.
  • Ensure compliance with quality management systems, regulatory requirements, and validation standards.
  • Lead technical projects, mentor team members, and communicate project progress, risks, and solutions.
  • Support research, product development, and continuous improvement initiatives for medical devices.

Required Skills:

  • Process Development & Validation (DOE, IQ/OQ/PQ, TMV)
  • Statistical Analysis
  • Root Cause Analysis
  • Medical Device Manufacturing
  • Cross-Functional Project Leadership
  • Quality Management Systems (QMS)
  • Technical Problem Solving
  • Project Management
  • Risk Management
  • Technical Documentation

Preferred Skills:

  • HPLC, LCMS, FTIR, Mass Spectrometry
  • Lean Six Sigma / DFSS / DRM
  • Green Belt Certification
  • Technical Writing
  • Investigation & CAPA
  • Medical Device Regulatory Compliance

Education:

  • Advanced degree in Mechanical Engineering, Biomedical Engineering, Materials Science, Physics, Chemistry, Chemical Engineering, or a related engineering/science discipline.

Experience:

  • 7+ years of relevant R&D or manufacturing engineering experience, or
  • 5+ years of relevant experience with an advanced degree.
  • Experience in medical device process development, validation, and cross-functional project leadership is required.

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