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Contract Capa Engineer Jobs (NOW HIRING)

Quality Engineer

San Jose, CA · On-site

$84K - $109K/yr

... a contract manufacturing environment focused on precision metal components for medical devices ... Own and execute CAPA and continuous improvement actions to improve process control and prevent ...

Quality Engineer

San Jose, CA · On-site

$84K - $109K/yr

... a contract manufacturing environment focused on precision metal components for medical devices ... Own and execute CAPA and continuous improvement actions to improve process control and prevent ...

Quality Engineer

San Jose, CA · On-site

$84K - $109K/yr

... a contract manufacturing environment focused on precision metal components for medical devices ... Own and execute CAPA and continuous improvement actions to improve process control and prevent ...

W2 Contract Industry: Medical Devices We are looking for a Failure Analysis Engineer with ... • Support CAPA activities and work with R&D, Manufacturing, Service, and Quality teams.

Quality Engineer, Sustaining

Carlsbad, CA · On-site

$74K - $96K/yr

Working closely with our NPI QE team, contract manufacturers and quality control, you will ensure ... CAPA and SCAR ownership, and change control activities. This role liaisons with R&D, Quality NPI ...

Controls Engineer

North Haven, CT · On-site

$83K - $107K/yr

My name is Vyshu, and I'm reaching out from Intellectt Inc. regarding an exciting contract ... Perform root cause analysis, CAPA, and continuous improvement initiatives * Collaborate with ...

Senior Quality Engineer

New Hope, MN · On-site

$91K - $124K/yr

... CAPA activities. They should also have experience providing effective technical support and ... Previous experience with Class II or Class III medical device contract manufacturing complex ...

Controls Engineer

Concord, NC · On-site

$77K - $100K/yr

Concord, NC (Onsite) Duration: Long Term Contract Job Summary: We are seeking a Controls Engineer ... Support change control, deviation investigations, and CAPA activities Required Qualifications

Quality Engineer

Neenah, WI · On-site

$45 - $55/hr

Knowledge in quality tools and methodologies such as Root Cause Analysis, SPC, CAPA, APQP, PPAP ... Job Type & Location This is a Contract to Hire position based out of Neenah, WI. Pay and Benefits ...

MES Validation Engineer

Hillsboro, OR · Remote

$75 - $84/hr

... Contract (Possibility Of Extension) Pay Rate: $75/hr - $84/hr on W2 DOE Company Benefits: Medical ... Support change controls, deviations, CAPA investigations, and audit readiness activities. * Manage ...

Product Quality Engineer

San Jose, CA · On-site

$150K - $225K/yr

Partner with suppliers and contract manufacturers to oversee SMT processes, including SPI, AOI, and ... Deep knowledge of structured quality methodologies including 8D, CAPA, FMEA, SPC, Cpk, control ...

Product Quality Engineer

San Jose, CA · On-site

$150K - $225K/yr

Partner with suppliers and contract manufacturers to oversee SMT processes, including SPI, AOI, and ... Deep knowledge of structured quality methodologies including 8D, CAPA, FMEA, SPC, Cpk, control ...

Manufacturing & Industrial Engineer

Dublin, CA · On-site

$79K - $104K/yr

... contract opportunity for a Manufacturing & Industrial Engineer based in Dublin, CA (Onsite) with ... RCA), CAPA, and Industry 4.0 * Bachelor's degree in Manufacturing, Industrial Engineering, or a ...

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Contract Capa Engineer information

See salary details

$39K

$101.8K

$137.5K

How much do contract capa engineer jobs pay per year?

As of Jul 11, 2026, the average yearly pay for contract capa engineer in the United States is $101,752.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What is a Contract CAPA Engineer?

A Contract CAPA Engineer is a professional hired on a temporary or project basis to manage and oversee Corrective and Preventive Action (CAPA) processes within an organization, typically in regulated industries such as pharmaceuticals, medical devices, or manufacturing. Their primary responsibility is to investigate issues, identify root causes, and implement solutions to prevent recurrence of non-conformities. They ensure that CAPA processes meet regulatory standards and help maintain compliance with industry guidelines. Contract CAPA Engineers often work with cross-functional teams to drive continuous improvement and ensure product quality.

What are the key skills and qualifications needed to thrive as a Contract CAPA Engineer, and why are they important?

To excel as a Contract CAPA Engineer, you need a strong background in quality engineering, root cause analysis, and regulatory compliance, often supported by a degree in engineering or a related field. Expertise in CAPA management systems, quality management software (like TrackWise), and knowledge of ISO 13485 or FDA regulations are typically required. Strong analytical thinking, attention to detail, and effective communication skills help drive successful corrective and preventive actions. These competencies ensure regulatory compliance, minimize risks, and maintain product quality in regulated industries.

What are some common challenges faced by a Contract CAPA Engineer when implementing corrective and preventive actions across multiple client sites?

As a Contract CAPA Engineer, one of the main challenges is adapting to different organizational processes and quality management systems at each client site. Each company may have unique documentation standards, regulatory requirements, and communication protocols, which can complicate the investigation and resolution of quality issues. Balancing multiple projects, aligning stakeholders, and ensuring timely closure of CAPA actions while strictly adhering to compliance standards requires strong organizational and interpersonal skills. Successful engineers proactively build rapport with client teams and remain detail-oriented to ensure all corrective and preventive actions are both effective and audit-ready.

What jobs pay 4000 a week without a degree?

A Contract Capa Engineer typically earns a high weekly income through specialized skills in regulatory compliance and quality assurance in the pharmaceutical or biotech industries. Such roles often require technical expertise, industry certifications, and experience rather than a traditional degree, and they may involve contract or freelance work with flexible schedules. High-paying contract engineering roles can also include fields like software development, IT consulting, or skilled trades, which prioritize experience and skills over formal education.

What engineer makes $500,000 a year?

A Contract Capa Engineer typically does not earn $500,000 annually; such high salaries are more common in executive or specialized roles in the tech or finance industries. Senior engineers with extensive experience, advanced certifications, or leadership responsibilities may reach high six-figure incomes, but $500,000 is rare for standard engineering positions. Compensation depends on factors like location, company size, and industry demand.

What is the difference between Contract Capa Engineer vs Contract Failure Analysis Engineer?

AspectContract Capa EngineerContract Failure Analysis Engineer
Required CredentialsBachelor's in Engineering, Six Sigma, Root Cause AnalysisBachelor's in Engineering, Six Sigma, Root Cause Analysis
Work EnvironmentManufacturing, Aerospace, AutomotiveManufacturing, Aerospace, Automotive
Employer & Industry UsageQuality departments, Reliability teamsQuality departments, Reliability teams
Common Search & ComparisonYesYes

Both roles focus on quality and reliability, requiring similar certifications and working in manufacturing or aerospace industries. The Contract Capa Engineer primarily manages corrective and preventive actions to address issues, while the Contract Failure Analysis Engineer investigates root causes of failures. They often collaborate but serve distinct functions within quality assurance teams.

What engineers make $300,000 a year?

Senior contract Capa engineers with extensive experience, specialized skills in regulatory compliance, and advanced certifications can earn salaries approaching or exceeding $300,000 annually, especially in high-demand industries like aerospace or pharmaceuticals. Compensation often depends on factors such as location, company size, and project complexity.

What does a capa engineer do?

A CAPA (Corrective and Preventive Action) engineer is responsible for investigating quality issues, identifying root causes, and implementing corrective and preventive measures to ensure product compliance and safety. They often analyze data, collaborate with cross-functional teams, and use quality management tools to improve processes and prevent recurrence of problems.
More about Contract Capa Engineer jobs
What cities are hiring for Contract Capa Engineer jobs? Cities with the most Contract Capa Engineer job openings:
What are the most commonly searched types of Capa Engineer jobs? The most popular types of Capa Engineer jobs are:
What states have the most Contract Capa Engineer jobs? States with the most job openings for Contract Capa Engineer jobs include:
Infographic showing various Contract Capa Engineer job openings in the United States as of July 2026, with employment types broken down into 12% Locum Tenens, 82% Full Time, 1% Part Time, 1% Temporary, 3% Contract, and 1% Summer. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $101,752 per year, or $48.9 per hour.

Quality Engineer

Vantedge

San Jose, CA • On-site

$84K - $109K/yr

Full-time

Posted 29 days ago


Job description

Job Type
Full-time
Description
Quality Engineer
Full-time Permanent On-site
Salaried $85k - $105k
*We are not accepting candidates from third party agencies.
About Us:
Vantedge Medical is the premier metals-based med-tech solutions partner from concept to full-scale manufacturing. We are at the forefront of precision engineering and innovation, specializing in the development and manufacturing of vital components for medical markets such as Robotic Assisted Surgery, Orthopedics, Surgical Instruments, Dental, and more. Our teams work in unison, collaborating and problem-solving to serve the manufacturing needs of the top Medical Original Equipment Manufacturers (OEMs) around the globe. Making a difference in the lives of patients and their families drives us to go above and beyond every day. With a steadfast commitment to advancing medical technology, we take immense pride in the work we do - and have a lot of fun doing it.
About this Opportunity:
The Quality Engineer supports product quality, process improvement, and compliance activities within a contract manufacturing environment focused on precision metal components for medical devices. This role is responsible for driving quality performance through nonconformance management, root cause analysis, CAPA, MRB support, process monitoring, and continuous improvement initiatives.
The QE will work closely with Manufacturing Engineering, Inspection, Production, Supplier Quality, and Operations to identify quality issues, interpret inspection and measurement data, support containment and corrective actions, and improve process stability. A strong understanding of CNC machining processes, dimensional inspection, GD&T, and CMM measurement data is preferred to support effective troubleshooting and data-driven decision making.
Responsibilities:
  • Own and support investigation and documentation of nonconformances in systems such as ETQ, including defect analysis, containment, root cause, corrective action, and effectiveness verification.
  • Support timely MRB activities and complaint dispositions, including coordination with cross-functional teams, follow-up on actions, and documentation of decisions.
  • Lead root cause analysis using tools such as 5 Whys, Fishbone, Pareto analysis, process mapping, and data-driven problem solving.
  • Drive continuous improvement projects focused on defect reduction, rework reduction, process stability, inspection efficiency, and overall quality performance.
  • Partner with Manufacturing Engineering and Production to troubleshoot CNC machining-related quality issues, including dimensional variation, process drift, tooling-related defects, setup issues, and repeat nonconformances.
  • Review and interpret engineering drawings, specifications, GD&T requirements, inspection plans, and customer quality requirements.
  • Analyze dimensional inspection results, including CMM reports, to identify trends, measurement concerns, process capability gaps, and potential root causes.
  • Work with Inspection and CMM teams to support measurement data interpretation, inspection method reviews, and troubleshooting of questionable or inconsistent results.
  • Support First Article Inspection, validation activities, process qualification, and capability studies through dimensional review, data analysis, and documentation.
  • Support incoming inspection and supplier quality activities, including supplier issue investigation, SCAR support, and defect trend analysis.
  • Own and execute CAPA and continuous improvement actions to improve process control and prevent recurrence of quality issues.
  • Maintain and improve quality documentation, including procedures, work instructions, inspection checklists, control plans, and quality records.
  • Support internal and external audits, including preparation, evidence gathering, audit response, and corrective action follow-up.
  • Track, analyze, and report quality metrics such as defects, rework trends, yield, MRB aging, repeat issues, and process performance.
  • Knowledge of process capability, GR&R, measurement system analysis, and statistical process control.

Requirements
  • Bachelor's degree in Engineering, Manufacturing, Mechanical Engineering, Biomedical Engineering, or related technical field; equivalent technical experience may be considered.
  • 3+ years of experience in Quality Engineering, Manufacturing Engineering, or related engineering role in a manufacturing environment.
  • Strong understanding of engineering drawings, specifications, GD&T, and dimensional inspection methods.
  • Experience supporting nonconformance management, MRB, CAPA, root cause analysis, and corrective action implementation.
  • Working knowledge of CNC machining processes and common machining-related defects preferred.
  • Ability to interpret inspection and measurement data, including CMM reports, dimensional results, and trend data.
  • Strong problem-solving skills with the ability to connect measurement data to potential process, tooling, setup, material, or inspection method issues.
  • Experience using data analysis tools such as Excel and/or Minitab to identify trends and support decision making.
  • Strong communication skills and ability to work effectively with Manufacturing, Inspection, Engineering, Quality, and Operations teams.
  • Ability to manage multiple priorities and drive actions to completion in a fast-paced manufacturing environment.
  • Strong understanding of inspection planning, FAI requirements, validation support, and customer quality expectations.
  • Experience leading continuous improvement, Kaizen, Lean, Six Sigma, or defect reduction projects.

Preferred Qualifications
  • Experience in medical device manufacturing or another regulated industry.
  • Familiarity with ISO 13485, ISO 9001, and/or FDA 21 CFR Part 820 requirements.
  • Hands-on experience with CNC machining, precision metal components, sheet metal, or metal fabrication processes.
  • Experience reviewing CMM reports and working with inspection teams to troubleshoot measurement results.
  • Experience with ETQ, Visual ERP, or similar quality/ERP systems.