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Contract Capa Engineer Jobs (NOW HIRING)

Dawar Consulting, Inc.

Validation Engineer

Tucson, AZ

$39 - $42/hr

Job Duration: Long Term Contract (Possibility Of Extension & FT Conversion) Rate: $39-$42/hr on W2 ... Experience supporting audits, CAPA activities, and process improvement initiatives * Familiarity ...

BioPhase Solutions

Validation Engineer

Los Angeles, CA · On-site

$115K/yr

... contract development and manufacturing organization. Salary: $100-115k+/year depending on ... Familiarity with deviation investigations, CAPA processes, and audit responses. * Basic vendor ...

Talent Groups

Supplier Quality Engineer

Waltham, MA · Hybrid

This hybrid contract role will focus on supplier qualification, supplier audits, corrective action ... Hands-on experience with SCAR, NCMR, CAPA, Root Cause Analysis * Familiarity with FDA and GMP ...

Alphatec Spine

Quality Engineer, Sustaining

Carlsbad, CA

$74.70K - $96.50K/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 ...

Ageatia Global Solutions

Portsmouth NH ,03801 Duration: 06 Months Contract (REMOTE) * MES Engineer is responsible for ... Participate in RCAs as MES representative * Assist with completion of CAPA actions * Participates ...

Kymanox

(Contract) CQV Engineer

Charlottesville, VA · On-site

The (Contract) CQV Engineer will have direct experience in Commissioning, Qualification or ... Generate, investigate, and resolve deviations; support change control and CAPA processes in ...

Kymanox

(Contract) CQV Engineer

Kenosha, WI

The (Contract) CQV Engineer will have direct experience in Commissioning, Qualification or ... Generate, investigate, and resolve deviations; support change control and CAPA processes in ...

Kymanox

(Contract) CQV Engineer

Indianapolis, IN

The (Contract) CQV Engineer will have direct experience in Commissioning, Qualification or ... Generate, investigate, and resolve deviations; support change control and CAPA processes in ...

Cypress HCM

Senior Quality Engineer

New Hope, MN · On-site

$91.90K - $124.70K/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 ...

Stark Pharma Solutions Inc

Controls Engineer

Concord, NC · On-site

$77.80K - $100.60K/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

Intellectt INC

Controls Engineer

North Haven, CT · On-site

$83.10K - $107.40K/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 ...

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All JobsContract Capa Engineer Jobs

Contract Capa Engineer information

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$39K

$101.8K

$137.5K

How much do contract capa engineer jobs pay per year?

As of May 28, 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 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 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 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.

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:
What job categories do people searching Contract Capa Engineer jobs look for? The top searched job categories for Contract Capa Engineer jobs are:
Contract Capa Engineer jobs near you
Infographic showing various Contract Capa Engineer job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 1% Internship, 3% Full Time, 83% Part Time, 2% Temporary, and 10% Contract. Highlights an 83% Physical, and 17% Remote job distribution, with an average salary of $101,752 per year, or $48.9 per hour.
Validation Engineer

Validation Engineer

Dawar Consulting, Inc.

Tucson, AZ

$39 - $42/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 5 days ago

Job description

Our client, a world leader in biotechnology and life sciences, is looking for a “Validation Engineer" based out in Tucson, AZ.

Job Duration: Long Term Contract (Possibility Of Extension & FT Conversion)

Rate: $39-$42/hr on W2

Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

Job Summary:

We are seeking a proactive Validation Engineer with 1–3 years of experience in a regulated manufacturing environment such as medical devices, pharmaceuticals, or biotechnology. This on-site role focuses on process validation activities to ensure compliance with FDA, ISO, cGMP, and internal quality standards while supporting continuous improvement and operational excellence.

Key Responsibilities:
  • Develop, write, review, and execute process validation and process verification protocols and reports
  • Conduct risk assessments and support validation strategies for new and existing manufacturing processes
  • Analyze and interpret validation data to ensure compliance with regulatory and internal quality requirements
  • Collaborate with Manufacturing, Quality, and Design Transfer teams to resolve validation issues and implement corrective actions
  • Support process optimization and continuous improvement initiatives to improve quality and efficiency
  • Ensure compliance with FDA, ISO, cGMP, and internal regulatory standards
  • Maintain validation documentation, traceability records, and audit-ready files
  • Provide training and guidance on validation processes, procedures, and compliance requirements
Required Qualifications:
  • Bachelor’s degree in Engineering, Life Sciences, or related field
  • 1–3 years of experience in validation within a regulated manufacturing environment
  • Knowledge of process validation principles, verification techniques, and industry standards
  • Familiarity with FDA regulations, ISO standards, and cGMP requirements
  • Strong technical writing, analytical, and problem-solving skills
  • Excellent communication and cross-functional collaboration abilities
Preferred Experience:
  • Medical device, biotech, or pharmaceutical industry experience
  • Experience supporting audits, CAPA activities, and process improvement initiatives
  • Familiarity with risk assessments and validation documentation practices
Key Skills:

Process Validation | Process Verification | FDA Compliance | cGMP | ISO Standards | Validation Protocols | Risk Assessments | CAPA | Technical Writing | Root Cause Analysis | Quality Systems | Continuous Improvement | Manufacturing Validation | Regulatory Compliance

If interested, please send us your updated resume at hr@dawarconsulting.com/kavitha@dawarconsulting.com .