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Contract Capa Engineer Jobs in Mount Prospect, IL

Actalent

Quality Engineer

Chicago, IL

$36 - $41/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... CAPA). * Lead and drive corrective actions across engineering, purchasing, manufacturing, and ... Job Type & Location This is a Contract to Hire position based out of Chicago, IL. Pay and Benefits ...

New

Actalent

Senior Supplier Quality Engineer

Elk Grove Village, IL · Hybrid

$55 - $70/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Partner with contract manufacturers to resolve manufacturing issues. * Coordinate directly with ... Provide sustaining engineering support, including root cause analysis, CAPA execution, and MRB ...

Actalent

Application Engineer

Barrington, IL

$31.25 - $36.05/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... CAPA) processes. * Adhere to company policies, safety standards, and quality requirements in all engineering and quotation activities. Job Type & Location This is a Contract to Hire position based ...

Actalent

Quality Engineer

Waukegan, IL · On-site

$42 - $46/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... CAPA) for non-conformances. * Analyze production and development data to identify trends, defects ... Job Type & Location This is a Contract position based out of Park City, IL. Pay and Benefits The ...

System One

Senior Document Control Coordinator

Cary, IL · Remote

$23 - $28.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Contract Compensation: $23-$28.25 Work Model: Hybrid - onsite and remote Hours: 40.0 Overview ... Coordinate Change Control, Nonconformance, and CAPA workflows to ensure timely progression, closure ...

System One

Senior Document Control Coordinator

Cary, IL · Remote

$23 - $28.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Contract Compensation: $23-$28.25 Work Model: Hybrid - onsite and remote Hours: 40.0 Overview ... Coordinate Change Control, Nonconformance, and CAPA workflows to ensure timely progression, closure ...

System One

Senior Document Control Coordinator

Cary, IL · Remote

$23 - $28.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Contract Compensation: $23-$28.25 Work Model: Hybrid - onsite and remote Hours: 40.0 Overview ... Coordinate Change Control, Nonconformance, and CAPA workflows to ensure timely progression, closure ...

System One

Senior Document Control Coordinator

Cary, IL · Remote

$23 - $28.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Contract Compensation: $23-$28.25 Work Model: Hybrid - onsite and remote Hours: 40.0 Overview ... Coordinate Change Control, Nonconformance, and CAPA workflows to ensure timely progression, closure ...

System One

Senior Document Control Coordinator

Cary, IL · Remote

$23 - $28.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Contract Compensation: $23-$28.25 Work Model: Hybrid - onsite and remote Hours: 40.0 Overview ... Coordinate Change Control, Nonconformance, and CAPA workflows to ensure timely progression, closure ...

System One

Senior Document Control Coordinator

Cary, IL · Remote

$23 - $28.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Contract Compensation: $23-$28.25 Work Model: Hybrid - onsite and remote Hours: 40.0 Overview ... Coordinate Change Control, Nonconformance, and CAPA workflows to ensure timely progression, closure ...

System One

Senior Document Control Coordinator

Cary, IL · Remote

$23 - $28.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Contract Compensation: $23-$28.25 Work Model: Hybrid - onsite and remote Hours: 40.0 Overview ... Coordinate Change Control, Nonconformance, and CAPA workflows to ensure timely progression, closure ...

System One

Senior Document Control Coordinator

Cary, IL · Remote

$23 - $28.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Contract Compensation: $23-$28.25 Work Model: Hybrid - onsite and remote Hours: 40.0 Overview ... Coordinate Change Control, Nonconformance, and CAPA workflows to ensure timely progression, closure ...

System One

Senior Document Control Coordinator

Cary, IL · Remote

$23 - $28.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Contract Compensation: $23-$28.25 Work Model: Hybrid - onsite and remote Hours: 40.0 Overview ... Coordinate Change Control, Nonconformance, and CAPA workflows to ensure timely progression, closure ...

CMA CGM

QHSE Healthcare Expert - Chicago, IL

Chicago, IL · On-site

$120K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... contract logistics and air, ocean, ground, and finished vehicle transport. That is why CEVA ... Monitor quality metrics, customer feedback, CAPA trends, audit results, training compliance, and ...

Nemera

Quality Engineer - Validation

Buffalo Grove, IL · On-site

$73K - $95K/yr

... and contract manufacturing. Nemera's manufacturing sites are located in the US, France, Germany ... Utilize CAPA problem solving techniques to reduce internal and external failures, selects sound ...

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Showing results 1-20

All JobsContract Capa Engineer JobsContract Capa Engineer Jobs in Mount Prospect, IL

Contract Capa Engineer information

See Mount Prospect, IL salary details

$38.7K

$101.1K

$136.6K

How much do contract capa engineer jobs pay per year?

As of Aug 20, 2026, the average yearly pay for contract capa engineer in Mount Prospect, IL is $101,090.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,500.00 and $115,700.00 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?

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 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 are popular job titles related to Contract Capa Engineer jobs in Mount Prospect, IL?

For Contract Capa Engineer jobs in Mount Prospect, IL, the most frequently searched job titles are:

What job categories do people searching Contract Capa Engineer jobs in Mount Prospect, IL look for?

The top searched job categories for Contract Capa Engineer jobs in Mount Prospect, IL are:

What cities near Mount Prospect, IL are hiring for Contract Capa Engineer jobs?

Cities near Mount Prospect, IL with the most Contract Capa Engineer job openings:

Contract Capa Engineer jobs near you

Validation Engineer

Sterling Engineering Inc.

Buffalo Grove, IL

$55 - $65/hr

Full-time

Re-posted yesterday

Job description

Validation Engineer – Injection Molding
Location: Buffalo Grove Il
Hire Type: Contract
Shift: 1st Shift | Monday–Friday
Compensation: $55–$65/hour
Overview
We are seeking a hands-on Validation Engineer with experience supporting plastic injection molding manufacturing within a regulated environment. This individual will lead equipment, process, and manufacturing validations while partnering closely with Manufacturing Engineering, Quality, Operations, and Automation teams to ensure new and existing molding processes meet quality and regulatory requirements.
The ideal candidate will have experience developing and executing IQ/OQ/PQ protocols, validating injection molding equipment and processes, troubleshooting manufacturing issues, and supporting continuous improvement initiatives in a medical device, pharmaceutical, or similarly regulated manufacturing environment.
Key Responsibilities
Develop, execute, and approve IQ, OQ, and PQ validation protocols for injection molding equipment, automation, and manufacturing processes.
Lead validation activities for new product introductions, equipment installations, process transfers, and manufacturing changes.
Validate injection molding processes including process windows, machine qualifications, tooling, auxiliary equipment, and automation systems.
Perform risk assessments utilizing FMEA and other risk management tools.
Investigate validation failures, process deviations, and nonconformances while implementing effective corrective actions.
Analyze process capability, statistical data, and validation results to ensure robust manufacturing processes.
Collaborate with Manufacturing Engineering to optimize molding parameters, cycle times, and process performance.
Support mold qualifications, process characterization, and production readiness activities.
Prepare validation reports, technical documentation, protocols, and supporting engineering documentation.
Participate in equipment FAT/SAT activities when applicable.
Ensure validation documentation complies with FDA, ISO 13485, GMP, and internal quality standards.
Support CAPA investigations, change control activities, and regulatory audits.
Work cross-functionally with Engineering, Quality, Production, Tooling, Automation, and Regulatory Affairs teams.

Qualifications
Bachelor's degree in Engineering or related technical discipline.
3+ years of validation engineering experience within a manufacturing environment.
Hands-on experience validating plastic injection molding processes and equipment.
Strong knowledge of IQ/OQ/PQ methodologies and validation lifecycle documentation.
Experience with process validation, equipment qualification, and manufacturing process development.
Familiarity with scientific molding principles and process optimization.
Experience with statistical analysis tools and process capability studies.
Knowledge of risk management methodologies including PFMEA/FMEA.
Strong technical writing and documentation skills.

Preferred Qualifications
Medical device, pharmaceutical, or highly regulated manufacturing experience.
Experience with automated manufacturing equipment, robotics, vision systems, and PLC-controlled equipment.
Knowledge of FDA 21 CFR Part 820, ISO 13485, GMP, and GAMP guidance.
Experience with injection mold qualification, tooling validation, and mold transfers.
Familiarity with cleanroom manufacturing environments.
Experience supporting CAPA, NCR investigations, and change control processes.
Working knowledge of Minitab or other statistical software.

Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.