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Contract Capa Engineer Jobs in Andover, MN (NOW HIRING)

Cypress HCM

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 ...

TiltEdge Solutions LLC

Manufacturing Engineer

Wyoming, MN · On-site

$45 - $55/hr

Wyoming, MN Duration: 3 Months contract & Extendable Key Responsibilities: * Plan, coordinate, and ... 8D, and CAPA, and ensure closure of corrective actions. * Manage pre-production pilot builds ...

Actalent

Quality Engineer

Anoka, MN

$95K - $120K/yr

Strong knowledge of FDA regulations, risk management, CAPA, SPC, FMEA, and root cause analysis ... Medical device CDMO or contract manufacturing experience. * CQE, Lean Six Sigma, or related quality ...

Laborie

Supplier Quality Engineer

Plymouth, MN · On-site

$95K - $105K/yr

... contract manufacturer evaluation procedures, use of risk management tools, and auditing of current ... and CAPA fulfillment. * Participate in product design and development projects as needed and ...

VitalPath

Quality Engineer II

Saint Paul, MN · On-site

$69K - $87K/yr

... contract manufacturing partner that delivers high-quality complex catheter solutions around the ... CAPA activities. Work Location/Schedule * This position requires the employee to be onsite at our ...

Actalent

Supplier Quality Engineer

Hamel, MN

$40 - $53/hr

Ensure suppliers develop, implement, and execute effective Corrective and Preventive Action (CAPA ... This is a Contract position based out of Hamel, MN. Pay and Benefits The pay range for this ...

Actalent

Supplier Quality Engineer

Hamel, MN · On-site

$40 - $53/hr

Ensure suppliers develop, implement, and execute effective Corrective and Preventive Action (CAPA ... This is a Contract position based out of Hamel, MN. Pay and Benefits The pay range for this ...

Actalent

Supplier Quality Engineer

Hamel, MN · On-site

$40 - $53/hr

Ensure suppliers develop, implement, and execute effective Corrective and Preventive Action (CAPA ... This is a Contract position based out of Hamel, MN. Pay and Benefits The pay range for this ...

Actalent

Quality Technician

Maple Grove, MN · On-site

$19 - $25/hr

Support engineers in failure analysis and CAPA activities, including serving as a CAPA project ... Job Type & Location This is a Contract position based out of Maple Grove, MN. Pay and Benefits The ...

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Showing results 1-20

All JobsContract Capa Engineer JobsContract Capa Engineer Jobs in Andover, MN

Contract Capa Engineer information

See Andover, MN salary details

$40.3K

$105.1K

$142K

How much do contract capa engineer jobs pay per year?

As of Aug 30, 2026, the average yearly pay for contract capa engineer in Andover, MN is $105,055.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,700.00 and $120,300.00 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 Andover, MN?

For Contract Capa Engineer jobs in Andover, MN, the most frequently searched job titles are:

What job categories do people searching Contract Capa Engineer jobs in Andover, MN look for?

The top searched job categories for Contract Capa Engineer jobs in Andover, MN are:

What cities near Andover, MN are hiring for Contract Capa Engineer jobs?

Cities near Andover, MN with the most Contract Capa Engineer job openings:

Contract Capa Engineer jobs near you
Infographic showing various Contract Capa Engineer job openings in Andover, MN as of August 2026, with employment types broken down into 86% Full Time, 9% Part Time, and 5% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $105,055 per year, or $50.5 per hour.

Quality Engineer - Medical Devices

Stark Pharma Solutions Inc

Minneapolis, MN • On-site

$75K - $97K/yr

Contractor

Re-posted 10 days ago

Job description

Job Title: Quality Assurance Engineer – Medical Devices

Location: Northwest Minneapolis Metro Area

Type: 6-Month Contract-to-Hire

Job Summary

Seeking a Quality Assurance Engineer to support quality systems, manufacturing operations, CAPA, validation, audits, and DHF activities within a medical device environment. This role will partner cross-functionally to ensure compliance with FDA and ISO standards throughout the product lifecycle.

Key Responsibilities

  • Manage CAPAs, nonconformances, root cause investigations, and change controls
  • Support IQ/OQ/PQ validation activities and review quality documentation
  • Maintain DHF documentation and support product lifecycle activities
  • Review batch records, work orders, and manufacturing documentation for GMP compliance
  • Support incoming inspection, supplier quality, and audit readiness
  • Analyze quality metrics and drive continuous improvement initiatives
  • Support customer complaint investigations and PLM system updates

Required Qualifications

  • Bachelor’s degree in Engineering, Life Sciences, or related field
  • 5+ years of medical device quality or design assurance experience
  • Strong knowledge of FDA 21 CFR 820, ISO 13485, and ISO 14971
  • Experience with CAPA, NCs, DHF, audits, and validation activities
  • Familiarity with PLM systems such as Windchill, Agile, or Propel