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Capa Engineer Jobs in Florida (NOW HIRING)

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Validation Engineer Location: Jackson, FL Duration: 1.5-year contract Hours per week: 40+ We are ... Experience with risk assessments, FMEA, and deviation/CAPA management * Proficient in authoring and ...

21891-1 Quality Assurance Engineer Level 2, Orlando, FL (Secret/Ability to Obtain) Description ... CAPA) implementation, guaranteeing reliability and regulatory compliance. Drive continuous ...

... Engineering Change Requests, and Non-Conforming Materials Reports, CAPA Reports, Complaint investigations and Supplier Corrective Action Reports to ensure operational support and compliance.

Sr. Quality Engineer

Gainesville, FL · On-site

$80K - $108K/yr

The Sr. Quality Engineer serves as the Quality owner for a defined orthopedic joint product ... CAPA and root cause analysis * Change control systems * Familiarity with GD&T and inspection ...

Manufacturing Engineer Location: Orlando, FL 32826 Pay Rate: $40.00-55.00/hour Shift: 1st ... Perform root cause analysis (RCCA/CAPA) and drive issues to closure * Support incoming, in-process ...

Sr. Quality Engineer

Gainesville, FL · On-site

$79K - $108K/yr

Sr. Quality Engineer Department: Quality Employment Type: Full Time Location: Gainesville, FL ... CAPA and root cause analysis * Change control systems * Familiarity with GD&T and inspection ...

Job #218833 Chipton-Ross is seeking a Quality Assurance Engineer for a contract opportunity in ... action (CAPA) implementation, guaranteeing reliability and regulatory compliance. * Drive ...

Manufacturing Engineering Job Category: Scientific/Technology All Job Posting Locations ... CAPA's, etc). Utilizes cross functional collaboration with safety, quality, and operations to meet ...

Quality Engineer - Manufacturing

Seminole, FL · On-site

$64K - $83K/yr

... for CAPA/SCAR implementation. * Lead implementations of improvement plans and actions that shall ... Bachelors in Engineering (Industrial/Mechanical/Materials or Electronics) and 3+ years of Quality ...

Manufacturing Engineering Job Category: Scientific/Technology All Job Posting Locations ... CAPA's, etc). Utilizes cross functional collaboration with safety, quality, and operations to meet ...

Manufacturing Engineering Job Category: Scientific/Technology All Job Posting Locations ... CAPA's, etc). * Utilizes cross functional collaboration with safety, quality, and operations to ...

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Capa Engineer information

See Florida salary details

$29.1K

$76K

$102.8K

How much do capa engineer jobs pay per year?

As of Jul 5, 2026, the average yearly pay for capa engineer in Florida is $76,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,800.00 and $87,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Capa Engineer position, and why are they important?

To thrive as a CAPA Engineer, you need a solid background in quality engineering, root cause analysis, and process improvement, typically supported by a degree in engineering or a related technical field. Familiarity with CAPA management systems, quality standards such as ISO 13485 or ISO 9001, and tools like Six Sigma or FMEA is highly valuable. Strong problem-solving abilities, attention to detail, and effective communication skills distinguish top performers in this role. These competencies ensure effective identification, documentation, and resolution of quality issues, helping organizations maintain regulatory compliance and deliver high-quality products.

What is a CAPA Engineer job?

A CAPA (Corrective and Preventive Action) Engineer is responsible for identifying, investigating, and resolving quality issues in manufacturing or engineering processes. They analyze root causes of defects, implement corrective measures, and develop preventive strategies to ensure compliance with industry regulations. CAPA Engineers work closely with cross-functional teams to improve product quality, streamline processes, and maintain regulatory compliance. They also document findings, track action plans, and support continuous improvement initiatives to reduce future risks.

What are the main daily responsibilities of a CAPA Engineer?

A CAPA Engineer's daily responsibilities typically include investigating potential or actual nonconformities, conducting root cause analyses, and developing corrective and preventive action plans to resolve and prevent future issues. They also collaborate closely with cross-functional teams such as manufacturing, quality assurance, and regulatory affairs to ensure solutions are practical and compliant with industry standards. Additionally, CAPA Engineers monitor the progress and effectiveness of implemented actions, prepare documentation for audits, and participate in continuous process improvement initiatives. This role is crucial for maintaining the highest quality standards and ensuring compliance in regulated industries such as medical devices or pharmaceuticals.

What are the most commonly searched types of Capa Engineer jobs in Florida? The most popular types of Capa Engineer jobs in Florida are:
Infographic showing various Capa Engineer job openings in Florida as of June 2026, with employment types broken down into 87% Full Time, 4% Part Time, 3% Contract, and 6% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $76,039 per year, or $36.6 per hour.

Manufacturing Engineer -Medical Devices (IQ/OQ/PQ Focus)

Hirekeyz Inc

Gainesville, FL • On-site

$66K - $85K/yr

Contractor

Posted 21 days ago


Job description

Title: Manufacturing Engineer – Medical Devices (IQ/OQ/PQ Focus)

Location: Gainesville, FL (On-site)

Duration: Long Term Contract

Position Summary:

Our client is seeking a highly skilled Manufacturing Engineer with a strong background in the medical device industry and extensive experience in IQ/OQ/PQ validation activities. The successful candidate will ensure that manufacturing processes meet regulatory requirements, improve efficiency, and maintain the highest quality standards.

Key Responsibilities:

  • Lead and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for new and existing equipment and processes.
  • Develop and maintain process validation protocols, reports, and associated documentation in compliance with ISO 13485, FDA 21 CFR Part 11, and GMP requirements.
  • Collaborate with Quality, R&D, and Production teams to ensure smooth transfer of new products into manufacturing.
  • Conduct root cause analysis and implement corrective and preventive actions (CAPA) for process deviations.
  • Optimize manufacturing processes to improve yield, reduce cost, and maintain compliance.
  • Support equipment selection, procurement, and installation.
  • Ensure adherence to environmental, health, and safety (EHS) guidelines.

Qualifications:

  • Bachelor’s degree in Mechanical, Manufacturing, Industrial Engineering, or related field.
  • Experience: 6-8 years
  • 6+ years of experience in manufacturing engineering within the medical device industry.
  • Proven experience with IQ/OQ/PQ execution and documentation.
  • Strong understanding of validation requirements under FDA and ISO regulations.
  • Excellent problem-solving and documentation skills.