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Capa Jobs in Florida (NOW HIRING)

CAPA (Corrective and Preventive Actions) Nonconformance (NCR) management Document Management / Change control Document and record control Training and competency systems Drive continuous improvement ...

New

Sr. Quality Engineer

Fort Lauderdale, FL · On-site

$84K - $114K/yr

Know GD&T, Solidworks (read drawings), root cause analysis and CAPA * Can move NC from beginning to end, can come up with solutions * Exp with Critical to Quality Attributes (CTQ) - tolerances on ...

... CAPA closure rate, and warranty cost drivers. · Partner with Project Engineering and Product Quality to translate field learnings into design improvements, reliability enhancements, service ...

... CAPA closure rate, and warranty cost drivers. · Partner with Project Engineering and Product Quality to translate field learnings into design improvements, reliability enhancements, service ...

Showing results 41-60

Capa information

What are the typical daily responsibilities of a CAPA specialist?

A CAPA specialist is responsible for investigating quality issues, identifying root causes, and implementing corrective and preventive actions to ensure ongoing compliance and product integrity. Their typical day involves reviewing nonconformance reports, collaborating with cross-functional teams, documenting findings, and tracking the progress of CAPA initiatives using specialized software. CAPA specialists also prepare reports for audits and may facilitate meetings to drive continuous improvement activities. This role often requires balancing multiple projects and deadlines in a regulated environment, making organizational and communication skills crucial for success.

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

To thrive as a CAPA (Corrective and Preventive Action) specialist, you need expertise in quality management systems, root cause analysis, and compliance with industry standards, typically backed by a degree in engineering, life sciences, or a related field. Familiarity with CAPA software, regulatory frameworks (such as ISO 13485 or FDA 21 CFR Part 820), and document control systems is essential. Strong analytical thinking, attention to detail, and effective communication skills are vital soft skills for this role. These skills ensure effective problem-solving and sustained compliance, which are essential for maintaining product quality and meeting regulatory requirements.

What is a CAPA?

A CAPA (Corrective and Preventive Action) job involves identifying, investigating, and resolving quality issues in industries like manufacturing, healthcare, and pharmaceuticals. CAPA professionals analyze root causes of defects or process failures and implement corrective actions to prevent recurrence. They ensure compliance with regulatory standards, document findings, and improve overall quality management systems. Their role is critical in maintaining product safety, efficiency, and regulatory adherence.

What are the most commonly searched types of Capa jobs in Florida? The most popular types of Capa jobs in Florida are:
What cities in Florida are hiring for Capa jobs? Cities in Florida with the most Capa job openings:
Infographic showing various Capa job openings in Florida as of July 2026, with employment types broken down into 87% Full Time, 6% Part Time, 2% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution.

Principal, Corporate Quality Engineer

chromalloy

Tampa, FL • On-site

Other

Posted 17 days ago


Chromalloy rating

8.1

Company rating: 8.1 out of 10

Based on 26 frontline employees who took The Breakroom Quiz

151st of 487 rated machine equipment manufacturers


Job description

We are hiring a Principal Corporate Quality Engineer to advance our enterprise Quality Management System across a global network of manufacturing and repair sites. In this deployable, strategic role, you'll standardize quality processes, lead complex investigations, strengthen supplier quality, support PMA Continued Operational Safety (COS), and serve as our enterprise eQMS administrator and SME.

What You'll Do
  • Drive standardization and continuous improvement of quality systems, processes, and tools across manufacturing, repair, and PMA operations.
  • Deploy to sites facing capacity constraints, customer escalations, audits, or business-critical projects to stabilize performance and implement sustainable corrective actions.
  • Lead complex investigations and RCCA/CAPA using structured problem-solving (8D, 5 Why, Fishbone, FTA, statistical methods); coach site teams on investigation discipline.
  • Support PMA COS activities—partnering with Airworthiness, Engineering, and Site Quality on field events, risk assessments, and lessons learned deployment.
  • Execute enterprise supplier quality strategy through audits, assessments, risk reviews, and corrective action closure.
  • Own eQMS implementation, configuration, governance, workflows, and network adoption.
  • Support internal, supplier, customer, and regulatory audits.
What You Bring
  • Bachelor's degree in Engineering (Aerospace, Mechanical, Industrial, Quality, or related).
  • 8+ years in aerospace quality, manufacturing/repair station quality, quality systems, or supplier quality.
  • Strong working knowledge of AS9100, ISO 9001, Nadcap, FAA Part 145, and FAA Part 21 PMA.
  • Proven track record leading investigations, RCCA/CAPA, audits, and cross-site quality projects.
  • Ability to influence results across sites without direct authority.
  • Willingness to travel extensively up to 75% globally (must have active passport or the ability to obtain)
Preferred Qualifications
  • PMA Continued Operational Safety (COS) program experience.
  • Enterprise eQMS deployment and administration experience.
  • Background across both aerospace manufacturing and repair/MRO.
  • ASQ CQE, CQA, CMQ/OE, Lean Six Sigma Green/Black Belt, or Lead Auditor certification.

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