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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 ...

Manufacturing Engineer

Melbourne, FL · On-site

$80 - $110/hr

Lead root cause analysis for defects and non-conformances, driving corrective and preventive actions (CAPA) to resolution and verifying effectiveness. * Manage analysis and disposition of units ...

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

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

Showing results 41-60

Capa information

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 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 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 August 2026, with employment types broken down into 90% Full Time, 4% Part Time, 5% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Senior Manager, Quality Systems

Arthrex GmbH

Naples, FL • On-site

$140 - $210/hr

Other

Medical, Dental, Vision, Life, Retirement

This job post has expired today. Applications are no longer accepted.


Job description

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Senior Manager, Quality Management Systems for our global headquarters in Naples, Florida. The Senior Manager, Quality Management Systems is responsible for leading, maintaining, and continuously improving the Arthrex Quality Management System (QMS) to ensure compliance with global regulatory requirements including FDA 21 CFR Part 820, ISO 13485, and other applicable standards. This role drives quality system effectiveness across core processes such as CAPA, change management, audits, document control, and training, while supporting inspection readiness and enabling business growth. This position requires a strategic leader who can balance compliance with operational efficiency, foster cross-functional collaboration, and elevate quality systems as a proactive enabler of organizational excellence. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.

Duties and Responsibilities: Quality System Leadership

Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO 13485, and global regulatory requirements

Establish and drive quality strategy, governance, and system performance metrics

Ensure alignment and scalability of quality systems across sites and functions

Core QMS Process Ownership

Provides oversight of critical quality system elements:

CAPA (Corrective and Preventive Actions)

Nonconformance (NCR) management

Document Management / Change control

Document and record control

Training and competency systems

Drive continuous improvement initiatives to enhance system effectiveness and reduce risk

Audit & Inspection Readiness

Lead and develop risk-based internal audit program and schedules

Ensure ongoing inspection readiness and lead FDA, notified body, and other regulatory inspections

Partner with site leadership to address audit findings and drive sustainable corrective actions

Compliance & Risk Management

Implement risk-based approaches to quality system monitoring and decision-making

Ensure timely identification, escalation, and resolution of compliance gaps

Monitor regulatory changes and drive system updates accordingly

Establish and monitor KPIs for QMS effectiveness (e.g., CAPA cycle time, audit trends, training compliance)

Leverage data analytics to identify trends, systemic issues, and improvement opportunities

Coordinate and support all QMS Management Review activities.

Lead, develop, and mentor a team of quality professionals

Build a culture of ownership, accountability, and continuous improvement

Drive capability development in auditing, compliance, and quality system processes

Education and Experience:
  • Bachelor’s degree required, preferably in an Engineering or Science discipline
  • 15 years related experience required in a medical device or similar regulated environment
  • 8 years of quality leadership experience required
  • Experience with global/multi-site quality systems
  • Experience supporting FDA or notified body inspections
Knowledge and Skill Requirements/Specialized Courses and/or Training:
  • Strong working knowledge of FDA QSMR, ISO 13485 and applicable international regulations.
  • Proven experience leading audits and regulatory inspections
  • Strong leadership and people development skills
  • Ability to influence cross-functional stakeholders at all levels
  • Strategic thinker with strong execution and problem-solving capabilities
  • Experience driving system improvements and transformation initiatives
Machine, Tools, and/or Equipment Skills:

Proficiency in the use of PC and programs, particularly Excel, Word (or equivalents if changed by the Company), PowerPoint, SAP or similar business software.

Reasoning Ability:

Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.

Mathematical Skills

Ability to comprehend and apply mathematical principles to the degree required to perform the job based upon job requirements.

Language and Communication Skills:

Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above. Ability to verbally communicate ideas and issues effectively to other team members and management. Ability to write and record data and information as required by procedures.

  • Medical, Dental and Vision Insurance
  • Company-Provided Life Insurance
  • Voluntary Life Insurance
  • Flexible Spending Account (FSA)
  • Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)
  • Matching 401(k) Retirement Plan
  • Annual Bonus
  • Wellness Incentive Program
  • Free Onsite Medical Clinics
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