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Remote Quality Management System Jobs in Florida

Refresco

Quality Systems Platform Manager

Tampa, FL · On-site +1

$89K - $123K/yr

Ensure proper change management and communication during system updates./ Data & Reporting * Develop dashboards and reporting tools to support quality performance monitoring and leadership visibility.

Verify Inc.

Certified Auditor

Sarasota, FL · Remote

Strong working knowledge of AS9100 and quality management systems. * Experience conducting supplier ... Conduct on-site and remote audits of suppliers to verify compliance with AS9100 requirements.

Verify

Certified Auditor

Sarasota, FL · Remote

Strong working knowledge of AS9100 and quality management systems. * Experience conducting supplier ... Conduct on-site and remote audits of suppliers to verify compliance with AS9100 requirements.

Verify

Certified Auditor

Sarasota, FL · Remote

Strong working knowledge of AS9100 and quality management systems. * Experience conducting supplier ... Conduct on-site and remote audits of suppliers to verify compliance with AS9100 requirements.

Phsorg

... management of the Plan's quality improvement and accreditation activities including NCQA ... Remote: Open to applicants in the United States, excluding CA, IL, ND, NY, WA, and WY. Hybrid: For ...

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Remote Quality Management System information

What is a remote quality management system?

A Remote Quality Management System (QMS) is a set of processes and tools that help organizations maintain quality standards for their products or services, even when teams are working remotely or from different locations. It typically involves digital platforms that allow for documentation, tracking, auditing, and continuous improvement activities to be conducted online. This enables companies to ensure compliance with industry regulations, improve efficiency, and maintain product or service quality without the need for on-site supervision. Remote QMS solutions are especially important for distributed teams or organizations with global operations.

What are the key skills and qualifications needed to thrive as a remote quality management system specialist?

To thrive as a Remote Quality Management System Specialist, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 9001), and experience with QMS implementation or auditing. Proficiency with digital QMS platforms (e.g., MasterControl, Veeva), document control systems, and relevant certifications like Certified Quality Auditor (CQA) are typically required. Strong attention to detail, analytical thinking, and clear communication skills help you excel in virtual collaboration and problem-solving. These skills ensure compliance, continuous improvement, and effective maintenance of quality standards in a remote work environment.

How does a remote quality management system professional typically collaborate with cross-functional teams to maintain compliance and quality standards?

As a Remote Quality Management System professional, collaboration with cross-functional teams—such as engineering, regulatory affairs, and production—is primarily facilitated through virtual meetings, shared documentation platforms, and project management tools. You will regularly coordinate with these teams to ensure that quality protocols are followed and that any process improvements or corrective actions are implemented efficiently. Clear communication and proactive follow-up are essential, especially when addressing compliance issues or preparing for audits. Despite working remotely, strong digital collaboration skills help maintain the integrity of the quality system and ensure organizational standards are consistently met.

What is the difference between Remote Quality Management System vs Remote Quality Assurance Specialist?

AspectRemote Quality Management SystemRemote Quality Assurance Specialist
CertificationsISO 9001, CQE, Six SigmaISO 9001, CQE, Six Sigma
Work EnvironmentSoftware-focused, process-orientedProduct-focused, testing and compliance
Industry UsageManufacturing, healthcare, techManufacturing, software, healthcare

Both roles often require similar certifications and work in industries emphasizing quality standards. However, Remote Quality Management System professionals focus on implementing and maintaining quality management software and processes, while Remote Quality Assurance Specialists concentrate on testing, inspections, and ensuring product compliance remotely.

What are the most commonly searched types of Quality Management System jobs in Florida?

The most popular types of Quality Management System jobs in Florida are:

What are popular job titles related to Remote Quality Management System jobs in Florida?

For Remote Quality Management System jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Remote Quality Management System jobs in Florida look for?

The top searched job categories for Remote Quality Management System jobs in Florida are:

What cities in Florida are hiring for Remote Quality Management System jobs?

Cities in Florida with the most Remote Quality Management System job openings:

Remote Quality Management System jobs near you
Infographic showing various Remote Quality Management System job openings in Florida as of September 2026, with employment types broken down into 56% Full Time, 13% Part Time, 2% Temporary, and 29% Contract. Highlights an 22% In-person, 2% Hybrid, and 76% Remote job distribution.

Quality Management System Specialist II (34866)

Jacksonville, FL • On-site, Remote

KLS MARTIN LP
Manufacturing • 1 - 5K employees
Learn more about KLS MARTIN LPexternal

Full-time

Posted 4 days ago

KLS Martin rating

9.1

Company rating: 9.1 out of 10

Based on 7 frontline employees who took The Breakroom Quiz

Job description

Job Summary

The Quality Management System Specialist II supports the development, implementation, maintenance, and continual improvement of the Quality Management System for medical devices. This role independently leads complex assigned QMS processes, evaluates quality system needs and risks, leads and supports audits, analyzes quality data, and partners with cross-functional teams to implement practical, compliant improvements. The position provides technical guidance and supports the development of lower-level QMS team members. This position requires flexible hours to support, monitor, and ensure regulatory compliance.  Additionally, the position will require both onsite and local remote work. 

Essential Functions, Duties, and responsibilities

  • Support the administration, maintenance, and continual improvement of the Quality Management System (QMS) at KLS. 
  • Lead implementation and monitoring of assigned QMS processes, procedures, quality plans, and improvement initiatives. 
  • Independently manage complex or multiple assigned QMS processes, records, projects, and action items.
  • Support recalls and advisory notices, including coordination of assigned activities.  
  • Maintains and applies current knowledge of FDA and international regulations, guidance, and standards applicable to company products (medical devices).
  • Plan, conduct, document, and follow up on risk-based process audits, and lead or support internal and external audits, including MDSAP audits. 
  • Coordinate audit evidence and capture accurate and timely minutes during audits, including observations, commitments, action owners, and due dates. 
  • Provide oversight of assigned document management activities and SharePoint libraries. 
  • Draft, review, and approve quality documents and procedures.  
  • Evaluate, document and communicate QMS impacts and recommend appropriate actions or controls. 
  • Provide oversight and support for assigned calibration and supplier control activities. 
  • Lead assigned corrective and preventive action, nonconformity, investigation, and effectiveness-check activities.
  • Lead planning and preparation of Management Review meetings. 
  • Analyze, trend, and communicate quality system data (i.e., NCMRs, Adverse Events, Supplier Ratings, etc.) 
  • Perform other related duties as assigned.

Education and Experience Requirements

  • Knowledge of device regulations and device applications ISO 13485, FDA, SOR 98 282
  • 4 year degree plus 3 to 5 years of work experience in a regulated industry or
  • 5 years of experience in regulated industry 
  • Proficient user of Microsoft Office applications, with intermediate knowledge of MS Excel

Knowledge, Skills, and Abilities

  • Maintains high integrity and confidentiality of company and department information 
  • Ability to work effectively with all levels of internal and external associates, customers, and colleagues 
  • Excellent interpersonal skills with the ability to effectively communicate at all levels internally as well as externally 
  • Ability to follow through on issues, make informed decisions that comply with policies and procedures, complete tasks and problem solve 
  • Ability to retrieve and interpret documentation 
  • Ability to work with minimal supervision 
  • Ability to manage multiple priorities  
  • Ability to work both independently and within a team environment 

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