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Remote Quality Management System Jobs in Florida

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ATR - QUALITY MANAGER ATR AMERICAS

Miami, FL · On-site +1

ATC Management system training: E-learning updates on iSpring & Docebo Mission#2 Support ATC ... remote working, generous paid time off...) Well-being / health (supplementary health & welfare ...

Airbus

ATR - QUALITY MANAGER ATR AMERICAS

Miami, FL · On-site +1

ATC Management system training: E-learning updates on iSpring & Docebo Mission#2 Support ATC ... remote working, generous paid time off...) Well-being / health (supplementary health & welfare ...

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.

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Remote Quality Management System information

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 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.

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 are the key skills and qualifications needed to thrive as a Remote Quality Management System (QMS) Specialist, and why are they important?

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.
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 July 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 100% Remote job distribution.
Director, Quality Assurance (Quality Systems)

Director, Quality Assurance (Quality Systems)

Syncromune

Fort Lauderdale, FL • On-site, Remote

$2/hr

Full-time

Posted 24 days ago

Job description

The Director, Quality Assurance (Quality Systems) will be primarily responsible for the implementation and maintenance of Phase-appropriate Quality processes and procedures in accordance with Good Industry Practices (GXP) for Syncromune's programs and products. The Director, QA (Quality Systems) will continue to build and cultivate GXP through organizational processes, including training programs and implementation and management of the electronic Quality Management System (eQMS) for the Drug division.
This role will serve as the primary interface and administrator for the Pharmaceutical Quality System (PQS) at Syncromune, with responsibility for establishing conformance to quality system requirements and ensuring system-level alignment with vendor, supplier, and CDMO quality activities. The role will lead the project team for the implementation of Syncromune's electronic Quality Management System (eQMS).
Principal Duties and Responsibilities include the following:
  • Lead administration and continuous improvement of Syncromune's global Pharmaceutical Quality System (PQS), focusing on quality processes and infrastructure that support the company's progression from startup to commercial operations. Enable compliant scalable growth across programs, sites and geographies in accordance with applicable regulations and standards.
  • Serve as Business Owner, Administrator, and Subject Matter Expert (SME) for the PQS and eQMS, including system level elements such as Document Control, Training, Deviation Management, Risk Management, CAPA, Change Management, Internal Audit, External Audit support, Vendor/Supplier Quality Systems Requirements, and the quality system components of Pharmacovigilance, Product Surveillance/ Complaints, and Recalls, while coordinating with Quality Management for operational and product-level activities.
  • Lead the evaluation, validation, implementation, and administration of an electronic Quality Management System (eQMS).
  • Manage the internal audit program.
  • Support and co-host GXP-focused audits, inspections, and assessments of Syncromune in partnership with Quality Management for auditors including, but not limited to:
    • Notified Bodies
    • Regulatory Authorities
    • Customers
    • Potential partners
  • Partner with Supplier Quality Management, Drug Development, and other internal functions to ensure alignment between PQS requirements and external manufacturing quality activities, maintaining clear process ownership between system-level QA and operational QA.
  • Build and develop a high performing team to support and advance Syncromune's business objectives.
Supervisory Responsibilities:
  • Direct reports: to be defined as the team grows.
Qualification Requirements:
Education:
  • Bachelor's degree in Life Sciences, Engineering, Medical Technology, or related scientific discipline required. Advanced degree preferred.
  • Professional certifications such as ASQ Certified Quality Auditor (CQA), Regulatory Affairs Certification (RAC), or other GXP certification a plus.
Experience:
  • Approximately 10 years of progressively responsible experience in quality assurance within the pharmaceutical or biotechnology industry.
  • At least 5 years of experience in a leadership or management role of a PQS with direct report responsibilities.
  • Positive experience in hosting and managing regulatory authority inspections and completing remediation activities.
  • Demonstrated success in leading the implementation of an electronic Quality Management System (eQMS).
Knowledge/Skill:
  • High degree of technology proficiency and fluency in Enterprise platforms.
  • Excellent project management skills with ability to manage multiple priorities in a fast-paced environment.
  • Commitment to integrity, ethics, and quality culture development.
  • Expertise in the US FDA Code of Federal Regulations and International Council on Harmonisation (ICH) as applicable to the pharmaceutical industry.
  • Exceptional leadership abilities with proven success building and motivating high-performing teams as well as turnaround teams.
  • Outstanding written and verbal communication skills with ability to influence at different functional and organizational levels both internally and with Vendor/ Contractor/ Supplier partners.
  • Demonstrated ability to work collaboratively across functions and across geographies, and skill in building effective partnerships for successful outcomes.
  • Proactive mindset, driving projects forward and providing recommendations to Leadership based on anticipated compliance challenges and industry trends.
Working Conditions:
Specify work environment:
  • The work environment is remote, and must be in a suitable location that allows focused output and video meetings.
  • Domestic travel may be required up to 10% of time.
  • This role requires a high degree of computer screen time and the individual will be regularly required to see, talk, hear, read, and type.

Syncromune is an Equal Opportunity Employer.
Expected US salary range: $210,000-$230,000
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to, the primary work location and the chosen candidate's relevant skills, experience, and education.
This position generally is eligible for cash incentive compensation, equity incentive compensation, and employee benefits under the Company's benefit plans.

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