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Remote Quality Management System Jobs in Pennsylvania

Working knowledge of ISO quality management systems and quality auditing practices strongly preferred. * Experience collaborating across multiple business entities, functions, and global teams. What ...

... Quality Management System (QMS). This individual will be part of the broader Global Quality ... Willingness to travel globally up to 50%; role may be remote or site-based within the EU/UK. Pay ...

... for Onsite System Administrators on extended leave, providing remote backfill coverage when ... Adhears to Motorola and the Customer's Change management policies and procedures * Builds and ...

Quality Specialist

Pittsburgh, PA · On-site +1

$26.50 - $28.20/hr

Hybrid or remote work flexibility may be available based on organizational needs Make a Meaningful ... Obtain and maintain Quality Management (QM) certification. * Obtain and maintain Certified ...

Conduct quality assurance and rubric-based evaluations of AI-generated outputs. * Annotate data ... management consulting, corporate strategy, business transformation, or operations. * Experience ...

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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 Pennsylvania?

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

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

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

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

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

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

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

Infographic showing various Remote Quality Management System job openings in Pennsylvania as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.

GLP Quality Assurance Manager, Contract Research Organization

RPM ReSearch

Scranton, PA • Remote

$90K - $115K/yr

Full-time

Re-posted 8 days ago


Job description

Job Title: Quality Assurance Manager GLP


About the Role: The Quality Assurance Manager is responsible for managing daily QA activities and leading a small team of QA Associates. Reporting remotely to the QA Director, this role involves ensuring comprehensive audits of nonclinical and laboratory studies to verify compliance with protocols, Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP) (21 CFR Part 58 and Part 11), and applicable regulatory requirements. The QA Manager will also provide leadership, mentorship, and guidance to team members, driving quality assurance best practices within the facility.


Key Responsibilities:


  • Oversee and manage QA operations, ensuring thorough audits across various disciplines including non-clinical GLP studies, method validations, vendor qualifications, and equipment/software validations.
  • Act as the primary onsite QA leader, addressing day-to-day operational issues and compliance questions in the absence of the remote QA Director.
  • Conduct and oversee in-life, process, data, and facility audits to verify adherence to regulatory standards.
  • Lead audits and supervise QA investigations, ensuring robust documentation and timely resolution.
  • Maintain accurate, organized audit records and computerized documentation systems to effectively support audit activities and regulatory inspections.
  • Identify and communicate quality and compliance trends, proactively recommending and implementing process improvements.
  • Provide expert guidance and interpretations of GLP regulations, supporting the development and execution of corrective actions and SOP enhancements.
  • Serve as the primary point of contact during external client and regulatory audits, effectively representing the QA department.
  • Participate in project planning, risk assessments, and strategic implementation activities.
  • Develop and deliver GLP compliance training to facility staff, ensuring alignment with regulatory requirements and industry best practices.
  • Engage actively in professional development activities, including industry seminars, certification programs, and ongoing training.


Qualifications and Experience:


  • Bachelor's degree or higher in a scientific discipline or an equivalent combination of education and experience.
  • Minimum of 5 years of Quality Assurance experience, specifically within GLP-regulated environments, including experience in a supervisory or management role.
  • Professional certification such as RQAP-GLP (Registered Quality Assurance Professional-GLP) or ASQ-CQA (Certified Quality Auditor) strongly preferred.
  • Proven experience managing QA teams, leading audits, managing investigations, and independently hosting client or regulatory audits in a contract research organization
  • Familiarity with computerized system validation processes and requirements is advantageous.
  • Comprehensive understanding of the preclinical drug development process and associated regulatory expectations.


Skills and Competencies:


  • Strong leadership and team management capabilities.
  • Excellent organizational, problem-solving, and decision-making skills.
  • Exceptional communication and interpersonal abilities, able to effectively engage stakeholders across all organizational levels.
  • High level of detail orientation and ability to manage multiple tasks in a fast-paced environment.
  • Proficiency with Microsoft Office Suite and QA documentation management systems.


Join Our Team: If you're an experienced Quality Assurance professional passionate about leading teams and driving compliance excellence, we invite you to apply. Become a key leader in our organization, ensuring the integrity and quality of groundbreaking preclinical research.