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Remote Quality Management System Jobs in Pennsylvania

YO AI Labs

AI Consulting Expert - Remote

Philadelphia, PA · Remote

$100 - $200/hr

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

Solventum

CPO Quality

Pittsburgh, PA · On-site +1

Lead product lifecycle management from ideation through implementation and optimization. * Ensure ... Remote USA Travel: No travel required Relocation Assistance: Not authorized Must be legally ...

Healthcare

CPO Quality

Pittsburgh, PA · Remote

Lead product lifecycle management from ideation through implementation and optimization. * Ensure ... Remote USA Travel: No travel required Relocation Assistance: Not authorized Must be legally ...

Premier Orthopaedics

Coder I - Remote

West Chester, PA · On-site +1

$17.75 - $23.75/hr

Utilizes practice management system (PMS) to accurately account for demographics and services ... high-quality, patient-focused care. Philadelphia Hand to Shoulder Center (PHSC), a division of ...

The Pennsylvania State University

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... Advising clients on water quality management, conservation strategies, and water reuse initiatives.

NETZSCH Group

Compliance & Contract Manager

Exton, PA · On-site +1

Develop, maintain, and continuously improve the Compliance Management System, Risk Management ... Collaborate closely with Legal, Finance, HR, Procurement, Sales, IT, Quality Management, and ...

TAD PGS, Inc

Quality Auditor

Philadelphia, PA · On-site +1

Perform regularly scheduled qualifying, surveillance and sampling, both on-site, in-plant or remote ... with department managers. * Recommend improved systems, policies, and procedures for the ...

TAD PGS, Inc.

Quality Auditor

Philadelphia, PA · On-site +1

Perform regularly scheduled qualifying, surveillance and sampling, both on-site, in-plant or remote ... with department managers. * Recommend improved systems, policies, and procedures for the ...

Thermo Systems

Engineering Manager

Fort Washington, PA · On-site +1

$150K - $170K/yr

Lead adherence to Thermo Systems Quality Management System (QMS) and engineering standards. * Promote continuous improvement in engineering workflows and project execution methodologies. * Review ...

Thermo Systems

Engineering Manager

Duquesne, PA · On-site +1

$150K - $170K/yr

Lead adherence to Thermo Systems Quality Management System (QMS) and engineering standards. * Promote continuous improvement in engineering workflows and project execution methodologies. * Review ...

Harris

$19/hr

Communicates frequently with the Identity Manager. * Monitors remote team quality results ... Demonstrated understanding of a variety of hospital health information systems. * Strong Excel ...

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All JobsQuality Management System JobsRemote Quality Management System JobsRemote Quality Management System Jobs in Pennsylvania

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:

Remote Quality Management System jobs near you
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.

Manager, GLP Compliance

Cabaletta Bio Inc.

Philadelphia, PA • On-site, Remote

Full-time

PTO

Re-posted 16 days ago

Job description

Job Description - Manager, GLP Compliance- Remote- Philadelphia, PA
Philadelphia, PA
Cabaletta Bio (Nasdaq: CABA) is a clinical-stage biotechnology company focused on developing and launching the first curative targeted cell therapies designed specifically for patients with autoimmune diseases. The CABA™ platform encompasses two complementary strategies which aim to advance the discovery and development of engineered T cell therapies with the potential to become deep and durable, perhaps curative, treatments for a broad range of autoimmune diseases. The lead CARTA (Chimeric Antigen Receptor T cells for Autoimmunity) strategy is prioritizing the development of rese-cel, a 4-1BB-containing fully human CD19-CAR T cell investigational therapy. Rese-cel is currently being evaluated in the RESET™ (REstoring SElf-Tolerance) clinical development program spanning multiple therapeutic areas, including rheumatology, neurology and dermatology. Cabaletta Bio's headquarters and labs are located in Philadelphia, PA. For more information, please visit www.cabalettabio.com and connect with us on LinkedIn.
Uniquely Differentiated. Rapid. Elegant.
At Cabaletta, we are driven by the shared mission of developing cures, where a patients' own cells are used to fight disease. We are building a culture grounded in the knowledge that successful cures can be achieved for patients if every member of the Cabaletta is focused on the success of the team. To nurture this, we make an active commitment to the well-being and continuous growth of each employee who joins the team. In this way, we are not only working to improve the lives of patients, but of everyone involved. #CabalettaCrew.
We're proud to be a Great Place to Work-Certified™ company! #GPTWcertified Check out what our employees say makes working here so great: Working at Cabaletta Bio Inc | Great Place to Work®
Manager, GLP Compliance
Reporting to the Senior Director of GCP Compliance, the GLP Quality Control Specialist is responsible for supporting and maintaining compliance with Good Laboratory Practice (GLP) requirements across laboratory operations that support clinical development. This role is responsible for developing, implementing, and maintaining quality control processes that promote regulatory compliance, data integrity, and operational excellence. The Manager, GLP Compliance partners closely with cross-functional teams to assess, monitor, and continuously improve laboratory quality systems, ensuring laboratory activities are conducted in accordance with applicable regulatory requirements, company policies, and industry best practices.
Responsibilities
GLP Compliance
  • Ensure internal, central, and local clinical laboratory activities are conducted in compliance with applicable Good Laboratory Practice (GLP) regulations, GCP requirements where applicable, company procedures, and industry standards.
  • Monitor regulatory updates and emerging industry trends to ensure continued compliance and implementation of best practices.
  • Support quality oversight of laboratory activities throughout the clinical study lifecycle.

Quality Control & Quality Systems
  • Develop, implement, maintain, and continuously improve laboratory quality control processes and procedures.
  • Perform routine quality reviews and assessments to identify compliance gaps and opportunities for process improvement.
  • Support the implementation of corrective and preventive actions (CAPAs) to address identified issues.

Audits & Inspection Readiness
  • Assist in planning, coordinating, and conducting internal laboratory audits to evaluate compliance with GLP requirements.
  • Support regulatory inspections and external audits by preparing documentation, coordinating responses, and tracking commitments through completion.
  • Participate in inspection readiness activities and support continuous audit preparedness.

Documentation Management
  • Review, maintain, and oversee controlled laboratory documentation, including Standard Operating Procedures (SOPs), protocols, reports, specifications, and quality records.
  • Ensure laboratory documentation is accurate, complete, current, and compliant with GLP requirements and internal Quality Management System (QMS) procedures.
  • Ensure laboratory-related Trial Master File (TMF) documentation is complete, accurate, and filed in a timely manner.

Training & Compliance
  • Support the development and delivery of GLP training for laboratory personnel.
  • Provide guidance on quality processes, documentation standards, and regulatory expectations.
  • Promote a culture of quality, compliance, and continuous learning across laboratory operations.

Risk Management
  • Assist in identifying, assessing, and documenting quality and compliance risks related to laboratory activities.
  • Support the development and implementation of risk mitigation strategies.
  • Monitor quality trends and recommend improvements to reduce compliance risk.

Continuous Improvement
  • Participate in continuous improvement initiatives that enhance laboratory quality systems, operational efficiency, and regulatory compliance.
  • Collaborate with cross-functional stakeholders to implement process improvements and share best practices.
  • Support quality metrics, trend analysis, and effectiveness monitoring.

Cross-Functional Collaboration & Communication
  • Partner with Clinical Operations, Translational Medicine, Regulatory Affairs, and laboratory vendors to support quality initiatives.
  • Communicate quality-related issues, compliance status, risks, and improvement opportunities to management and key stakeholders.
  • Foster collaborative relationships that support high-quality laboratory operations and inspection readiness.

Required Qualifications
  1. Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Life Sciences, or a related scientific discipline.
  2. Minimum of two (2) years of hands-on experience in biopharmaceutical operations, laboratory operations, technical operations, quality operations, or a related GxP environment.
  3. Minimum of one (1) year of experience supporting Document Control within a GxP environment, including experience with controlled documents, electronic document management systems, and Trial Master File (TMF) documentation.
  4. Working knowledge of Good Laboratory Practice (GLP), Good Clinical Practice (GCP), ICH guidelines, and applicable FDA regulations.
  5. Understanding of Quality Management Systems (QMS) and electronic document management systems.
  6. Familiarity with Trial Master File (TMF) requirements and laboratory documentation best practices.
  7. Cell and Gene Therapy experience is preferred.
  8. Strong organizational skills with exceptional attention to detail and the ability to manage multiple priorities.
  9. Excellent written, verbal, and interpersonal communication skills.
  10. Demonstrated ability to work independently while collaborating effectively within cross-functional teams.
  11. Proficiency in Microsoft Office applications and electronic quality management systems.
  12. Commitment to continuous learning, professional development, and promoting a culture of quality and compliance.

Our name - Cabaletta - is derived from the operatic term that represents a rapid, repetitive, and technically challenging section of an operatic aria, designed to showcase the skills of the lead singer. Analogously, Cabaletta Bio strives to achieve rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the driver of specific autoimmune diseases without the need for long-term immunosuppression.
For more information, please visit https://www.cabalettabio.com/join-our-crew
Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans.
Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law.
Cabaletta Bio, Inc. does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Cabaletta, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Cabaletta shall not be responsible to any individual or entity for any payment relating to any form of fee or compensation.
And, if a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Cabaletta has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm.
#LI-REMOTE

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