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Remote Gxp Systems Jobs (NOW HIRING)

Remote Overview Product Master Data Management (MDM) is a highly cross-functional and critical ... GxP Validation Experience (Non-Negotiable) * Hands-on experience with GxP-regulated systems

GxP quality systems, including GCP/GLP audit processes * Regional/international knowledge of GCP ... Remote-Eligible Flex Eligibility Status: In this Remote-Eligible role, you can choose to be ...

Remote Duration: Long-Term Contract Role Overview Design, configure, and maintain LIMS (version 12 ... systems Ensure compliance with laboratory and business processes Required Skills Strong knowledge ...

**This role is open to remote candidates who have availability to travel to the client in Bloomington ... Ensure compliance with industry regulations (e.g., GxP, FDA, ISO standards) through proper system ...

**This role is open to remote candidates who have availability to travel to the client in Bloomington ... Ensure compliance with industry regulations (e.g., GxP, FDA, ISO standards) through proper system ...

**This role is open to remote candidates who have availability to travel to the client in Bloomington ... Ensure compliance with industry regulations (e.g., GxP, FDA, ISO standards) through proper system ...

QMS Team Lead or Architect

Port Henry, NY · On-site +1

$56.50 - $77.50/hr

Remote Duration: 6+ Months Contract Team Lead or Architect (exp with Trackwise is a must which is a ... Experience with Computer Systems Validation for GxP-relevant systems and associated activities i.e.

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Remote Gxp Systems information

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$36K

$68.4K

$116K

How much do remote gxp systems jobs pay per year?

As of Jun 7, 2026, the average yearly pay for remote gxp systems in the United States is $68,438.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,500.00 and $85,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote GxP Systems Specialist, and why are they important?

To thrive as a Remote GxP Systems Specialist, you need a strong understanding of GxP regulations (such as GMP, GLP, and GCP), quality assurance principles, and experience in life sciences or pharmaceutical environments, often supported by a relevant degree. Familiarity with validated computerized systems, compliance software (e.g., Veeva Vault, TrackWise), and certifications like Certified Quality Auditor (CQA) are highly valuable. Excellent attention to detail, problem-solving skills, and strong remote communication abilities help you effectively manage compliance tasks and collaborate with global teams. These skills ensure that regulated systems meet stringent quality standards and regulatory requirements, minimizing compliance risks for the organization.

What are some common challenges faced by professionals working in remote GxP systems roles, and how can they be addressed?

One common challenge in remote GxP systems roles is maintaining clear communication and coordination across distributed teams, especially when ensuring compliance with regulatory standards. Professionals often need to navigate time zone differences, secure data handling, and remote validation processes. These challenges can be addressed by using robust project management tools, regular virtual meetings, and secure collaboration platforms. Establishing clear documentation and protocols also helps ensure compliance and smooth workflows while working remotely.

What is the difference between Remote Gxp Systems vs Remote Quality Assurance Specialist?

AspectRemote Gxp SystemsRemote Quality Assurance Specialist
CertificationsGxP-related certifications (e.g., GxP, CSV)ISO, GxP, or QA certifications
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, or healthcare sectors
Industry UsageCommon in pharmaceutical and biotech companiesWidespread in healthcare, manufacturing, and software
Job FocusEnsuring GxP compliance in systems and processesQuality assurance and process validation

Remote Gxp Systems roles focus on maintaining GxP compliance within regulated industries, while Remote Quality Assurance Specialists concentrate on overall quality processes across various sectors. Both roles require similar certifications and often overlap in industry usage, but their primary focus differs: Gxp Systems emphasizes system compliance, whereas QA Specialists focus on quality assurance practices.

What are Remote GxP Systems?

Remote GxP systems refer to software or technological platforms used to manage Good Practice (GxP) compliance activities—such as Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and Good Manufacturing Practice (GMP)—from a remote or offsite location. These systems enable organizations in regulated industries, like pharmaceuticals and biotechnology, to securely access, monitor, and control quality and compliance data without being physically present on site. Remote GxP systems often include features for electronic records, audit trails, and real-time collaboration to ensure regulatory standards are consistently met, even when teams are distributed.
More about Remote Gxp Systems jobs
What cities are hiring for Remote Gxp Systems jobs? Cities with the most Remote Gxp Systems job openings:
What are the most commonly searched types of Gxp Systems jobs? The most popular types of Gxp Systems jobs are:
What states have the most Remote Gxp Systems jobs? States with the most job openings for Remote Gxp Systems jobs include:
Infographic showing various Remote Gxp Systems job openings in the United States as of May 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $68,438 per year, or $32.9 per hour.

Job description

Role: Product MDM Specialist (Pharma Domain)
Location: Remote
Overview
Product Master Data Management (MDM) is a highly cross-functional and critical domain within pharma. The product master serves as a GxP-regulated asset,
Core Responsibilities
  • Manage and design Product Master Data across the full pharmaceutical lifecycle
  • Ensure GxP compliance and validation for all product data processes
  • Enable data availability and consistency across business functions (R&D, Regulatory, Manufacturing, Commercial)
  • Support real-time data integration with downstream enterprise systems
  • Design scalable data models representing product entities across multiple domains
  • Collaborate with cross-functional teams to align product data standards and usage
Mandatory Skills
  1. IDMP Compliance (Critical)
    • Strong understanding of Identification of Medicinal Products (IDMP) standards
    • Experience aligning product data with regulatory requirements
  2. GxP Validation Experience (Non-Negotiable)
    • Hands-on experience with GxP-regulated systems
    • Knowledge of validation processes (IQ/OQ/PQ, documentation, audits)
  3. Pharma Product Lifecycle Knowledge
    • Understanding of:
      • Discovery (compound/molecule)
      • Clinical (IND)
      • Regulatory (NDA/BLA)
      • Commercial/Supply Chain (SKU)
  4. MDM Architecture Expertise
    • Experience with federated or hub-of-hubs MDM architecture
    • Ability to manage cross-domain master data integration
  5. System Integration Experience
    • Integration with:
      • ERP systems (SAP preferred)
      • LIMS (Laboratory systems)
      • Regulatory platforms
    • Real-time or near real-time data synchronization
  6. Data Modeling
    • Ability to design complex product data models
    • Experience handling product representation across multiple business contexts