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
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
Director, QualityComputer System Assurance (CSA),DataIntegrity(DI) & Digital Health Technologies ...
South San Francisco, CA · On-site +1
Senior Director, GxP Quality Systems Location: South San Francisco, CA - On-site 4 days per week ... Ensure that products and clinical trial activities and use of DHTs, wearable devices, remote ...
Director, QualityComputer System Assurance (CSA),DataIntegrity(DI) & Digital Health Technologies ...
South San Francisco, CA · On-site +1
Senior Director, GxP Quality Systems Location: South San Francisco, CA - On-site 4 days per week ... Ensure that products and clinical trial activities and use of DHTs, wearable devices, remote ...
SAP S/4HANA PP & QM
San Diego, CA · Remote
Role: SAP S/4HANA PP & QM with Pharma & GXP experience Location: Remote Duration: 6+ months ... Integration with serialization and compliance systems
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SAP S/4HANA PP & QM
San Diego, CA · Remote
Role: SAP S/4HANA PP & QM with Pharma & GXP experience Location: Remote Duration: 6+ months ... Integration with serialization and compliance systems
Remote (EST time) Duration: Long term Overview The Senior Configuration Specialist is responsible ... GxP and industry standards. Key Responsibilities * Lead system configuration and enhancements ...
New
Remote (EST time) Duration: Long term Overview The Senior Configuration Specialist is responsible ... GxP and industry standards. Key Responsibilities * Lead system configuration and enhancements ...
New
Perform system validation, testing, and documentation as per regulatory requirements. * Collaborate ... Familiarity with GxP compliance and validation processes. * Prior experience in an Agile ...
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Perform system validation, testing, and documentation as per regulatory requirements. * Collaborate ... Familiarity with GxP compliance and validation processes. * Prior experience in an Agile ...
Remote (EST time) Duration: Long term Note: We need resource in US and LATAM both the locations ... GxP and industry standards. Key Responsibilities * Lead system configuration and enhancements ...
New
Remote (EST time) Duration: Long term Note: We need resource in US and LATAM both the locations ... GxP and industry standards. Key Responsibilities * Lead system configuration and enhancements ...
New
Enterprise Product Data Lead - Life Sciences
Somerset, NJ · On-site +1
USA (Remote) Employment: Full-Time Eligibility: US Citizen or Green Card Holders Only Seeking a ... Implement and manage GxP validation for product data processes and systems (non-negotiable)
Enterprise Product Data Lead - Life Sciences
Somerset, NJ · On-site +1
USA (Remote) Employment: Full-Time Eligibility: US Citizen or Green Card Holders Only Seeking a ... Implement and manage GxP validation for product data processes and systems (non-negotiable)
USA (Remote) Employment: Full-Time Eligibility: US Citizen or Green Card Holders Only Seeking a ... Implement and manage GxP validation for product data processes and systems (non-negotiable)
Quick apply
USA (Remote) Employment: Full-Time Eligibility: US Citizen or Green Card Holders Only Seeking a ... Implement and manage GxP validation for product data processes and systems (non-negotiable)
Associate Director, Audit Management
Boston, MA · Remote
$154K - $231K/yr
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 ...
Associate Director, Audit Management
Boston, MA · Remote
$154K - $231K/yr
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 ...
Technical Product Owner (Remote)
Raleigh, NC · Remote
$66.50/hr
Adhering to external regulatory and statutory requirements (e.g., GxP, Sarbanes Oxley), as well as ... Optimizing data flow between upstream and downstream systems through secure and accurate ...
Technical Product Owner (Remote)
Raleigh, NC · Remote
$66.50/hr
Adhering to external regulatory and statutory requirements (e.g., GxP, Sarbanes Oxley), as well as ... Optimizing data flow between upstream and downstream systems through secure and accurate ...
... all system modifications and recording this according to GxP standards. * Handover of all ... Location: 100% Remote Start: 01.06.2026 Duration: till end of 2026 Capacity: 40 hours per week
... all system modifications and recording this according to GxP standards. * Handover of all ... Location: 100% Remote Start: 01.06.2026 Duration: till end of 2026 Capacity: 40 hours per week
Senior Engineering/ IT Program Manager
Ponce, PR · On-site +1
$113K - $113K/yr
Medical Device Manufacturing Company Duration: 12 Months Location: 100% Remote (Travel to Ponce ... Support manufacturing, digital transformation, and regulated systems * Work across Engineering ...
Senior Engineering/ IT Program Manager
Ponce, PR · On-site +1
$113K - $113K/yr
Medical Device Manufacturing Company Duration: 12 Months Location: 100% Remote (Travel to Ponce ... Support manufacturing, digital transformation, and regulated systems * Work across Engineering ...
Strong understanding of clinical trial operations and clinical systems workflows * Strong technical ... As needed, partner with QA, Val, and IT to ensure delivery aligns with GxP and validation ...
Strong understanding of clinical trial operations and clinical systems workflows * Strong technical ... As needed, partner with QA, Val, and IT to ensure delivery aligns with GxP and validation ...
Veeva Project Lead
Foster City, CA · On-site +1
Remote Duration: Full Time * Bachelor's degree preferably in Computer Science, Information ... across GxP-regulated systems. * 4+ years leading project execution and management including ...
Veeva Project Lead
Foster City, CA · On-site +1
Remote Duration: Full Time * Bachelor's degree preferably in Computer Science, Information ... across GxP-regulated systems. * 4+ years leading project execution and management including ...
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 ...
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 ...
Sr. Application Administrator (Remote) Southern Research + You Discover a career where your work ... They are responsible for the overall validated state of the system within a GxP Environment. The ...
Sr. Application Administrator (Remote) Southern Research + You Discover a career where your work ... They are responsible for the overall validated state of the system within a GxP Environment. The ...
Veeva QMS Consultant
Bloomington, IN · On-site +1
**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 ...
Veeva QMS Consultant
Bloomington, IN · On-site +1
**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 ...
Veeva QMS Consultant
Bloomington, IN · Remote
**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 ...
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Veeva QMS Consultant
Bloomington, IN · Remote
**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 ...
Veeva QMS Consultant
Bloomington, IN · On-site +1
**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 ...
Veeva QMS Consultant
Bloomington, IN · On-site +1
**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.
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.
Remote Gxp Systems information
See salary details
$36K - $43.3K
23% of jobs
$44.3K is the 25th percentile. Wages below this are outliers.
$43.3K - $50.5K
15% of jobs
$50.5K - $57.8K
6% of jobs
The median wage is $64.1K / yr.
$57.8K - $65.1K
7% of jobs
$65.1K - $72.4K
11% of jobs
$72.4K - $79.6K
7% of jobs
$82.9K is the 75th percentile. Wages above this are outliers.
$79.6K - $86.9K
11% of jobs
$86.9K - $94.2K
5% of jobs
$94.2K - $101.5K
8% of jobs
$101.5K - $108.7K
3% of jobs
$108.7K - $116K
2% of jobs
$36K
$68.4K
$116K
How much do remote gxp systems jobs pay per year?
What are the key skills and qualifications needed to thrive as a Remote GxP Systems Specialist, and why are they important?
What are some common challenges faced by professionals working in remote GxP systems roles, and how can they be addressed?
What is the difference between Remote Gxp Systems vs Remote Quality Assurance Specialist?
| Aspect | Remote Gxp Systems | Remote Quality Assurance Specialist |
|---|---|---|
| Certifications | GxP-related certifications (e.g., GxP, CSV) | ISO, GxP, or QA certifications |
| Work Environment | Regulated industries like pharma, biotech, medical devices | Manufacturing, software, or healthcare sectors |
| Industry Usage | Common in pharmaceutical and biotech companies | Widespread in healthcare, manufacturing, and software |
| Job Focus | Ensuring GxP compliance in systems and processes | Quality 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?
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Full-time
Posted 9 hours ago
Job description
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
- IDMP Compliance (Critical)
- Strong understanding of Identification of Medicinal Products (IDMP) standards
- Experience aligning product data with regulatory requirements
- GxP Validation Experience (Non-Negotiable)
- Hands-on experience with GxP-regulated systems
- Knowledge of validation processes (IQ/OQ/PQ, documentation, audits)
- Pharma Product Lifecycle Knowledge
- Understanding of:
- Discovery (compound/molecule)
- Clinical (IND)
- Regulatory (NDA/BLA)
- Commercial/Supply Chain (SKU)
- Understanding of:
- MDM Architecture Expertise
- Experience with federated or hub-of-hubs MDM architecture
- Ability to manage cross-domain master data integration
- System Integration Experience
- Integration with:
- ERP systems (SAP preferred)
- LIMS (Laboratory systems)
- Regulatory platforms
- Real-time or near real-time data synchronization
- Integration with:
- Data Modeling
- Ability to design complex product data models
- Experience handling product representation across multiple business contexts