... GxP systems. • Implement and monitor strict QC processes for all deployments, including peer review, QA validation, and change control sign-off prior to production release. • Oversee all ...
... GxP systems. • Implement and monitor strict QC processes for all deployments, including peer review, QA validation, and change control sign-off prior to production release. • Oversee all ...
The Position The GxP Laboratory Systems Administrator position is responsible for supporting the development and delivery of various laboratory systems including daily system administration of GxP ...
The Position The GxP Laboratory Systems Administrator position is responsible for supporting the development and delivery of various laboratory systems including daily system administration of GxP ...
Oversee all operating system deployments and in-place upgrades (IPU) for validated systems, ensuring consistent execution under GxP change control. * Manage patching cycles, including Microsoft and ...
Oversee all operating system deployments and in-place upgrades (IPU) for validated systems, ensuring consistent execution under GxP change control. * Manage patching cycles, including Microsoft and ...
The Position The GxP Laboratory Systems Administrator position is responsible for supporting the development and delivery of various laboratory systems including daily system administration of GxP ...
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The Position The GxP Laboratory Systems Administrator position is responsible for supporting the development and delivery of various laboratory systems including daily system administration of GxP ...
Oversee all operating system deployments and in-place upgrades (IPU) for validated systems, ensuring consistent execution under GxP change control. * Manage patching cycles, including Microsoft and ...
Oversee all operating system deployments and in-place upgrades (IPU) for validated systems, ensuring consistent execution under GxP change control. * Manage patching cycles, including Microsoft and ...
Job Title: GxP Project Manager Location: Bay Area, CA Duration: 6+ months with possible of ... Experience managing Computer System Validation (CSV) projects. * Experience delivering projects ...
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Job Title: GxP Project Manager Location: Bay Area, CA Duration: 6+ months with possible of ... Experience managing Computer System Validation (CSV) projects. * Experience delivering projects ...
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Senior Manager, GxP Systems & Validation Verona, Wisconsin, United States
Verona, WI · On-site
$145 - $165/hr
Senior Manager, GxP Systems & Validation Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by ...
Senior Manager, GxP Systems & Validation Verona, Wisconsin, United States
Verona, WI · On-site
$145 - $165/hr
Senior Manager, GxP Systems & Validation Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by ...
Senior GxP Engineer, Endpoint Engineer
Cambridge, MA · On-site
$130.80 - $209.40/hr
Oversee all operating system deployments and in‑place upgrades (IPU) for validated systems, ensuring consistent execution under GxP change control. * Manage patching cycles, including Microsoft and ...
Senior GxP Engineer, Endpoint Engineer
Cambridge, MA · On-site
$130.80 - $209.40/hr
Oversee all operating system deployments and in‑place upgrades (IPU) for validated systems, ensuring consistent execution under GxP change control. * Manage patching cycles, including Microsoft and ...
Partner with QA and Regulatory teams to support GxP computerized systems, including Quality Management Systems (QMS) and regulated documentation platforms. * Gather and document business requirements ...
Partner with QA and Regulatory teams to support GxP computerized systems, including Quality Management Systems (QMS) and regulated documentation platforms. * Gather and document business requirements ...
Maintain the GxP Systems Inventory and User Access Management, creating and maintaining roles and privileges, including activation and/or deactivation of users * Support configuration management of ...
Maintain the GxP Systems Inventory and User Access Management, creating and maintaining roles and privileges, including activation and/or deactivation of users * Support configuration management of ...
Provide Tier 1+ support for GxP and non-GxP systems, endpoint devices, business applications, and user access issues. * Troubleshoot and resolve incidents affecting GxP-regulated applications ...
Provide Tier 1+ support for GxP and non-GxP systems, endpoint devices, business applications, and user access issues. * Troubleshoot and resolve incidents affecting GxP-regulated applications ...
This role is ideal for a professional with minimum 2 years experience administering and supporting laboratory computerized systems in a GxP regulated environment.The candidate manages day-to-day ...
This role is ideal for a professional with minimum 2 years experience administering and supporting laboratory computerized systems in a GxP regulated environment.The candidate manages day-to-day ...
Specialist, IT - GxP Technical Support
Cranbury, NJ · On-site
$54K - $72K/yr
Provide Tier 1+ support for GxP and non-GxP systems, endpoint devices, business applications, and user access issues. * Troubleshoot and resolve incidents affecting GxP-regulated applications ...
Specialist, IT - GxP Technical Support
Cranbury, NJ · On-site
$54K - $72K/yr
Provide Tier 1+ support for GxP and non-GxP systems, endpoint devices, business applications, and user access issues. * Troubleshoot and resolve incidents affecting GxP-regulated applications ...
Specialist, IT GxP Technical Support
Cranbury, NJ · On-site
$54K - $82K/yr
Provide Tier 1+ support for GxP and non-GxP systems, endpoint devices, business applications, and user access issues. * Troubleshoot and resolve incidents affecting GxP-regulated applications ...
Specialist, IT GxP Technical Support
Cranbury, NJ · On-site
$54K - $82K/yr
Provide Tier 1+ support for GxP and non-GxP systems, endpoint devices, business applications, and user access issues. * Troubleshoot and resolve incidents affecting GxP-regulated applications ...
Senior Computer Systems Validation Engineer
San Carlos, CA · Hybrid
$164K - $190K/yr
The Senior Computer Systems Validation (CSV) Engineer is responsible for leading validation activities for cloud based GxP systems to ensure they meet regulatory, quality, and operational ...
Senior Computer Systems Validation Engineer
San Carlos, CA · Hybrid
$164K - $190K/yr
The Senior Computer Systems Validation (CSV) Engineer is responsible for leading validation activities for cloud based GxP systems to ensure they meet regulatory, quality, and operational ...
Max Rate $$.$$$.$$ Onsite Princeton NJ 1. hands-on experience in Computer System Validation as a Validation Analyst/Lead working experience in GxP systems. 2. Hands on Applications knowledge on GxP ...
Max Rate $$.$$$.$$ Onsite Princeton NJ 1. hands-on experience in Computer System Validation as a Validation Analyst/Lead working experience in GxP systems. 2. Hands on Applications knowledge on GxP ...
System Test and Validation Lead
Miami, FL · On-site
$95 - $145/hr
... GxP systems as a Senior Consultant, Regulatory, Risk, and Compliance. This role supports system validation strategy, audit readiness, CAPA management, and risk-based compliance activities across ...
System Test and Validation Lead
Miami, FL · On-site
$95 - $145/hr
... GxP systems as a Senior Consultant, Regulatory, Risk, and Compliance. This role supports system validation strategy, audit readiness, CAPA management, and risk-based compliance activities across ...
System Test and Validation Lead
Westlake, TX · On-site +1
Lead end-to-end validation activities for GxP systems, including validation plans, IQ/OQ/PQ protocols, summary reports, user requirements specifications, functional specifications, design ...
System Test and Validation Lead
Westlake, TX · On-site +1
Lead end-to-end validation activities for GxP systems, including validation plans, IQ/OQ/PQ protocols, summary reports, user requirements specifications, functional specifications, design ...
System Test and Validation Lead
Jericho, NY · On-site +1
Lead end-to-end validation activities for GxP systems, including validation plans, IQ/OQ/PQ protocols, summary reports, user requirements specifications, functional specifications, design ...
System Test and Validation Lead
Jericho, NY · On-site +1
Lead end-to-end validation activities for GxP systems, including validation plans, IQ/OQ/PQ protocols, summary reports, user requirements specifications, functional specifications, design ...
System Test and Validation Lead
Richmond, VA · On-site +1
Lead end-to-end validation activities for GxP systems, including validation plans, IQ/OQ/PQ protocols, summary reports, user requirements specifications, functional specifications, design ...
System Test and Validation Lead
Richmond, VA · On-site +1
Lead end-to-end validation activities for GxP systems, including validation plans, IQ/OQ/PQ protocols, summary reports, user requirements specifications, functional specifications, design ...
GXP Systems information
See salary details
$46K - $55.7K
5% of jobs
$55.7K - $65.5K
6% of jobs
$65.5K - $75.2K
12% of jobs
$76.6K is the 25th percentile. Wages below this are outliers.
$75.2K - $84.9K
11% of jobs
$84.9K - $94.6K
12% of jobs
The median wage is $98.2K / yr.
$94.6K - $104.4K
12% of jobs
$104.4K - $114.1K
11% of jobs
$121.1K is the 75th percentile. Wages above this are outliers.
$114.1K - $123.8K
10% of jobs
$123.8K - $133.5K
9% of jobs
$133.5K - $143.3K
10% of jobs
$143.3K - $153K
4% of jobs
$46K
$102.1K
$153K
How much do gxp systems jobs pay per year?
What is a GxP Systems?
A GxP Systems job involves managing, implementing, and maintaining computerized systems that comply with regulatory standards like FDA, EMA, and other industry guidelines. These systems support Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP) in industries such as pharmaceuticals and biotechnology. Responsibilities typically include validation, documentation, compliance assessments, and ensuring data integrity. The role requires knowledge of regulatory requirements, IT systems, and quality assurance principles.
What are the main responsibilities of someone working in GxP Systems?
Professionals in GxP Systems are responsible for implementing, validating, and maintaining computerized systems used in regulated environments, ensuring these systems comply with industry regulations such as FDA, EMA, or ICH guidelines. Their daily tasks typically include managing system validation projects, performing risk assessments, handling documentation, supporting audits, and collaborating with IT, Quality Assurance, and business users. The role also involves troubleshooting issues, keeping up with regulatory updates, and providing user training. Given the critical nature of compliance in life sciences and healthcare, attention to detail and cross-functional teamwork are crucial for success.
What are the key skills and qualifications needed to thrive in the GxP Systems position, and why are they important?
To thrive in a GxP Systems role, strong knowledge of GxP (Good Practice) regulations, computer system validation (CSV), and IT compliance are essential, usually supported by a degree in a scientific or technical field. Familiarity with quality management systems (QMS), 21 CFR Part 11, audit processes, and common validation and documentation tools is typically required, and certifications such as PMP or GAMP can be advantageous. Excellent problem-solving, attention to detail, and communication skills help professionals manage highly regulated projects and collaborate across departments. These capabilities are vital to ensure technology systems meet regulatory standards, reduce compliance risks, and maintain data integrity in regulated environments.
What cities are hiring for Gxp Systems jobs?
Cities with the most 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 Gxp Systems jobs?
States with the most job openings for Gxp Systems jobs include:
What job categories do people searching Gxp Systems jobs look for?
The top searched job categories for Gxp Systems jobs are:

Moderna rating
9.2
Based on 10 frontline employees who took The Breakroom Quiz
5th of 86 rated pharmaceutical
Job description
Moderna is a leading biopharmaceutical company focused on mRNA technology. The GxP Endpoint Engineer will be responsible for managing the SCCM environment to support GxP operations, ensuring compliance with quality assurance standards and maintaining a validated infrastructure.
Responsibilities:
• Own and manage the SCCM GxP environment, ensuring all configurations, task sequences, and deployments comply with QA guidance and validation standards.
• Design, document, and maintain standard operating procedures (SOPs) and configuration baselines specific to GxP systems.
• Implement and monitor strict QC processes for all deployments, including peer review, QA validation, and change control sign-off prior to production release.
• Oversee all operating system deployments and in-place upgrades (IPU) for validated systems, ensuring consistent execution under GxP change control.
• Manage patching cycles, including Microsoft and third-party updates, coordinating with QA, GxP Support, and Application Owners to plan, validate, and document each phase.
• Create and maintain deployment and compliance reports, providing transparency to QA and management on patch and configuration status across the GxP fleet.
• Collaborate with Application Owners and GxP Support teams to coordinate deployments, validate installations, and resolve environment-specific issues.
• Develop and publish Knowledge Base (KB) articles and operational guides for support teams and end users related to SCCM processes, patching, and imaging.
• Serve as the escalation point for packaging, deployment, and compliance failures impacting GxP systems.
• Partner with QA to participate in audits, provide system validation evidence, and ensure documentation accuracy across all controlled activities.
• Contribute to the ongoing evolution of how SCCM operates in Moderna’s validated environment, helping to design scalable, compliant frameworks for automation and reporting.
Qualifications:
Required:
• 6+ years of experience in SCCM/MECM administration, including task sequences, OSD, collections, compliance baselines, and application deployments.
• Proven experience managing systems in regulated (GxP, GMP, or validated) environments, adhering to QA and change control processes.
• Strong understanding of QA, QC, and validation principles within endpoint management.
• Experience performing in-place upgrades (IPUs), PXE imaging, and patch management in controlled environments.
• Hands-on experience with third-party patching tools and their integration with SCCM.
• Familiarity with ServiceNow for change control, approval workflows, and incident tracking.
• Ability to produce comprehensive documentation, SOPs, and KBs aligned with GxP validation standards.
• Strong collaboration skills to engage with QA, Application Owners, and Support teams on validation, testing, and incident management.
Preferred:
• Analytical mindset and attention to detail to ensure every configuration and deployment meets compliance and performance expectations.
• Bachelor’s degree in Information Technology, Computer Science, or a related technical discipline.
• Experience with co-managed SCCM + Intune environments in validated systems.
• Familiarity with JAMF Pro for cross-platform GxP compliance awareness.
• Knowledge of GAMP 5 validation principles or equivalent regulated system frameworks.
• Prior experience generating QA audit documentation or participating in validation testing for endpoint systems.
• Understanding of Windows OS lifecycle management and modern endpoint management best practices.
• Certifications such as Microsoft Endpoint Manager, ITIL, or CompTIA Security+.
• A proactive, methodical approach to process improvement and compliance-driven automation.
Company:
Moderna Therapeutics is a biotechnology company that develops medicines and vaccines based on messenger RNA (mRNA) technology. Founded in 2010, the company is headquartered in Cambridge, USA, with a team of 1001-5000 employees. The company is currently Late Stage.
About Moderna
Sourced by ZipRecruiter
In just over a decade, Moderna has evolved from a research-focused company in the messenger RNA (mRNA) field to a leading enterprise with a diverse clinical portfolio of vaccines and therapeutics. With a strong intellectual property portfolio and state-of-the-art manufacturing capabilities, Moderna collaborates with global partners to advance groundbreaking science and achieve rapid scaling of production. Notably, Moderna's mRNA platform has enabled the development of therapies for various diseases, including infectious diseases, immuno-oncology, and cardiovascular conditions. Recognized as a top biopharmaceutical employer, Moderna fosters an inclusive and smoke-free work environment. The company is dedicated to equal employment opportunities and non-discrimination, ensuring that all employees and applicants are treated with respect and without bias based on factors like race, gender, religion, disability, or sexual orientation. Moderna is also committed to providing reasonable accommodations for individuals with disabilities, in accordance with applicable laws. To know more, visit www.modernatx.com.
Industry
Manufacturing
Company size
501 - 1,000 Employees
Headquarters location
Cambridge, MA, US
Year founded
2010