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Gxp Systems Jobs (NOW HIRING)

ACL Digital

GxP System admininstrator

San Mateo, CA · On-site

... systems. Responsibilities include leading validation activities (authoring, execution, and review of protocols), project management and administering both GxP and business applications. Key ...

Vaxcyte

Manager, IT Quality & Compliance

San Carlos, CA · On-site +1

This is a hands-on role requiring expertise in IT system validation, auditing, vendor management, and compliance operations within a regulated GxP environment. Essential Functions: IT Validation ...

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$46K

$102.1K

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How much do gxp systems jobs pay per year?

As of Jun 23, 2026, the average yearly pay for gxp systems in the United States is $102,067.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $125,000.00 per year, depending on experience, location, and employer.

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 is a GxP Systems job?

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 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.

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Gxp Systems jobs near you
Infographic showing various Gxp Systems job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 2% Internship, 15% As Needed, 3% Full Time, 73% Contract, and 6% Nights. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $102,067 per year, or $49.1 per hour.
GxP Systems Engineer

GxP Systems Engineer

Preferred Staffing & Recruiting, LLC

Norwood, MA • On-site

Other

Posted 27 days ago

Job description

Job Description:

We are seeking an experienced GxP Systems Engineer to support the design, deployment, integration, and management of Digital Quality Automation Systems and laboratory instrumentation within GMP-regulated environments. The ideal candidate will have strong experience working with laboratory automation systems, analytical instruments, system integrations, validation, and GxP compliance.

Key Responsibilities:
  • Support implementation, optimization, maintenance, and upgrades of Digital Quality Automation Systems such as Hamilton Venus, Scitara DLX, and analytical laboratory instrumentation
  • Collaborate with business analysts, software engineers, automation teams, and digital stakeholders throughout the system lifecycle
  • Translate system, equipment, and data integration requirements into scalable digital lab solutions within GMP environments
  • Support integration of laboratory systems with connected digital platforms, robotics, automation systems, and future AI initiatives
  • Manage and support change controls, SOPs, work instructions, KB articles, and regulatory documentation
  • Ensure systems comply with GxP, GAMP, and FDA regulatory requirements
  • Participate in system validation, implementation, maintenance, and inspection readiness activities
  • Support troubleshooting, optimization, and continuous improvement of laboratory digital workflows
  • Collaborate with cross-functional teams including Quality, Validation, IT, and Laboratory Operations
  • Participate in internal and external audits as Digital Quality Systems SME
Required Qualifications:
  • Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field
  • 5+ years of experience supporting life sciences analytical instruments and laboratory systems within GMP environments
  • Experience with Digital Quality Automation Systems such as Hamilton Venus, Scitara DLX, or similar laboratory automation platforms
  • Strong understanding of laboratory systems integration, digital workflows, and data integrity requirements
  • Experience with GxP, GAMP, FDA 21 CFR Part 11, and compliance regulations
  • Experience supporting cloud-hosted and on-prem laboratory systems integration
  • Strong troubleshooting, documentation, and communication skills
Preferred Qualifications:
  • Experience with Linux/Ubuntu environments
  • Experience with robotics, automation, and connected instrument platforms
  • Experience supporting AI-enabled laboratory initiatives
  • Strong understanding of laboratory quality management workflows and analytical instrumentation

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