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How much do gxp systems jobs pay per year?

As of Jul 14, 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 July 2026, with employment types broken down into 2% Locum Tenens, 20% Internship, 60% As Needed, 16% Full Time, 1% Contract, and 1% Summer. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $102,067 per year, or $49.1 per hour.

GxP Systems Admin

Stark Pharma Solutions Inc

Lexington, MA • On-site

Contractor

Posted 20 days ago

Job description

Hi,

My name is Sravani Dasari, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on GxP Application System Administrator position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows.

Job Title: GxP Systems Admin
Location: Lexington, MA
Duration: Long Term

Position Overview

We are seeking a GxP Systems Admin to support and maintain regulated manufacturing, laboratory, and automation systems within a pharmaceutical or biotechnology environment. This role will be responsible for system administration, user support, compliance activities, troubleshooting, and ensuring systems remain in a validated and compliant state.

Key Responsibilities

• Administer and support GxP-regulated computerized systems across manufacturing, laboratory, and automation environments.
• Manage user accounts, system access, permissions, and security controls.
• Perform system maintenance, monitoring, troubleshooting, backups, and routine health checks.
• Support periodic system reviews, audits, inspections, and compliance activities.
• Maintain system administration records, logs, and documentation.
• Participate in change control, deviation investigations, and CAPA activities.
• Ensure compliance with data integrity principles, CSV requirements, and regulatory standards.
• Collaborate with Quality, Manufacturing, IT, Validation, and Engineering teams to support business operations.

Required Qualifications

• Bachelor's Degree in Information Technology, Engineering, Life Sciences, Computer Science, or a related field.
• 2–4+ years of experience administering GxP-regulated computerized systems in pharmaceutical, biotechnology, or life sciences environments.
• Experience supporting manufacturing, laboratory, or automation applications.
• Working knowledge of DCS/SCADA Systems such as DeltaV, FactoryTalk, or Metasys.
• Experience with Historian Systems (PI) and laboratory applications including LabX, Unicorn, Sartocheck, Nova Biomass, or ThinManager.
• Strong understanding of Data Integrity principles (ALCOA+), Computerized System Validation (CSV), and Change Control & CAPA processes (TrackWise).
• Experience managing user access, system security, troubleshooting, backups, and routine system maintenance activities.
• Strong troubleshooting, documentation, communication, and problem-solving skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/