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How much do gxp jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for gxp in the United States is $14.66, according to ZipRecruiter salary data. Most workers in this role earn between $12.98 and $15.38 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a GxP (Good Practice) Compliance Specialist, and why are they important?

To thrive as a GxP Compliance Specialist, you need a solid understanding of regulatory standards (such as GMP, GLP, and GCP), quality management systems, and often a degree in life sciences or a related field. Familiarity with audit management tools, electronic quality management systems (eQMS), and relevant certification (like RAC or ASQ CQA) is highly valued. Strong attention to detail, analytical mindset, and effective communication skills help ensure regulatory adherence and facilitate cross-functional collaboration. These competencies are crucial for maintaining product quality, patient safety, and compliance with industry regulations.

How does a GxP professional typically collaborate with cross-functional teams to ensure regulatory compliance?

GxP professionals regularly work alongside teams such as quality assurance, manufacturing, research and development, and regulatory affairs to ensure all processes and documentation meet regulatory standards. This collaboration often involves facilitating audits, reviewing protocols, and providing training on compliance requirements. Effective communication and a proactive approach are key, as GxP professionals must ensure that all stakeholders understand and adhere to the relevant guidelines throughout the product lifecycle.

What are GxP jobs?

GxP jobs refer to roles that operate under 'Good Practice' guidelines in the life sciences and pharmaceutical industries, where 'GxP' stands for 'Good [x] Practice' (such as Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), or Good Clinical Practice (GCP)). These jobs are responsible for ensuring that products are developed, tested, manufactured, and distributed in compliance with regulatory standards to guarantee safety, quality, and integrity. GxP professionals may work in areas like quality assurance, laboratory management, clinical trials, and manufacturing. Their work is critical for meeting regulatory requirements set by agencies like the FDA or EMA. Adherence to GxP standards helps protect patient safety and product quality throughout the product lifecycle.

What is the difference between Gxp vs Quality Assurance Specialist?

AspectGxpQuality Assurance Specialist
Required CredentialsGxp compliance training, industry-specific certificationsQuality assurance certifications, such as CQE or CQA
Work EnvironmentRegulated industries like pharmaceuticals, biotech, and medical devicesManufacturing, healthcare, or software industries
Employer & Industry UsageUsed in industries with strict regulatory standardsCommon in quality-focused roles across various sectors
Comparison Search IntentUnderstanding Gxp compliance rolesComparing quality assurance roles with Gxp responsibilities

Gxp professionals focus on ensuring compliance with Good Practice standards in regulated industries, while Quality Assurance Specialists oversee quality processes across various sectors. Both roles require quality-related certifications, but Gxp roles emphasize regulatory compliance specific to industries like pharmaceuticals and biotech. Understanding these differences helps job seekers identify the right career path based on industry and certification requirements.

More about Gxp jobs
What cities are hiring for Gxp jobs? Cities with the most Gxp job openings:
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What job categories do people searching Gxp jobs look for? The top searched job categories for Gxp jobs are:
Gxp jobs near you
Infographic showing various Gxp job openings in the United States as of May 2026, with employment types broken down into 91% Full Time, 1% Part Time, and 8% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $30,498 per year, or $14.7 per hour.
GxP System Endineer

GxP System Endineer

Career Soft Solutions Inc

Boston, MA • On-site

Full-time

Posted 7 days ago

Job description

Job Title: GxP System Engineer Work Location: Norwood (Boston), MA (Onsite) The Role Client is seeking a GxP Systems Engineer, who will be responsible for the design, deployment and management of our expanding portfolio of first-in-kind automation and digital enterprise instrumentation systems that support the Quality Control GMP laboratories and system integration with our connected Digital platforms. This role will be a member of the Digital Quality team and requires both strong intellectual agility and hands-on technical skills. Who You Are: You are passionate about quality, continuous improvement, and enhancing systems to ensure optimal user experience and business efficiency.

You thrive in a fast-paced environment and are comfortable rolling up your sleeves – if a process doesn't exist yet, you define it. You collaborate well amongst a team of expert peers. Here's What You'll Do • Collaborate with a team of internal and external business analysts and other software/automation engineers in the complete product lifecycle management of various Digital Quality Automation Systems (Hamilton Venus, Scitara DLX, etc.) and Standalone Analytical Instrumentation (SpectraMax M5, Hamilton Liquid Pipetting systems, etc.) including implementation, optimization, support, maintenance updates and version upgrades.

• Translate system/equipment/data integration requirements from various Digital and Business teams to be able to deploy the appropriate Digital Lab System solution in a GMP environment. • Manage or assist in necessary change control/regulatory Digital documentation (living documents, SOPs, work instructions, KB articles, etc.) required to demonstrate appropriate compliance. • Partner with digital stakeholders to ensure successful validation and integration of key systems into the connected instrument pipeline, future robotics/automation capabilities, and any artificial intelligence initiatives.

• Foster a culture of innovation within the team and with stakeholders to challenge the status quo leveraging both new technologies and creative solutions within existing systems. • Apply an operational excellence mindset to help Identify, devise and recommend new opportunities to optimize current processes. • Ensure GMP compliance is built into the design, delivery and maintenance of all systems.

• Maintain inspection readiness through adherence to internal quality policies, procedures and training. • Participate in internal and external audits as digital quality expert for portfolio of systems. • On-site presence is required with possible travel between regional sites.

• Additional duties may be assigned from time to time. Here's What You'll Need (Minimum Qualifications) • Bachelor's degree or equivalent in science, engineering or computer science • 5 to 7+ years' experience designing, implementing, and managing life sciences Analytical Instruments in a in biopharmaceutical GMP environment • Direct experience with automation solutions such as Hamilton Venus preferred • Experience with Linux Ubuntu SUDO commands a plus • Experience with GAMP and GxP compliance regulations • Experience in laboratory systems including data integrity regulations, instrument integration, and laboratory digital workflow optimization • Experience working with Digital systems hosted in cloud and understanding of connectivity between on-prem systems and SaaS/Cloud. Here's What You'll Bring to the Table (Preferred Qualifications) • Creative/innovative/problem solver that actively drives progress • Ability to work independently and make sound and timely decision to achieve expected results • Strong understanding of core laboratory systems, related processes, and quality management workflows • Strong interpersonal skills with the ability to build successful professional working relationships • Ability to participate on multiple concurrent projects in a fast-paced environment.

• Ability to effectively collaborate in a dynamic, cross-functional matrix environment. • A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

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