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Diverse Lynx

GxP Test Lead

Boca Raton, FL · On-site

$45 - $61.25/hr

Strong expertise in GxP , CSV . * Experience in functional testing of custom built applications, mobile testing. * In-depth understanding of Software Testing Life Cycle (STLC) process, QA tools and ...

Marriott

FLEX GXP Support Agent

Bethesda, MD · Hybrid

The GXP Agent works closely with on-property teams to uphold service standards, streamline communication, and maximize operational efficiency. Key Responsibilities: * Manage room inventory and ...

Amgen, Inc.

Senior Director, R&D GxP Audit

Senior Director, R&D GXP Audit What you will do Let's do this! Let's change the world! The Senior Director, R&D GxP Audit will lead the global strategy, execution, and continuous improvement of the ...

Regeneron Pharmaceuticals

The Director, GxP Enterprise Architecture leads the IT architecture practice for manufacturing and operations (e.g., manufacturing, QA, QC, process sciences, supply chain). This role defines ...

Amgen

Senior Director, R&D GxP Audit

Juncos, PR

Senior Director, R&D GXP Audit What you will do Let's do this! Let's change the world! The Senior Director, R&D GxP Audit will lead the global strategy, execution, and continuous improvement of the ...

JLL

Lab Services GXP Media Technician

North Brunswick, NJ · On-site

$20 - $26.50/hr

Lab Services (GXP) Media Prep Technician - JLL What this job involves: The Lab Services Media Prep Technician plays a critical role in supporting laboratory research operations within a highly ...

Yochana

GxP Test Lead

Boca Raton, FL · On-site

$45 - $61.25/hr

• 15+ years of software QA/testing experience, with at least 10+ years in regulated environments like life sciences, pharma, healthcare. • Strong expertise in GxP compliance, CSV, and FDA 21 CFR ...

Marriott

FLEX GXP Support Agent

Bethesda, MD · Hybrid

The GXP Agent works closely with on-property teams to uphold service standards, streamline communication, and maximize operational efficiency. Key Responsibilities: * Manage room inventory and ...

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How much do gxp jobs pay per hour?

As of Jun 26, 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.

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.

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.
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 June 2026, with employment types broken down into 92% Full Time, 1% Part Time, and 7% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $30,498 per year, or $14.7 per hour.
GxP & Lab Systems Administrator

GxP & Lab Systems Administrator

Supernus Pharmaceuticals, Inc.

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 29 days ago

Job description

Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. We currently have 8 products in the market that are making a real impact on patient outcomes.
Job Summary:
The GxP and Lab Systems Administrator will provide skilled implementation, operational, and maintenance support for lab computer applications. This position will employ skilled systems knowledge to ensure proper daily operation of lab systems and will troubleshoot and remediate application issues.
Essential Duties & Responsibilities:
  • Troubleshoots, diagnoses, and resolves lab software application-specific support issues.
  • Monitors the performance, availability, and usage of enterprise lab software applications, identifying and troubleshooting any issues or anomalies, and collaborating with relevant teams to resolve them promptly.
  • Performs system owner/ business administrator duties to support GxP validated computer systems (e.g. LIMS, Empower, and MassLynx).
  • Works with the CSV and IT teams to support the generation of computer system validation deliverables.
  • Configures lab software applications to meet specific business needs, including workflows, reports, and other settings, in collaboration with stakeholders and end-users.
  • Collaborates with vendors and the internal IT team to plan and execute application upgrades, patches, and maintenance activities, ensuring minimal end-user disruption.
  • Coordinates with the internal IT team to support the qualification of new or changed lab computer systems.
  • Initiates and manages quality records (e.g. change control, deviation, CAPA actions) and create or revise Standard Operating Procedures (SOPs).
  • Creates and maintains documentation following Good Documentation Practices, to ensure efficient application management and support processes.
  • Reviews vendor/contractor documentation for services provided.
  • Supports and assists in performing Periodic Reviews of GxP lab computer systems.
  • Ensures GxP lab systems remain in a validated state.

Supervisory Responsibilities:
  • N/A.

Knowledge & Other Qualifications:
  • BA/BS degree or equivalent experience/ certification in a computer science or other science-related discipline.
  • 2+ years of practical related IT systems administration experience.
  • Knowledge of Windows desktop and server operating systems.
  • Knowledge of LIMS and Empower systems as well as other laboratory data systems.
  • Strong documentation skills are necessary to maintain accurate records of the lab application's configuration, user guides, and any customizations or integrations implemented.
  • Ability to diagnose problems and define/resolve/coordinate the implementation of solutions with other groups.
  • Ability to troubleshoot and resolve various application problems working with our IT systems/network administration personnel and software vendors.
  • Self-motivated with the initiative to see issue resolution through to completion.
  • Business-focused approach with strong interpersonal skills.
  • Positive attitude with a commitment to a high quality of work.
  • Demonstrated competency to learn new technical skills.

Other Characteristics:
  • Ability to quickly learn new or unfamiliar technology and applications using documentation and internet resources.
  • Ability to work independently and as part of a team and maintain high ethical standards of quality, data integrity, and security.
  • Good analytical thinker who possesses problem-solving skills, can visualize solutions, and can use an innovative and dynamic approach to work.
  • Ability to consistently exhibit Supernus Values in interactions with employees at all levels of the organization, customers, and others.
  • Dependable, reliable, and flexible, when necessary, with excellent time management skills.
  • Good communication skills being able to communicate via various methods including electronic, in person, or via telephone.
  • Capable of performing other duties and responsibilities as assigned or directed by Management.
  • Authorized to legally work in the United States without visa sponsorship.

Physical Requirements/Work Environment/Travel Requirements:
  • Candidate should be comfortable moving throughout a five-floor, connected two-building complex.
  • Position may require prolonged sitting, standing, walking, reaching, twisting, turning, kneeling, and bending; the ability to push, pull, drag, and/or lift to 20 pounds; normal manual dexterity and hand/eye coordination; repetitive hand movement using a computer keyboard and mouse.
  • Required to have close visual acuity to perform activities such as viewing a computer monitor and reading.
  • The worker is not substantially exposed to adverse environmental conditions.

Compensation:
At Supernus, we offer a competitive compensation package that reflects your experiences and contributions. The expected salary range for fully qualified candidates applying for this role is $77,000 to $95,000. This range is what the Company reasonably expects to offer for the position and is not reflective of the full compensation scale of the role. This range may be modified in the future. An individual's salary within the range is based on multiple factors, which may include and are not limited to education, relevant experience, knowledge, length of industry experience and organizational needs.
You also will be able to participate in a competitive benefits package, including but not limited to: health, dental, vision, paid time off, 401k company match, company paid life insurance and health and wellness benefits. The total compensation package for this position also includes other compensation elements such as stock equity awards, employee stock purchase programs and participation in our Company's discretionary annual bonus program.
Supernus Pharmaceuticals is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, disability, protected veteran status, age or any other characteristic protected by law.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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