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Full Time Gxp Systems Jobs (NOW HIRING)

Agilent

$116K - $219K/yr

Ensure systems meet GxP, FDA 21 CFR Part 11, and other regulatory requirements as required based on ... The full-time equivalent pay range for this position is $116,800.00 - $219,000.00/yr plus ...

WinWire

Business Analyst

Foster City, CA · On-site

Job Type : Full-Time / Contract Location : Foster City, CA We are seeking a Business Analyst with ... Must understand GXP system validation process and familiar with AWS environments * Experience ...

Nihon Kohden USA

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Strong knowledge of GxP, ISO 13485, ISO 14971, and FDA 21 CFR 820. * Able to apply Canadian Medical ... The regular hours for this full-time position are 8:00 a.m. to 5:00 p.m., Monday-Friday, unless ...

Nihon Kohden America

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Strong knowledge of GxP, ISO 13485, ISO 14971, and FDA 21 CFR 820. * Able to apply Canadian Medical ... The regular hours for this full-time position are 8:00 a.m. to 5:00 p.m., Monday-Friday, unless ...

Nihon Kohden

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Strong knowledge of GxP, ISO 13485, ISO 14971, and FDA 21 CFR 820. * Able to apply Canadian Medical ... The regular hours for this full-time position are 8:00 a.m. to 5:00 p.m., Monday-Friday, unless ...

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Full Time Gxp Systems information

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$46K

$102.1K

$153K

How much do full time gxp systems jobs pay per year?

As of Sep 2, 2026, the average yearly pay for full time 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 GxP systems?

GxP systems are specialized software and processes used in industries like pharmaceuticals, biotechnology, and healthcare to ensure compliance with regulatory standards such as Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and Good Manufacturing Practice (GMP). A full-time GxP systems role typically involves maintaining, validating, and supporting these systems to ensure they meet strict quality and compliance requirements. Professionals in this role work closely with quality assurance, IT, and regulatory teams to ensure data integrity and regulatory compliance throughout the product lifecycle.

What are the key skills and qualifications needed to thrive as a full time GxP Systems professional?

To thrive as a Full Time GxP Systems professional, you need a solid background in computer science or life sciences, experience with regulatory compliance (such as FDA, EMA), and knowledge of Good Practice (GxP) guidelines. Familiarity with validated systems, electronic records management tools, and common industry software like Veeva Vault or SAP is typically required. Attention to detail, strong problem-solving skills, and the ability to communicate effectively with cross-functional teams set top candidates apart. These competencies ensure systems are compliant, reliable, and support the integrity of regulated processes within the life sciences industry.

What are some common challenges faced by professionals working in full time GxP Systems roles, and how can they be addressed?

Professionals in full-time GxP Systems roles often face challenges related to maintaining regulatory compliance in a constantly evolving landscape. Staying current with global regulations, ensuring data integrity, and managing system validation can be demanding. Collaboration with quality assurance, IT, and business stakeholders is crucial to anticipate compliance risks and implement effective controls. Regular training, robust documentation practices, and proactive system monitoring are key strategies to overcome these challenges and support successful audits and inspections.

What is the difference between Full Time Gxp Systems vs Gxp Compliance Specialist?

AspectFull Time Gxp SystemsGxp Compliance Specialist
CertificationsGxP-related certifications, Good Practice trainingGxP certifications, regulatory compliance training
Work EnvironmentPharmaceutical or biotech manufacturing facilities, laboratoriesRegulatory departments, quality assurance teams
Employer & Industry UsagePharmaceutical companies, biotech firms, CROsRegulatory agencies, pharmaceutical companies

Full Time Gxp Systems roles focus on managing and maintaining GxP systems within manufacturing or laboratory environments, ensuring compliance and system integrity. Gxp Compliance Specialists primarily handle regulatory adherence, audits, and documentation. Both roles require similar certifications and work in related settings, but their core responsibilities differ in scope and focus.

What cities are hiring for Full Time Gxp Systems jobs?

Cities with the most Full Time 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 Full Time Gxp Systems jobs?

States with the most job openings for Full Time Gxp Systems jobs include:

Full Time Gxp Systems jobs near you

Business Application & Systems Administrator

Agilent

On-site, Remote

$116K - $219K/yr

Full-time

Re-posted 25 days ago

Agilent Technologies rating

8.5

Company rating: 8.5 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers

Job description

Job Description

The Business Applications & Systems Administrator is responsible for managing, implementing, and optimizing business applications. The role will develop & coordinate testing with impacted departments, including specifically coordinating with IT and Quality for validation & compliance. Manages business application projects, ensuring effective communication across teams/functions as well as informing management of progress and key issues.

Key Responsibilities

Application Management:

  • Administer and maintain core business owned applications (e.g. Project & Portfolio Management, Electronic Lab Notebook, Lab Management, Image Management, Spotfire business intelligence).

Configuration & Customization:

  • Configure applications to support business workflows, including directly configuring and through available technical resources.

Compliance & Validation:

  • Write test plans and testing scripts in support of Computer System Validation (CSV) team
  • Ensure systems meet GxP, FDA 21 CFR Part 11, and other regulatory requirements as required based on application upgrades.
  • Collaborate with IT and QA on compliance and security attestations.

Support & Troubleshooting:

  • Provide first line support for application-related questions, including directing to appropriate subject matter experts.

Upgrades & Patches:

  • Plan and execute upgrades and patches and ensure validation compliance

Data Integrity:

  • Ensure data integrity and traceability across systems.

Training:

  • Train end-users and maintain user guides.
Qualifications

  • Bachelor's degree in Information Technology, Computer Science, or related field.

  • 8+ years in application administration.

  • Familiarity with validated systems and regulatory compliance.

  • Strong understanding of GxP, FDA 21 CFR Part 11 compliance.

  • Excellent problem-solving and communication skills.


Preferred Qualifications:

  • 10+ years in business applications management.

  • Experience within a life sciences environment.

  • Experience with cloud-based pharmaceutical applications.

  • Knowledge of change control in regulated environments.

  • Familiarity with CSV (Computer System Validation) processes.

  • Experience with leading cloud based business systems implementation.

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least August 27, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $116,800.00 - $219,000.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: OccasionalShift: DayDuration: No End DateJob Function: Administration

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