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Full Time Gxp Systems Jobs (NOW HIRING)

VBB

Field Calibration Technician - Seattle, WA

Tacoma, WA · On-site

$70K - $82K/yr

... | Full-Time Join a growing field service team supporting critical environmental monitoring systems ... Maintain compliance with GMP, GxP, FDA, ISO, and regulatory standards * Travel to customer sites ...

VBB

Field Calibration Technician - Seattle, WA

Renton, WA · On-site

$70K - $82K/yr

... | Full-Time Join a growing field service team supporting critical environmental monitoring systems ... Maintain compliance with GMP, GxP, FDA, ISO, and regulatory standards * Travel to customer sites ...

Pace Analytical Services

PLS Scientist III

Oakdale, MN

$85K - $95K/yr

This is a full-time, onsite, Scientist 3 position located in Oakdale, MN, Monday through Friday, 8 ... Ensure compliance with all safety regulations, GxP standards, and internal quality policies.

Pacelabs

PLS Scientist III

Oakdale, MN · On-site

$85K - $95K/yr

This is a full-time, onsite, Scientist 3 position located in Oakdale, MN,Monday through Friday, 8 ... Ensure compliance with all safety regulations, GxP standards, and internal quality policies.

Pace

PLS Scientist III

Oakdale, MN · On-site

$85K - $95K/yr

This is a full-time, onsite, Scientist 3 position located in Oakdale, MN, Monday through Friday, 8 ... Ensure compliance with all safety regulations, GxP standards, and internal quality policies.

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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 Jul 15, 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 in a full-time role?

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 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 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 are the key skills and qualifications needed to thrive as a Full Time GxP Systems professional, and why are they important?

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 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
Senior Manager, R&D Quality - Document Control & Training

Senior Manager, R&D Quality - Document Control & Training

BIOMARIN PHARMACEUTICAL

San Rafael, CA • On-site

Full-time

Re-posted 4 days ago

BioMarin Pharmaceutical rating

8.3

Company rating: 8.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

23rd of 74 rated pharmaceutical

Job description

Who We Are
BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.
Guided by our purpose to develop medicines that make a profound impact on people's lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.
Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.
About Technical Operations
BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

We are seeking a Senior Manager, R&D Quality - Document Control & Training to lead and continuously improve critical GxP quality system processes supporting our R&D organization. This role is responsible for document lifecycle management, training governance, inspection readiness support, process standardization, metrics/reporting, and cross-functional quality systems partnership.
The ideal candidate brings strong experience in controlled document management, training administration/governance, and GxP quality systems within biotech, pharma, or life sciences. This is a highly collaborative role requiring partnership across Quality, Clinical, Nonclinical, Regulatory, Safety/Pharmacovigilance, and other stakeholders to ensure compliant, scalable, and efficient processes.
What you'll do
  • Lead controlled document and training processes in a GxP-regulated environment
  • Drive process improvements across document control, training, and quality systems workflows
  • Support audit and inspection readiness activities
  • Monitor and trend quality system metrics and identify opportunities for improvement
  • Partner cross-functionally to improve compliance, standardization, and operational effectiveness
  • Provide subject matter expertise on document control and training systems/processes
What we're looking for
  • Experience in Quality, Quality Systems, Compliance, or related functions in biotech/pharma/life sciences
  • Strong experience with document control and training processes in a regulated environment
  • Knowledge of GxP requirements relevant to R&D/development organizations
  • Ability to work cross-functionally and influence in a matrixed environment
  • Experience supporting inspections, audits, and continuous improvement initiatives
Strongly preferred
  • Direct experience with Veeva Vault
  • Direct experience with ComplianceWire
  • Experience in R&D, clinical, nonclinical, or development-phase quality environments
  • Experience with metrics, reporting, and process harmonization
Keywords: Quality Systems, Document Control, Training, GxP, R&D Quality, Veeva Vault, ComplianceWire, Inspection Readiness, Audit Support, SOPs, Controlled Documents, LMS, Biotech, Pharmaceutical, Quality Management Systems


Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Employment Type: Fulltime-Regular

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