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Full Time Gxp Systems Jobs (NOW HIRING)

Secura Bio

Manager, Document Control and Training

$121K - $142K/yr

Employment Type Full-time Reports To Senior Director, Quality Assurance Key Responsibilities ... Record Archival in Ace: Ensuring GxP records are stored in the ACE system. Utilizing the ...

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 ...

Systimmune

Director, Information Technology

Redmond, WA · On-site

$180K - $250K/yr

... systems in regulated (GxP) environments. This position is based full-time onsite at our Redmond, WA office and will then move to our new Bothell, WA facility in fall 2026 and will lead the IT design ...

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.

Pacelabs

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.

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 ...

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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 Aug 7, 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 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?

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 QA Specialist, Global Document Control Management

Revolution Medicines

Redwood City, CA • On-site

Full-time

Re-posted 19 days ago

Job description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
  • Support the development, implementation, and continuous improvement of the global GxP Document Management Program, ensuring document control processes, governance, and systems remain compliant, efficient and aligned with regulatory requirements and industry standards.
  • Review and coordinate Document Change Controls (DCCs) and document workflows to ensure GxP procedures, forms, templates, and other controlled documents are managed throughout their lifecycle in accordance with global requirements and company procedures.
  • Serve as the subject matter expert (SME) for the electronic Document Management System (eDMS/eQMS), driving global standardization, governance, system optimization, user support, and continuous improvement initiatives.
  • Partner cross-functionally with global RevMed functions, sites, and affiliates to evaluate document management process effectiveness, identify improvements, and implement sustainable solutions that enhance the operational excellence.
  • Support strategic document management initiatives, including workflow optimization, system enhancements, document migrations, periodic reviews, global expansion activities, training programs, and process improvement projects.
  • Monitor, analyze, and communicate key quality metrics and KPIs related to document lifecycle management and process performance, driving appropriate corrective and preventive actions.
  • Support the development, implementation, and maintenance of global SOPs, work instructions, governance frameworks, and best practices supporting document management of quality systems while promoting process consistency, governance, and user adoption.
  • Support internal audits, regulatory inspections, and inspection readiness activities and foster a culture of quality, accountability, and continuous improvement.

Required Skills, Experience and Education:
  • BA/BS degree in Biological Sciences, Chemistry, or related field and/or equivalent experience and education.
  • Minimum 5 years of Pharma/Biotech industry experience in Quality Assurance (QA) in a GxP environment.
  • Experience in developing and implementing GxP quality systems to meet current regulatory and industry standards.
  • Direct experience managing global GxP document management and training systems.
  • Excellent working knowledge and understanding of GxP requirements, proficiency in applying regulatory requirements, and ICH guidelines.
  • Direct experience working with Veeva QualitySuite electronic platforms (QualityDocs, Training, QMS).
  • Proficient with Microsoft Office including Word, Excel, PowerPoint experience is a plus.
  • Excellent communication skills, both oral and written to clearly and concisely communicate with internal and external team members.
  • Ability to work independently and collaboratively across cross-functional teams in a dynamic environment

Preferred Skills:
  • Strategic thinking and project management skills.
  • Direct experience with handling and/or participating in regulatory body inspections.
  • A continuous improvement mindset and willingness to take initiative in solving problems.
  • Experience in both virtual sponsor and scaling global organization models.
    #LI-Hybrid #LI-JC1

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
Base Pay Salary Range
$120,000-$150,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

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