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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

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.

Zifo

GxP Lab Computing Analyst

Framingham, MA · On-site

This role will require full-time on-site presence at our client site in Framingham, MA.** **This ... Liaise between System/Lab owners and third parties to coordinate best times for services * Provide ...

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

As of Jun 9, 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
Business Analyst Veeva Vault Clinical (CTMS/eTMF) - Remote - Full time

Business Analyst Veeva Vault Clinical (CTMS/eTMF) - Remote - Full time

Lorven Technologies

Remote

Full-time

Posted 19 days ago

Job description

Our client seeks an Business Analyst Veeva Vault Clinical (CTMS/eTMF) for a Full Time Project in Remote . Below is the detailed requirement
Job Title: Business Analyst Veeva Vault Clinical (CTMS/eTMF)
Work location : Remote
Duration: Full Time
Job Description:
  • Bachelor's degree preferably in Computer Science, Information technology, Computer Engineering, or related IT discipline or equivalent experience with 12+ Minimum Experience

Skills & Experience
  • Business Analyst with 10-12+ years of experience delivering or leading regulated enterprise or clinical systems initiatives
  • Hands-on experience with Veeva Vault Clinical (CTMS and eTMF)
  • Strong understanding of clinical trial operations and clinical systems workflows
  • Strong technical fluency to partner effectively with internal and external teams in Business, IT, Data, Infrastructure, and QA
  • Demonstrated experience overseeing release and environment management in a GxP-regulated environment
  • Proven ability to lead complex, cross-functional initiatives and drive clarity from ambiguity
  • Excellent executive communication, documentation, and stakeholder management skills

Business Analysis Leadership/Execution & Veeva Vault Clinical Expertise
  • Lead complex, cross-functional initiatives related to Veeva Vault Clinical (CTMS/eTMF), including implementation, optimization efforts, migrations, and strategic enhancements
  • Convert ambiguity into clear problem statements, scope, success criteria, execution plans, timelines, risks, and decision points
  • Proactively manage dependencies, trade-offs, and risks; elevate decisions with clear recommendations to Clinical Systems LT
  • Serve as a SME for Veeva Vault Clinical (CTMS/eTMF), advising on configuration implications, functional capabilities, and downstream system impacts
  • Partner with development and support teams on complex or systemic issues, contributing to root-cause analysis and long-term solutions
  • Participate in enhancement definition, prioritization, solution design, and validation strategy
  • Collaborate closely with integration and data teams on end-to-end clinical system workflows
  • Review key technical and functional documentation, including business and system requirements, design specifications, release notes, validation plans, and SOPs
  • Ensure documentation is complete, accurate, and aligned with intended business outcomes, system behavior, and regulatory expectations
  • Act as a translator between technical and business audiences, validating that documentation clearly reflects scope, assumptions, risks, and downstream impacts
  • Partner with CS Leads, QA, Val, and IT to ensure documentation supports validation, inspection readiness, and audit traceability

Migration and Transformation Leadership -- Lead/contribute to large-scale system migration, of Client legacy CTMS Gilda (Siebel) to Veeva Vault Clinical and related transformation efforts; Drive/participate in migration planning, including cutover strategy, data validation approach, reconciliation methods, rollback planning, communications, change management, and archiving strategy; Help to coordinate technical and business readiness across all stakeholder groups
Validation, Compliance, Release and Environment Management -- Provide oversight and coordination for Veeva Vault Clinical releases across non-production and production environments; As needed, partner with QA, Val, and IT to ensure delivery aligns with GxP and validation expectations; Drive release impact assessments, cross-functional readiness reviews, and deployment sequencing in partnership with IT, QA, Val and development teams; Ensure appropriate governance and usage of development, test, and UAT environments to support parallel workstreams and testing cycles; Act as a single point of orchestration for release- and environment-related dependencies, risks, and conflicts; Ensure releases are executed in a compliant, predictable, and business-aligned manner; Provide oversight and contribution to validation approaches, UAT strategy, and release documentation
Executive Communication and Clinical Systems Leadership Enablement -- Operate as a trusted advisor and analyst for Clinical Systems LT; Lead routine internal Clinical Systems Meeting to ensure internal alignment on technical and operational decisions/risks/updates on the Vault Clinical program; Deliver concise, executive-ready communication on progress, risks, trade-offs, and decisions required; Influence with minimal oversight to gain alignment and drive outcomes across senior stakeholder groups
Preferred / Nice-to-haves
  • Experience with system integrations (e.g., CTMS ↔ eTMF/EDC/Data Lakes & repositories)
  • Experience working with Siebel (CTMS), working with Veeva Managed Services or vendor escalations
  • Familiarity with Agile or DevOps methodologies; Knowledge of clinical metrics and reporting tools
  • Siebel CTMS experience, particularly in migration or decommissioning efforts
  • Experience with system integrations, APIs, middleware, and data platforms
  • Experience with Veeva Managed Services or external vendors
  • Exposure to operational metrics, reporting, or analytics in a clinical systems setting
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About Lorven technologies

Sourced by ZipRecruiter

Lorven Technologies, headquartered in Plainsboro, New Jersey, United States, is a reputable company in the technology industry, specializing in providing effective IT solutions and consulting services. The company's official website, lorventech.com, offers comprehensive insights into its offerings which include but are not limited to software development, IT consulting, project management, and business analysis. Since its inception, Lorven Technologies has been committed to ensuring efficiency and reliability in delivering IT services to its global clientele, establishing itself as a trusted name in the industry.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Plainsboro, NJ, US

Year founded

2001

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