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Veeva Lms Jobs (NOW HIRING)

Align Technology, Inc.

Global QMS Engineer

Morrisville, NC · On-site

$67K - $87K/yr

Experience working with electronic QMS tools (e.g., Arena PLM, Agile, Veeva, MasterControl, or similar) and/or LMS platforms (e.g., Docebo, Cornerstone). * Experience with Business Intelligence (BI ...

Align Technology

Global QMS Engineer

Raleigh, NC · On-site

$78K - $107K/yr

Experience working with electronic QMS tools (e.g., Arena PLM, Agile, Veeva, MasterControl, or similar) and/or LMS platforms (e.g., Docebo, Cornerstone). * Experience with Business Intelligence (BI ...

Align Technology

Global QMS Engineer

Raleigh, NC · On-site

$70K - $90K/yr

Experience working with electronic QMS tools (e.g., Arena PLM, Agile, Veeva, MasterControl, or similar) and/or LMS platforms (e.g., Docebo, Cornerstone). * Experience with Business Intelligence (BI ...

Revance

Associate Director, IT R&D

Newark, CA · On-site

... LMS. * Extensive experience in IT R&D lab systems, laboratory informatics, and CSV in regulated ... Experience with Veeva applications Company Summary: Revance is a global company developing ...

Edwards Lifesciences Corporation

... LMS and regulatory requirements. Lead audit preparation efforts for TMTT including team education ... processes (e.g., Trifecta, Veeva Vault, Litmos) for both internal and external training.

Edwards Lifesciences Corporation

... LMS and regulatory requirements. Lead audit preparation efforts for TMTT including team education ... processes (e.g., Trifecta, Veeva Vault, Litmos) for both internal and external training.

Edwards Lifesciences Corporation

... LMS and regulatory requirements. Lead audit preparation efforts for TMTT including team education ... processes (e.g., Trifecta, Veeva Vault, Litmos) for both internal and external training.

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How much do veeva lms jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for veeva lms in the United States is $37.28, according to ZipRecruiter salary data. Most workers in this role earn between $28.12 and $46.88 per hour, depending on experience, location, and employer.

What is the difference between Veeva Lms vs Veeva Vault Administrator?

FeatureVeeva LmsVeeva Vault Administrator
Primary RoleManage learning management systems and training programsManage Veeva Vault content management and related workflows
CertificationsVeeva LMS certifications, eLearning developmentVeeva Vault certifications, content administration
Work EnvironmentTraining departments, eLearning teamsContent management teams, regulatory compliance
Industry UsagePharmaceutical, biotech, life sciencesPharmaceutical, biotech, life sciences

While both roles involve Veeva platforms, Veeva Lms specialists focus on training and learning management, whereas Veeva Vault Administrators handle content and data within Veeva Vault. Understanding these differences helps organizations assign the right expertise for their needs.

What are some common challenges faced by professionals working with Veeva LMS, and how can they be overcome?

Professionals working with Veeva LMS often encounter challenges such as adapting to frequent platform updates, ensuring seamless integration with other enterprise systems, and managing user adoption across diverse teams. To overcome these, it's helpful to stay current with Veeva's release notes, participate in community forums, and collaborate closely with IT and training teams. Additionally, clear communication and tailored training programs can significantly boost user engagement and smooth the transition during system changes.

What are the key skills and qualifications needed to thrive as a Veeva LMS Administrator, and why are they important?

To thrive as a Veeva LMS Administrator, you need a solid understanding of learning management systems, experience with Veeva Vault platform, and a background in training or compliance, often supported by a related degree or certifications. Familiarity with Veeva Vault QMS/LMS modules, data management tools, and regulatory compliance systems is typically required. Attention to detail, strong problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies ensure accurate training record management, regulatory compliance, and efficient support for organizational learning initiatives.

What is a Veeva LMS specialist?

A Veeva LMS specialist is a professional who manages, implements, and supports the Veeva Learning Management System (LMS) within organizations, particularly in the life sciences industry. This role involves overseeing training programs, ensuring compliance with regulatory standards, and optimizing the use of Veeva LMS for employee development. Specialists often handle user administration, course creation, reporting, and troubleshooting system issues. Their expertise helps organizations streamline training and maintain robust documentation for audits and quality assurance.
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Veeva Lms jobs near you
Senior Manager, R&D Quality - Document Control & Training

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

BioMarin Pharmaceutical Inc.

San Rafael, CA • On-site

Full-time

Re-posted 3 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

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.

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