Veeva

61 Veeva Jobs Hiring Near You

OR · On-site

: The Veeva Administrator is responsible for ensuring the Veeva Vault Applications are maintained in a compliant manner. Responsibilities encompass administration of Veeva Vault Regulatory Information ...

Veeva Specialist

Morristown, NJ · On-site +1

$18.50 - $24.75/hr

Veeva Specialist Location: Morristown, NJ (Remote) Duration: 12 Months (Possibility of extension) Work Schedule: 9 AM - 5 PM EST, 40 hours per week Overview: We are seeking a detail-oriented and ...

Veeva vault

Waukegan, IL · Remote

$94.10K - $119.70K/yr

Job Title: Veeva vault Job Location: Waukegan, IL(Remote working fine for now) Job Type: Contract * Veeva vault * Experiences in Veeva Vault Promomats. * Responsible for migration deliverables

Veeva BA

Dallas, TX · On-site

$85.40K - $110.30K/yr

They have used Veeva QMS Vaults * They understand Veeva's structure * They are a current Wipro employee * I'm sure you have ideas of other requirements * Need Immediately

Veeva Solution Architect

Raritan, NJ · On-site

$64.50 - $85/hr

Veeva Solution Architect Location: Raritan, NJ Duration: Duration: 6-12 Months [Possible Extension] Primary skills: Veeva Vault Architect, Solution Architect, Integration Specialist, Vault SDK ...

Position Summary The Veeva RIM Specialist will provide expertise and guidance in the management and publishing of regulatory documents ensuring their conformance with Health Authority requirements.

Veeva Vault Quality Docs * Experience in Veeva Vault Q Docs/QMS configuration - Must * Experience in Compliance Wire configuration - Must * Systems IQ/OQ/PQ in the Pharma industry Responsibilities:

Veeva Solution Architect Duration: 6-12 months Location: Cupertino, CA Pay range: $60 to $64/hr on W2 all inclusive. Experience: Deep and strong experience with Veeva Vault configuration and ...

Veeva Vault Solution Architect

Avenel, NJ · On-site

$64 - $84.50/hr

Support all assigned development activities for the Veeva Vault implementation program under the leadership of the client Quality Veeva team. * Coordinate with Business analysts to outline the ...

Veeva Specialist

Morristown, NJ · On-site +1

$18.50 - $24.75/hr

Veeva Specialist Location: Morristown, NJ (Remote) Duration: 12 Months (Possibility of extension) Work Schedule: 9 AM - 5 PM EST, 40 hours per week Overview: We are seeking a detail-oriented and ...

Veeva Systems is building the industry cloud for Life Sciences to help companies work in a more efficient and connected way. Learn more about our products, vision and values, and status as a public ...

Veeva Systems is building the industry cloud for Life Sciences to help companies work in a more efficient and connected way. Learn more about our products, vision and values, and status as a public ...

Veeva Clinical Consultant

Nashville, TN · Hybrid

$70.35K - $196K/yr

An experienced Veeva Clinical Consultant The work: Designing, configuring, and implementing Clinical Vault solutions to meet our business needs. This role involves collaborating with cross-functional ...

New

Veeva Vault Admin Job Location: Summit, NJ or Remote Job Type: Contract Job Summary: Candidate should have at least 2 years of experience in supporting Veeva Vault application Roles and ...

Showing results 21-40

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Infographic showing various job openings at Veeva in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 21% Physical, 72% Hybrid, and 7% Remote job distribution.
Veeva Safety Specialist

Other

Posted 8 days ago


Job description

Job Summary:
  • The Veeva Safety Specialist will be responsible for the implementation, administration, configuration, and ongoing support of Veeva Vault Safety solutions within a pharmaceutical or life sciences environment.
  • This role involves managing safety processes, resolving system issues, supporting regulatory compliance activities, and ensuring smooth operation of safety workflows on the Veeva Vault platform.
  • The specialist will collaborate with cross-functional teams to support pharmacovigilance operations, system enhancements, audit readiness, and compliance initiatives while maintaining high standards of GxP compliance and data integrity.
Roles & Responsibilities:
  • Administer, configure, and maintain Veeva Vault Safety applications, including account management, workflows, issue resolution, transmission records, and regulatory submissions.
  • Support implementation and ongoing maintenance activities for Veeva Safety and related platform features.
  • Manage and troubleshoot support tickets, system issues, and enhancement requests within the Veeva environment.
  • Participate in SDLC activities, system updates, Release Impact Assessments (RIA), and validation support.
  • Support safety and compliance processes, including change control, deviation management, CAPA workflows, periodic reviews, and user access reviews.
  • Ensure system compliance with GxP and regulatory requirements for pharmacovigilance and safety operations.
  • Collaborate with business users, IT teams, and stakeholders to gather requirements and implement system improvements.
  • Monitor system performance and maintain system documentation, SOPs, and user manuals.
  • Conduct user training sessions and provide end-user support for Veeva Safety applications.
  • Analyze data, troubleshoot system issues, and provide data-driven recommendations for process improvements.
  • Support audit and inspection readiness activities related to Veeva Safety and safety operations.
  • Maintain effective communication and knowledge sharing across project and operational teams.
Education & Experience:
  • Bachelor's or Master's degree in Engineering, Technology, Life Sciences, Pharmacy, or related field preferred.
  • 10+ years of experience in Veeva Vault Safety administration, support, or implementation within pharmaceutical or life sciences organizations.
  • Strong experience with Veeva Vault Safety, including workflow configuration, issue resolution, and regulatory submission processes.
  • Good understanding of pharmacovigilance processes, including ICSR case processing and safety operations.
  • Hands-on experience with SDLC processes, Release Impact Assessment (RIA), and Veeva platform features.
  • Knowledge of GxP compliance, CAPA, deviation management, change control, and audit processes.
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Excellent communication, documentation, and collaboration skills.
  • Preferred Certifications:
    • Veeva Technical Foundation Certification
    • Administer Veeva Safety Certification

Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

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Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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