Veeva Safety Specialist

Karwell Technologies

Boston, MA

JOB DETAILS
SKILLS
Administrative Skills, Analysis Skills, Biology, Biotech and Pharmaceutical, Change Control, Communication Skills, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Data Analysis, Data Quality, Documentation, Environmental Sciences, GxP, Help Desk, Identify Issues, Maintain Compliance, Operational Support, Performance Analysis, Pharmacovigilance, Pharmacy, Problem Solving Skills, Process Improvement, Process Safety Management, Regulatory Compliance, Regulatory Requirements, Regulatory Submissions, Requirements Management, Rich Internet Application (RIA), Safety Compliance, Safety Process, Sales Management, Software Administration, Software Development Lifecycle (SDLC), Standard Operating Procedures (SOP), Systems Maintenance, Team Player, Training/Teaching
LOCATION
Boston, MA
POSTED
30+ days ago
Job Description:
  • 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.

Requirements:

  • 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

About the Company

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Karwell Technologies