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Computer System Validation Lead / Program Manager

Veeva Systems Inc.California - San Francisco
On-site Full-time

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Experience Level

Manager

Qualifications

Proven experience in computer system validation within the pharmaceutical or biotechnology industry. Strong understanding of regulatory requirements and guidelines (e.g., FDA, GxP). Exceptional project management skills with the ability to lead diverse teams. Excellent communication and interpersonal skills. Bachelor's degree in a relevant field; advanced degree preferred.

About the job

Veeva Systems seeks a Computer System Validation Lead / Program Manager based in San Francisco, California. This role shapes and guides validation programs for cloud-based solutions used in the life sciences industry, with an emphasis on regulatory compliance and operational efficiency.

Role overview

This position leads the validation of computer systems to ensure they meet regulatory standards. The work spans the entire validation process, from initial planning through final execution. Collaboration with teams across the company is central to aligning on quality expectations and maintaining best practices.

Main responsibilities

  • Direct validation efforts for computer systems to satisfy regulatory requirements
  • Oversee all stages of the validation process, from planning to completion
  • Partner with internal teams to ensure quality standards are met
  • Monitor and refine validation practices to support business objectives

Requirements

  • Background in managing validation programs within regulated settings
  • Strong knowledge of quality standards for computer systems
  • Skilled at working with cross-functional stakeholders

About Veeva Systems Inc.

Veeva Systems is a leading provider of cloud-based software for the global life sciences industry. Our mission is to help our customers bring therapies to market faster and improve patient outcomes through innovative technology solutions.

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