drjobs Sr Veeva QMS Support Analyst

Sr Veeva QMS Support Analyst

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1 Vacancy
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Job Location drjobs

San Francisco, CA - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Job Summary:
We are seeking a detailoriented and technically skilled Veeva QMS Support Specialist to provide enduser support configuration assistance and continuous improvement for our Veeva Quality Management System (QMS). This role serves as a bridge between Quality IT and end users ensuring smooth implementation and operation of Veeva QMS modules including Change Control Deviations (QE) Continuous Improvement/CAPA.
Responsibilities:
  • Serve as primary point of contact for Veeva QMS expertise.
  • Configure and maintain Veeva QMS modules in alignment with business requirements and best practices.
  • Manage user accounts roles permissions and security settings.
  • Support the rollout of new Veeva QMS features releases and enhancements.
  • Collaborate with Quality Regulatory and IT teams to gather requirements and implement workflows and process improvements.
  • Monitor system performance and data integrity ensuring compliance with applicable regulations (e.g. 21 CFR Part 11 GxP).
  • Provide training documentation and user guidance for internal stakeholders.
  • Work with Veeva support and implementation partners to resolve technical issues and drive system optimization.
Requirements:
  • Bachelors degree in Life Sciences Computer Science Information Systems or related field.
  • 4 years of experience supporting Veeva QMS.
  • Strong understanding of quality processes in regulated industries (pharma biotech).
  • Familiarity with GxP compliance electronic records/signatures 21 CFR Part 11 and validation principles.
  • Excellent problemsolving communication and interpersonal skills.
  • Experience with system administration configuration and ticket tracking.
Preferred:
  • Veeva Vault Admin Certification or equivalent experience.
  • Experience with Veeva Vault API or integrations.
  • Background in quality assurance regulatory affairs or IT in a life sciences environment.

Employment Type

Full Time

Company Industry

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