Senior Quality Systems Consultant, Veeva

Clarkston Consulting

. Participate in projects at life sciences and consumer products companies designing and deploying Veeva .

Posted 10/24/2026full-timeUnited StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in implementing Veeva Quality suite and Veeva Vault RIM capabilities within life sciences, alongside strong project management skills including defining deliverables and managing project scope. Proven ability to develop client relationships and provide training and guidance to team members.

Highest-signal resume keywords

Veeva Quality Suite ImplementationRegulatory Information Management SystemsDocument Management SystemsTeam LeadershipGood Manufacturing Practices (GMP) Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Veeva VaultEtQTrackWiseOpenTextSharePointDocumentumFirstDoc/FirstPointNextDocsContent Management SolutionsQuality Management Systems

Soft Skills

Analytical SkillsClient Services OrientationFlexibilityAdaptabilityCommunication Skills

Certifications & Qualifications

4-Year Degree

Industry Keywords

Life SciencesConsumer ProductsGlobal Quality RequirementsCompliance ConsiderationsStandard Operating Procedures (SOPs)

Tech Stack

Tools & technologies

Vault

About the role

Key responsibilities & impact

Participate in projects at life sciences and consumer products companies designing and deploying Veeva
Support configuration and implementation of Veeva Quality suite and Veeva Vault RIM capabilities
Lead requirements workshops
Design, prototype, configure, and document content management/QMS data solutions
Develop trusted client relationships beyond the project lifecycle
Create and oversee project or workstream plans and timelines
Define deliverables, assign team roles and resources, track issues and resolutions, and help manage project scope and requirements
Assist in validating computer systems for use in a Good Manufacturing Practices (GMP) environment
Create and revise Standard Operating Procedures (SOPs)
Conduct knowledge transfer and train end-users, including sharing best practices
Provide guidance to junior systems analysts and client personnel assigned to projects

Requirements

What you’ll need

5+ years of experience working with or for life sciences companies
Experience implementing Document or Quality Management systems for life sciences as a consultant, business, or IT representative
Experience with regulatory information management systems, including registrations and submissions, preferred
Understanding of global quality requirements, compliance considerations, and processes
Firsthand experience with systems such as Veeva Vault, EtQ, TrackWise, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, or other quality information or content management systems
Team Lead experience
Flexibility and adaptability, including design through hands-on configuration and ability to stretch into new roles
Thorough client services orientation and active participation in engagements and project plans/tasks
Excellent analytical skills
Ability to present and write at publication quality level
4-year degree from an accredited college or university

Benefits

Comp & perks

Comprehensive Health and Wellness Benefits (Medical, Dental, Vision, and more)
401k with company contributions
Paid vacation, personal days, holidays, and sick leave
Paid Parental Leave and Family Building Benefits (Adoption, Surrogacy, and Infertility Support)
Life and Disability Insurance
Training and Professional Development investments
Tuition Assistance
Interview-process accommodation support
Inclusive and equitable workplace