Senior Quality Systems Consultant, Veeva

Clarkston Consulting

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

Posted 10/10/2026full-timeUnited StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in implementing Veeva Quality suite and Veeva Vault RIM capabilities, along with strong project management skills in life sciences and consumer products sectors. Proficient in regulatory information management systems and creating Standard Operating Procedures (SOPs) while fostering client relationships and leading teams.

Highest-signal resume keywords

Veeva Quality Suite ImplementationRegulatory Information Management SystemsProject ManagementTeam LeadershipClient Relationship Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Document Management SystemsQuality Management SystemsComputer-System ValidationStandard Operating Procedures (SOPs)Analytical Skills

Soft Skills

FlexibilityAdaptabilityClient Services OrientationCommunication Skills

Tools & Technologies

Veeva VaultEtQTrackWiseOpenTextSharePointDocumentumFirstDoc/FirstPointNextDocs

Industry Keywords

Life SciencesConsumer ProductsGMP EnvironmentsGlobal Quality RequirementsCompliance Considerations

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 the 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 extending beyond project lifecycles
Create and oversee project or workstream plans and timelines
Define deliverables, assign team roles and resources, identify and track issues and resolutions, and help manage project scope and requirements
Assist in computer-system validation for GMP environments
Create and revise Standard Operating Procedures (SOPs)
Conduct knowledge transfer and end-user training, including sharing best practices
Provide guidance to junior systems analysts and client personnel
Work with market-leading clients in life sciences, consumer products, and retail industries
Travel an estimated 30–50% based on client and project needs; work from a home office when not traveling

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; ability to work from design through hands-on configuration and stretch into new roles
Thorough client services orientation and active participation in executing engagements and project plans/tasks
Excellent analytical skills
Ability to present and write at publication quality level to communicate findings and recommendations
4-year degree from an accredited college or university
Responsible, authentic use of AI; real-time AI-generated or scripted interview answers are prohibited

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