Senior Consultant, Quality Systems – Veeva

Clarkston Consulting

Quality Systems Senior Consultant at Clarkston delivering business solutions for life sciences and consumer products companies. Collaborating with clients on Veeva implementations and project management.

Posted 6/19/2026full-timeRaleigh • Montana, North Carolina, Ohio, Pennsylvania, Wisconsin • 🇺🇸 United StatesSeniorWebsite

ATS Keywords

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Hard Skills

VeevaQuality Management SystemsDocument Management SystemsRegulatory Information Management SystemsGood Manufacturing PracticesStandard Operating ProceduresAnalytical SkillsProject ManagementConfigurationImplementation

Soft Skills

Team LeadClient Services OrientationFlexibilityAdaptabilityCommunicationKnowledge TransferRelationship BuildingProblem SolvingTrainingDocumentation

Tools & Technologies

Veeva VaultEtQTrackWiseOpenTextSharePointDocumentumFirstDocFirstPointNextDocs

Certifications & Qualifications

4-year degree

Industry Keywords

Life SciencesConsumer ProductsComplianceGlobal Quality RequirementsQuality Information SystemsContent Management SystemsGMP EnvironmentProject ScopeRequirements WorkshopsBest Practices

Tech Stack

Tools & technologies

Vault

About the role

Key responsibilities & impact

**What You’ll Do**
As a Quality Systems (Veeva) Senior Consultant at Clarkston, you will:
- Participate in projects at life sciences and consumer products companies designing and deploying Veeva
- Support the 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
- Earn trusted client status and develop relationships that extend beyond the project’s life cycle
- Create and oversee project or workstream plans and timelines, define deliverables, assign team roles and resources, identify and track issues and their resolution, and help manage project scope and requirements.
- Assist in validation of computer systems for use in a Good Manufacturing Practices (GMP) environment and creating and revising Standard Operating Procedures (SOPs)
- Conduct knowledge transfer and training of end-users, including sharing best practices
- Provide guidance to junior systems analysts and client personnel assigned to projects

Requirements

What you’ll need

*What We’re Looking For*
- 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 - our consultants work on everything from design to hands-on configuration and can stretch into new roles
- Thorough client services orientation and accustomed to taking an active role in executing engagements and project plans/tasks
- Excellent analytical skills and the ability to present and write at publication quality level to communicate findings and recommendations
- 4-year degree from an accredited college or university

Benefits

Comp & perks

*Our benefits include:*
- 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, and more