Senior Quality Systems Consultant, Veeva

Clarkston Consulting

Quality Systems (Veeva) Senior Consultant at Clarkston delivering business solutions for life sciences and retail clients. Supporting Veeva implementation and fostering client relationships.

Posted 5/19/2026full-timeRaleigh • North Carolina, Pennsylvania • 🇺🇸 United StatesSeniorWebsite

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
**How You’ll Grow**
Beyond your day-to-day responsibilities, throughout your career at Clarkston you will:
- Receive the support and mentorship of your Clarkston colleagues and leaders
- Expand your existing skillset with internal and external professional development opportunities

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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

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

Soft Skills

Team LeadershipClient Services OrientationFlexibilityAdaptabilityCommunicationKnowledge TransferMentorshipRelationship BuildingProblem SolvingTraining