Quality Systems (Veeva) Senior Consultant
Role details
Job location
Tech stack
Job description
Clarkston Consulting is seeking motivated, self-driven leaders who are energized by team results and interested in joining a firm that values its culture and people as its biggest strengths. Come join us as a Quality Systems (Veeva) Senior Consultant, and in this role, you will deliver creative business solutions to our market-leading clients in the life sciences, consumer products, and retail industries.
Together, we can find the answers to our clients' most challenging business problems through a combination of our industry expertise, business process knowledge, and consulting excellence.
What You'll Do
As a Quality Systems (Veeva) Senior Consultant at Clarkston, you will:
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Participate in projects at life sciences and consumer products companies designing and deploying Veeva
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Support the configuration and implementation of Veeva Quality suite and Veeva Vault RIM capabilities
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Lead requirements workshops, design, prototype, configure and document content management/QMS data solutions
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Earn trusted client status and develop relationships that extend beyond the project's life cycle
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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.
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Assist in validation of computer systems for use in a Good Manufacturing Practices (GMP) environment and creating and revising Standard Operating Procedures (SOPs)
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Conduct knowledge transfer and training of end-users, including sharing best practices
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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:
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Receive the support and mentorship of your Clarkston colleagues and leaders
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Expand your existing skillset with internal and external professional development opportunities
Requirements
What We're Looking For
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5+ years of experience working with or for life sciences companies
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Experience implementing Document or Quality Management systems for life sciences as a consultant, business, or IT representative
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Experience with regulatory information management systems, including registrations and submissions, preferred
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Understanding of global quality requirements, compliance considerations, and processes
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Firsthand experience with systems such as Veeva Vault, EtQ, TrackWise, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, or other quality information or content management systems
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Team Lead experience
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Flexibility and adaptability - our consultants work on everything from design to hands-on configuration and can stretch into new roles
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Thorough client services orientation and accustomed to taking an active role in executing engagements and project plans/tasks
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Excellent analytical skills and the ability to present and write at publication quality level to communicate findings and recommendations
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4-year degree from an accredited college or university
Benefits & conditions
Travel is an integral part of this role and is estimated to average 30-50%. This may vary based upon client and project needs. When not traveling, consultants work from their home office. Relocation is not required., Our benefits include:
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Comprehensive Health and Wellness Benefits (Medical, Dental, Vision, and more)
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401k with company contributions
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Paid vacation, personal days, holidays, and sick leave
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Paid Parental Leave and Family Building Benefits (Adoption, Surrogacy, and Infertility Support)