Job Details

ID #23797211
State New Jersey
City Southplainfield
Job type Permanent
Salary USD TBD TBD
Source Robert Half
Showed 2021-12-03
Date 2021-12-02
Deadline 2022-01-31
Category Systems/networking
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Veeva Quality Docs Admin

New Jersey, Southplainfield, 07080 Southplainfield USA

Vacancy expired!

Description

Focus on business process re-engineering efforts and regulatory complianceEarn trusted client status and develop relationships that extend beyond the project'Microsoft life cycleParticipate in projects at life sciences and consumer products companies designing and deploying Quality systemsRapidly configure and implement the Vault Quality suite (Vault QMS, Vault QualityDocs) which is used to manage quality process and content in the cloudLead requirements workshops, design, prototype, configure and document content management/QMS data solutionsCreate and oversee project plans and timelines, define project deliverables, assign project team roles and resources, identify and track issues and their resolution, and 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 practicesProvide guidance to junior systems analysts and client personnel assigned to projects

Requirements

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 Understanding of global quality requirements, compliance considerations and processes for Quality process and content management, life sciences compliance, and/or computer systems validation Firsthand experience with systems such as Veeva Vault, EtQ, TrackWise, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, other quality information or content management systems

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Vacancy expired!

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