fme Life Sciences

fme US, LLC is a trusted advisor and partner specializing in Business Solution deployments for the Life Sciences Industry

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Open Positions4

United StatesFull-TimeLife SciencesPosted
  • Serve as a trusted expert in regulated data and content management with a focus on GxP, regulatory, clinical, and quality domains
  • Provide insight into the enterprise architecture and deployment of systems such as Veeva Vault, OpenText Documentum, Generis CARA, etc.
  • Leverage deep industry knowledge to define proven best practices in content and data migration and compliance validation
  • Partner with Account Managers and Client Engagement Managers to create client-tailored strategic migration roadmaps and drive value in pre-sales engagements
  • Lead client-facing pre-sales workshops to assess readiness, gather requirements, and advise future-state architectures for effective data and content migrations
  • Represent fme in strategic client conversations, aligning technical migration direction with business transformation goals
  • Architect end-to-end migration frameworks, including advising on known source system and target system limitations and best practice approaches
  • Lead solutioning efforts leveraging fme migration-center, proprietary accelerators, and client infrastructure
  • Contribute to, review, and approve all solution estimates and proposals
  • Advise on scalable, validated, and compliant architecture aligned with 21 CFR Part 11, Annex 11, and related frameworks
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About fme Life Sciences

fme US, LLC is a trusted advisor and partner specializing in Business Solution deployments for the Life Sciences Industry. Founded in 2010, the company offers consulting, systems integration, migration, and support services for critical solutions including RIM, Regulatory, Clinical, and QMS, collaborating with leading vendors such as Veeva and OpenText.

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