Senior Technical Lead, Veeva Vault Migrations - Life Sciences - EU

4 months, 1 week ago
Full-time
Lead
Software Development
FME US,

FME US,

fme US provides Enterprise Content Management Solutions for the Life Sciences Industry, helping clients optimize processes and embrace digital transformation to stay competitive globally.

Internet Software & Services
11-50
Founded 1995

Description

  • Partner with project managers and stakeholders to define project requirements, objectives, timelines, and resource plans.
  • Lead and manage a global technical team across onshore, offshore, and contractor resources.
  • Serve as the technical liaison between project teams and stakeholders, including business contacts and QA teams.
  • Provide technical guidance on architecture, design decisions, code reviews, documentation practices, and project execution standards.
  • Monitor project risks, escalate issues, and help evaluate solution options to address technical roadblocks.
  • Identify change orders and provide technical scope, estimates, and resource planning for proposed changes.
  • Work with QA teams to define test strategies, review test plans, and support defect and performance issue resolution.
  • Lead implementation and migration efforts for content management solutions across life sciences clients.
  • Collaborate with business and IT stakeholders in Clinical, Regulatory, and Quality domains to translate business objectives into system requirements.
  • Support pre-sales activities by contributing technical expertise, solution design input, and estimates for proposals.

Requirements

  • Bachelor’s degree in Computer Science, Information Technology, Life Sciences, or a related field.
  • Minimum of 8 years of experience in data and document migration, ECM implementation, or related fields.
  • At least 3 years of leadership experience within the life sciences industry.
  • Extensive experience architecting, installing, designing, implementing, configuring, and troubleshooting ECM systems and applications.
  • Advanced experience with ECM platforms such as Veeva Vault, OpenText Documentum, or Generis CARA.
  • Experience with data and document migration tools, SQL, XML, and scripting languages.
  • Experience with both cloud-based and on-premise solutions.
  • Strong understanding of life sciences regulations, compliance requirements, validation processes, and GxP-validated systems and documentation.
  • Experience working with clients across international markets and managing globally distributed technical teams, including offshore resources and external providers.
  • Must be available for occasional domestic and international travel and flexible work hours to meet program timelines and deadlines.

Benefits

  • Remote position.
  • Occasional international and domestic travel may be available/required depending on project needs.
  • Flexible work hours may be necessary to accommodate program timelines and deadlines.

Interested in this position?

Apply directly on the company website

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