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Role Description

fme Life Sciences is seeking a highly experienced Global Solution Architect to serve as a Subject Matter Expert (SME) in regulated data management and content migration, as part of a client’s digital transformation process. This is a senior role in our organization and is ideal for professionals with deep domain knowledge in life sciences, a client-first mindset, strong technical proficiency, and a track record of designing scalable, compliant migration solutions.

This position emphasizes strategic thinking, cross-functional collaboration, and dedication to delivering impactful results in global transformation initiatives for top-tier pharmaceutical leaders. This role will play a dual function, contributing to strategic sales efforts and providing subject matter expertise and executive technical oversight of active projects.

Key Responsibilities

• Subject Matter Expertise
  • 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.
• Business Development and Client Advocacy
  • 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.
• Technical Solution Design
  • 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.

Qualifications

• 20+ years of experience in enterprise data and content management platforms within the life sciences industry.
• Strong domain expertise with content and data migration in validated environments, including systems like Veeva Vault and OpenText Documentum.
• Demonstrated ability to bridge business objectives and technical solutions, especially in regulated domains.
• Experience in consulting or client advisory roles with a focus on digital transformation.
• Excellent communication, presentation, and executive briefing skills.

Preferred Attributes

• Experience with fme migration-center or other enterprise migration/ETL platforms.
• Exposure to emerging technologies such as AI-enabled content analysis, metadata enrichment, or automation in migration pipelines.
• Background in Computer Science, Life Sciences, Engineering, or related fields.
• Familiarity with change management and user adoption strategies in regulated industries.

Benefits

• Medical, Dental & Vision plans
• 401k with company match
• Life Insurance, Short & Long-term Disability Plans
• Paid Time Off (Vacation, Sick/Personal & 10 Paid Holidays)
• Employee Referral Program
• Training & Development & Company Retreats
• Wellness Resources/Employee Assistance Program
• Remote