Job Description
About fme
fme Life Sciences specializes in delivering high quality, complex migration services focusing on data and documents in regulated industries. We serve a diverse client base in the Life Sciences industry, ranging from innovative start-ups to large global pharmaceutical companies. As a recognized leader, we provide expert consulting, tailored data and document migration, and ongoing support to meet critical needs in their industries. Our strategic partnerships with leading platform vendors such as Veeva Vault, OpenText Documentum, and Generis CARA enable us to offer unparalleled expertise and service to our clients.
At fme, our priority is client satisfaction, assisting them in determining the most effective ways to deploy mission-critical technologies and support their ever-evolving business growth and needs. Our ability to provide business insight as a complement to our clients’ internal expertise, combined with our capacity to execute efficiently and cost-effectively, is a key feature of our services and differentiates us from our competition.
Job 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.
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.
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
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