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 like 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.
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 migration
* 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 approach
* 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
Required Qualifications and Skills
* 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
* Expected travel is up to 20% for client workshops and strategy sessions
* Business fluent-level English proficiency (spoken and written) is required
Your fme-benefits
* Remote work (up to 100%) as well as an annual mobile work bonus
* Individual working time and part-time models
* Equipment with current devices (at choice: Apple, Google Pixel or HP) also for private use
* An annual training budget and individual career and development planning
* Discounts via corporate benefits
* An annual budget for innovation management to shape creative brainstorming processes within the company
Curious now? We will be happy to give you further insights into our company and your area of responsibility during a personal meeting.
We are looking forward to meeting you
Contact person for questions:
Ansprechpartner für Fragen: Ute