Job Description

*This is a fully remote role The Veeva Migration Consultant will lead customer migration implementations by providing expertise with data and document content migration, Vault migration tools and APIs, and Vault Platform best practices to ensure customer success. We are seeking a motivated and experienced individual with a proven technical background in Enterprise Content Management Migration and Life Sciences to become a key member of our Migration Services Practice. They should possess strong analytical and technical skills, a robust and relevant background, strong communication abilities and a team-oriented attitude. The candidate should possess technical knowledge of the leading content management platforms and will ideally have work experience in the Life Sciences industry. The successful candidate will be confident working with business and IT groups in R&D and Q&M application business areas. They will be the migration lead for migrating ECM solutions for a wide range of clients. They will engage with clients to understand their business needs, translate those needs into migration requirements and lead the migration initiative to meet those requirements. An understanding of pharmaceutical validation and documentation practices as well as regulations is key. Requirements This role requires exceptional verbal and written communication skills and the candidate must have the ability to converse with people from all levels within an organization. We are looking for a creative and dedicated individual who will fit with our collaborative culture. Work with clients to analyze their migration needs and define requirements for migrating leading Content Management solutions in the Life Sciences industry; Minimum 7 years of document/content migration experience with enterprise content management systems (Documentum, OpenText, Box, SharePoint, etc.) ; Minimum 7 years of customer-facing technical consulting experience; Translate requirements into migration plans and mapping specifications and ensure delivery to the client including reporting the migration progress; Liaise with and lead offshore migration team during migration execution and verification; ability to work well with a diverse and globally distributed team; Service as the Subject Matter Expert (SME) for the migration of Content Management solutions; supporting multiple projects simultaneously; Lead migration projects and escalate migration project risks/issues in a timely manner, as necessary to management; Ability to learn new concepts, source and target systems, and software independently and quickly; Eagerness to learn and apply new emerging technologies to solve complex business requirements; Proven track record meeting with senior management and executives as the subject matter expert. Further requirements: Bachelor\'s Degree in Computer Science or related field; 7-10 years experience in the Life Sciences industry or consulting (R&D and Q&M business processes); Minimum 5 years of experience migrating ECM solutions; Advanced knowledge (5+ years) of the Veeva Clinical, Regulatory, and Quality suites; specific experiences within the Regulatory Vaults are highly desired especially RIM; Experience migrating from and to Documentum content management systems to Veeva is a plus; Advanced database skills including knowledge of Oracle/SQL Architecture; ability to write complex SQL statements experience helpful; Experience with validated systems with the ability to produce quality documentation deliverables and execute installation procedures and test cases; Experience with migration verification procedures; Excellent client-facing and interpersonal communication skills; The candidate must be strong at communicating with stakeholders of all levels; They will possess extensive interpersonal skills and must be able to prepare regular written and verbal presentations, technical documents, and reports; The candidate must be self-driven but must also work well in a team, taking on different roles as needed (dependent on the project situation) ; The candidate must be flexible and able to multi-task; can work within an ambiguous, fast-paced environment, while also driving toward clarity and solutions; demonstrated resourcefulness in setting priorities; General experience in Veeva Quality, Clinical, or Safety business processes; Experience with GxP and software validation regulations. Nice to have: Experience with Veeva Regulatory (RIM, Submission, Submission Archive) is a plus; Familiarity with other platforms such as Generis CARA/ OpenText D2/ FirstDoc would be beneficial. Here\'s our part of the deal: You\'ll be part of a mature, stable company, with more than 15 years on the market; You\'ll get to play with cool stuff like Enterprise Content Management (ECMs), Business Intelligence and Cloud technologies; Competitive salary; Training & Development; Flexible work schedule. We are fme, an innovative environment within a young team. We are part of fme Group headquartered in Braunschweig, Germany, with subsidiaries in Germany, Romania and United States. For more than 15 years we have helped enterprises speed up critical business processes, improve operative decision making and ensure information security and compliance using Enterprise Content Management, Business Intelligence and Cloud technologies.

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