Senior Technical Lead - Veeva Vault Migrations

5 days ago

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fme US, LLC

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OpenText • Documentum • InfoArchive • Digital Transformation • Life Sciences

11 - 50 employees

Founded 2010

Description

•About fme Life Sciences •fme Life Sciences focuses on Business Solution technology implementations that leverage Content Services (Document Management) platforms for clients in the Life Sciences Industry. •fme is increasingly regarded as a trusted vendor and partner by its clients, who range from small and emerging start-ups to large global pharmaceutical companies. •The company is widely regarded as a leader in providing business consulting, systems integration and ongoing support services focused on Content Services and its applicability to business-critical solutions including RIM, Regulatory, Clinical and QMS. •fme’s priority is client satisfaction and assisting them with determining the most effective way to deploy mission critical technologies. •We focus on three aspects, business process consulting, technology platform implementations and managed services, and data/document migration services. •This ability to provide business insight as a supplement to the clients’ internal expertise, and then to execute efficiently and cost effectively on the technical implementation, is a key feature of our services and differentiates us from our competition. •We are seeking a highly skilled and experienced Senior Technical Lead to oversee and drive data and document migration projects, along with enterprise content management (ECM) implementations. •This role requires deep technical expertise, strong leadership abilities, and a thorough understanding of the life sciences landscape. •As a Senior Technical Lead, you will serve as the subject matter expert, overseeing and managing all technical aspects of the project and leading the technical team. •This role requires close collaboration with the Project Manager (PM) and engagement with both internal and external stakeholders, including contractors, to ensure project success. •You will work in tandem with the Project Manager, Business Analysts and Technical Consultants to ensure seamless project progression, provide strategic guidance, address technical challenges, and achieve project objectives within the established constraints. •The ideal candidate will have in-depth technical expertise with leading content management platforms and the Life Sciences industry. •The successful candidate will be adept at collaborating with both business and IT teams within Clinical, Regulatory, or Quality domains. •As the technical lead, you will be responsible for implementing and migrating Content Management solutions for a diverse range of Life Sciences clients, including small, medium, and large enterprises. •You will work closely with clients to understand their business objectives, translate those objectives into system requirements, and lead the successful implementation and migration of solutions. •This role involves coordinating with our offshore team and partners to ensure seamless execution. •A strong understanding of pharmaceutical validation, documentation practices, and relevant regulations is essential. •This role demands outstanding verbal and written communication skills, with the ability to engage effectively with individuals at all levels of an organization. •We seek a creative and committed individual who will thrive in and contribute to our collaborative culture. •Key Responsibilities / Qualifications

Requirements

•Education: Bachelor’s degree in Computer Science, Information Technology, Life Sciences, or a related field. •Experience: Minimum of 8 years of experience in data and document migration, ECM implementation, or related fields, with at least 3 years in a leadership role within the life sciences industry. Extensive experience in architecting, installing, designing, implementing, configuring, and troubleshooting ECM systems and applications. •Technical Skills: Advanced experience in ECM platforms (e.g., Veeva Vault, OpenText Documentum, Generis CARA), data and document migration tools, SQL, XML, and scripting languages. Experience with cloud-based solutions as well as on-premise solutions. •Regulatory Knowledge: Strong understanding of life sciences regulations and compliance requirements, including experience with validation processes as well as with GxP-validated systems, processes, and documentation requirements. •This is a REMOTE position but may require occasional international and domestic travel to project sites or client meetings. Flexible work hours may be necessary to accommodate program timelines and deadlines

Benefits

•#LIREMOTE