About fme Life Sciences
fme Global Life Sciences specializes in delivering comprehensive business solutions with a focus on data and document migration, enterprise content management (ECM) system implementation, and business consulting services. 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 Regulatory Information Management (RIM), Clinical, and Quality Management System (QMS) domains. Our strategic partnerships with leading ECM vendors like Veeva Vault, OpenText Documentum, Generis CARA, Ephesoft, and Alfresco 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 sets us apart from our competition.
Job Description
As a Technical Consultant, you will work on the implementation aspects of the project and you will use your skills, knowledge and experience to bring a technology project (implementation or migration) to success. You will collaborate closely with the Project Manager and Technical Lead to ensure that the project progresses smoothly, technical challenges are addressed, and the project objectives are met within the defined constraints.
The candidate should possess basic technical knowledge of at least one of the leading content management platforms and will ideally have work experience in at least one of the business areas in the Life Sciences industry. The candidate will be a technical consultant for implementing, migrating, testing and documenting ECM solutions for a wide range of clients based on provided user requirements. An understanding of pharmaceutical validation and documentation practices is helpful.
This role requires good 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.
Key Responsibilities
• Implementation and Migration – Work on the implementation and migration of technical solutions and applications that fulfill the client’s needs. This can include but is not limited to customizing and configuring software applications, configuring migration utilities and creating additional supporting scripts to fulfill migration scope, as well as offering technical support and troubleshooting assistance within the project scope. The technical work will be related to a specific domain or technology and to one or multiple of our partner platforms (Veeva Vault, OpenText Documentum, Generis CARA).
Requirements
Benefits
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