fme Life Sciences is a leading provider of business and technology services supporting the deployment of Business Applications and Content Services/ECM solutions to its clients in the Life Sciences Industry. We act as a trusted advisor and systems integration specialist across the Clinical, Regulatory and Quality and Manufacturing domains in Europe and North America. fme is partnered with the leading ECM vendors supporting the Life sciences industry, including Veeva, OpenText/Documentum, Sparta, Generis (CARA), Ennov and Alfresco.
fme’s priority is client satisfaction and assisting organizations with determining the most effective way to deploy mission critical Content Services related technologies. We focus on both the business process aspects of technology platform implementations and data/document migrations, in addition to delivering high quality technical resources. 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 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 have 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. He/She will be the migration lead for migrating ECM solutions for a wide range of clients. He/She 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.
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.
To perform this job successfully, an individual must be willing and able to perform each essential responsibility satisfactorily.
Got curious? We would be happy to give you further insights into our company and your area of responsibility during a personal interview.
We are looking forward to meeting you!