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 is partnered with the leading Business Solutions and ECM vendors supporting the Life Sciences Industry, including Veeva, OpenText/ Documentum, Generis (Cara), Sparta.
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 motivated, inquiring and communicative individual with a strong vision being part of an aspiring team.
The candidate should be an experienced professional with a proven technical background in Enterprise Content Management and Life Sciences to become a key member of our Technology Services Practice.
The ideal candidate should possess strong analytical and technical skills, a robust and relevant background, strong communication abilities and have a team-oriented attitude.
The candidate should have 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 technical lead for implementing ECM solutions for a wide range of clients. He/She will engage with clients to understand their business needs, translate those needs into system requirements and lead the implementation of the system 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.
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!