IT Technical Writer

For our client, a pharmaceutical company in Switzerland, we are looking for a motivated and ambitious:

IT Technical Writer

BACKGROUND:
This Validated M&S Environment project will identify the processes and systems gaps, analyze and address them and establish a fully operational environment for the Clinical Modeling and Simulation (M&S) team. It aims at building a secure, reliable, scalable and Good Clinical Practice (GCP) compliant working environment for the M&S.
The project is in its delivery phase. An external company has been identified and we are working closely with the vendor to implement the business requirements and to achieve the full implementation of the system by the end of 2017.
The main goal of the project is to comply with the mandated GCP requirements from the Regulatory Authorities and to harmonize exploratory and M&S workflows and tools.

TASKS & RESPONSIBILITIES:

- Preparation of the complete project development life cycle documentation
- Coordination and tracking of activities associated with the delivery of documentation, eg adequate review and approval process is followed
- Support the project team in documenting testing activities and setting up appropriate test cases and scripts
- Support the Informatics Project Leader in coordinating and attending project team meetings, writing of meeting minutes and follow-up of action items
- Analyzing existing documentation and consolidation

MUST HAVES:

- Sufficient technical background (+7 years' experience in the Informatics/Information Management area) and knowledge to write documents for the complete Software Development Lifecycle
- Good knowledge of the full Lifecycle of an Information Management (IM) project and supporting a project methodology
- Extensive knowledge of the MS Office tools
- Flexible and able to work on many tasks at the same time
- Team player with very good communication skills
- Excellent written and spoken English language skills

NICE TO HAVES:

+++ Experience with computer systems validation (CSV) including knowledge of how to test software packages in a validated environment (particularly 21 CFR Part11)
+++ Experience in using HP Application Lifecycle Management (HP ALM)
++ Experience in the Pharmaceutical industry

START DATE: 01.06.2017
END DATE: 10.11.2017
LOCATION: BASEL

Are you interested to work in this challenging position? Alessia Biassoli, Talent Resourcer, is looking forward to receiving your complete profile. Please send an e-mail (see below)