Consultant Validation de Systèmes informatisés (VSI) H/F
Offer details
Wanted profile
And what about you?
- 5 years' higher education / Engineering or equivalent
- Good understanding of the pharmaceutical industry and its processes
- At least 5 years' experience in IT project management in the pharmaceutical industry: knowledge of one or more ERPs and Computerised Systems Validation (CSV) processes.
- A culture of quality and project management (quality, cost, deadlines, planning, workload, management of deliverables, communication, regular reporting),
- Sense of service - Results-oriented personality
- Strong interest in cross-functional work
- A good level of English
Are you ready to take on new challenges and start a new adventure? Don't hesitate to contact us!
Context
At Anywr.Life - brand of the ANYWR group, we specialise in the manufacture of Life Sciences We work closely with our customers in the pharmaceutical, biotechnology and medical device sectors.
As part of our expansion, we are recruiting profiles of Computerised Systems Validation Consultant (VSI) for the pharmaceutical industry.
Mission
Your main task will be to provide technical and management solutions for our customers in the pharmaceutical industry to improve the performance and quality of their environment.
You will work directly on our partners' sites in a GMP environment, in project mode.
Your role as Computerised Systems Validation Consultant (VSI) will be to contribute to our customers' projects such as :
- Supervision of ERP implementation,
- Identifying and defining all the interfaces required,
- Identifying, defining, coordinating and monitoring the work packages to be carried out,
- Creating and monitoring the required project documentation,
- Identifying and communicating any project risks,
- ERP updates and maintenance
