Beschreibung
Are you looking for a challenging and interesting project in Switzerland? Are you an experienced CSV consultant ?General information:
- Start date: 20.05.2019
- Latest start date: 27.05.2019
- End date: 31.12.2019
- Extension: An extension is possible, but needs to be approved.
- Work load: 100%
- Work location: Basel, Switzerland
- Deadline to submit profiles: 8:00AM GMT on 29th April
- Travel: Not required.
Tasks & Responsibilities:
- Computerized system validation of stand-alone systems according to company requirements
- Authoring of the system dedicated SOPs and other CSV documentation
- Communication with stakeholders across the organization
- Collaboration with the project team
- Report to the CSV Lead
Must Haves:
- +8 years of experience as CSV Specialist (requirements below included)
- Experience with validation of lab systems in a GMP environment
- More than 4 years of experience in regulated environments
- Project management experience
- Experience in cooperation with lab and service technicians
- Experience in operating different Lab IT systems
- Strong communication skills (very important for this Senior role)
- Fluent in German and English (both mandatory)
Nice to Haves:
+++ Experience with validation of PAT systems is a plus
++ Experience in Pharmaceutical industry is a plus
+ Experience with HP ALM Software is a plus