Beschreibung
CSV (Computer Systems Validation) Consultant, Electronic Record/Signature Compliance, GxP IT Compliance Regulations
Experience of Validation Testing of IT applications for Pharma applications
Good Knowledge and hands of Experience in Computer Systems Validation (CSV), CAPA, 21 CFR, GAMP, GxP, IQ/OQ/PQ, LIMS and Electronic Laboratory Notebook (ELN)
Good Communication and managerial skills to Lead the Validation Team
Ability to manage multiple tasks and projects simultaneously, and to prioritize work, goals and tasks per the divisional and corporate objectives.
Develop the validation testing strategy for large and medium sized projects and develop the overall Validation plans and timetables.
Experience with Quality Center (HP Quality Center), HP ALM, HP QTP Preferable
- Knowledge of German is highly advantageous, although not mandatory.
Please send your CV for immediate consideration.