Beschreibung
Must have experience on TrackWise (SPARTA) QMS systems - at least 4 years on TRACKWISE
Domain:
Pharmaceutical/Biotech/Process Industries
Must Have:
Application Design, Architecture and Development, Configuration experience
Experience in IT functional design and effort estimates
4+ years of relevant experience with compliance/quality management software
3+ years of relevant experience with TRACKWISE Quality Management System (version 8.5+), including creation of process groups, workflows, notifications, coordinator activities & group categories.
3+ years working in a GMP validated software environment
1+ years working with Crystal Reports or exposure to TRACKWISE Analytics
1+ years working with SQL to query, create, update tables, materialized views, database links.
Working knowledge of TRACKWISE migrator and Import utilities
Experience troubleshooting TrackWise applications.
Experience writing/analysing TrackWise web services a plus.
L2 or L3 support experience on TW
Good to have:
Experience with TrackWise implementations that have interfaced with multiple other applications (eg ERP, MES)
Experience working with offshore delivery team
Life Sciences experience
Experience presenting to IT stakeholders.
Consultative skills
Good listening skills with ability to make timely well-informed decisions.
Ability to translate business requirements and architecture designs into system designs.
Ability to track project activities and track progress
Willingness and ability to train and offshore mentor staff.