Experience in providing services such as large-scale business and technology transformation, targeted business performance improvement and post-merger integration for R&D functions (includes Pharmacovigilance, Clinical, Regulatory, Pre-clinical and research, QC and research laboratories).
- Profound experience in the development, implementation and lifecycle management of key computerized systems in the Pharmaceutical Development, Manufacturing and Quality space (e.g. ERP/SAP, CTMS, MES, LIMS)
- Excellent background and experience in project management of large global IT projects
- Extensive track record of successful cross-divisional/cross-functional work with complex international and multidisciplinary teams
- Profound understanding of global regulations and Health Authorities expectations governing computerized systems incl. computerized systems validation, lifecycle management and 21 CFR Par 11 requirements.
Vacancy Type: Full Time
Job Location: London, England
Application Deadline: N/A