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Site IT Director
2 maanden geleden
Bristol Myers Squibb is a global biopharmaceutical company that is dedicated to transforming patients' lives through science. We are inspired by a single vision - to make a meaningful difference in the lives of patients.
Director, IT Cell Therapy Manufacturing Site LeadThis role plays a critical part in managing all corporate and locally supported infrastructure and software at the Leiden, NL Cell Therapy manufacturing site. The IT team is committed to achieving excellence, measured by their effectiveness in supporting business functions and related business processes across the company.
Key Responsibilities- Lead a matrixed organization to deliver effective, innovative, and stable solutions that meet the needs of the site.
- Collaborate with site leadership to develop, support, and align strategies for business process improvements through information systems automation.
- Function as the liaison and single point of contact between site leadership and corporate IT.
- Accountable for continuous operation and maintenance of ERP, MES, LIMS, local manufacturing, quality control, and quality management site IT systems as well as associated site infrastructure.
- Lead Cell Therapy site service level management scope and process with IT groups and/or vendor managed services.
- Provide IT leadership to site inspection readiness and data integrity initiatives.
- Participate in high-level strategic communications with the business and site leadership teams.
- Manage new demand from the various site functions through the IT stage gate process.
- Identify key technology trends and how new technologies might be leveraged to provide better solutions to the manufacturing site.
- Bachelor's degree in a life sciences or engineering discipline or a minimum of 10 years of equivalent biotechnology or pharmaceutical industry experience.
- Greater than 10 years in multiple organizational contexts, including IT, CSV, linking technology to business needs in the biopharmaceutical industry.
- Experience in information technology, preferably within a pharmaceutical technical operations environment. Experience should range from manufacturing and quality control systems to GxP quality management systems.
- Demonstrated effective leadership skills in building high-performance teams.