Director, Site IT Lead

5 dagen geleden

Leiden, Nederland Bristol Myers Squibb Voltijd

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb Netherlands

Bristol Myers Squibb has been active in the Dutch market for over 50 years, employing people across a range of activities and business units in Utrecht, The Netherlands.

The Netherlands is also home to our first European Cell Therapy facility, located at the Leiden Bio Science Park, the largest life sciences cluster of The Netherlands. This new state of the art facility is focused on commercial manufacturing with capabilities for multi-product Cell Therapy manufacturing. You can become part of this exciting journey. if you want to know more about it

The Netherlands has everything it takes to become the medicines hub of Europe, the so-called Boston by the North Sea. As we continue to expand our footprint by building this new site, we are looking to grow our team.

Would you like to become an important chain in our worldwide network to bring this new personalized treatment to patients suffering from blood cancer? Join us and be a game changer

Position Summary

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology, and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

The Director, IT Cell Therapy Manufacturing Site Lead position plays a critical role in managing all corporate & locally supported infrastructure and software at the Leiden, NL Cell Therapy manufacturing site. IT is committed to achieving excellence as measured (in part) by their effectiveness in supporting business functions and related business processes across the company. The role must excel at supporting the site’s daily operations while also developing a strategic IT roadmap for the site.

This role will report to the Exec. Director, IT Business Partner for Cell Therapy & Digital Manufacturing and will also be part of CTGM IT Leadership Team.

Key Responsibilities

Lead a matrixed organization composed of both site direct reports and groups of indirect reports to deliver effective, innovative, and stable solutions that meet the needs of the site. Active member of the Site Leadership team. Collaborate with site leadership to develop, support, and align strategies for business process improvements through information systems automation. Function as the liaison and the 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, i.e. Service Level Agreements (SLA’s), Disaster Recovery/Service Continuity, etc. 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 (Manufacturing Operations, Quality, Supply Chain, Manufacturing Science & Technology) 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

Qualifications & Experience

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.

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