Senior Director, Cell Therapy Devens Manufacturing Site IT Lead
4 weeks ago
Bristol-Myers Squibb is a global biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled and experienced IT Platform and Product Manager to oversee the IT operations at our Devens, MA Cell Therapy manufacturing site.
Key Responsibilities:- Lead a matrixed organization composed of site direct reports and indirect reports to deliver effective, innovative, and stable solutions that meet the site's needs.
- Develop and implement comprehensive IT strategies that support the organization's business objectives and growth plans.
- Oversee the development, implementation, and maintenance of IT platforms to support manufacturing operations.
- Collaborate with stakeholders to define product requirements, prioritize features, and create product roadmaps.
- Manage new demand from site functions through the IT stage gate process.
- Negotiate and manage contracts with IT vendors, service providers, and consultants.
- Bachelor's degree in an Information Technology, life sciences, or engineering discipline (Master's Degree preferred) or a minimum of 12 years of equivalent biotechnology or pharmaceutical industry experience.
- Proven experience in IT platform management, product management, and manufacturing site IT operations.
- Extensive experience in a senior IT leadership role, with a proven track record of successful IT strategy development and execution preferably within a pharmaceutical technical operations environment.
- Demonstrated strong leadership and team management skills, with the ability to inspire and motivate a diverse team.
- Excellent project management skills, with the ability to manage multiple projects simultaneously.
- Strong analytical and problem-solving skills.
- In-depth knowledge of IT infrastructure systems, change management, staff mentoring, performance evaluation, life-long learning, and diagnosis of sources of problems in both technology and business processes.
- Deep knowledge of regulatory requirements in the areas of current Good Manufacturing Process (cGMP).
- Understanding of regulatory requirements and the role technology plays in satisfying those requirements is essential to this position.
- Thorough understanding of best practices in SDLC and ITIL.
- Effective communication and interpersonal skills, with the ability to influence and engage stakeholders at all levels.
Bristol-Myers Squibb is an equal opportunity employer and welcomes applications from diverse candidates. We are committed to creating an inclusive work environment that values diversity, equity, and inclusion. If you are passionate about transforming patients' lives through science, we encourage you to apply for this exciting opportunity.
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