Chad Kowieski
Transformational Leader in Pharmaceutical Facilities Management | Expertise in IFM & Regulatory Compliance
- Role
- Executive Director Global Facilities Operations at Bristol Myers Squibb
- Location
- Princeton, NJ, US
- LinkedIn followers
- 500 followers
About Chad Kowieski
With over 25 years of experience in facilities management and strategic operations, I specialize in delivering innovative, cost-effective solutions that align facilities strategies with organizational goals. My career spans leadership roles in global pharmaceutical and biotechnology companies, overseeing portfolios exceeding 4 million square feet and managing budgets of $300M+ annually.I excel in driving operational excellence, building high-performing teams, and implementing Integrated Facilities Management (IFM) models that streamline processes and reduce costs. My expertise extends to regulatory compliance, where I’ve successfully led global health authority inspections (FDA, EMA, MHRA, and more) and acted as a Subject Matter Expert (SME) for high-purity water systems.Adept at navigating complex matrix organizations, I thrive in fostering cross-functional collaboration with procurement, finance, and operational teams to achieve business objectives. Whether leading transformative infrastructure projects, developing long-term capital improvement strategies, or ensuring audit readiness, I am committed to enhancing operational reliability and sustainability.
Experience
Executive Director Global Facilities Operations
Feb 2026 — Present
Education
University of Wisconsin-Platteville
Bachelor of Science (BS)
1996 — 2001
University of Wisconsin-Platteville
Bachelor of Science (B.S.)
1996 — 2001
Skills
- 21 Cfr Part 11
- Aseptic Processing
- Biotechnology
- Capa
- Change Control
- Engineering
- Manufacturing
- Fda
- Mhra
- Regulatory Requirements
- Vaccines
- Cross-Functional Team Leadership
- Formulation
- Quality Auditing
- Validation
- V&V
- Ema
- Quality Assurance
- Sop
- Lean Manufacturing
- Management
- Trackwise
- Technology Transfer
- Clinical Operations
- Gmp
- Lims
- Project Engineering
- Root Cause Analysis
- Generic Programming
- Regulatory Affairs
- Software Documentation
- Tga
- R&D
- Automation
- Glp
- Quality Control
- Fda Gmp
- Gamp
- Commissioning
- Iso 13485
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