Salvatore Mancini
Facilities Manager | Streamlining Operations, Driving Safety, Reducing Costs & Ensuring Regulatory Excellence
- Role
- Facilities Manager at Cryoport Systems
- Location
- New York, NY, US
- LinkedIn followers
- 500 followers
About Salvatore Mancini
I lead facilities and operations for highly regulated life sciences environments, with…
Experience
Facilities Manager
Mar 2021 — Present · Morris Plains, NJ, US
Lead facilities and operations management for a regulated life sciences logistics provider, overseeing all aspects of site infrastructure, compliance, and operational efficiency.Key Achievements:Facility Buildout & Commissioning: Directed the startup, commissioning, and construction of a sq. ft. facility including office, production, and critical infrastructure spaces—delivered on time and to full compliance standards.Facilities & Infrastructure Leadership: Manage maintenance, repair, and calibration of site-wide systems including HVAC, generators, life safety systems, security, and monitoring systems to ensure 24/7 operational readiness.Vendor & Contract Management: Oversee third-party service providers and vendor contracts; implement cost controls and negotiate service agreements to improve performance and reduce expenses.Budgeting & Resource Management: Develop and manage operational budgets, aligning expenditures with business objectives while maintaining compliance and safety standards.Fleet & Logistics Oversight: Direct fleet management, ensuring critical, life-saving shipments are delivered reliably and efficiently.Team Leadership: Lead, mentor, and develop a cross-functional facilities team, fostering a culture of accountability, safety, and continuous improvement.Multi-Site Oversight: Managed facilities operations across multiple locations prior to transition into a centralized flagship site.
Education
Ramapo College of New Jersey
Bachelor of Science (B.S.), Engineering Physics
2013 — 2015
Bergen Community College
Associate of Science (A.S.), Natural Sciences and Mathematics
2010 — 2013
Skills
- Cross-Functional Team Leadership
- Root Cause Analysis
- Regulatory Affairs
- Validation
- Quality Assurance
- U.s. Title 21 Cfr Part 11 Regulation
- Corrective and Preventive Action (Capa)
- Lean Manufacturing
- Change Control
- Biotechnology
- Capa
- U.s. Food and Drug Administration (Fda)
- Manufacturing
- Gmp
- 21 Cfr Part 11
- Pharmaceutics
- Quality System
- Pharmaceutical Industry
- Sop
- Fda
- Standard Operating Procedure (Sop)
- Management
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