David Santoro
Materials Management Supervisor at Alnylam Pharmaceuticals
- Role
- Materials Management Supervisor at Alnylam Pharmaceuticals
- Location
- Cambridge, MA, US
- LinkedIn followers
- 500 followers
About David Santoro
I have many years of experience in regulated industrial climates, from plant start up activities to multiple production facilities. Here are some highlights of my ability, knowledge, and expertise in customer service, inventory control, product receiving, warehousing, and materials distribution. During this time I was able to develop many systems and procedures that improved productivity, and efficiency. I am confident that I would be a great addition to any team. Highlights • 12 years of distribution management experience• 30 years of warehousing experience • Proven record in work, manpower planning and quality improvement• Experience in inventory control software development and application• Background in GMP products and equipment including chemicals, hazardous materials, diagnostic instruments, clean room and lab supplies, sterile items in both refrigerated, and ambient conditions. • Highly effective in MRP / ERP system troubleshooting• Independently resolved complex system issues • Responsible for the procurement of raw materials, and general supplies• Worked in FDA, USDA and cGMP compliant warehousing for over twenty two years. Excellent communication skills• Ability to work in a fast paced environmentSpecialties: •Overseen process order / work order creation for projected production demand.•Streamlined inventory stocking levels by creating minimum and maximum standard levels.•Hazardous Material Incident Commander •Standardized receiving, stocking, checking, and disposal of materials in production areas. •Implemented hazardous material stock rotation plan.•Conducted hazardous material/safety training for employees.•Cut disposal of hazardous materials 20% by implementing maximum stocking level
Experience
Materials Management Supervisor
Mar 2019 — Present · Boston, MA, US
Skills
- Gmp
- Sop
- Fda
- Change Control
- Pharmaceutical Industry
- Troubleshooting
- Capa
- Quality Control
- Quality Assurance
- Biotechnology
- Procurement
- 21 Cfr Part 11
- Validation
- Manufacturing
- Lims
- Gxp
- Aseptic Processing
- Quality System
- Laboratory
- Glp
- V&V
- Corrective and Preventive Action (Capa)
- U.s. Food and Drug Administration (Fda)
- Standard Operating Procedure (Sop)
- U.s. Title 21 Cfr Part 11 Regulation
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