Tyrone Ortiz
Operations I Supply Chain I Continuous Improvement Senior Leader
- Role
- Associate Director at Eli Lilly and Company
- Location
- Hillsborough, NC, US
- LinkedIn followers
- 500 followers
About Tyrone Ortiz
Industrial Engineer with over twenty years of experience in the Pharmaceutical, Biopharma and Medical Device industries, including direct managerial/supervisory experience; working in Quality Assurance, Manufacturing and Packaging (Operations), and Supply Chain roles. Broad experience in cGMP environment and in high and low volume production. A committed team player and creative analytical problem solver with demonstrated success in managing new processes to improve quality, efficiency and productivity. Hands-on experience Lean Six Sigma (Kanban, Kaizen, 5S, Just-in-time) and Strategic Planning (Hoshin Kanri).Specialties: Certified Lean Six Sigma Black Belt Certified Quality Improvement Associate Deviations or Non-Conformance, CAPA and Change Control Batch Record / DHR and SOP development. Statistics softwares (Minitab, Statgraphics and QI Macros) ERP systems: JD Edwards, SAP (P34) and SAP-APO (P38) Capacity Analysis and / Planning and Scheduling Root Cause Analysis (RCA) and Statistical Process Control (SPC) Knowledge using TrackWise, Master Control and Documentum programs. Employee Management, Engagement and Communication (Tier Management System). Production performance (financial and operational) Continuous Improvement - Lean Manufacturing ISO and cGMP Team Development/Building Strategic Planning (Hoshin Kanri)
Experience
Associate Director
Jun 2023 — Present · NC, US
Education
Polytechnic University of Puerto Rico
MEM, Manufacturing Management
2005 — 2007
Polytechnic University of Puerto Rico
BS, Industrial Engineer
1996 — 2002
Skills
- Fda Gmp
- Sop Development
- Kaizen
- 5 Why
- Statistical Process Control (Spc)
- Standard Operating Procedure (Sop)
- Spc
- 5s
- Deviations
- Engineering
- Cgmp Manufacturing
- Change Control
- Manufacturing Operations
- Inspection
- Sop
- Fda
- Value Stream Mapping
- 21 Cfr
- 21 Cfr Part 11
- Quality Assurance
- Root Cause Analysis
- Industrial Engineering
- Design Control
- U.s. Title 21 Cfr Part 11 Regulation
- Medical Devices
- Capa
- Manufacturing
- Iso 13485
- Kanban
- Dmaic
- Gmp
- Lean Manufacturing
- Cgmp Practices
- Pharmaceutics
- Trackwise
- Process Excellence
- Validation
- Six Sigma
- Gxp
Find verified contacts for anyone on LinkedIn
Unifers gives sales teams verified emails and direct dials, enriched profiles, and outreach that lands in the inbox.
Free plan included · No credit card required
This profile is compiled from publicly available professional sources. Unifers is not affiliated with or endorsed by LinkedIn. Request removal of this profile.