Overview
In 2023, our operation needed to deliver significant cost savings. I identified a high‑impact opportunity to increase the speed of a frequently run medical‑grade polyester style without compromising quality, chemistry %, or regulatory compliance.
Problem
A high‑volume, high‑cost product was running significantly slower than another style with nearly identical characteristics. Because the product was chemistry‑sensitive and medical‑grade, changes were historically avoided.
Goal: Increase speed safely and deliver $100K+ in savings while maintaining all quality and regulatory requirements.
Aproach
Learned from a fabric‑formation class that similar fabrics can run with similar specs
Noticed two polyester styles with nearly identical GSM, width, and shrinkage behavior
Ran a small, no‑risk test on scrap material to validate feasibility
Chose this style because it was high‑volume, high‑cost, and in high market demand
I designed a two‑phase experimental plan:
Phase 1 — Exploratory Trials (5 recipes)
Created five recipes with different combinations of speed, temperature, and pad pressure
Operators placed physical flags on the fabric to mark each recipe change
Tested each section for:
Shade
Weight
Width
Chemistry % (silver content)
This phase confirmed the product remained stable even at higher speeds.
Standardized temperature and pad pressure based on Phase 1 results
Selected an average temperature using heat‑history analysis (internal fabric temperature during drying)
Ran a second set of trials where speed was the only variable
Conducted full lab testing to confirm product integrity
Scheduled initial trials during a low‑production weekend to minimize operational risk
Coordinated with supply chain to ensure no impact on weekly production goals
Gained supervisor buy‑in by presenting projected savings vs. controlled risk
Engaged operators directly — they placed flags, monitored checkpoints, and ran the machine with me
Built trust through transparency and previous successful projects
Validated that increased speed produced no negative impact on quality metrics
Created a one‑page operator guide with key checkpoints for smooth running
Updated SOPs and completed a full ISO 13485‑compliant change request
Established a control chart and assigned ongoing monitoring to the quality facilitator
Results
Speed increased from 18 → 27 ypm (50% improvement)
Daily output doubled (12 → 24 sets), effectively adding a full day of production capacity
$170K annual savings from:
Reduced energy use
Fewer overtime hours
Increased throughput
Better workforce allocation
No impact on scrap, rework, or first‑pass yield
Recognized by leadership and the medical group
Invited to present the project multiple times
Contributed to promotion readiness
Key Skills Demonstrated
Experimental trial design
Heat‑history and moisture‑profile analysis
Statistical validation of quality metrics
Cross‑functional collaboration
ISO 13485‑compliant documentation and change control
Operator engagement and change management
Throughput improvement and cost‑savings analysis