Beruflich Dokumente
Kultur Dokumente
SCOTTON
12574 Traverse Place
(317) 845-9571
Fishers, Indiana 46038
ssd1326@westpost.net
PROFILE
Hands-on senior level manufacturing professional with a solid background in prog
ram management, process engineering, operations, quality, and regulatory complia
nce in electronics assembly and medical device industries. Over ten years exper
ience with SMT and Thru Hole process development and process control at the engi
neering and management levels. Proven problem solving skills and team building
ability. Solid track record of successful experience in optimizing productivity
and improving profitability.
Core Competencies Include:
Productivity & Cost Reduction Improvements * Strategic Planning * Change Agent
Forecasting * Safety Performance * Organizational Development * Asset Management
Project Management * Six Sigma * 5S * Resource Allocation * Project Quoting
Organizational Leadership & Development
PROFESSIONAL DEVELOPMENT
Symbios Medical
Indianapolis, Indiana
Director of Operations 2006-Present
Coordinated and managed the transition into a new facility. This included plann
ing and executing critical moves of existing manufacturing and production areas
and office spaces. Retained original production staffing to accomplish startup
operations while meeting customer requirements.
Key Accomplishments Include:
* Specified, purchased and constructed a class 1000 cleanroom environment manufa
cturing space.
* Constructed none cleanroom manufacturing spaces including warehouse and office
spaces and loading docks.
* Assumed responsibility for all purchasing of all critical materials for buildi
ng product. Defined and built a non traditional excel based MRP material tracki
ng and trigger mechanism for parts replenishment as the initial material control
system while continuing to research the best solution for our needs.
* Successfully qualified the manufacturing spaces and processes which allowed pr
oduction samples to be shipped to customers for their qualification and ultimate
FDA approval.
* Instituted a formal production schedule to drive the production ramp, matching
the sales forecast to meet projected requirements including sterilizing specifi
cations.
*
Catheter Research Inc.
Indianapolis, Indiana
Director of Engineering / Operations
2005-200
6
Managed all production activities for medical life sciences products with staff
of 83 employees. Accountable for process improvement activities, quality, and r
egulatory requirements. Managed all product development activities including pr
oviding product quotes and initiation of new contracts. Supported all metrology
activities.
Key Accomplishments Include:
* Increased production by 25% by implementing a defined schedule based on the us
e of similar materials, minimizing the changeover of parts and equipment.
* Reduced scrap by 60% for molded parts supplied for a catheter device.
* Worked closely with major customer to develop a process and qualify process su
pport for the launch of a new device. Generated $80K in additional revenue.
* Coordinated and implemented a plant move to a different location over a holida
y weekend. Critical processes were setup and re-qualified to start on the first
workday.
* Transferred a major device product line to the customer's Mexico facility. Al
l tooling, documentation, history files, etc. were moved without incident.
EDUCATION
Bachelor of Science in Electrical Engineering Technology
Old Dominion University, Norfolk, Virginia
Associate of Science in Electronics Technology
Delaware Technical and Community College, Newark DE
Two Years of General Business Management course study at The University of Delaw
are