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Paul Carl Wood
Professional experience
Thermo Fisher Scientific Rockwood, TN
Industrial Project Engineer
Developed SOP documentation and line balancing for newly
implemented processes.
Successfully managed multiple production and product launch
projects to fruition, several over $1 million in annual
revenue.
Implemented Project Management fundamentals (PMBOK) to guide
project analysis and management: (Charters, Scope, WBS, Risk
Analysis, etc.)
Created and maintained project team budgets and tracked
expenses, within budget, successfully.
Trained production groups on process improvement methodology,
and shepherded process improvement teams to implement
solutions.
Thermo Fisher 2013 CAS award nominee
NemcoMed (through Allegiant International) Ft. Wayne, IN
2009
Validation Engineer
Cleaning/Passivation validation protocol development and
successful process runs within a month.
Updated controls for better process capability, understanding
and monitoring to ASTM A 380, & A 967.
Cooper Standard Automotive Auburn, IN
2007-2009
Lean Industrial Engineer
Analyzed production methods and established production goals
for shop floor, leading to increased throughput and level
production loads.
Establish process and labor cost levels for plant.
Produced process maps to outline improved production flow.
Utilized Kaizens, work balancing, level loading, and OEE
analysis to implement production cost savings for major
production lines (over $1 million procured)
Implemented 5-S line up for production cells after Kaizen
completion, and created better quality and functioning of the
production floor.
Conducted new product launches, on time, and under budget.
Produced work cell production boards for visual management by
supervisors.
Developed standard and visual SOPs for new and existing
product lines.
Evaluate equipment and work spaces for ergonomic efficiencies.
DePuy, a Johnson & Johnson Co. Warsaw, IN
1991-2007
Manufacturing Engineer
Designed, executed, and documented cleaning equipment,
computer PLC software, distribution equipment and utility
validations to ensure safety and cleanliness of medical
implant product. Performed IQs, OQs and PQs complying with
FDA and J&J validation specifications.
Engineered finishing equipment processes to 21 CFR 820 & ISO
13485.
Specified, recommended, supervised installation of new
finishing process equipment that increased production by 20%.
Supported Calibration methods and procedures initiated within
validation protocols.
Familiar with R.O. water systems, Gamma/EtO sterilization and
their related validation techniques
Conducted DOEs using Minitab software for validation prep.
Maintained quality controls on production processes through
SPC and problem analysis.
Completed FMEAs for new product launches and existing product
re-evaluations
Designed fixturing for ease of use through changeover and
throughput improvements
Identified and lead $100,000 per year process improvement
savings
Implemented Lean Manufacturing concepts with value stream map
analysis. After improvements, process flow was improved by up
to 98%.
Programmed CNC Swiss lathes, and machining centers for Trauma
production cells.
Enhanced AutoCAD layouts to maximize cellular flow for
improved production
Supervised 35 production personnel for management on leave (up
to 6 months)
Received J&J President's Award for Distribution Reorganization
Team
DePuy, Inc. Warsaw, IN 1988-1991
Time Study Engineer
Regulated process time studies
Produced departmental efficiency studies to better control
production flow.
Developed quarterly cost reduction analysis
Education
Purdue University West Lafayette, IN
Bachelor of Science Degree in Supervision
Emphasis in Industrial Engineering
References
References Available Upon Request